Actively Recruiting
Home Tele Rehabilitation Therapy for Vascular Dementia and Stroke Patients
Led by The Methodist Hospital Research Institute · Updated on 2026-03-02
120
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the feasibility and impact of home telerehabilitation therapy on caregiver burden in patients who have had a stroke more than six months ago, including those with and without vascular dementia. This controlled, evaluator-masked parallel study focuses on chronic ischemic or hemorrhagic stroke patients, aiming to compare remote rehabilitation therapy targeting the weaker arm to usual care. The study includes baseline assessments and follows a structured timeline to monitor therapy effects and safety. Participants will first continue their usual home rehabilitation care for one month. This is followed by four weeks of telerehabilitation therapy using a treatment application, where patients perform occupational therapist-prescribed hand and arm exercises for about 90 minutes per day with appropriate rest. Treatments are scheduled Monday through Friday and can be divided into multiple sessions to fit patient and caregiver preferences. Detailed records of motor tasks, repetitions, and performance levels will be maintained throughout the therapy period. Participants will undergo initial evaluations including questionnaires, functional and impairment scales, and brain imaging data collection. Demographic, medical history, stroke history, and medication information will be recorded from electronic medical records. Safety, comfort, and any adverse events will be monitored during all study visits. The primary outcomes measured include the Burden Scale for Family Caregivers and adverse events at three to four months, with secondary measures assessing upper extremity motor function. The entire study participation spans approximately four months with multiple follow-up evaluations.
CONDITIONS
Brief Title
Home Tele Rehabilitation Therapy for Vascular Dementia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Symptomatic ischemic or hemorrhagic stroke confirmed by CT or MRI
- Stroke occurred at least 6 months ago
- Some active movement in the affected upper arm, elbow, or wrist (MRS 1 or more)
- Ability to provide informed consent or have a legal representative provide consent
- Willingness of patient and at least one caregiver to comply with all study procedures and attend visits
- Age 18 years or older
- Ability to follow one-step commands
- Living in the community with transportation to evaluation sessions
- Ability to use the therapy system with minimal assistance and sufficient corrected vision
- Modified Ashworth Scale score 3 or less in the affected arm
- Passive range of motion within functional limits at shoulder, elbow, wrist, and hand
You will not qualify if you...
- History of severe alcohol or drug abuse, severe psychiatric illness, poor motivation, or severe language or cognitive deficits preventing study participation
- Bilateral paresis or weakness due to peripheral nerve or muscle injury
- Severe uncontrolled medical conditions making intensive rehabilitation unsafe or unfeasible
- Current participation in other experimental upper limb rehabilitation trials
- Non-English speakers without a translator for all sessions
- Pregnancy
- Prisoners
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) for screening and enrollment
Duration - 1 day
Participants undergo initial evaluation including questionnaires, impairment and functional scales, and medical record review.
1 baseline evaluation visit
Duration - 4 weeks
Participants perform conventional home rehabilitation exercises for the weaker arm as prescribed by an occupational therapist.
Home exercises Monday through Friday for 4 weeks
Duration - 4 weeks
Participants perform application-driven home telerehabilitation therapy with occupational therapist prescribed hand/arm exercises guided by a treatment app.
Treatment sessions Monday through Friday, approximately 1 hour 45 minutes each, with flexibility to split sessions
Duration - 1 day
Participants complete follow-up evaluations including functional assessments and questionnaires approximately 1 month after treatment ends.
1 follow-up evaluation visit
Trial Site Locations
Total: 1 location
1
Houston Methodist Hospital
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
D
Darrel W Cleere, MPH
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SEQUENTIAL
Primary Purpose
TREATMENT
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here