Virtual Reality for Reducing Anxiety and Improving Sleep in Cholecystectomy Patients
VR patient education video
Treatment Adherence and Compliance+8
+ Anxiety Disorders
+ Behavior
Services Research Study
Summary
Study start date: January 5, 2025
Actual date on which the first participant was enrolled.This study explores the use of virtual reality (VR) to enhance patient education and family communication for patients undergoing gallbladder removal surgery, known as cholecystectomy. The aim is to see if using VR can help reduce stress and anxiety, improve sleep quality, and increase satisfaction with the surgical preparation process. It is especially relevant for patients preparing for surgery, as it might provide a more relaxed and informed experience, potentially leading to better outcomes and recovery. The study will involve 60 patients who will be divided into three groups to compare different approaches: standard care, VR education, and VR education with a virtual family meeting. Participants will be assigned to one of three groups randomly. In the standard care group, patients will undergo routine procedures with no VR intervention. In the VR education group, patients will watch an educational video using VR goggles before surgery to help them understand the procedure better. The VR education and interview group will additionally have a virtual family meeting, where patients can interact with their families in a simulated home environment using VR technology. Throughout the process, participants will complete questionnaires to assess their stress, anxiety, sleep quality, and satisfaction, both before and after the surgery. The study aims to provide insights into how VR can support patients' emotional and informational needs during surgical preparation.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Marmara University Pendik Training and Research Hospital Prof. Dr. Asaf Ataseven Additional Service Building
Istanbul, Turkey (Türkiye)Open Marmara University Pendik Training and Research Hospital Prof. Dr. Asaf Ataseven Additional Service Building in Google Maps