[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"depression-disorder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:depression-disorder":680},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,22,0,[8,55,79,108,135,175,196,230,259,298,324,343,370,408,441,489,517,555,579,603,635,661],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100577061",false,"NCT06793397","A Study of a Deuterated Psilocin Analog (CYB003) in Humans With Major Depressive Disorder","An Efficacy and Safety, Phase III, Multi-center, Double-Blind, Randomized Controlled Study Comparing 2 Active Doses of CYB003 and Placebo in Eligible Participants With Major Depressive Disorder","EMBRACE","Inclusion Criteria:\n\nParticipants must meet all the following criteria to be included in the trial:\n\n* Age18 to 85 years.\n* Participant has a diagnosis of MDD (single or recurrent episode as defined by DSM-5 TR \\[if single episode, duration of ≥4 weeks and ≤24 months\\] and established as per evaluation by the Investigator. The first MDD episode must have occurred prior to age 60.\n* Moderate to severe depression at Screening and Baseline, independently confirmed.\n* Participants have been on a stable dose of antidepressant medication (label specified) at an adequate dose in the last 4 weeks prior to Screening and has had an inadequate response (less than 50% improvement), as judged by the Investigator.\n* Participant has a body mass index (BMI) of 40 kg\u002Fm2 or less (BMI ≤40 kg\u002Fm2), inclusive, at Screening.\n* Participant is able to refrain from nicotine use during the dosing session (up to 8 hours).\n* Participants capable of producing sperm must use a condom plus spermicide during the trial and for 12 weeks after their final dose of trial medication, if their partner is a person of childbearing potential.\n* Participants of childbearing potential who have a partner capable of producing sperm must agree to use a highly effective method of contraception in combination with the use of a condom plus spermicide during the trial and for 12 weeks after their final dose of trial medication. Such participants must have a negative pregnancy test at Screening and Day 1 prior to dosing.\n* Participants of non-childbearing potential who are or were capable of producing eggs (ova) must have been postmenopausal or permanently sterile following hysterectomy, bilateral salpingectomy, or bilateral oophorectomy.\n* Participants have provided written informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form.\n\nExclusion Criteria\n\nParticipants with any of the following characteristics\u002Fconditions will be excluded from trial participation:\n\n* Current or previously diagnosed schizophrenia spectrum or other psychotic disorders, including schizophrenia, schizoaffective disorder, schizotypal disorder, schizophreniform disorder, brief psychotic disorder, current or previous history of bipolar disorder, or current borderline personality disorder.\n* Participants with a medical diagnosis of attention deficit hyperactivity disorder (ADHD) will be excluded if currently taking medication for ADHD.\n* Family history of schizophrenia, schizoaffective disorder, or bipolar disorder type 1 (first-degree relatives).\n* Significant suicide risk within the past 6 months, during the Screening Period, or at Baseline; or (b) suicidal behaviors within 12 months of Screening; or (c) clinical assessment of significant suicidal risk during clinical interview; or (d) non-suicidal self-injury within 12 months of Screening.\n* Current or previous diagnosis of treatment-resistant MDD, defined as failure to respond to 2 or more antidepressant treatments of 2 different classes given at an adequate dose (label specified) for an adequate duration as judged by the Investigator and clinical interview.\n* Has had electroconvulsive treatment, transcranial magnetic stimulation, deep brain stimulation, or vagal nerve stimulation for any episode of MDD in the last 6 months.\n* Currently receiving a monoamine oxidase inhibitor, tricyclic antidepressants, mirtazapine, trazodone, moclobemide, buspirone, or an antipsychotic or mood stabilizer. Note: if receiving these medications are for another indication, they must be discontinued ≥ 14 days or 5 half-lives, whichever is longer, prior to Day 1.\n* Participant report of (or if available in medical record) exposure to psilocin, or 5-HT2a receptor agonists, or any other psychedelics, such as ayahuasca, mescaline, lysergic acid diethylamide, peyote, or 3,4-methylenedioxymethamphetamine, more than 10 times over the participant's lifetime or any psychedelic use within 12 months prior to Screening.\n* Participant report of (or if available in medical record) treatment with ketamine or S-ketamine use within 6 months prior to Screening.\n* Clinically relevant history of abnormal physical health interfering with the trial (including but not limited to, neurological, cardiovascular, respiratory, gastrointestinal \\[including dyspepsia or gastroesophageal reflux disease\\], hepatic, or renal disorder).\n* Has hypothyroidism or hyperthyroidism, unless controlled on appropriate medication.\n* Current diagnosis of uncontrolled hypertension or an arrhythmia, or clinically relevant abnormal results for heart rate.\n* Participants have a presence or relevant history of organic brain disorders.\n* Participant is taking or has taken OTC doses of 5-HTP or St John's Wort within prior to trial medication administration.\n* Donation of blood or plasma within 4 weeks prior to first dosing and until 4 weeks after final dosing.\n* Participants capable of producing sperm who will not abstain from sperm donation between first dosing and 12 weeks after final dosing.\n* Participants of childbearing potential who are pregnant, breastfeeding, planning to conceive or unwilling to abstain from egg (ova) donation between first dosing and 12 weeks after final dosing.\n* History of serotonin syndrome.\n* Unwilling to consent to audio and video recording of psychological support and dosing sessions.","ALL","18 Years","85 Years",{"count":20,"type":21},330,"ESTIMATED","INTERVENTIONAL",[24],"PHASE3","The purpose of this study is to determine the efficacy, safety and tolerability of CYB003 compared to matching placebo as adjunctive treatment in patients with MDD.\n\nFor more information about the EMBRACE study, including participating study locations, and to register your interest in learning more about participation, please visit the study website: https:\u002F\u002Fembrace-mdd-trial.com\u002F",[27,28,29,30,31,32],"Major Depressive Disorder (MDD)","Depression in Adults","Depression - Major Depressive Disorder","Depression Disorders","Depression Disorder","Depression",[34,35,32,36,37,38,39,40,41],"MDD","Psychedelic","Major Depressive Disorder","CYB003","CYB003-001","CYB003-002","Psilocybin","psilocin-7438","RECRUITING","2026-06-29",{"date":45,"type":46},"2026-06-30","ACTUAL",{"date":48,"type":46},"2025-12-10",{"date":50,"type":21},"2027-05-08",{"name":52,"class":53},"Cybin IRL Limited","INDUSTRY",68,{"id":56,"slug":4,"hasResults":10,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":60,"sex":16,"minAge":17,"maxAge":61,"enrollmentInfo":62,"targetDuration":4,"studyType":22,"phases":64,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":4},"100645223","NCT07678242","The Lucida Project","Inclusion Criteria - all participants:\n\n* Age 18 to 84\n* Elevated depressive symptoms: PHQ-9 ≥ 10; Healthy controls: PHQ-9 \\\u003C5\n\nInclusion Criteria - randomized participants:\n\n* Proficient in English to try to unsure understanding of study requirement, consent forms and questionnaires that can often us medical terms not routinely used in general conversation.\n* Able to provide informed consent\n* Have access to a smartphone that can download apps from Google Play or the Apple App Store\n* Ability to receive text messages\n* Indicate interest in participation after being informed of restrictions to payment\n\nExclusion Criteria:\n\n* Regular daily meditation practice for past 6 months or regular weekly meditation practice for past 12 months\n* Attended a meditation retreat or a yoga\u002Fbody practice retreat with a significant meditation component\n* Previous use of Healthy Minds Program app\n* Current suicidal intent and\u002For high self-injury risk (determined by PHQ-9 item 9 and BDI item 9)\n* Self-reported history of psychosis\n* Self-reported history of mania\n* Living or traveling outside the US during the whole study participation period (trips outside US after the interview phase is not an exclusion)\n* Hearing impairments\n* Prior participation\n* Self report pregnancy",true,"84 Years",{"count":63,"type":21},1500,[65],"NA","The purpose of this clinical trial is to learn about the impact of the Healthy Minds Program (HMP) on measurements of well-being. The main question it aims to answer is:\n\n* Does use of HMP reduce symptoms of depression?\n\nParticipants will complete a 4-week well-being program.",[31],"NOT_YET_RECRUITING","2026-06-24",{"date":71,"type":46},"2026-07-01",{"date":73,"type":21},"2026-08",{"date":75,"type":21},"2028-08",{"name":77,"class":78},"University of Wisconsin, Madison","OTHER",{"id":80,"slug":4,"hasResults":10,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":85,"targetDuration":87,"studyType":88,"phases":4,"briefSummary":89,"conditions":90,"keywords":92,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":107},"100618546","NCT07333027","Lonely in Depression","Effects of Loneliness in the Treatment of Depression","Inclusion Criteria:\n\n* primary diagnosis of depression according to ICD-10 (F32 or F33), as diagnosed by a physician or clinical psychologist in conjunction with the M.I.N.I. Mini-International Neuropsychiatric Interview diagnostic tools\n* inpatient elective or emergency admission to one of the two psychiatric clinics; - age over 18 years\n* sufficient understanding of spoken and written German\n* informed voluntary consent\n\nExclusion Criteria:\n\n* a current lack of capacity to provide consent (e.g., pronounced psychotic symptoms, stuporous depressive syndrome, and thought constriction to suicidality)\n* previous participation in the study\n* pregnancy or breastfeeding\n* inpatient stay of less than 7 days, even if the patients initially met the inclusion criteria.",{"count":86,"type":21},200,"3 Months","OBSERVATIONAL","The goal of this prospective study is to better understand the link between loneliness and depression in the inpatient psychiatric treatment of depression. It aims to answer:\n\nDo lonely and not lonely persons benefit the same way from inpatient depression treatment? Is loneliness a clinical relevant factor in inpatient treatment of depression? What are the underlying biopsychosocial mechanisms?\n\nParticipants will be asked to do some\n\n* self-report questionnaires\n* clinical interview\n* biosampling (blood, saliva, stool) at three main measurement timepoints (1. begin of inpatient treatment, 2. day of discharge, 3. three months after discharge).",[31,91],"Loneliness",[93,94,95,96,97],"loneliness","depression","prospective","biosampling","clinical","2026-06-11",{"date":100,"type":46},"2026-06-15",{"date":102,"type":46},"2026-02-05",{"date":104,"type":21},"2027-09",{"name":106,"class":78},"Friedrich-Alexander-Universität Erlangen-Nürnberg",2,{"id":109,"slug":4,"hasResults":10,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":22,"phases":118,"briefSummary":120,"conditions":121,"keywords":123,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":107},"100643335","NCT07639359","Subanesthetic Ketamine Infusions for Depressive Symptoms in Intensive Care Unit Patients","Ketamine In Depression - Intensive Care Unit Trial (KID-ICU): A Phase II Randomized, Double-Blind, Placebo-Controlled Multicenter Study of Ketamine Infusion for Depressive Symptoms in Intensive Care Unit Patients","KID-ICU","\\*\\*Inclusion Criteria:\\*\\*\n\n* Age 18 to 99 years.\n* Male or female.\n* Admission to an intensive care unit for 6 or more days at the time of screening.\n* Moderate to severe depressive symptoms, defined as a Patient Health Questionnaire-9 score of 10 or greater at screening.\n* Ability to provide informed consent.\n\n\\*\\*Exclusion Criteria:\\*\\*\n\n* History of psychosis or hallucinations, as assessed by review of the electronic medical record and patient interview during screening.\n* History of prolonged QT interval.\n* History of dementia.\n* History of major depressive disorder before the current intensive care unit admission.\n* History of psychiatric diagnosis, including dissociative disorder, primary psychotic disorder, mania with psychosis, pervasive developmental disorder, cognitive disorder, or anorexia nervosa.\n* Known allergy to ketamine or diphenhydramine.\n* History of increased intracranial pressure, hypertensive hydrocephalus, or increased intraocular pressure.\n* Hemodynamic instability at the time of screening, defined as peripheral oxygen saturation \\\u003C95%, systolic blood pressure \\\u003C90 mmHg or \\>180 mmHg, heart rate \\\u003C50 or \\>120 beats\u002Fmin, or respiratory rate \\\u003C10 or \\>30 breaths\u002Fmin.\n* Patient refusal to participate or to provide informed consent.\n* Pregnancy, postpartum period within 2 months, or breastfeeding.\n* Presence of intracranial mass or vascular lesion.\n* Altered mental status precluding informed consent.\n* Body weight \\>115 kg or \\\u003C45 kg.\n* Active psychosis.\n* Current treatment with medications that may interfere with the N-methyl-D-aspartate receptor system, including lamotrigine, acamprosate, memantine, riluzole, or lithium.\n* Current treatment with aminophylline or theophylline.\n* Active substance withdrawal or use of hallucinogens, including cannabis, in the past month, as determined by clinical interview and urine drug screening.","99 Years",{"count":117,"type":21},50,[119],"PHASE2","\\*\\*Brief Summary\\*\\*\n\nDepressive symptoms are frequent among patients admitted to the intensive care unit (ICU) and may be associated with worse clinical outcomes, reduced participation in care, lower treatment adherence, and increased mortality. Conventional antidepressants, including selective serotonin reuptake inhibitors (SSRIs), have limited utility in this setting because of their delayed onset of action, incomplete efficacy, and potential drug interactions in medically complex patients.\n\nKetamine, an N-methyl-D-aspartate (NMDA) receptor antagonist, has emerged as a rapid-acting antidepressant when administered at subanesthetic doses. Preliminary evidence suggests that intravenous ketamine may improve mood-related symptoms within a short time frame and may have an acceptable safety profile in selected critically ill patients.\n\nThe KID-ICU trial (Ketamine In Depression - Intensive Care Unit) is a Phase II randomized, double-blind, placebo-controlled multicenter trial designed to evaluate the efficacy and safety of subanesthetic intravenous ketamine infusions for moderate-to-severe depressive symptoms in adult ICU patients. Eligible participants are adults who have been admitted to the ICU for 6 or more days and have moderate-to-severe depressive symptoms, defined as a Patient Health Questionnaire-9 (PHQ-9) score of 10 or greater.\n\nParticipants will be randomized in a 1:1 ratio to receive either intravenous ketamine at 0.5 mg\u002Fkg, with a maximum dose of 60 mg per day, administered over 40 to 60 minutes on 2 consecutive days, or placebo with normal saline in an identical presentation. The primary efficacy outcome is the change in PHQ-9 score from baseline to Day 30 after the last infusion. Safety outcomes include prespecified hemodynamic, neuropsychiatric, and treatment-discontinuation events during and after infusion. Secondary outcomes include anxiety and depression symptoms assessed with the Hospital Anxiety and Depression Scale (HADS), clinical severity and improvement assessed with Clinical Global Impression scales, intensive care unit and hospital length of stay, and mortality.\n\nA total of 50 participants will be enrolled across intensive care unit sites at Hospital Italiano de Buenos Aires. Psychiatric and clinical follow-up will be provided to all participants regardless of treatment assignment.",[31,122],"Ketamine",[124,125,94],"ketamine","intensive care","2026-06-05",{"date":128,"type":46},"2026-06-10",{"date":130,"type":46},"2026-05-14",{"date":132,"type":21},"2027-10-01",{"name":134,"class":78},"Hospital Italiano de Buenos Aires",{"id":136,"slug":4,"hasResults":10,"nctId":137,"briefTitle":138,"officialTitle":139,"acronym":140,"eligibilityCriteria":141,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":142,"targetDuration":4,"studyType":22,"phases":144,"briefSummary":145,"conditions":146,"keywords":150,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":174},"100643231","NCT07637097","VOCALE LBD: Online Peer Support for Caregivers of People With Lewy Body Dementia","Reducing Depression in Family Caregivers of Persons Living With Lewy Body Dementia Through Tailored Asynchronous Online Intervention.","VOCALE LBD","Inclusion Criteria:\n\n* Current family member or informal (unpaid) caregiver of a person with a confirmed diagnosis of Lewy Body Dementia (LBD) or LBD mixed pathology\n* Experiences depressive symptoms as defined by a score of 5 or higher on the Patient Health Questionnaire-9 (PHQ-9)\n* Able to read, write, and speak English\n* Has access to a device (computer, tablet, or smartphone) that can connect to the internet and be used for videoconferencing or phone calls, OR is interested in using a loaner device\n\nExclusion Criteria:\n\n* Active suicidal ideation as indicated by endorsement of PHQ-9 Item 9 (thoughts that you would be better off dead, or thoughts of hurting yourself)\n* Paid or professional caregiver (must be unpaid family\u002Finformal caregiver)\n* Unable to read, write, or speak English",{"count":143,"type":21},220,[65],"This study tests whether a tailored, fully asynchronous online group intervention (VOCALE LBD) reduces depression in family caregivers of people with Lewy Body Dementia (LBD), compared to standard educational materials. LBD is the second most common form of degenerative dementia and causes distinct challenges, including visual hallucinations, REM sleep disorder, and severe motor symptoms, that are not addressed by generic caregiver interventions. Depression rates in LBD caregivers reach 40-50%, double the rate seen in Alzheimer's disease caregivers, yet no rigorous digital interventions exist specifically for this population. VOCALE LBD is a text-based, low-bandwidth platform (Discourse) that brings groups of 10-15 caregivers together in an 8-week moderated online community. Weekly topics address LBD-specific challenges (sleep problems, hallucinations, self-care) and problem-solving skills using the ADAPT method. A pilot study (n=54) showed strong effects on depressive symptoms (Cohen's d=0.54 at 1-month follow-up), near-perfect engagement, and high participant satisfaction. This RCT (N=220) will test efficacy, examine mechanisms of action (self-efficacy and problem-solving), and explore analytics approaches for pragmatic monitoring, laying groundwork for future implementation in clinics and community organizations.",[147,31,148,149],"Lewy Bodies Disease","Caregiver Burden","Caregivers",[151,152,153,154,155,156,157,158,159,160,161,162,163,164],"Lewy body disease","LBD","Family caregivers","Caregiver Depression","Online Intervention","Asynchronous","Digital Health","Peer Support","Problem-solving therapy","VOCALE","Telehealth","Dementia caregiver","ADAPT method","Discourse Platform","2026-06-03",{"date":167,"type":46},"2026-06-09",{"date":169,"type":21},"2026-12-01",{"date":171,"type":21},"2030-11-30",{"name":173,"class":78},"University of Washington",1,{"id":176,"slug":4,"hasResults":10,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":22,"phases":183,"briefSummary":184,"conditions":185,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":187,"lastUpdatePostDateStruct":188,"startDateStruct":190,"completionDateStruct":192,"leadSponsor":194,"locationsCount":4},"100637513","NCT07618312","Improving Patient Engagement in Mental Health Services","Improving Patient Engagement in Mental Health Services: Adaptation and Implementation of a Behavioral Activation Intervention","Inclusion Criteria:\n\n* Age 18 years or older\n* Spanish-speaking adult who prefers to receive services in Spanish\n\nResident of a rural or frontier community in Montana or New Mexico\n\nPositive screen for depressive symptoms at or above study eligibility threshold on Spanish-language screening measure\n\nAble and willing to participate in telehealth sessions\n\nAble to provide informed consent\n\nExclusion Criteria:\n\n* Active suicidal intent requiring immediate emergency intervention\n\nCurrent psychosis or mania\n\nSevere cognitive impairment that would prevent participation\n\nCurrently receiving intensive psychiatric treatment that would conflict with the intervention\n\nUnable to participate in telehealth sessions\n\nUnable to provide informed consent",{"count":182,"type":21},100,[65],"Hybrid Type II Implementation Trial",[31,186],"Engagement","2026-05-26",{"date":189,"type":46},"2026-06-01",{"date":191,"type":21},"2027-03",{"date":193,"type":21},"2030-02",{"name":195,"class":78},"Montana State University",{"id":197,"slug":4,"hasResults":10,"nctId":198,"briefTitle":199,"officialTitle":200,"acronym":4,"eligibilityCriteria":201,"healthyVolunteers":10,"sex":202,"minAge":17,"maxAge":4,"enrollmentInfo":203,"targetDuration":4,"studyType":22,"phases":205,"briefSummary":206,"conditions":207,"keywords":216,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":222,"startDateStruct":224,"completionDateStruct":226,"leadSponsor":228,"locationsCount":174},"100629899","NCT07480668","Aromatherapy for Mental Health Promotion in IVF Patients","Aromatherapy for Mental Health Promotion in In Vitro Fertilization Patients: a Randomized Clinical Trial","Inclusion Criteria:\n\n* Female gender, age over 18 years.\n* Diagnosis of infertility with indication for In Vitro Fertilization (IVF).\n* Patients on the waiting list at HC-UFMG.\n* Agreement not to practice other mind-body or herbal complementary therapies during the study.\n* DASS-21 screening score compatible with at least mild anxiety, stress, and\u002For depression.\n* No aversion to inhaling essential oil or synthetic lavender essence.\n\nExclusion Criteria:\n\n* Severe neurological, psychiatric, or clinical disorders (e.g., schizophrenia, severe depression) that prevent participation.\n* Use of medications that could confound the primary outcome (e.g., sleep medications, anxiolytics, antidepressants, neuroleptics) in the 30 days prior to or during the study.\n* Known allergy to lavender products.\n* Pregnancy during the study period.\n* Use of essential oils in the last 90 days.","FEMALE",{"count":204,"type":21},120,[65],"The experience of infertility can cause significant emotional instability, especially for patients awaiting In Vitro Fertilization (IVF) treatment, generating anxiety, stress, and depressive symptoms. This study is a randomized clinical trial assessing the effectiveness of aromatherapy in improving mental health and quality of life in women undergoing infertility treatment. 120 participants will be randomized into three groups (Intervention, Placebo, and Control). The intervention involves the inhalation of true lavender essential oil (Lavandula angustifolia) for four weeks.",[208,209,31,210,211,212,213,214,215],"Anxiety","Stress","Quality of Life","Aromatherapy","IVF","Complementary Therapies","Spirituality","Infertility",[217,211,218,219,214,212,208,209,32,220],"Infertility, Female","Lavender Oil","Complementary Therapy","In Vitro Fertilization","2026-04-24",{"date":223,"type":46},"2026-04-29",{"date":225,"type":46},"2026-03-01",{"date":227,"type":21},"2026-12",{"name":229,"class":78},"Federal University of Minas Gerais",{"id":231,"slug":4,"hasResults":10,"nctId":232,"briefTitle":233,"officialTitle":233,"acronym":4,"eligibilityCriteria":234,"healthyVolunteers":60,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":235,"targetDuration":4,"studyType":22,"phases":237,"briefSummary":238,"conditions":239,"keywords":242,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":250,"lastUpdatePostDateStruct":251,"startDateStruct":253,"completionDateStruct":255,"leadSponsor":257,"locationsCount":107},"100634341","NCT07538427","Enhancing Health in Rural Populations: Music as Therapy","Inclusion Criteria:\n\n* residency at one of the two elder care facilities\n* ability to communicate in English.\n\nExclusion Criteria:\n\n* not a resident at one of the two elder care facilities\n* inability to communicate in English.",{"count":236,"type":21},60,[65],"The goal of this clinical trial is to learn whether a music-based intervention can improve mental and physical health and strengthen coping skills among adults living in residential care settings in northern Arizona. The main questions it aims to answer are: Does participation in the music-based intervention reduce stress, anxiety, depression, and pain?, and Does participation increase the use of music as a coping strategy and improve overall well-being?\n\nResearchers will compare participants' pre-intervention and post-intervention responses to determine whether the music classes are associated with improvements in health and coping outcomes. Participants will: Attend a 6-week music class held once per week for one hour; participate in active music activities such as drumming and rhythm exercises; complete a brief survey before and after the intervention. Some participants are also invited to complete a short interview about their experiences.",[209,240,241,31],"Generalized Anxiety","Chronic Pain",[243,244,245,246,247,248,249],"Music-based intervention","Active music therapy","Drumming","Non-pharmacological intervention","behavioral therapy","Aging populations","Community-based intervention","2026-04-15",{"date":252,"type":46},"2026-04-20",{"date":254,"type":46},"2026-03-12",{"date":256,"type":21},"2027-05-30",{"name":258,"class":78},"Northern Arizona University",{"id":260,"slug":4,"hasResults":10,"nctId":261,"briefTitle":262,"officialTitle":263,"acronym":4,"eligibilityCriteria":264,"healthyVolunteers":60,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":265,"targetDuration":267,"studyType":88,"phases":4,"briefSummary":268,"conditions":269,"keywords":281,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":250,"lastUpdatePostDateStruct":292,"startDateStruct":293,"completionDateStruct":294,"leadSponsor":296,"locationsCount":4},"100630769","NCT07491978","Development and Multicenter Validation of an AI-Based Remote Photoplethysmography (rPPG) Facial Scan for Multimodal Health Assessment","Development and Multicenter Validation of an AI-Based Remote Photoplethysmography (rPPG) Facial Scan for Multimodal Health Assessment: Agreement With Clinical, Laboratory, and Psychological Parameters in an Urban Population","Inclusion Criteria:\n\n1. Adults aged ≥18 years.\n2. Able and willing to provide written informed consent.\n3. Able to comply with study procedures, including face scan, physical examination, blood sampling, and questionnaire completion.\n4. Clinically stable at the time of assessment.\n\nExclusion Criteria:\n\n1. Facial conditions affecting the region of interest (ROI), such as injury, deformity, or impaired circulation, that may interfere with rPPG signal acquisition.\n2. Presence of facial tattoos or coverings that obstruct optical signal detection.\n3. Inability to remain still or comply with measurement procedures during data acquisition.\n4. Severe medical conditions that preclude safe participation, as judged by the investigator.\n5. Incomplete data or withdrawal of consent during the study.\n\n   \\-",{"count":266,"type":21},1000,"1 Day","The goal of this observational study is to learn if a non-contact facial scan using artificial intelligence (AI) can be used to check health status in adults living in urban areas such as Jakarta. The facial scan uses a method called remote photoplethysmography (rPPG), which measures small changes in blood flow from the face using a camera.\n\nThe main questions this study aims to answer are:\n\n1. How close are the results from the facial scan to standard medical measurements, such as heart rate, breathing rate, blood pressure, and oxygen levels?\n2. Can the facial scan estimate other health indicators, such as blood sugar, lipid profile, HbA1c, and hemoglobin levels?\n3. Is there a relationship between the facial scan results and mental health, such as stress, anxiety, and depression?\n\nParticipants will take part in several simple and mostly non-invasive procedures:\n\n1. Answer questionnaires about their mental health and daily habits\n2. Have basic health checks, such as blood pressure, heart rate, and body measurements\n3. Provide a blood sample for laboratory testing\n4. Complete a facial scan using a camera for about 1 to 3 minutes\n\nResearchers will compare the results from the facial scan with standard clinical and laboratory tests to see how well the technology works.\n\nThis study may help develop a simple and accessible screening tool that can be used for early detection of health risks. It may also support the use of digital health and telemedicine in community and clinical settings.",[270,271,272,273,274,31,208,275,276,277,278,279,280],"Metabolic Syndrome","Hypertension","Diabetes (DM)","Tachycardia","ASCVD","Stress (Psychology)","Obesity & Overweight","Cardiometabolic Risk Factors","Cardiometabolic Health Indicators","Sleep","Wellness",[282,283,284,285,286,287,288,289,290,291],"remote photoplethysmography","rPPG","artificial intelligence","digital biomarker","telemedicine","vital signs","cardiometabolic risk","machine learning","facial scan","screening tool",{"date":252,"type":46},{"date":221,"type":21},{"date":295,"type":21},"2027-03-30",{"name":297,"class":78},"Tarumanagara University",{"id":299,"slug":4,"hasResults":10,"nctId":300,"briefTitle":301,"officialTitle":302,"acronym":4,"eligibilityCriteria":303,"healthyVolunteers":60,"sex":16,"minAge":304,"maxAge":4,"enrollmentInfo":305,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":307,"conditions":308,"keywords":310,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":316,"lastUpdatePostDateStruct":317,"startDateStruct":319,"completionDateStruct":321,"leadSponsor":322,"locationsCount":174},"100633684","NCT07529886","Symptoms of Anxiety and\u002For Depression and SDM in Older Patients With CLTI","Symptoms of Anxiety and\u002For Depression and the Shared Decision Making (SDM) Process in Older Patients With Critical Limb Threatening Ischaemia (CLTI)","Inclusion Criteria:\n\n* Patients\n\n  * Aged ≥65 years old\n  * CLTI\n  * Active symptoms of anxiety or depression (clinician concern)\n* Carers\n\n  o In a non-paid caring role for a patient aged ≥65 years with CLTI and active symptoms of anxiety or depression\n* Staff o Healthcare professional (vascular surgeons, therapists, clinical nurse specialists, geriatricians, anaesthetists, pharmacists) providing care for people aged ≥65 years with CLTI\n\nExclusion Criteria:\n\n* Patients\n\n  * Palliative - death anticipated within one month\n  * Clinical and research team identify as lacking capacity to participate\n* Carers\n\n  o Clinical and research team identify as lacking capacity to participate\n* Staff o Not providing care for older people with CLTI","65 Years",{"count":306,"type":21},30,"Mental health disorders are common in older people and are often unrecognised. Those living with mental health disorders who are being considered for vascular surgery have worse post operative outcomes, including longer length of hospital stay, higher readmission rates and emergency admissions to hospital. These patients also have more medical conditions contributing to their post surgery complications and poor health outcomes.\n\nSurgery for vascular patients can include life changing operations, such as amputation, which impacts mental health and quality of life.\n\nShared decision making is the process whereby patients and clinicians work together to make evidence based decisions centred on patient values and preferences and is part of the Comprehensive Geriatric Assessment and optimisation (CGA) model of care. SDM has been shown to improve patient experience through provision of realistic choice, enhanced interaction with clinicians, greater empowerment and increased confidence and trust in healthcare provision. Implementing SDM in vascular patients can be particularly challenging. Evaluating and communicating benefits and risks of available treatments for CLTI in a complex older patient population requires additional consideration beyond the inherent surgical risks. To achieve truly informed SDM, the clinician requires knowledge of the impact of co-existing conditions on postoperative recovery, the natural history of the surgical pathology with and without surgery and an awareness of the benefits and risks of alternative treatments underpinned by skilful communication.",[309,31,208],"Critical Limb Threatening Ischaemia",[311,312,313,314,315],"Shared decision making","Perioperative medicine","Geriatrics","Mental health problems","Vascular surgery","2026-04-14",{"date":318,"type":46},"2026-04-17",{"date":320,"type":21},"2026-06",{"date":227,"type":21},{"name":323,"class":78},"Guy's and St Thomas' NHS Foundation Trust",{"id":325,"slug":4,"hasResults":10,"nctId":326,"briefTitle":327,"officialTitle":328,"acronym":4,"eligibilityCriteria":329,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":304,"enrollmentInfo":330,"targetDuration":4,"studyType":22,"phases":332,"briefSummary":333,"conditions":334,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":254,"lastUpdatePostDateStruct":335,"startDateStruct":337,"completionDateStruct":339,"leadSponsor":341,"locationsCount":107},"100618664","NCT07334561","Transcranial Electrical Stimulation for Comorbid Depression and Chronic Pain","Transcranial Electrical Stimulation for Comorbid Depression and Pain: From Technological Development to Clinical Translation in a Multicenter Trial","Inclusion Criteria:\n\n1. Aged 18-65 years;\n2. Meet the diagnostic criteria for a depressive episode according to DSM-5, with current mild-to-moderate depressive symptoms (HAMD-17 score ≥8 and ≤23);\n3. Report persistent pain lasting ≥3 months and score ≥4 on item 5 of the Brief Pain Inventory (BPI);\n4. Maintain a stable anti-depression drug and psychological treatment plan (including dosage, drug type, or therapeutic approach) for at least four weeks prior to enrollment;\n5. Right-handed, with normal hearing, vision, or corrected vision;\n6. Able to voluntarily provide written informed consent to participate in the study and willing and capable of complying with all study procedures.\n\nExclusion Criteria:\n\n1. Diagnosed with other psychiatric disorders, including schizophrenia spectrum disorders, bipolar I disorder (due to potential risk of manic episodes and contraindication of lithium or anticonvulsants), primary anxiety disorders, depression associated with severe somatic illness, etc.\n2. Active suicidal ideation, defined as a score of 4 on item 3 of the HAMD-17.\n3. Severe or treatment-resistant depression (HAMD-17 score ≥23, with current depressive episode lasting at least 2 years or failure to respond to two or more antidepressant treatments during the current episode).\n4. Substance use disorder within the past 3 months.\n5. Experience of malignant pain due to cancer pain syndrome, visceral pain (e.g., gastric pain), or referred pain (e.g., back pain from pancreatitis).\n6. Neurological disorders associated with structural brain abnormalities (e.g., traumatic brain injury, recent stroke, brain tumor).\n7. Having undergone neuromodulation treatments within the past 3 months, including electroconvulsive therapy (MECT), repetitive transcranial magnetic stimulation (rTMS), or transcranial electrical stimulation (tES).\n8. Contraindications to transcranial electrical stimulation (e.g., intracranial metal implants, cardiac pacemaker, cochlear implant, skin lesions at stimulation sites, personal or family history of epilepsy).\n9. Current or within the past 1 month use of medications affecting central nervous system excitability or pain, such as anticonvulsants, lithium, opioids, nonsteroidal anti-inflammatory drugs, and antipsychotics. Occasional as-needed use of acetaminophen as rescue medication is permitted but must be documented in detail in the study diary.\n10. Signs of dementia or other severe cognitive impairment (MMSE score \\\u003C24).\n11. Severe or unstable somatic diseases, including but not limited to: neurological disorders (e.g., epilepsy, stroke, migraine, history of cranial surgery); cardiovascular diseases (e.g., uncontrolled hypertension, heart failure, arrhythmia, myocardial infarction); respiratory disorders (e.g., severe sleep apnea syndrome); malignancy or immunocompromised status; uncontrolled diabetes (fasting blood glucose \\>12 mmol\u002FL).\n12. Pregnancy or lactation.\n13. Concurrent participation in another clinical trial, participation in any clinical trial within the past 90 days, or planned participation in another trial during the study period.\n14. Any contraindications to magnetic resonance imaging (e.g., metal implants, claustrophobia, respiratory or motor impairments).\n15. Inability to cooperate with study assessments.",{"count":331,"type":21},240,[65],"This clinical trial aims to investigate a novel non-pharmacological intervention, transcranial electrical stimulation (tES), for the treatment of comorbid depression and chronic pain. The primary objectives are to optimize neurostimulation parameters through a multicenter randomized controlled design and to elucidate the underlying neural circuit-immune interaction mechanisms of this comorbidity. Participants with comorbid depression and chronic pain will be randomly assigned to receive one of four interventions: (1) anodal tDCS unilateral hemispheric concurrent dual-site stimulation (a-tDCS UHCDS) targeting the left DLPFC and M1; (2) single-target anodal tDCS over the left DLPFC; (3) 40 Hz gamma transcranial alternating current stimulation (tACS); or (4) sham stimulation. The intervention period will last for 2 weeks, followed by a series of post-treatment follow-up assessments. Researchers will compare the changes in depression severity (e.g., assessed by HAMD-17) and pain intensity (e.g., NRS, BPI) across groups to evaluate the efficacy. Secondary outcomes include pain perception, quantitative sensory testing (QST), fMRI, MEG, metabolic markers, neurotransmitter and inflammatory biomarkers. This study aims to provide a precise, individualized therapeutic strategy, reduce reliance on pharmacotherapy, and promote the development of domestic high-end medical devices.",[31,241],{"date":336,"type":46},"2026-03-16",{"date":338,"type":21},"2026-05",{"date":340,"type":21},"2027-12",{"name":342,"class":78},"Shanghai Mental Health Center",{"id":344,"slug":4,"hasResults":10,"nctId":345,"briefTitle":346,"officialTitle":347,"acronym":4,"eligibilityCriteria":348,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":349,"enrollmentInfo":350,"targetDuration":4,"studyType":22,"phases":351,"briefSummary":352,"conditions":353,"keywords":356,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":361,"lastUpdatePostDateStruct":362,"startDateStruct":364,"completionDateStruct":366,"leadSponsor":368,"locationsCount":174},"100625429","NCT07422519","Virtual Reality-Based Mindfulness as an Adjunct to Treatment as Usual in Treatment-Resistant Depression","A Pilot Randomised Controlled Study Evaluating the Efficacy and Tolerability of Virtual Reality-Based Mindfulness as an Adjunct to Treatment as Usual in Treatment-Resistant Depression","Inclusion Criteria:\n\n* Age between 18 and 74 years, inclusive\n* Diagnosis of treatment-resistant Major Depressive Disorder (MDD), single or recurrent episode, in accordance with DSM-5 diagnostic criteria.\n* Inadequate response to two or more oral antidepressants during the current depressive episode\n* Inadequate response to at least one pharmacological combination or augmentation strategy\n* Ability and willingness to provide written informed consent for participation and data collection\n\nExclusion Criteria:\n\n* Presence of any contraindication to esketamine administration according to the approved product label\n* Current participation in another interventional clinical study involving antidepressant medication\n* Any medical, psychiatric, or other condition that, in the opinion of the investigator, could: (a) compromise participant safety or well-being, or (b) interfere with, limit, or confound study assessments or outcomes","74 Years",{"count":306,"type":21},[65],"The primary aim of this study is to evaluate the efficacy and tolerability of a combined Virtual Reality (VR)-based mindfulness intervention and pharmacological treatment compared with pharmacological treatment alone in reducing depressive symptoms in patients with Treatment-Resistant Depression (TRD).\n\nSecondary questions this study aims to address include:\n\n1. Does the combined intervention lead to changes in inflammatory blood parameters compared with pharmacological treatment alone?\n2. Does the addition of a VR-based mindfulness intervention prolong remission of depressive symptoms six months after treatment completion?\n3. Is the combined treatment with mindfulness and esketamine well-tolerated, and how does its adverse effect profile compare with esketamine treatment alone?\n4. Is there an association between changes in mindfulness trait levels, assessed using the FFMQ-SF, and reductions in depressive symptom severity?\n\nParticipants will be recruited from a Treatment-Resistant Depression Programme and randomly assigned to receive either VR-based mindfulness intervention in addition to treatment as usual or treatment as usual alone. The mindfulness intervention will last one month and include a total of 8 sessions. All participants will undergo comprehensive assessments at baseline and at predefined follow-up time points to evaluate clinical outcomes, inflammatory markers, tolerability, and remission duration.",[29,31,354,355],"Depression Chronic","Treatment-Resistant Major Depressive Disorder",[357,36,358,359,360],"Treatment-Resistant Depression","Mindfulness-Based Intervention","Virtual Reality","Esketamine","2026-02-25",{"date":363,"type":46},"2026-02-27",{"date":365,"type":46},"2025-09-18",{"date":367,"type":21},"2026-12-15",{"name":369,"class":78},"Hospital Universitari Vall d'Hebron Research Institute",{"id":371,"slug":4,"hasResults":10,"nctId":372,"briefTitle":373,"officialTitle":374,"acronym":375,"eligibilityCriteria":376,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":304,"enrollmentInfo":377,"targetDuration":4,"studyType":22,"phases":379,"briefSummary":380,"conditions":381,"keywords":382,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":399,"lastUpdatePostDateStruct":400,"startDateStruct":402,"completionDateStruct":404,"leadSponsor":406,"locationsCount":174},"100624985","NCT07416747","GynMDD Add-On to Supportive Psychotherapy in Mild to Moderate Depression","Multicenter Interventional Real-world Study Evaluating the Impact of the Dietary Supplement GynMDD Administered as an add-on to Supportive Psychotherapy in Patients With Mild to Moderate Depression.","SWING","Inclusion Criteria:\n\n* Adults aged 18 to 65 years, inclusive\n* The main reason for consultation is a suspected depressive episode\n* MADRS score between 15 and 34, indicating mild to moderate depression\n* No suicidal risk, defined as a score of 0 on item 10 of the MADRS scale\n* Body Mass Index (BMI) between 19 and 29 (inclusive)\n* Signed informed consent, confirming that the participant understands the purpose and requirements of the study and agrees to comply with the procedures (including scheduled supportive psychotherapy sessions)\n* Affiliation with the French national health insurance system or beneficiary of such coverage\n\nExclusion Criteria:\n\n* History of severe psychiatric disorders or currently undergoing supportive psychotherapy\n* Confirmed suicidal risk, defined as a score between 1 and 6 on MADRS item 10\n* Current treatment with antidepressants (AD)\n* MADRS score \\> 34\n* Conditions in which probiotic administration is not recommended (e.g., immunodeficiency, presence of a venous catheter)\n* Allergy to any component of the placebo or the GynMDD dietary supplement\n* Current consumption of probiotic-based dietary supplements\n* Recent infectious episodes that may require antibiotic therapy\n* Current treatment with anxiolytics\n* Long-term chronic anti-inflammatory treatment\n* Alcohol abuse, defined as a consumption of 10 standard drinks per week or more\n* Use of illicit drugs or substances of abuse\n* Inability to provide informed consent\n* Participation in another clinical study within the past 12 months\n* Pregnant or breastfeeding women\n* Patients without health insurance\n* Individuals under legal protection, guardianship, trusteeship, or any other protective measure",{"count":378,"type":21},168,[65],"The goal of this clinical trial is to learn whether the dietary supplement GynMDD, when taken as an add-on to supportive psychotherapy, can improve symptoms of mild to moderate depression in adults aged 18 to 65. The main questions it aims to answer are:\n\nDoes adding GynMDD to supportive psychotherapy lead to a greater reduction in depressive symptoms (measured by the MADRS scale) compared with supportive psychotherapy plus placebo?\n\nDoes the supplement also improve digestive well-being and influence gut microbiota profiles over the course of treatment?\n\nResearchers will compare patients receiving supportive psychotherapy + GynMDD to those receiving supportive psychotherapy + placebo to see if GynMDD provides additional benefits beyond standard care.\n\nParticipants will:\n\n* Attend regular appointments with their general practitioner\n* Complete one supportive psychotherapy session per week for 8 weeks\n* Take a daily dose of GynMDD or placebo\n* Complete weekly self-assessment questionnaires on mood, digestive symptoms, and any side effects via a mobile app\n* Provide two stool samples (at the start and end of the study) for microbiota analysis",[32,31,28],[383,384,385,386,387,388,389,390,391,392,393,394,395,396,397,398],"Gut-Brain Axis","Gut Microbiota","GynMDD","Mild Depression","Moderate Depression","MADRS","Supportive Psychotherapy","Psychotherapy","Dietary Supplement","Probiotic Supplement","Real-World Study","Mental Health","Curcumin","L-Glutamine","Randomized Controlled Trial","PHQ-9","2026-02-13",{"date":401,"type":46},"2026-02-18",{"date":403,"type":21},"2026-03",{"date":405,"type":21},"2027-11",{"name":407,"class":78},"Fondation FondaMental",{"id":409,"slug":4,"hasResults":10,"nctId":410,"briefTitle":411,"officialTitle":412,"acronym":413,"eligibilityCriteria":414,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":415,"targetDuration":4,"studyType":22,"phases":417,"briefSummary":418,"conditions":419,"keywords":424,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":433,"lastUpdatePostDateStruct":434,"startDateStruct":436,"completionDateStruct":437,"leadSponsor":439,"locationsCount":4},"100623547","NCT07398053","General Practitioner & Pharmacist Support for Discontinuing Long-term Antidepressants in Clinically Stable Patients","General Practitioner & Pharmacist Support for Discontinuing Long-term Antidepressants in Clinically Stable Patients: a Cluster Randomised Pragmatic Trial in Primary Care","GPS-AD","Inclusion Criteria:\n\nPatients will be eligible for inclusion in the study if they meet all of the following criteria:\n\n* Are 18 years or older and capable of providing informed consent.\n* Have their Global Medical File (GMD) managed by one of the participating GPs.\n* Have been prescribed AD (any type) by their GP for the treatment of depression, with:\n\n  * at least 6 months of continuous daily use following a first depressive episode, or\n  * at least 2 years of continuous daily use in the context of a relapsed depression\u002Frecurrent episode\n* Are judged by their GP as no longer meeting the criteria for a current depressive disorder.\n\nExclusion Criteria:\n\nPatients will be excluded from participation in the study if they meet any of the following criteria:\n\n* AD discontinuation is considered contra-indicated by the treating GP.\n* The patient is judged by the GP to be at high risk of relapse. This includes any of the following:\n\n  * Current significant depressive symptoms, defined as a score of ≥12 on the PHQ-9\n  * Current significant anxiety symptoms, defined as a score of ≥10 on the Generalised Anxiety Disorder-7 (GAD-7) scale.\n  * Current suicidal ideation, defined as a score \\>0 on item 9 (suicidality) of the PHQ-9.\n  * The patient is currently receiving only psychiatric treatment (out- or inpatient) for depression\n\nIn addition to the criteria increasing the risk of relapse, the following will also be an exclusion criteria:\n\n* The patient has a current psychiatric comorbidity (e.g. bipolar disorder, psychosis, substance use)\n* The patient has a diagnosis of dementia or significant cognitive impairment (assessed by GP judgement) or is living in a nursing home.\n* The AD is prescribed for a primary indication other than depression, such as anxiety alone without comorbid depressive disorder, or chronic pain.\n* The patient has insufficient language proficiency in Dutch or French to participate in the study procedures (e.g. providing consent, completion of questionnaires, interviews).\n* use of trazodon as AD as this is mainly used for sleep problems",{"count":416,"type":21},324,[65],"In Belgium, many adults who have suffered from depression keep using antidepressants on a daily basis for years afterwards, sometimes longer than guidelines recommend. Yet for some people who have been feeling well for a long time, this is no longer necessary, while the continued use of antidepressants can lead to side effects and causes additional costs for the healthcare system.\n\nHowever, reducing the doses of antidepressants or stopping altogether is not always easy. Some patients are afraid that their depression will return, and GPs and pharmacists often find the subject difficult to broach.\n\nThis is why the GPS-AD study is investigating a new approach in which GPs and pharmacists work more closely together to provide better support to patients. First, the GP invites patients who have been taking antidepressants for a long time for a consultation. Together, they discuss whether tapering of the medication is reasonable and feasible. If they agree to stop the treatment, the GP draws up a tapering plan tailored to the patient. The pharmacist helps monitor this process, offering advice and support to the patient while the doses are gradually reduced.\n\nThe study will extend over a period of two years and will take place in GP practices throughout Belgium. The new approach based on closer collaboration between GPs and pharmacists will be compared to the current standard of care, to determine whether it helps more long-term users to stop taking antidepressants without experiencing a recurrence of depressive symptoms.\n\nThe name of the study, GPS-AD (General Practitioner and Pharmacist Support for Antidepressant Discontinuation), refers to the collaboration between GPs and pharmacists in tapering of antidepressants, and also symbolises the support and guidance (the 'GPS') provided to patients and healthcare providers in assessing whether long-term use of antidepressants is still necessary.",[420,421,31,422,423],"Deprescribing","Antidepressant","Discontinuation","Primary Care",[425,426,427,94,428,429,430,431,432],"deprescribing","discontinuation","tapering","antidepressants","long-term use","chronic use","medication review","primary care","2026-02-02",{"date":435,"type":46},"2026-02-09",{"date":225,"type":21},{"date":438,"type":21},"2028-05-31",{"name":440,"class":78},"University Ghent",{"id":442,"slug":4,"hasResults":10,"nctId":443,"briefTitle":444,"officialTitle":445,"acronym":446,"eligibilityCriteria":447,"healthyVolunteers":10,"sex":16,"minAge":448,"maxAge":17,"enrollmentInfo":449,"targetDuration":4,"studyType":22,"phases":451,"briefSummary":452,"conditions":453,"keywords":460,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":480,"lastUpdatePostDateStruct":481,"startDateStruct":483,"completionDateStruct":485,"leadSponsor":487,"locationsCount":174},"100620990","NCT07364799","Effectiveness of the SoundHeal Multi-Sensory Integrative Therapy Among Justice-Involved Youth","Effectiveness of the SoundHeal (Heal) Multi-Sensory Integrative Therapy in Enhancing Emotional Regulation Among Justice-Involved Youth and Its Effect on Therapeutic Alliance and Mental Health Outcomes","HEAL-SLOJSC","Inclusion Criteria:\n\n* Age: Youth 12-18 years old. All participants enrolled in this study will be under the age of 18 at time of enrollment.\n* Custody: Detained in SLO County, CA Juvenile Hall with at least 8 weeks of expected stay at the time the clinical trial starts\n* Diagnosis: Documented history of being at risk or of having a history or current diagnosis of a mental health disorder (depression, anxiety, stress) and\u002For SUD\n* Language\u002FComprehension: Basic English understanding; accommodations for limited literacy allowed\n* Consent\u002FAssent: Eligible juveniles must provide assent, with parent\u002Fguardian or Legally Authorized Representative (LAR) consent.\n* Ensure that the person providing informed consent understands the information provided, even if that person providing informed consent agrees to be in the research.\n* Participation: Willingness to comply with the Heal intervention, journaling, and questionnaires\n* Recruitment and selection participation: Eligible participants will be selected in collaboration with facility behavioral-health staff using objective inclusion criteria only. Recruitment procedures are designed to be fair and free from arbitrary influence by facility administrators or peers.\n\nSpecial Considerations: Because participants are minors and incarcerated, safeguards ensure voluntary participation, protection from coercion, age-appropriate communication, and accommodations for literacy or comprehension limits.\n\nExclusion Criteria:\n\n* Age\u002FStatus: Not between 12-18 years old, or not currently detained in SLO County Juvenile Hall\n* Length of Stay: Expected detention is less than 8 weeks at start of clinical trial\n* Clinical Stability: Determined by onsite staff to be medically or psychiatrically unable to participate safely\n* Consent\u002FAssent: Unable to provide assent, or if parent\u002Fguardian or LAR does not provide consent\n* If the person providing informed consent needs more time than is allowed by the research design.\n* Language\u002FComprehension: Cannot understand basic English, even with literacy accommodations\n* Participation: Unwilling to comply with the Heal intervention, journaling, or questionnaires\n* Research staff will not personally use the device for research purposes. Their role is limited to facilitating device use for participants and monitoring protocol adherence.\n* While the Healpod may be available for non-research use in other settings, this protocol strictly limits its use to the described research procedures. Any non-research use will be separated from this study, and no data will be collected from individuals outside of the study.\n* Currently pregnant or becomes pregnant during the study period: If pregnant or pregnancy is discovered during participation, the individual will be withdrawn from the study to prevent any potential discomfort or unknown risk exposure related to the device environment (sound, vibration, or lighting).\n\nSpecial Exclusions\n\n* Juveniles whose participation may be influenced by coercion (e.g., enrollment tied to privileges or probation decisions)\n* Juveniles with severe cognitive or behavioral impairment that prevents safe or meaningful participation","12 Years",{"count":450,"type":21},12,[65],"Emotional dysregulation in justice-involved youth (JIY) is a condition that significantly impacts young people, their families, and juvenile justice and public health systems. Affecting an estimated 60-70% of detained Attention deficit hyperactivity disorderadolescents, it is a major driver of aggression, substance use, school failure, and later recidivism. Despite available treatments, managing emotional dysregulation in custody remains challenging, with youth often enduring high arousal, anger, and anxiety that persist into adulthood. Current popular therapies, including Cognitive Behavioral Therapy (CBT) and Dialectic Behavioral Therapy (DBT), often fall short in detention because they rely on verbal processing, require multiple scheduled sessions, and\u002For need highly trained staff. Other technologies, like biofeedback and neurostimulation techniques, are still under scrutiny for adolescents, given their higher-than-usual Adverse Events (AEs).\n\nThis SoundHeal study aims to evaluate a sensory intervention using the Healpod, a distraction-free physical space where a participant sits, delivering sound, music, gentle vibrations, and ambient light. Following this is a brief expressive journaling exercise to compare any before, during and after experience changes from the sensory immersion.\n\nThis prospective, single-center cohort study hypothesizes that these sessions will improve juveniles' ability to emotionally regulate, improve therapeutic alliance, mental health outcomes and build coping skills that can potentially help in long-term mental health and substance abuse treatment in JIY and beyond.",[454,455,31,456,457,458,459],"Emotional Dysregulation","Therapeutic Alliance","Anxiety Disorders","Stress Disorders","Substance Use Disorders","Mental Health Disorders",[461,462,463,464,465,466,467,468,469,470,471,472,473,474,475,476,477,478,479],"Emotional regulation","Emotional dysregulation","Justice-involved youth","Juvenile detention","Sensory-based intervention","multi-sensory stimulation therapy","Multisensory therapy","Sound therapy","music therapy","Vibroacoustic therapy","Therapeutic alliance","Therapy readiness","Mental health outcomes","substance use disorder","Coping skills","Non-verbal intervention","Journaling","Expressive Writing","Mindfulness","2026-01-16",{"date":482,"type":46},"2026-01-23",{"date":484,"type":21},"2026-01-30",{"date":486,"type":21},"2026-04",{"name":488,"class":53},"SoundHeal",{"id":490,"slug":4,"hasResults":10,"nctId":491,"briefTitle":492,"officialTitle":493,"acronym":494,"eligibilityCriteria":495,"healthyVolunteers":60,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":496,"targetDuration":4,"studyType":22,"phases":498,"briefSummary":499,"conditions":500,"keywords":503,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":508,"lastUpdatePostDateStruct":509,"startDateStruct":511,"completionDateStruct":513,"leadSponsor":515,"locationsCount":174},"100600442","NCT07097545","Change in Social Media Use and Well-being Among College Students Receiving a Two-week Exercise or Mindfulness Intervention","Social Media Use Study","SMUS","Inclusion Criteria:\n\n* The participant is 18 or older.\n* The participant must be a Johns Hopkins University student.\n* Owning an iPhone or Android smartphone, with frequent use of social media use daily (\\>\n\n  1 hour)\n* Enabling and sharing screenshots of the participant's smartphone use metrics, including number of last-week pickups, notifications received, and average screen time.\n* Providing consent to participate.\n* Only exercising 1 hour or less daily, on average.\n\nExclusion Criteria:\n\n* younger than 18\n* Not a Johns Hopkins University Student\n* Doesn't own a smart phone\n* Uses smartphone less than 1 hour daily\n* Exercises more than 1 hour daily",{"count":497,"type":21},300,[65],"The investigators will be randomizing 300 college student participants with high levels of social media use into either a 1) control condition (no intervention), a 2) mindfulness meditation cognitive intervention, or 3) a social media reduction + exercise replacement intervention. Participants complete intervention activities daily for two weeks. The investigators will collect self-report and behavioral measures of social media use and related psychological constructs at three time points: baseline, immediately after the intervention period, and one-week after the intervention period (three weeks from baseline).",[501,208,31,502],"Social Media Addiction","Wellbeing",[504,505,506,507],"digital media reduction intervention","mindfulness","behavioral intervention","digital wellbeing","2025-12-16",{"date":510,"type":46},"2025-12-17",{"date":512,"type":46},"2025-08-24",{"date":514,"type":21},"2027-01",{"name":516,"class":78},"Johns Hopkins Bloomberg School of Public Health",{"id":518,"slug":4,"hasResults":10,"nctId":519,"briefTitle":520,"officialTitle":521,"acronym":522,"eligibilityCriteria":523,"healthyVolunteers":60,"sex":16,"minAge":17,"maxAge":524,"enrollmentInfo":525,"targetDuration":4,"studyType":22,"phases":527,"briefSummary":528,"conditions":529,"keywords":533,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":546,"lastUpdatePostDateStruct":547,"startDateStruct":549,"completionDateStruct":551,"leadSponsor":553,"locationsCount":174},"100615438","NCT07292610","Impact of Nut Consumption on Mental Health in Young Adults","Impact of Nut Consumption on Mental Health in Young Adults: a Randomized Controlled Trial","NUTS4BRAIN-RCT","Participants must meet all the following criteria to be considered eligible for selection and randomization:\n\nInclusion Criteria:\n\n* Age: Participants must be between 18 and 25 years old.\n* Academic Status: Participants must be enrolled as university students.\n* Field of Study: Participants may come from any academic program offered at the Cuenca Campus, including Nursing, Social Work, Education, Fine Arts, Engineering, Journalism, and Teaching.\n\nParticipants will be excluded from the study if they have any of the following conditions, based on self-reported information:\n\nExclusion Criteria:\n\n* Allergies: Known nut allergy.\n* Self-reported cardiovascular, metabolic, gastrointestinal or mental health disorder.","24 Years",{"count":526,"type":21},135,[65],"Nuts have a high nutrient density, and numerous studies have reported their cardiometabolic benefits. Although observational studies in adults have indicated a potential link between nut consumption and improved mental health, there is still insufficient evidence from experimental studies to draw firm conclusions about this association.",[31,208,394,209,530,531,532],"Cognition","BDNF","General Wellbeing",[534,535,536,537,538,394,32,208,530,539,540,541,542,543,544,545,531],"RCT","Dietary Intervention","Nut consumption","young adults","Randomized controlled trial","University students","Sleep quality","Academic performance","Walnuts","Almonds","Pistachios","Hazelnut","2025-12-15",{"date":548,"type":46},"2025-12-18",{"date":550,"type":46},"2025-11-24",{"date":552,"type":21},"2027-04",{"name":554,"class":78},"University of Castilla-La Mancha",{"id":556,"slug":4,"hasResults":10,"nctId":557,"briefTitle":558,"officialTitle":559,"acronym":4,"eligibilityCriteria":560,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":304,"enrollmentInfo":561,"targetDuration":4,"studyType":22,"phases":563,"briefSummary":564,"conditions":565,"keywords":566,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":570,"lastUpdatePostDateStruct":571,"startDateStruct":573,"completionDateStruct":575,"leadSponsor":577,"locationsCount":4},"100612465","NCT07253935","Impact of Therapeutic Exercise Integrated With Psychotherapy and Education in Patients With Depression","Efficacy of a Combined Approach of Therapeutic Exercise, Psychotherapy, and Therapeutic Education in Patients With Depression: The ACTIDEP Randomized Controlled Trial","Inclusion Criteria:\n\n* Diagnosis of depression or dysthymia according to the ICD-11 criteria (including unspecified depressive disorder, code 6A7Z) or DSM-5-TR criteria confirmed by their referring physician.\n* A patient currently undergoing psychological treatment for depression with a score above the established cutoff in a validated depression questionnaire.\n\nExclusion Criteria:\n\n* Pregnancy.\n* Presence of neurological comorbidities or neurological signs.\n* Systemic rheumatic diseases, including fibromyalgia.\n* Central nervous system disorders.\n* Severe cognitive impairment.\n* Schizophrenia, psychotic disorders, or bipolar spectrum disorders.",{"count":562,"type":21},112,[65],"The goal of this clinical trial is to evaluate whether a combined approach including therapeutic exercise, psychotherapy, and therapeutic education can improve depressive symptoms and quality of life in adults diagnosed with depression.\n\nThe main questions it aims to answer are:\n\nDoes a biobehavioral intervention that integrates exercise, psychotherapy, and education reduce depressive symptoms more effectively than psychotherapy alone? Does this combined approach improve quality of life, physical function, and sleep quality compared with standard psychological therapy? Researchers will compare the intervention group (therapeutic exercise + psychotherapy + education) to the control group (psychotherapy alone) to determine whether the integrated program provides greater improvements in mental health and well-being.\n\nParticipants will:\n\nComplete an initial assessment including demographic data, physical tests, and validated questionnaires.\n\nBe randomly assigned to one of the two groups. If in the intervention group, take part in an 8-week telematic program consisting of graded activity, therapeutic exercise, and educational sessions.\n\nUndergo post-intervention assessments and a follow-up evaluation 12 weeks after the program ends.\n\nThis study aims to provide evidence on whether combining therapeutic exercise and education with psychotherapy can enhance treatment outcomes and promote long-term adherence to physical activity in people with depression.",[31],[567,32,568,569],"Mental disorders","Exercise","Physical activity","2025-11-26",{"date":572,"type":46},"2025-11-28",{"date":574,"type":21},"2025-12-01",{"date":576,"type":21},"2027-05",{"name":578,"class":78},"MarcoMateoRiera",{"id":580,"slug":4,"hasResults":10,"nctId":581,"briefTitle":582,"officialTitle":582,"acronym":4,"eligibilityCriteria":583,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":304,"enrollmentInfo":584,"targetDuration":4,"studyType":22,"phases":585,"briefSummary":586,"conditions":587,"keywords":588,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":594,"lastUpdatePostDateStruct":595,"startDateStruct":597,"completionDateStruct":599,"leadSponsor":601,"locationsCount":174},"100599323","NCT07082998","Comparing the Efficacy of Heated Yoga and Sauna as a Treatment for Depression","Subject Characteristics\n\nInclusion Criteria:\n\n1. adults (18-65 years old)\n2. Ability to provide informed consent\n3. English language proficiency\n4. PHQ-9 score \\> 10, indicating at least moderate depressive symptoms 21\n5. Must have filled out the waiver for the community-based partners prior to enrolling in the study\\*\n6. Individuals of childbearing potential must use an acceptable form of birth control\n7. (if applicable) willingness to keep psychiatric medications and psychotherapy stable throughout the course of the study\n8. Must be able to access mindfulness app on a device (i.e., smartphone, iPad, etc.)\n9. Can travel to Breathe in Harvard Square and at least one Restore location (i.e., Hingham, Somerville, Dedham, Newton, Lynnfield)\n\nExclusion Criteria:\n\n1. Pregnant or planning to become pregnant\n2. Breast feeding\n3. Active suicidal thinking (i.e., PHQ-9 item 9 ≥1 and a positive response to C-SSRS screener items 3, 4, 5, or 6)\n4. Active eating disorders or substance use disorders within the past 12 months, as per the MINI\n5. Primary OCD or PTSD, as per the MINI\n6. History of bipolar disorder, psychotic disorders, as per the MINI\n7. ≥25% drop in PHQ-9 score from screen to baseline\n8. Under the influence or withdrawal of drugs or alcohol\n9. Positive urine toxicology screen due to illicit drug use or other exclusionary medications. (Potential false positives will be addressed on a case-by-case basis at the discretion of the PI or designee)\n10. have had a bone fracture or joint surgery in the past 6 months\n11. not able to walk freely or without difficulty\n12. any serious, unstable medical condition as determined by the revised Physical Activity Readiness Questionnaire (PAR-Q+) and do not have approval from their treating physician (we will check in with treating physician in the event that participants endorse any item on the PAR-Q+)\n13. participants must have a healthcare provider who they could contact if they needed medical care, such as a primary care doctor, a counselor, a psychiatrist, a nurse practitioner, or a clinic that you go to.\n14. Significant exposure to heated yoga classes in the past 3 months (i.e., more than 6 classes)\n15. Significant exposure to sauna sessions in the past 3 months (i.e., more than 6 sessions)\n16. Significant exposure to mindfulness app in the past 3 months (i.e., more than 6 uses of the app)\n17. are on medications that make dehydration more likely (e.g., lithium, antipsychotics, insulin-dependent) diuretics, barbiturates, b-blockers, anticholinergics, current ETOH acute intoxication, reduced ability to sweat, hemophilia, pacemaker (magnets used to assemble saunas can interrupt the pacer)\n18. antidepressant or psychiatric medications that are initiated less than 8 weeks or a dose change less than 4 weeks prior to screening visit\n19. psychotherapy that has been initiated within the past 3 months\n20. psychiatric hospitalization within the past year\n21. diagnosed with any neurological disorders that would impact participation or make participation unsafe\n22. are currently in active ketamine, Electroconvulsive therapy, or Transcranial Magnetic Stimulation treatments\n23. are unable to follow the study procedures (e.g., not able to travel to the heated yoga or sauna studios)\n24. A subject who in the opinion of the Principal Investigator would not be able to safely complete the study or would jeopardize study integrity",{"count":204,"type":21},[65],"This project explores whether heated yoga, sauna, and a mindfulness app reduce depressive symptoms",[30,29,31,354,32,28],[94,589,590,591,505,592,593],"heated yoga","yoga","sauna","mindfulness app","clinical trial","2025-11-11",{"date":596,"type":46},"2025-11-13",{"date":598,"type":46},"2025-09-12",{"date":600,"type":21},"2027-07-31",{"name":602,"class":78},"Massachusetts General Hospital",{"id":604,"slug":4,"hasResults":10,"nctId":605,"briefTitle":606,"officialTitle":607,"acronym":608,"eligibilityCriteria":609,"healthyVolunteers":10,"sex":202,"minAge":610,"maxAge":524,"enrollmentInfo":611,"targetDuration":4,"studyType":22,"phases":613,"briefSummary":614,"conditions":615,"keywords":619,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":627,"lastUpdatePostDateStruct":628,"startDateStruct":630,"completionDateStruct":632,"leadSponsor":633,"locationsCount":174},"100603160","NCT07132905","Mpata Yathu Trial for Young Women in Zambia","Randomized Pilot Trial of Church-Based Problem-Solving Therapy for Adolescent Girls and Young Women With a History of Gender-Based Violence in Zambia","MYT","Inclusion Criteria:\n\nTo be eligible for enrollment in the RCT, participants must meet the following criteria:\n\n1. aged 15 to 24 years;\n2. Speak Nyanja, Bemba, and\u002For English fluently;\n3. Reside in the Matero or Chawama constituency area during the time of recruitment;\n4. Report lifetime exposure to GBV, as assessed by the following sections of the WHO Multi-country Study on Women's Health and Domestic Violence Against Women instrument:\n\n   * Section 7 (Physical Violence by Intimate Partner): Reports of being slapped, pushed, hit with a fist, kicked, dragged, choked, or threatened\u002Fattacked with a weapon by a husband or partner.\n   * Section 8 (Sexual Violence by Intimate Partner): Reports of being physically forced to have sex, having sex out of fear, or being forced to engage in degrading sexual acts by a husband or partner.\n   * Section 9 (Emotional Abuse by Intimate Partner): Reports of being insulted, belittled, intimidated, or threatened by a partner.\n   * Section 10 (Physical Violence by Non-Partner): Lifetime experiences of being beaten or physically mistreated by someone other than a partner since age 15.\n   * Section 11 (Sexual Violence by Non-Partner): Forced sex or sexual acts since age 15 by a non-partner, and childhood sexual abuse before age 15.\n5. Exhibit moderate depressive symptoms indicated by a score of 10-14 on the 9-item Patient Health Questionnaire (PHQ-9), or common mental disorder (CMD) symptoms (e.g., depression, anxiety) as indicated by a score of 9 or higher on the 14-item Shona Symptom Questionnaire (SSQ-14); and\n6. Be living with HIV or demonstrate HIV risk behaviors, as defined by validated items from the World AIDS Foundation survey,25 including unprotected sex, multiple sexual partners, coerced sex, or transactional sex.\n\nExclusion Criteria:\n\nWomen will be excluded if they:\n\n1. Require emergency treatment for any crisis (mental, physical, emotional) at the time of screening\n2. Report severe symptoms of depression (score \\> 14 on PHQ-9) or no to mild depression symptoms (PHQ-9 score \\\u003C10), and\u002For severe anxiety symptoms using the Generalized Anxiety Disorder 7-item scale or GAD-7 (score \\>14 on GAD-7)\n3. Have intellectual or cognitive disabilities that limit their ability to complete the screening tools, interact with a lay counselor and\u002For provide informed consent; and\u002For\n4. Are considered in immediate danger (e.g., reoccurring physical violence) during time of the study.\n5. Are currently receiving formal mental health counseling or psychotherapy (to avoid duplication of care and potential confounding effects).","15 Years",{"count":612,"type":21},180,[65],"This study aims to improve mental health and HIV-related outcomes among adolescent girls and young women (AGYW) in Zambia who have experienced gender-based violence (GBV). GBV includes physical, sexual, or emotional violence from partners or others and is known to increase the risk of depression, anxiety, post-traumatic stress, and HIV infection. In Zambia, access to mental health services is limited, especially for young women in low-resource communities. This study tests a counseling program called Mpata Yathu, which means \"Our Space\" in Chinyanja, designed to provide psychological support and improve well-being for young women who have faced violence and may be living with or at risk for HIV.\n\nMpata Yathu is a culturally adapted version of the Friendship Bench, a lay counselor-delivered mental health intervention originally developed in Zimbabwe. In this adapted version, trained community lay counselors will deliver six individual problem-solving therapy (PST) sessions over a three-month period. Sessions will be delivered in private spaces within local Catholic churches in the Matero and Chawama areas of Lusaka, Zambia. Counseling sessions will also include referral options for participants who may need further support related to HIV care, GBV, or mental health concerns.\n\nThe study is a two-arm randomized controlled trial. Participants will be randomly assigned to either:\n\n1. Immediate Intervention Group - Receives the Mpata Yathu intervention between baseline and 3-month follow-up\n2. Waitlist Control Group - Receives usual care for the first 3 months and then receives the Mpata Yathu intervention between 3- and 6-month follow-up\n\nA total of 180 young women (90 per group) will participate in the trial. To be eligible, participants must be between the ages of 15 and 24, reside in the Matero or Chawama area, report lifetime GBV exposure, and show moderate depressive symptoms or symptoms of common mental disorders (CMDs). They must also be living with HIV or report behaviors that place them at risk for HIV.\n\nThe primary outcome is symptoms of CMDs, assessed using the Shona Symptom Questionnaire (SSQ-14). Secondary outcomes include depression, anxiety, and PTSD symptoms, as well as HIV-related outcomes such as clinic attendance, antiretroviral therapy (ART) adherence, and prevention behaviors such as condom use or PrEP readiness. The study will also measure feasibility, acceptability, and fidelity of the intervention.\n\nData will be collected through surveys at baseline, 3 months, and 6 months. The research team will also monitor how the intervention is implemented, how participants respond to counseling, and whether counselors follow the therapy protocol. Participants will receive a small stipend for their time and transport at each counseling session and follow-up visit.\n\nThis study is designed to test whether a trauma-informed, church-based mental health intervention can improve psychological well-being and HIV engagement among young women who are often underserved in traditional healthcare systems. If successful, this model could be expanded to other churches or schools in Zambia and similar settings. The results will inform future large-scale evaluations and could help shape new strategies for addressing GBV, mental health, and HIV among youth in sub-Saharan Africa.",[616,617,618,31,208],"HIV","Common Mental Health Problems","PTSD - Post Traumatic Stress Disorder",[620,159,621,622,623,624,625,626],"Gender-based violence","Adolescent girls and young women","Zambia","Lay counselors","Mental health","HIV treatment engagement","HIV prevention","2025-08-13",{"date":629,"type":46},"2025-08-20",{"date":631,"type":21},"2025-09-22",{"date":45,"type":21},{"name":634,"class":78},"University of California, San Francisco",{"id":636,"slug":4,"hasResults":10,"nctId":637,"briefTitle":638,"officialTitle":638,"acronym":639,"eligibilityCriteria":640,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":641,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":643,"conditions":644,"keywords":648,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":652,"lastUpdatePostDateStruct":653,"startDateStruct":655,"completionDateStruct":657,"leadSponsor":659,"locationsCount":174},"100602931","NCT07129928","Organizational Strategies and Psychosocial Skills for Maintaining Physical Activity After a Depressive Episode: a 3-month Post-rehabilitation Study.","AP&Depression","Inclusion Criteria:\n\n* Patient over 18 years old\n* French-speaking patient\n* Patient with a depressive episode diagnosed by a physician\n* Patient who completed a stay at the Rehabilitation Center (CDR) at the Clinique des Portes de l'Eure\n* Patient at 3 months post-rehabilitation stay\n* Patient who completed an initial assessment (T0) at the Maison Sport Santé during the clinic stay\n\nExclusion Criteria:\n\n* Exacerbation of the condition\n* Patient who has already completed a 3-month follow-up assessment at the Maison Sport Santé (MSS)",{"count":642,"type":21},15,"With nearly 280 million people affected worldwide (2022), the management of depression represents a major public health issue. The study titled \"Organizational Strategies and Psychosocial Skills to Maintain Physical Activity after a Depressive Episode: A 3-Month Post-Rehabilitation Study\" (AP\\&Depression) fits within this context. Physical activity (PA) is now recognized as an effective complementary therapy to pharmacological and psychotherapeutic treatments, helping to regulate mood and reduce depressive symptoms. However, despite these proven benefits, individuals who have experienced a depressive episode often struggle to maintain regular physical activity once they leave the hospital setting. This study aims to identify the mechanisms that influence the continuation of PA after hospitalization by exploring organizational strategies, psychosocial skills, and individual determinants involved in this process.\n\nDepression is a debilitating illness characterized by persistent sadness, loss of interest, chronic fatigue, and impaired cognitive and physical abilities (DSM-5, 2013). Among the aggravating factors, sedentary behavior plays a key role, whereas PA is associated with a significant reduction in the risk of relapse. Yet, 67.8% of individuals with depression do not meet the recommended 150 minutes of weekly PA, and this figure rises to 85.7% when activity is measured objectively. This situation is explained by several barriers: lack of motivation, low self-efficacy, fluctuating mood disorders, social isolation, and limited access to exercise facilities. Conversely, certain factors facilitate the resumption of PA after a depressive episode, including structured support, the establishment of routines, social support, and therapeutic education.\n\nThe study relies on a qualitative methodology using semi-structured interviews conducted with 15 patients who stayed at the Rehabilitation Center of the Clinique des Portes de l'Eure. Participants are selected according to the following criteria: aged over 18, medically diagnosed with a depressive episode, underwent rehabilitation, and completed an initial assessment at the Maison Sport Santé. They will be interviewed three months after discharge to explore their PA practices. Data will be analyzed using NVivo software, following the COREQ (Consolidated Criteria for Reporting Qualitative Research) guidelines. The analysis of transcripts will help identify the organizational strategies implemented, the psychosocial skills involved, and the individual determinants influencing the maintenance of regular PA.\n\nThe expected results should highlight that patients adopt various strategies to maintain PA after hospitalization. Session planning, the gradual integration of PA into daily life, and the anticipation of obstacles are major levers for establishing a sustainable routine. In addition, psychosocial skills, such as stress management and interaction with a support network, emerge as essential elements for maintaining regular physical activity. However, several obstacles may be identified, including persistent fatigue, mood fluctuations, lack of organization, and social isolation. These findings underscore the importance of personalized support after rehabilitation, particularly through mechanisms such as Patient Therapeutic Education (PTE) or individualized follow-up in Maisons Sport Santé.\n\nThe aim of this study is to shed light on the mechanisms that enable individuals who have experienced a depressive episode to autonomously maintain physical activity after hospitalization. This research seeks to provide concrete recommendations for improving support during and after hospitalization to enhance adherence to PA. The study's conclusions could contribute to the development of new therapeutic approaches aimed at improving patients' quality of life.",[645,31,646,647],"Physical Activity","Rehabilitation","Organizational Behavior",[569,94,646,649,650,651],"Organizational strategies","Psychosocial skills","Determinants of physical activity","2025-08-11",{"date":654,"type":46},"2025-08-19",{"date":656,"type":21},"2025-09-01",{"date":658,"type":21},"2026-12-31",{"name":660,"class":78},"Hopital La Musse",{"id":662,"slug":4,"hasResults":10,"nctId":663,"briefTitle":664,"officialTitle":664,"acronym":4,"eligibilityCriteria":665,"healthyVolunteers":60,"sex":16,"minAge":17,"maxAge":666,"enrollmentInfo":667,"targetDuration":4,"studyType":22,"phases":668,"briefSummary":669,"conditions":670,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":672,"lastUpdatePostDateStruct":673,"startDateStruct":675,"completionDateStruct":677,"leadSponsor":679,"locationsCount":4},"100596704","NCT07048938","Clinical Effect and Mechanism Study of Five Elements Music Therapy(FEMT) on Depression Disorder","Inclusion Criteria:\n\n* Meet the diagnostic criteria for depressive episodes of ICD-10;\n* Hamilton Depression Scale -17 items score ≥14 points;\n* The diagnosis should be confirmed by at least two physicians with the title of attending physician or above.\n* Have sufficient visual and auditory levels to ensure that the necessary checks and experiments for the research can be completed;\n* Sign the written informed consent form and agree to be enrolled in the trial as required by the research plan.\n\nExclusion Criteria:\n\n* There are serious heart, liver and kidney diseases, organic brain diseases, serious cardiovascular diseases, tumors, blood history, rheumatism, malnutrition and neurodegenerative diseases, etc.\n* Depressive episodes secondary to other mental or physical illnesses;\n* There is a history of abuse of tobacco, alcohol and other psychoactive substances;\n* Those with comorbidities of other mental disorders;\n* Had participated in other drug clinical trials before inclusion.","60 Years",{"count":204,"type":21},[65],"The goal of this clinical trial is to learn if Five-Elements Music Therapy works to treat depression disorder. It will also learn about the mechanism of action of Five-Elements Music Therapy of Traditional Chinese Medicine (TCM) for depression disorder. The main questions it aims to answer is: Can Five-Elements Music Therapy, primarily using Gong-mode and Zhi-mode tones, improve Hamilton Depression Rating Scale (HAMD) scale scores in patients with depression disorder by regulating prefrontal cortex function?\n\nResearchers will compare customized five-element music 1 (featuring Gong-mode and Zhi-mode as the predominant tones) to customized five-element music 2 (featuring Shang-mode and Yu-mode as the predominant tones, with identical rhythm and pitch to music 1), while simultaneously observing electroencephalogram (EEG), eye movement, and pulse diagnostic data from a healthy control group, to see if customized five-element music 1 featuring Gong-mode and Zhi-mode as the predominant tones can significantly improve depressive states in patients with depressive disorder.\n\nParticipants will:\n\n1. Undergo Five-Element Music 1 or Five-Element Music 2 therapy twice daily for 4 weeks (28 days), with each session consisting of 30 minutes of music listening followed by 10 minutes of rest.\n2. Concurrently receive antidepressant therapy with fluoxetine hydrochloride.\n3. Undergo relevant examinations once every two weeks and record their levels of depression and anxiety (Hamilton Depression Rating Scale (HAMD) \\& Hamilton Anxiety Rating Scale (HAMA)).\n4. Undergo and record their post-intervention electroencephalogram (EEG), eye movement, and pulse characteristics after the 4-week period.",[31,30,671],"Depressive Disorder","2025-06-24",{"date":674,"type":46},"2025-07-03",{"date":676,"type":21},"2025-07-01",{"date":678,"type":21},"2026-03-31",{"name":342,"class":78},""]