Virtual reality may ease pain and speed recovery after bariatric surgery
NCT ID NCT04754165
First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time
Summary
This study tests whether using immersive virtual reality (VR) relaxation right after bariatric surgery can improve recovery. Participants choose calming scenes like mountains or beaches to help them relax. The trial measures how well patients feel they recover, their pain levels, and how much pain medication they need. If it works, VR could offer a simple, non-drug way to support recovery after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual Reality Immersive Relaxation
- What this could lead to
- If effective, VR could become a standard, drug-free tool to help people recover more comfortably after bariatric surgery.
- What could go wrong
- This is a small, early-stage study. The benefits may be modest, and VR may not work for everyone or significantly change recovery.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
66 people
The number who actually took part.
- Started
-
Mar 2022
- Expected to finish
-
Jun 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: \- Patients undergoing laparoscopic bariatric surgery at BIDMC under general anesthesia. Exclusion Criteria: * Age\<18 * Open wounds or active infection of the face or eye area * History of seizures or other symptom linked to an epileptic condition * Patients with hearing aids who are unable to tolerate wearing headphones with their hearing aids * Patients with a pacemaker or other implanted medical device * Droplet or airborne precautions (as determined by BIDMC infection control policy) * Non English Speaking or non Spanish Speaking * Chronic opioid dependence (existing oral opioid prescription for \>3 months, methadone, suboxone) Drop Out Criteria: (after enrollment and randomization, before intervention) \- Surgery is converted to an open procedure (laparotomy), the patient will be withdrawn from the study as these patients are treated in a manner that is different than standard ERAS protocols
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Bariatric surgery candidate are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Impact of Cross-Sectional design in Single-File rotary system on apical debris extrusion and postoperative pain following Single-Visit root canal treatment: an in vitro and randomized clinical study
- Comparison of perioperative analgesia nociception index (ANI) between preoperative and postoperative ultrasound-guided transversus abdominis plane Block(TAP block) in laparoscopic cholecystectomy
- Anrikefon injection for postoperative analgesia in thoracoscopic lung surgery: a randomized, Double-Blind, Active-Controlled, Parallel-Group, Single-Center clinical study
- Acupressure may offer drug-free relief after cesarean birth
- Can an extra nerve block cut opioid use after knee replacement?
- Can Weight-Loss surgery weaken protein digestion in older adults?