Virtual Reality for Chronic Pain in Younger Patients
This study is looking at whether using virtual reality (VR) games can help younger patients aged 7 to 21 manage chronic pain in their head, neck, or upper body. You would participate in 6 weekly sessions, each lasting about an hour. During these sessions, you would do physical therapy exercises and play VR games designed to help with movement. Researchers will measure your pain intensity using a Numeric Rating Scale and your ability to do daily activities using the Upper Extremity Functional Scale each week for 6 weeks to see if the interventions are helpful. This study is currently unclear on its recruitment status and plans to enroll 20 participants.
- Study design
- This is an interventional study with 20 planned participants. It is not specified if it is randomized or blinded.
- What's involved
- You would attend 6 once-weekly, hour-long sessions. Each session involves physical therapy exercises, virtual reality gaming, and completing questionnaires.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your pain and disability will be assessed weekly from enrollment to the end of treatment at 6 weeks.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Using Virtual Reality Applications for Younger Patients With Chronic Pain
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Elizabeth A Pickle, MD · PRINCIPAL_INVESTIGATOR · University of Pittsburgh Medical Center Children's Hospital of Pittsburgh
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Pain Intensity Based on Numeric Rating ScaleWeekly assessment from enrollment to the end of treatment at 6 weeks
Ranges from 0 (no pain) to 10 (worst pain imaginable)
- Disability Classification based on the Upper Extremity Functional ScaleWeekly assessment from enrollment to the end of treatment at 6 weeks
20-item questionnaire asking participant to rate difficulty of specified activities using the upper extremity with possible answers ranging from 1 (extreme difficulty or unable to perform activity) to 4 (no difficulty).