CompARing Long terM Outcomes in Chronic Stroke Survivors Across Investigational Assessments Following a Prescribed Upper Extremity Exercise Program
Purpose
The purpose of the study is to compare assessments of arm function following a standard exercise program in chronic stroke patients.
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 1 month post stroke - Score of at least 2-/5 on Manual Muscle Test for wrist flexors or extensors, indicating adequate movement to complete robotic device use - Able to follow written instructions
Exclusion Criteria
- Prior arm injury impacting available passive or active range of motion or significant arm pain with movement - Underlying brain pathologies such as metastatic or primary brain malignancies, comorbid multiple sclerosis, etc. - Prior significant drug or alcohol abuse - Diagnosed with dementia - Pre-stroke baseline modified Rankin Scale (mRS) >3 - History of seizure/epilepsy - History of clinically significant ischemic or hemorrhagic stroke prior to index stroke resulting in prior arm injury or weakness. - Pregnancy - Contraindication to MRI or Transcranial Magnetic Stimulation (TMS). - 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 ARM-program |
|
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