CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 34 enrolled
Drug / intervention
Pain Rehabilitation Virtual Reality (PRVR) +1 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04636177
NCT04636177N/ACompleted
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Pain Rehabilitation Virtual Reality (PRVR): Innovations to Enhance Mobility in the Presence of Pain

Stanford University·interventional·Posted Nov 19, 2020·Updated Nov 14, 2025

In Brief

A clinical study evaluating Pain Rehabilitation Virtual Reality (PRVR) and Standard Physiotherapy Rehabilitation (SPR) for Chronic Pain and 3 related conditions. Completed, enrolled 34 participants across 2 sites.

Detailed Summary

The proposed research is a single arm feasibility trial of pain rehabilitation virtual reality (PRVR) aimed at measuring feasibility, acceptability and utility of VR as well as changes in physical function and fear for adolescents with chronic musculoskeletal pain. The intervention includes standard physiotherapy treatment including functional goal setting and progressive exercise.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Pain, Musculoskeletal Pain, Fibromyalgia, Virtual Reality
CountriesUnited States
CollaboratorsNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedNov 19, 2020
Enrollment StartMar 10, 2022
Primary CompletionDec 7, 2024
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 5.6 years ago

Interventions

Pain Rehabilitation Virtual Reality (PRVR)behavioral

Participants will receive approximately 8, 1-hour physiotherapy sessions delivered over the course of 6-12 weeks. Adequate dose: 75% (6 of 8 sessions).

Standard Physiotherapy Rehabilitation (SPR)behavioral

Participants allocated to either intervention arm will receive 8, 1-hour physiotherapy sessions delivered over the course of 6-8 weeks. Adequate dose: 75% (6 of 8 sessions).