NCT05625438Recruiting
Telerehabilitation Early After Stroke
Bedside Telerehabilitation Early After Stroke
Source: ClinicalTrials.gov · Last updated 6 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The goal of this clinical trial is to assess the safety and feasibility of providing extra doses of rehabilitation therapy for persons with a recent stroke. The therapy treatment targets to improve arm function by introducing telerehabilitation to the bedside of participants during the inpatient rehab admission period. Participants will use a newly developed functional training system (HandyMotion) to access therapy treatment program directly from their hospital room. HandyMotion is a sensor-based training system that can connect to the TV set in the hospital room, enabling patients to access their therapy training program to practice rehab-oriented games and exercises ad libitum, at any time of the day.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- First submitted
- 1 Nov 2022
- Start date
- 19 Dec 2022
- Primary completion date
- Dec 2025
- Lead sponsor
- TRCare, Inc.
- Diseases
- Stroke
- NCT number
- NCT05625438
What you commit to
- Study type: Interventional
- Planned participants: 20
- From 19 Dec 2022 to the primary completion date, Dec 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Shoulder pain that in the judgement of the study team is likely to substantially limit the amount of telerehabilitation therapy completed
Other illness
- A major, active, coexistent neurological or psychiatric disease that would limit study participation, e.g., advanced dementia
Other
- Expectation that patient's cognitive status will likely interfere substantially with playing assigned games or exercises
- Deficits in communication that interfere with reasonable study participation
- Lacking visual acuity, with or without corrective lens, of 20/50 or better in at least one eye
- Subject does not speak sufficient English to comply with study procedures
Who the study is looking for
- Age 18 years or older
- 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.
- 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.
- Possess enough arm movement to participate in therapy
- Informed consent signed by the subject
- Able to follow simple instructions
- Study participation is not likely to be significantly limited by agitated behavior
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Providence St. Jude Medical Center Coordinator of this site? Confirm its status | Fullerton | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.