Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Telerehabilitation for stroke recovery

Official title: Bedside Telerehabilitation Early After Stroke

Run by TRCare, Inc. · NCT05625438 · Data updated 2026-11-12

This study tests if a new telerehabilitation program using a special training system can help people recovering from a stroke improve their arm function while they are still in the hospital.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment20 (estimated)
SponsorTRCare, Inc.
Industry-sponsored
Locations1 site (Fullerton, California)
StatusRecruiting
StartedDecember 19, 2022
Main results expectedDecember 2025
Study endsDecember 2025
Registry record updatedDecember 6, 2024
Trial IDNCT05625438 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older who have experienced a stroke within the last 30 days and have specific unilateral arm motor deficits.

Probably not a fit

Patients with significant cognitive impairments or major coexisting neurological or psychiatric conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the safety and feasibility of a telerehabilitation program designed for patients recovering from a recent stroke. Participants will engage in daily rehabilitation sessions using a sensor-based training system called HandyMotion, which allows them to access therapy exercises and games directly from their hospital room. The study aims to assess the effectiveness of this approach in improving arm function and overall motor outcomes during the inpatient rehabilitation period.

Why it matters

Potential benefit: If successful, this approach could enhance recovery outcomes for stroke patients by providing more accessible and engaging rehabilitation therapy.

How similar studies have gone: Other studies have shown promising results with telerehabilitation approaches, indicating potential for success in this novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age 18 years or older
2. Stroke that is radiologically verified, due to ischemia or to intracerebral hemorrhage, and with time of stroke onset \<30 days prior to enrollment; or traumatic brain injury.
3. Unilateral arm motor deficits that are neither trivial (no arm weakness) or devastating (arm plegia). This requires that the baseline Box \& Block Test score with affected arm to be at least 1 block in 60 seconds but no more than 90% of the number of blocks with the good arm.
4. Possess enough arm movement to participate in therapy
5. Informed consent signed by the subject
6. Able to follow simple instructions
7. Study participation is not likely to be significantly limited by agitated behavior

Exclusion Criteria:

1. A major, active, coexistent neurological or psychiatric disease that would limit study participation, e.g., advanced dementia
2. Expectation that patient's cognitive status will likely interfere substantially with playing assigned games or exercises
3. Deficits in communication that interfere with reasonable study participation
4. Lacking visual acuity, with or without corrective lens, of 20/50 or better in at least one eye
5. Subject does not speak sufficient English to comply with study procedures
6. Shoulder pain that in the judgement of the study team is likely to substantially limit the amount of telerehabilitation therapy completed

Where it's running

  • Providence St. Jude Medical Center
    Fullerton, California, United States
    Recruiting

Study contacts

  • Principal investigator: Natalia Covarrubias-Eckardt, MD — Providence St. Jude Medical Center
  • Study coordinator: Johnson K Sun
  • Email: kit@trcare.net
  • Phone: 650-300-2168

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Cerebrovascular Reactivity Testing with HD-DOT in Sickle Cell Patients

    This study tests whether high-density diffuse optical tomography can measure brain blood flow and oxygen use in people with sickle cell disease, to see how these signals relate to stroke risk.

    Recruiting Washington University School of Medicine · St Louis, Missouri · NCT07776444

  • Comparing Action Observation Therapy and Motor Relearning Program for Stroke Recovery

    This study is testing whether watching movements (Action Observation Therapy) or practicing movements (Motor Relearning Program) helps people recovering from a stroke improve their balance and mobility better.

    Recruiting Foundation University Islamabad · Islamabad · NCT06947343

  • Sovateltide treatment for acute ischemic stroke

    This test will try sovateltide in adults aged 18–80 who had an ischemic stroke within 24 hours to see if it helps improve recovery.

    Recruiting at 54 sites Phase 3 Pharmazz, Inc. · Tucson, Arizona and 53 other locations · NCT05691244

  • Enhanced imaging techniques for stroke diagnosis

    This study is testing whether new advanced imaging techniques can help doctors diagnose strokes faster and more accurately in patients who might have had a stroke.

    Recruiting Chinese PLA General Hospital · Beijing, Beijing Municipality · NCT05614193

  • Understanding brain blood flow and metabolism in children

    This study is trying to see how blood flow and metabolism in the brain affect development in children, especially those with sickle cell disease and stroke, by using advanced MRI techniques.

    Recruiting Washington University School of Medicine · St Louis, Missouri · NCT04157179

  • Registry connecting stroke survivors with research opportunities

    This study connects stroke survivors with research opportunities to help find new treatments that can improve their recovery.

    Recruiting University of California, San Francisco · San Francisco, California · NCT03318432

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.