WithdrawnNot Applicable

Augmented Reality-based Telerehabilitation Platform for Patients With Stroke

Stopped: Study did not receive funding

United States0Started 2025-06

Plain-language summary

The study is to 1) determine the feasibility of the use of our augmented reality (AR) rehabilitation program, including its preliminary efficacy, 2) determine the feasibility of obtaining an augmented reality assessment based on the Fugl-Meyer Assessment - Upper Extremity (FMA-UE).

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. 18 years or older
✓. ≥3 months post ischemic or hemorrhagic stroke
✓. Upper extremity deficit with an FMA-UE score between 20-50
✓. Able to operate the AR device independently or with the help of a caregiver
✓. Sufficiently proficient in the English language to follow instructions from Reia

Exclusion criteria

✕. History of developmental, neurological or psychological impairment leading to functional disability
✕. Vision or visual field impairment that interferes with the use of the AR headset
✕. Severe photosensitivity that makes use of the AR headset uncomfortable
✕. History of visually provoked seizures
✕. Hearing aids
✕. Cardiac pacemaker
✕. Implantable cardioverter-defibrillator (ICD)

What they're measuring

Adherence

Timeframe: 8 weeks

Percentage of participants who successfully complete the vFMA-UE

Timeframe: Day 70

Trial details

NCT IDNCT06963645

SponsorStanford University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-06

View on ClinicalTrials.gov More Stroke trials