This project will evaluate AppliedVR's EaseVRx - a multi-modal, skills-based, 8-week, virtual reality, home intervention - in an exploratory randomized controlled trial for self-management of chronic pain among Black, young adults (ages 18-50) with sickle cell disease.
Age range
18 Years – 50 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Pain Rating Using Numerical Pain Rating Scale (NPRS)
Timeframe: Baseline, up to week 4 or time period 1 (day 1-28), from week 4 to 8 or time period 2 (days 29-56)
Pain Intensity Subscale of the Chronic Pain Grade Questionnaire
Timeframe: Baseline, week 4, week 8, and 4 weeks post-intervention (week 12)
Participant Engagement: Minutes of Program Use Per Day
Timeframe: up to week 4 or time period 1 (day 1-28), from week 4 to 8 or time period 2 (days 29-56)
Participant Engagement: Duration in Days
Timeframe: Baseline, daily during treatment (4 weeks or time period 1, day 1-28), daily during treatment (8 weeks or time period 2, days 29-56)
Participant Engagement: Features Utilized
Timeframe: Daily during treatment (8 weeks)
Participant Engagement: Completion Rates
Timeframe: Daily average during treatment (up to 8 weeks)
Study Retention: Surveys
Timeframe: Baseline, 4 weeks, 8 weeks and 4 weeks post-intervention (week 12)
Study Retention: Daily Diaries
Timeframe: Up to 8 weeks
Participant Satisfaction
Timeframe: Post-treatment (up to 6 weeks post-treatment)
Frequency of Highest Satisfaction Scores
Timeframe: Post-treatment (up to 6 weeks post-treatment)
Safety: Number of Adverse Events
Timeframe: 4 weeks, 8 weeks, up to 6 weeks post-treatment