Home Tele Rehabilitation Therapy for Vascular Dementia
Part of paid clinical trials in Houston, Texas.
- Sponsor
- The Methodist Hospital Research Institute
- Study ID
- NCT06289569
- Status
- Recruiting
Conditions
- Dementia, Vascular
- Stroke Sequelae
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 110 Years
- Healthy Volunteers
- Not accepted
Interventions
- Home telerehabilitation therapy — OTHEROccupational therapist prescribed hand/arm exercises will be assigned to patients. Records of each subject's motor tasks, number of repetition and level of performance will be kept. Standard of care home therapy will be performed Monday-Friday for approximately 4 weeks, followed by 4 weeks of application-driven home teletherapy. It is expected that approximately 20 treatments will be finished in 4weeks, however the amount of therapy completed will be recorded to accommodate patients' schedules. Treatment times can be broken up into multiple treatment periods to accommodate patient and caregiver preferences.
Study Details
To determine whether the home telerehabilitation therapy is feasible and lessens caregiver burden in chronic stroke patients with and without vascular dementia (VaD)
Key Dates
- Start date
- Dec 14, 2024
- Status verified
- Feb 2026
- Primary completion
- Mar 14, 2028
- Completion
- Apr 1, 2028
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- NA
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Tele RehabilitationTelerehabilitation therapy Occupational therapist prescribed hand/arm exercises will continue for 90 minutes per day with adequate rest periods for 4 weeks, followed by telerehabilitation with the application for 4 weeks, when subjects will perform the tasks at home with the guidance of the treatment app. Detailed records of each subject's motor tasks, number of repetition and level of performance will be kept. Treatment will be performed Monday-Friday for approximately 4 weeks. Treatment times can be broken up into multiple treatment periods to accommodate patient and caregiver preferences.
Primary Outcome Measure
Burden Scale for Family Caregivers [ Time Frame: 3-4 months ]
Central Contacts
- Darrel W Cleere, MPH(713)-441-3770
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Houston Methodist Hospital | Houston | Texas | 77030 |
Find similar trials in Houston, TX
By research site
Related Studies
- Determinants of Incident Stroke Cognitive Outcomes and Vascular Effects on RecoverYRecruiting · Massachusetts General Hospital · Phoenix, Arizona
- The Diabetes Prevention Program Outcomes Study AD/ADRD ProjectEnrolling By Invitation · Marinella Temprosa · Phoenix, Arizona
- Imaging Post-Stroke Recovery: Using MEG to Evaluate CognitionRecruiting · Johns Hopkins University · Baltimore, Maryland
- TDCS to Improve Post-Stroke Cognitive ImpairmentRecruiting · Johns Hopkins University · Baltimore, Maryland