NCT06257472

Efficacy of Virtual Reality (VR) for Irritable Bowel Syndrome

Efficacy of Virtual Reality (VR) for Irritable Bowel Syndrome: A Randomized Trial Comparing Brain-Gut Directed VR vs. Sham VR
Anthony Lembo·ClinicalTrials.gov·device·Device trialRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Virtual Reality Headset
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Anthony Lembo
Funder
The Cleveland Clinic
Location
Los Angeles,Cleveland, United States of America
Timeline & enrollment
Phase
N/A
Start date
Jun 01, 2024
End date
Feb 01, 2025
Enrollment
75 participants
Primary outcome

IBS-targeted HRQOL (health-related quality of life)

Summary

In this study, the investigators conduct a remote, eight-week, two-arm, randomized controlled
 trial that assesses the benefits, primarily measured through the irritable bowel syndrome
 (IBS)-targeted HRQOL (health-related quality of life), of an immersive, disease-targeted
 virtual reality program compared to a non-immersive virtual reality program for patients with
 IBS.

ICD-10 classifications
Irritable bowel syndrome with predominant constipation [IBS-C]Irritable bowel syndromeIrritable bowel syndrome with predominant diarrhoea [IBS-D]Irritable bowel syndrome with mixed bowel habits [IBS-M]Other and unspecified irritable bowel syndrome
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06257472
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06257472 through Pure Global AI's free database. This phase not specified trial is sponsored by Anthony Lembo and is currently Recruiting. The study focuses on IBS - Irritable Bowel Syndrome. Target enrollment is 75 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.