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NCT04754165 · ClinicalTrials.gov registry record · NA
Postoperative VR for Recovery After Bariatric Surgery
A NA study of Postoperative Pain and Bariatric Surgery Candidate, sponsored by Beth Israel Deaconess Medical Center.
- Active
- Registry status
- NA
- Development phase
- 106
- Enrollment target
- 1
- Study location
NCT04754165: Active NA study of Postoperative Pain and Bariatric Surgery Candidate, sponsored by Beth Israel Deaconess Medical Center.
NCT04754165 is a NA study of Postoperative Pain and Bariatric Surgery Candidate that is active but no longer recruiting, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 106 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (54% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04754165, a NA study of Postoperative Pain and Bariatric Surgery Candidate, is active but no longer recruiting, sponsored by Beth Israel Deaconess Medical Center.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 106 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this study is to investigate whether the addition of immersive virtual reality (VR) in the immediate postoperative period to an enhanced recovery after surgery (ERAS) protocol could improve postoperative recovery from bariatric surgery.
Primary Outcome
The primary outcome of this study will be patient reported quality of recovery at time of PACU discharge, as assessed by the QOR-15. The QOR-15 is a validated instrument to assess postoperative recovery from the patient's perspective, assessing overall well-being, nausea, pain, and anxiety and depression following surgery.
Conditions Studied
Interventions
- OTHER Virtual Reality Immersive Relaxation
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 106 participants |
| Start Date | 2022-03-21 |
| Est. Completion | 2026-06-30 |
| Phase | NA |
What the registry record for NCT04754165 still lists
NCT04754165 is an interventional study that assigns participants to a tested intervention. The registered 106 participants enrollment target is mid-sized for trials with a published cap, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (54% lower).
The record links to 3 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 1 intervention - of which Virtual Reality Immersive Relaxation is the first listed.
NCT04754165 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT04754165 about?
NCT04754165 is a clinical study titled "Postoperative VR for Recovery After Bariatric Surgery". The objective of this study is to investigate whether the addition of immersive virtual reality (VR) in the immediate postoperative period to an enhanced recovery after surgery (ERAS) protocol could improve postoperative recovery from bariatric surgery.
What is the current status of trial NCT04754165?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 106 participants. The study started on 2022-03-21. Estimated completion is 2026-06-30.
What conditions does trial NCT04754165 study?
This clinical trial studies the following conditions: Postoperative Pain, Bariatric Surgery Candidate, Postoperative Complications.
What interventions are being tested in trial NCT04754165?
The interventions under investigation include: Virtual Reality Immersive Relaxation (OTHER).
Who is sponsoring clinical trial NCT04754165?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04754165 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postoperative Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT04754165's enrollment target sits among peer trials
106 53rd of 120 higher than 67 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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