Telerehabilitation In The Home After Stroke (NCT06682429)
Telerehabilitation In The Home After Stroke: A Randomized, Controlled, Assessor-Blind Clinical Trial
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this research study is to evaluate whether telerehabilitation targeting arm movement, when added to usual care, improves arm function and reduces global disability after stroke, compared to usual care alone. Patients with arm weakness due to stroke that happened in the past 90-150 days will be randomized into one of two groups: \[1\] TR and usual care; \[2\] usual care only (no TR), but people in the usual care group will be offered TR once the study is done. TR consists of 70 minutes/day of activities targeting arm function, 6 days a week for 6 weeks.
Who can join: Review the eligibility criteria below.
Location: Rancho Los Amigos Research Institute — Downey, California
Age range: 18 Years to 80 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (27 Sites)
Showing the first 25 of 27 sites.
- Rancho Los Amigos Research Institute — Downey, California
- University of California, Irvine — Irvine, California
- Keck Medical Center of USC — Los Angeles, California
- University of California, Los Angeles — Los Angeles, California
- Casa Colina Hospital and Centers for Healthcare — Pomona, California
- Hillcrest Medical Center at UC San Diego Health — San Diego, California
- Medstar Health Research Institute — Washington D.C., District of Columbia
- Brooks Rehabilitation Hospital — Jacksonville, Florida
- Jackson Memorial Hospital Christine E. Lynn Rehabilitation Center — Miami, Florida
- Emory Rehabilitation Hospital — Atlanta, Georgia
- University of Kansas Medical Center — Kansas City, Kansas
- Massachusetts General Hospital — Boston, Massachusetts
- Spaulding Rehabilitation Hospital — Charlestown, Massachusetts
- Baystate Medical Center — Springfield, Massachusetts
- University of Michigan University Hospital — Ann Arbor, Michigan
- Icahn School of Medicine at Mount Sinai — New York, New York
- NYP Columbia University Medical Center — New York, New York
- University of North Carolina Medical Center — Chapel Hill, North Carolina
- Duke University Hospital — Durham, North Carolina
- University of Cincinnati — Cincinnati, Ohio
- MetroHealth Old Brooklyn Health Center — Cleveland, Ohio
- Cleveland Clinic Foundation — Cleveland, Ohio
- Jefferson Moss Rehabilitation Research Institute — Elkins Park, Pennsylvania
- Medical University of South Carolina — Charleston, South Carolina
- The Institute for Rehabilitation and Research (TIRR) Memorial Hermann — Houston, Texas
📞 Contact the Study Coordinator
Phone: (424) 522-7874
Email: tr2trial@mednet.ucla.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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- Determining the Optimal Dose of Reactive Balance Training After Stroke — Toronto, Ontario
- AMPLATZER PFO Occluder Post Approval Study — Birmingham, Alabama
- Reflex Excitability in Post-stroke Stiff-Knee Gait — Cleveland, Ohio
- Group Lifestyle Balance™ for Individuals With Stroke (GLB-CVA) — Dallas, Texas
Explore by condition: All Stroke clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.