CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 20 enrolled
Drug / intervention
Control +1 moredevice
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/NCT06101264
NCT06101264N/ACompleted

Application of Virtual Reality in Post-Operative Recovery of a Pediatric Scoliosis Patient Population

Connecticut Children's Medical Center·interventional·Posted Oct 26, 2023·Updated Sep 22, 2025

In Brief

A clinical study evaluating Control and Virtual Reality for Adolescent Idiopathic Scoliosis. Completed, enrolled 20 participants across 1 site.

Detailed Summary

The purpose of this study is to assess the effect of virtual reality on subjective post-operative pain, total inpatient narcotic administration, and mobilization with physical therapy in pediatric patients who have undergone surgical correction for idiopathic scoliosis.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
202420252026
First PostedOct 26, 2023
Enrollment StartJan 1, 2024
Primary CompletionJun 1, 2025
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 2.7 years ago

Interventions

Controldevice

Control patients following spinal fusion for adolescent idiopathic scoliosis that receive no virtual reality sessions.

Virtual Realitydevice

Patients will undergo a 20 minute virtual reality session prior to each physical therapy session following spinal fusion for adolescent idiopathic scoliosis. Virtual reality sessions will continue until functionally cleared by physical therapy.