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NCT06289569Recruiting

Home Tele Rehabilitation Therapy for Vascular Dementia

Source: ClinicalTrials.gov · Last updated 2 Mar 2026

Brief summary (registry, in English)

To determine whether the home telerehabilitation therapy is feasible and lessens caregiver burden in chronic stroke patients with and without vascular dementia (VaD)

Status (registry)
Recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
21 Feb 2024
Start date
Dec 2024
Primary completion date
Mar 2028
Lead sponsor
The Methodist Hospital Research Institute
Diseases
Stroke
NCT number
NCT06289569

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From Dec 2024 to the primary completion date, Mar 2028
  • 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

  • Concurrent participation in other experimental upper extremity rehabilitation trials that would interfere with results.

Other illness

  • Patients with history of severe alcohol or drug abuse, psychiatric illnesses like severe depression, poor motivational capacity, or severe language disturbances, particularly of receptive nature or with serious cognitive deficits (defined as unable to follow study instructions even with help from caregiver).

Age

  • Patients with severe uncontrolled medical problems that would render intensive rehabilitation unfeasible or unsafe (e.g. cardiovascular disease, unstable cardiac arrhythmia, severe rheumatoid arthritis, active joint deformity of arthritic origin, active cancer or renal disease, any kind of end-stage pulmonary or cardiovascular disease, or a deteriorated condition due to age, epilepsy or others).

Other

  • Patients with bilateral paresis, or weakness or sensory damage due to peripheral causes (e.g. peripheral nerve injury, muscle or orthopedic injury etc.)
  • Non-English-speaking individuals will only be eligible if they can provide the appropriate translator for all the sessions of the study as no funding is available to pay for such services. However, we plan to include them once funding has been secured in the subsequent larger trial.
  • Pregnancy
  • Prisoners

Who the study is looking for

  • Symptomatic ischemic or hemorrhagic stroke verified by computerized axial tomography or magnetic resonance imaging
  • at least 6 months post stroke
  • At least some active movement in the affected upper extremity (MRS 1 or more in shoulder elbow or wrist)
  • Ability to provide informed consent, or LAR able to provide consent
  • Expressed willingness to comply with all study procedures and attend all study-related visits for both the patient and at least one caregiver.
  • Age ≥ 18.
  • Ability to follow one-step commands.
  • Community-dwelling with transportation to evaluation sessions.
  • Ability to operate the therapy system with minimal assistance, including sufficient corrected vision to perceive objects from a distance of 5 feet.
  • Modified Ashworth Scale Score 3 or less in the involved upper extremity
  • Passive range of motion within functional ranges at the shoulder, elbow, wrist and hand

Age in the registry: 18 years to 110 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Houston Methodist Hospital
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.