intenSive UpPer Extremity Recovery Program for Chronic Stroke (SUPER)
Purpose
The purpose of this study is to Investigate the feasibility of a high-quality, high-dose, high-intensity upper extremity therapy program and to assess the treatment effects of a high-quality, high-dose, high-intensity upper extremity therapy program on functional outcomes, motor impairment, and quality of life
Condition
- Chronic Stroke
Eligibility
- Eligible Ages
- Between 18 Years and 80 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Single qualifying stroke event as confirmed by CT or MRI - At least 6 months post stroke - Fugl-Meyer upper extremity (UE) score of 20-45 - Able to follow written instructions - Able to tolerate 6 hours of therapy a day
Exclusion Criteria
- Prior arm injury impacting available passive or active range of motion or significant arm pain with movement - Active drug or alcohol abuse - Diagnosed with advanced dementia - Pre-stroke baseline mRS>3 - History of clinically significant ischemic or hemorrhagic stroke resulting in prior arm weakness in the same territory as the index stroke - Medical instability assessed by the treating stroke physician to participate to the study.
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
Experimental Treatment |
|
Recruiting Locations
The University of Texas Health Science Center at Houston
Houston, Texas 77030
Houston, Texas 77030
More Details
- Status
- Recruiting
- Sponsor
- The University of Texas Health Science Center, Houston