Anxiety Preoperative

9

Review clinical trials related to Anxiety Preoperative. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Relationship Between Preoperative Anxiety Level and Frailty Score in Elderly Patients Scheduled for Elective Hip Arthroplasty: A Prospective Observational Study

Frailty is a state of vulnerability resulting from decreased physiological reserve across multiple organ systems, impairing an individual's ability to withstand stressors. As the elderly population grows worldwide, the proportion of older adults undergoing surgical procedures continues to rise, and frailty is expected to become increasingly prevalent among surgical candidates. Anxiety is one of the most common psychiatric conditions, affecting approximately one in three individuals globally. Preoperative anxiety may negatively influence surgical outcomes, particularly in older and more vulnerable patients. This prospective observational study aims to evaluate the relationship between preoperative anxiety level and frailty score in elderly patients aged 65 years and older scheduled for elective hip arthroplasty. Frailty will be assessed using the FRAIL Scale (Fatigue, Resistance, Ambulation, Illness, Loss of Weight), and anxiety will be measured using the Hamilton Anxiety Rating Scale (HAM-A). Secondary outcomes include the prevalence of frailty and anxiety, the effect of frailty on length of hospital stay, postoperative intensive care unit admission rates, and the relationship between frailty and preoperative laboratory and hemodynamic parameters.

Participants needed: 142
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Başakşehir Çam & Sakura City HospitalUpdated: Jun 8, 2026Locations: 1Duration: 1 Week
Eligibility criteria

Patients of both sexes aged 65 years and older [+3]

Patients with ASA physical status classification IV or V [+4]

Status: Recruiting

Auriculotherapy in the Treatment of Pre-Operative Anxiety

The goal of this clinical trial is to use the validated PROMIS Emotional Distress - Anxiety - Short Form 8a and PROMIS Emotional Distress-Depression-Short Form pre-and post-intervention to establish a superior correlation between the auriculotherapy treatment and the reduction of perioperative anxiety. Subject population will include those having a partial or total nephrectomy for cancer. Drawing the role that auriculotherapy may play in reducing perioperative anxiety related requirement after surgery may also help in reducing the risk of opioid use disorders (OUD) since anxiety has been found to be a major risk factor for OUD in surgical patients. Therefore, this trial will also examine the effect of the auriculotherapy intervention in reducing opioid requirement after surgery.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Jacques E. ChellyUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Greater than 18 years of age [+3]

Opioid dependence, based on the DSM definition of Opioid Use Disorder (OUD) [+6]

Status: Recruiting

Comparison of Two Relaxation Strategies Between Glasses, Virtual Reality Headset, and Without Relaxation Tool, in the Anxiety Preoperative of Orthopedic Adult Patients

In adults, the prevalence of preoperative anxiety related to surgery or anesthesia ranges from 60 to 80%, and context plays an important role. Patients with significant preoperative anxiety experience reduced sleep quality. In addition, high preoperative anxiety is linked to more severe postoperative pain and an increased need for painkillers. In addition, it is a source of dysfunction in care. Currently, there are no recommendations regarding the prevention of preoperative anxiety. New approaches have emerged that show some benefit: music, binaural auditory stimulation and hypnosis. In the UAC J0 unit of the Amiens-Picardie University Hospital, the caregivers offer the PSiO glasses, a tool combining three techniques: light therapy, relaxation and chromotherapy. This system has obtained CE and FCC markings and seems to be more or less effective on patients admitted to the CH . A pilot study evaluating the effects of virtual reality hypnosis on patients' preoperative anxiety has shown that this technology represents a non-invasive way to reduce preoperative stress levels without side effects and without the need for additional medical or paramedical staff. This study aims to improve the patient's well-being before their operation. Depending on the randomization, he will benefit from a relaxation session with the Psio glasses or a virtual reality hypnosis session with the Hypno VR headset. Follow-up of patients will be carried out on the basis of variation in an anxiety scale, physiological criteria, the amount of anesthetic products used, the time spent in the recovery room, and the evaluation of pain.

Participants needed: 632
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire, AmiensUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

Patient treated at the UAC D0 [+5]

Patient with deafness that does not allow him to perceive and understand sounds [+9]

Status: Recruiting

The Study Evaluates the Effect of an Interactive Projector as a Distraction for Children During Anesthetic Induction. The Primary Objective is to Reduce Perioperative Anxiety, Measured With the Modified Yale Preoperative Anxiety Scale (mYPAS).

This study is designed to evaluate the effect of technology as a distraction technique during anesthetic induction in children, starting from their arrival to the operating room. An interactive film will be displayed using a projector (BERT: Bedside Entertaining and Relaxation Tool) mounted on a whiteboard in front of the child's gurney. The primary outcome is perioperative anxiety, measured with the Modified Yale Preoperative Anxiety Scale (mYPAS).

Participants needed: 70
Trial details
Age: 2-6Biological sex: AllType: InterventionalSponsor: Clinica Alemana de SantiagoUpdated: Nov 17, 2025Locations: 1
Eligibility criteria

Patients undergoing elective procedures under general anesthesia at Clinica Alem... [+5]

Patient or parental does not consent [+6]

Status: Not yet recruiting

Effect of Virtual Reality on Patient Outcomes and Satisfaction in Total Knee Replacement

This study aims to evaluate the effectiveness of virtual reality (VR) in managing preoperative anxiety and postoperative pain in patients undergoing total knee replacement. Investigators will assess the impact of preoperative VR training on anxiety levels, explore the effectiveness of relaxing and distracting VR videos for pain management after surgery, and determine the optimal timing for VR application by comparing different VR intervention times. Our goal is to identify how VR can improve both the emotional and physical recovery process for patients undergoing knee replacement surgery.

Participants needed: 64
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Aykut TurgutUpdated: Sep 26, 2025Locations: 1
Eligibility criteria

Patients with an ASA score of 1, 2, or 3 [+2]

Using >30 mg of oral oxycodone or equivalent daily [+10]

Status: Not yet recruiting

The Efficacy of a Mindfulness-Based Virtual Reality Intervention to Reduce Pain in Postoperative Patients

The goal of this randomized clinical trial is to evaluate whether a virtual reality (VR) mindfulness intervention can reduce anxiety and postoperative pain in adults undergoing surgery, primarily hernia and varicose vein procedures. The main research questions are: * Does a preoperative VR mindfulness intervention reduce anxiety before surgery? * Does this reduction in anxiety result in lower postoperative pain compared to usual care? * Does the intervention help prevent chronic pain two weeks after surgery? Researchers will compare a VR mindfulness intervention group with a treatment-as-usual (TAU) group to assess the intervention's effectiveness. Participants will: * Be randomly assigned to one of two groups: * Experimental group: Receive a VR mindfulness session on the first day of hospitalization (one day before surgery). * Control group: Receive standard hospital care (no intervention). * Complete psychological and pain assessments at four time points: 1. Before the intervention (Day 1) 2. Immediately after the intervention (only the experimental group, Day 1) 3. After surgery (Day 2) 4. Two weeks after surgery (follow-up) * Report pain intensity using the Numeric Rating Scale (NRS) at four postoperative time points. Before enrollment, participants will undergo a structured interview to assess eligibility. This study aims to determine whether reducing preoperative anxiety through VR mindfulness contributes to improved pain management and a lower risk of developing chronic pain following surgery.

Participants needed: 64
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Babes-Bolyai UniversityUpdated: May 8, 2025
Eligibility criteria

The participant is scheduled for surgery and is currently hospitalized for herni... [+3]

Inability to provide informed consent due to mental incompetence (e.g., intellec... [+6]

Status: Recruiting

Audio Hypnosis for Reducing Anxiety in Children and Adolescents Undergoing MRI: A Randomized Controlled Trial

The goal of this clinical trial is to find out if listening to an audio hypnosis recording can help reduce anxiety in children and adolescents (ages 6-14) who are getting an MRI scan without sedation. The main questions the study will answer are: Does listening to a hypnosis audio before an MRI help children feel less anxious? Can hypnosis audio help reduce scan interruptions or early terminations? To find out, researchers will compare one group of children who listen to the hypnosis audio with another group who receive the usual explanation from medical staff to see if the audio helps lower anxiety and makes the MRI process smoother. What participants will do: Be randomly placed into either the hypnosis group (who get access to the hypnosis audio) or the control group (who receive the usual explanation). Listen to the hypnosis audio as many times as they like before the MRI (if in the hypnosis group). Fill out questionnaires before and after the MRI to measure anxiety (both children and parents). Have their MRI scan while researchers track any interruptions or early terminations. Have their anxiety levels rated by MRI technologists after the scan. This study aims to see if a simple, non-medication method like audio hypnosis can help children feel calmer during MRI exams.

Participants needed: 100
Trial details
Age: 6-14Biological sex: AllType: InterventionalSponsor: University of Witten/HerdeckeUpdated: Mar 21, 2025Locations: 1
Eligibility criteria

Age between 6 and 14 years [+2]

Severe cognitive impairment or mental retardation [+4]

Status: Recruiting

Management of Preoperative Anxiety in Children: Could a Lollipop Be the Solution?

The aim of the study is to evaluate the effectiveness of distraction using a lollipop versus premedication with intranasal midazolam to manage preoperative anxiety in pediatric anesthesia.

Participants needed: 63
Trial details
Age: 4-10Biological sex: AllType: InterventionalSponsor: Tunis UniversityUpdated: Nov 1, 2024Locations: 1
Eligibility criteria

Age > 4 ans , ASA 1 ou 2

Children who rejected premedication - The occurrence of perioperative complicati...

Status: Recruiting

The Effects of Wearing Operation Gown With Cartoon Characters on Reducing Preoperative Anxiety in Children: Randomized Controlled Study

The operating room environment can be frightening for pediatric patients. Many techniques have been used to make the operating room environment less intimidating, including allowing parents to accompany part of this procedure, play therapy and various distraction strategies during the entrance to the operating room. In a survey study, it was reported that parents were expected to create hospital conditions with a more child-friendly atmosphere. In this context, it is thought that creating a warmer environment for children, including the clothes worn in the operating room, may reduce the anxiety level of children. In this study, investigators' aim was to investigate the effect of wearing an hospital gown with cartoon characters on the reduction of preoperative anxiety in children scheduled for Orthopedic surgery by in the operating room.

Participants needed: 160
Trial details
Age: 4-12Biological sex: AllType: InterventionalSponsor: Uludag UniversityUpdated: Oct 8, 2024Locations: 1
Eligibility criteria

Patients who are planned to have elective orthopedic surgery [+2]

Motor and/or mentally retarded patients [+3]