Patient Targeted Upper Extremity Rehabilitation After Stroke
Completed · Not applicable
Conditions studied: Stroke
In brief
Each year in the US, approximately 795,000 people have a stroke, and the overwhelming majority of those who survive are unable to resume meaningful daily activities because of impaired movement in one arm/hand. This study will investigate the effects of a challenging 4-week physical rehabilitation therapy program that is targeted at specific movement impairments and systematically progressed to assure an ongoing "just right" level of rigor. The investigators anticipate that therapy targeted to address specific movement impairments will improve recovery of arm/hand movement in people who have had a stroke.
Key facts
- Study ID
- NCT01819506
- Run by
- VA Office of Research and Development
- People needed
- 103
- Starts
- 2013-03-01
- Expected to finish
- 2017-03-31
- Last updated by the study team
- 2019-08-08
Who can join
Age: 18 and older, up to 89. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Individuals are eligible for this study if they have:
- experienced a stroke at least 3 months prior that has resulted in unilateral hemiparesis.
- exhibit voluntarily paretic arm shoulder flexion 30 degrees with simultaneous elbow extension 20 degrees.
- impairment with overhead reach and wrist circumduction and fine motor dexterity.
- passive range of motion in affected shoulder, elbow and wrist within 20 degrees of normal values.
You may not qualify if…
- Individuals are not eligible for this study if they have:
- a lesion in the brainstem or cerebellum.
- another neurological disease that may impair motor skills (e.g., Parkinson's Disease).
- pain in the affected upper extremity that would limit participation in the study intervention.
- difficulty understanding and following 3-step directions.
- difficulty sitting independently without postural support.
- an orthopedic condition or impaired corrected vision that alters the kinematics of reaching.
- are unable to travel to and remain in Charleston SC for the duration of the 4-week study.
Where it is running
- Ralph H. Johnson VA Medical Center, Charleston, SC — Charleston, South Carolina, United States
Full record on ClinicalTrials.gov
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