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Virtual Reality for Post-Operative Recovery in Pediatric Scoliosis
N/A
Recruiting
Research Sponsored by Connecticut Children's Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
All pediatric patients (ages 13-18) at Connecticut Children's undergoing surgical correction for idiopathic scoliosis over a span of 12 months
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 times daily postoperatively until hospital discharge (up to 60 days postoperatively)
Awards & highlights
Study Summary
This trial looks at how virtual reality affects kids' post-op pain, drug use, and physical therapy after scoliosis surgery.
Who is the study for?
This trial is for pediatric patients aged 13-18 at Connecticut Children's who are undergoing surgery for idiopathic scoliosis. It excludes those with recent head or neck surgery, chronic opioid use, non-English speakers, seizure history, cognitive delays that affect VR use, and those with certain electronic medical devices.Check my eligibility
What is being tested?
The study is testing the impact of virtual reality on pain perception, narcotic medication needs, and physical therapy progress in children after scoliosis surgery. The goal is to see if VR can improve post-operative recovery experiences.See study design
What are the potential side effects?
Potential side effects may include discomfort from wearing a head-mounted display or specific reactions to virtual reality such as dizziness or nausea. However, these will be monitored during screening.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am a teen (13-18) at Connecticut Children's getting surgery for scoliosis.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 times daily postoperatively until hospital discharge (up to 60 days postoperatively)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 times daily postoperatively until hospital discharge (up to 60 days postoperatively)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Average subjective pain level on the 10-point Wong-Baker FACES pain scale
Secondary outcome measures
Average daily activity levels during the post-operative period measured through actigraphy.
Average number of physical therapy sessions prior to receiving clearance by physical therapy staff
Total amount of administered opioids during the post-operative period
Trial Design
1Treatment groups
Experimental Treatment
Group I: Virtual Reality InterventionExperimental Treatment1 Intervention
Participants will receive a post-operative virtual reality intervention following corrective surgery for idiopathic scoliosis.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Virtual Reality Intervention
2017
N/A
~240
Find a Location
Who is running the clinical trial?
University of ConnecticutOTHER
184 Previous Clinical Trials
158,233 Total Patients Enrolled
Connecticut Children's Medical CenterLead Sponsor
71 Previous Clinical Trials
31,454 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Does this trial welcome participants aged under 25 years?
"This trial is seeking participants that are between 13 and 18 years of age."
Answered by AI
How may I become involved in this research initiative?
"This clinical trial is searching for 60 patients who have adolescent idiopathic scoliosis and are aged between 13 and 18."
Answered by AI
Are new participants being enrolled in this experiment at present?
"According to clinicaltrials.gov, enrollment for this trial has closed since its inception on November 1st 2023 and latest update on October 19th 2023. However, there are 83 other clinical studies looking for participants at the moment."
Answered by AI
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