Using virtual reality to improve body image after bariatric surgery
Impact of the Use of Virtual Reality Exposure Therapy on Body Image After Bariatric Surgery
NA · University Hospital, Bordeaux · NCT05460104
This study is testing if virtual reality therapy can help people feel better about their body image after having weight loss surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Bordeaux (other) |
| Locations | 2 sites (Libourne and 1 other locations) |
| Trial ID | NCT05460104 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of Virtual Reality Exposure Therapy (VERT) in enhancing body image satisfaction among patients who have undergone bariatric surgery and are experiencing body image dissatisfaction. Participants will be assessed at 12 months post-intervention to determine the impact of VERT compared to standard follow-up care. The approach utilizes immersive virtual environments to help patients integrate their new body image and identity. Previous smaller studies have shown promise, but this study aims to provide more robust evidence with a larger sample size and longer follow-up.
Who should consider this trial
Good fit: Ideal candidates are patients who have undergone bariatric surgery and are in the weight stabilization phase, experiencing dissatisfaction with their body image.
Not a fit: Patients with motion sickness from virtual reality use, those who have had reconstructive surgery post-bariatric surgery, or those with certain psychiatric conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve body image satisfaction and overall quality of life for patients after bariatric surgery.
How similar studies have performed: While previous case reports have indicated positive outcomes with virtual reality therapy in similar contexts, this study represents a more rigorous approach to validate those findings.
Eligibility criteria
Show full inclusion / exclusion criteria
* inclusion criteria: patients who underwent bariatric surgery in the weight stabilization phase (between 18 and 30 months after surgery) presenting dissatisfaction with their body image according to the BSQ (score ≥ 111), to be affiliated to the French social security system. The prior, free and informed consent of the patient shall be obtained. * exclusion criteria: patients with disabling nausea (Motion Sickness) from previous use of a virtual reality headset, patients who had from post-bariatric reconstructive surgery, epileptic patients, decompensation of a psychiatric pathology
Where this trial is running
Libourne and 1 other locations
- CH de Libourne - Hôpital Robert BOULIN — Libourne, France (RECRUITING)
- CHU de Bordeaux - Hopital Haut-Lévêque — Pessac, France (RECRUITING)
Study contacts
- Study coordinator: Laurene BOSC, Dr
- Email: laurene.bosc@chu-bordeaux.fr
- Phone: 05.57.65.60.78
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Obesity, Bariatric Surgery Candidate, Virtual Reality Exposure Therapy, Body image, Dysmorphophobia