[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Lancaster General Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":95},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,69],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":34,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":68},"100609887",false,"NCT07220421","Foundational Programs to Combat Clinician Stress","Evaluate Foundational Wellness Programs to Help Reduce Clinician Burnout and Improve Professional Fulfilment in Health Care Professionals.","FACCTS","Inclusion Criteria:\n\n* 25-70 years of age,\n* UPHS or MGH clinician (physician, APP, CRNP, PA, psychologist),\n* Access to smart phone and internet,\n* Ability to give informed consent,\n* Interested in wearing an Oura ring and being part of a study to evaluate breath and meditation-derived exercises,\n* Willing to do relaxation exercise every day for 4 weeks.\n\nExclusion Criteria:\n\n* Currently maintaining a regular\u002Fdaily mind-body program practice (eg. meditation, yoga or breathing techniques),\n* Atrial fibrillation,\n* Pacemaker\u002Fdefibrillator,\n* Untreated or severe obstructive sleep apnea (AHI\\>=30),\n* History of diaphragm paralysis,\n* Unable or unwilling to complete the workshop,\n* Severe chronic obstructive pulmonary disease (COPD),\n* Severe valvular heart disease,\n* Prior or planned chest\u002Fabdominal or nasal\u002Ffacial surgery within 6 months,\n* Severe psychiatric illness (e.g. schizophrenia, schizoaffective disorder, bipolar disorder), active substance use, seizure disorder or major somatic illness (uncontrolled hypertension, lung disease, liver disease, cancer or heart disease).",true,"ALL","25 Years","70 Years",{"count":21,"type":22},180,"ESTIMATED","INTERVENTIONAL",[25],"NA","This is a prospective, randomized, controlled clinical trial in which clinicians from University of Pennsylvania Health Systems (UPHS) including Penn Medicine- Lancaster General Health (LGH) and Massachusetts General Hospital (MGH) are offered a well-known program to help reduce clinician burnout: Sudarshan Kriya Yoga (SKY) Breathing and Sahaj Meditation Intervention.",[28,29,30,31,32,33],"Burnout, Professional","Stress, Psychological","Stress, Physiological","Psychological Well-Being","Mind-Body Therapies","Work Related Stress",[35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55],"Sudarshan Kriya Yoga (SKY) Breathing and Sahaj Meditation","Stress Reduction","Healthcare Professional Burnout","Workplace Wellbeing","Work Life Balance","Physician","Healthcare Provider","Cognitive Performance","Cognitive Attention","Depression","Anxiety","Sleep","Heart Rate Variability","Resilience","Social Connection","Self-Valuation","Professional Fulfilment","Medical Errors","Physician Turnover","Healthcare Economics","Occupational Burnout","RECRUITING","2025-10-21",{"date":59,"type":60},"2025-10-23","ACTUAL",{"date":62,"type":60},"2025-09-15",{"date":64,"type":22},"2026-05",{"name":66,"class":67},"Lancaster General Hospital","OTHER",6,{"id":70,"slug":4,"hasResults":10,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":16,"sex":17,"minAge":76,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":23,"phases":79,"briefSummary":80,"conditions":81,"keywords":85,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},"100568988","NCT06688396","Dilated Cardiomyopathy Detection Using AI and Screening With Mobile Technology (DCM-DETECT)","Dilated Cardiomyopathy Detection Using Artificial Intelligence and Screening With Mobile Technology","DCM-DETECT","Inclusion Criteria (Proband)\n\n* Male or female age ≥ 18 years\n* Confirmed diagnosis of non-ischemic DCM determined at the discretion of the treating physician and defined as LVEF ≤ 45% at any time during the clinical course of the patient\n* Must have at least one living adult FDR\n* Able to provide informed consent\n\nInclusion Criteria (FDR)\n\n* Male or female age ≥ 18 years who are first-degree relatives of patients with DCM\n* Proband has provided informed consent\n* FDR able to provide informed verbal consent\n* Access to a smartphone or digital tablet with cellular data or Wi-Fi access\n\nExclusion Criteria (Proband)\n\n* DCM attributed to any other secondary form of cardiomyopathy per the investigator's determination\n* Proband has previously informed FDR to undergo cardiac screening\n* Ischemic cause of reduced LVEF\n\n  * evidence of myocardial infarction, inducible ischemia or chest pain on stress testing in absence of coronary angiogram to rule out ischemic disease\n  * history of acute coronary syndromes (STEMI (ST-Elevation Myocardial Infarction), NSTEMI (Non-ST-Elevation Myocardial Infarction) or unstable angina) revascularization or ≥75% stenosis of either left main or Left Anterior Descending (LAD) or ≥75% stenosis of 2 major epicardial vessels on angiogram\n* Moderate or greater primary valvular abnormality not due to underlying cardiomyopathy\n* Congenital structural heart disease\n* Severe and untreated or untreatable hypertension\n* Cardiomyopathy due to acute or reversible conditions; examples include tachyarrhythmias, thyroid disorders, iron overload\n* Any secondary cause of reduced LVEF such as pregnancy, myocarditis, amyloidosis, sarcoidosis, exposure to toxins including alcohol, substance abuse or chemotherapeutic drug\n* (CPC Participants only) Home address outside of traveling range\n\nExclusion Criteria (FDR)\n\n* Previously informed about cardiac screening or has completed cardiac screening by transthoracic echocardiogram (TTE)\n* Previously diagnosed with reduced LVEF\n* (CPC Participants only) Home address outside of traveling range","18 Years",{"count":78,"type":22},150,[25],"This is a prospective, single-arm clinical trial in which participants with dilated cardiomyopathy will invite their first degree relatives to undergo mobile cardiac, electrocardiogram screening.",[82,83,84],"Dilated Cardiomyopathy","Heart Failure","Heart Disease",[82,83,84],"2025-01-28",{"date":88,"type":60},"2025-01-30",{"date":90,"type":60},"2024-12-04",{"date":92,"type":22},"2026-12",{"name":66,"class":67},1,""]