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| Sponsored by: |
Department of Veterans Affairs |
| Information provided by: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT00013481 |
Purpose
This study will determine whether a therapeutic exercise program for improving motor coordination in locomotor tasks in post-stroke, hemiparesis patients will result in CNS recovery. The study will develop relationships between the improved motor performance and motor coordination during the locomotor task and the functional effects of the exercise program(e.g., gait variables.)
| Condition | Intervention | Phase |
|
Stroke |
Procedure: Stroke Rehabilitation |
Phase II |
| MedlinePlus related topics: | Rehabilitation |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study |
| Official Title: | Coordination of Hemiparetic Movement After Post-Stroke Rehabilitation |
| Estimated Enrollment: | 70 |
| Study Start Date: | January 2000 |
| Estimated Study Completion Date: | December 2002 |
Primary objective of this study is to determine whether a therapeutic exercise program which targets the functional recovery of persons with the post-stroke hemiparesis results in CNS recovery (improved motor coordination). They will determine whether motor coordination during a locomotor task is improved after an exercise program. They will then develop relationships between the improved motor performance and motor coordination during the locomotor task and the functional effects of the exercise program(e.g., gait variables) Overall goal is to develop a more rational basis for the design of stroke rehabilitation programs which target individuals most likely to recover and which are based on physiological principles. This study will supplement an NIH funded randomized clinical trial to evaluate a post-stroke exercise program designed to increase balance, strength, and endurance. Study will include 60-70 prospective patients enrolled in the randomized clinical trial at Kansas University Center on Aging. between Oct 1999 and Oct 2001.
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Functionally impaired elderly
Contacts and Locations| United States, Kansas | |||||
| VAMC, Kansas City | |||||
| Kansas City, Kansas, United States | |||||
| Investigator: | John Fryer, Ph.D., Asst. Director | Department of Veterans Affairs, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service |
| Investigator: | Victoria Mongiardo, Program Analyst | Department of Veterans Affairs, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service |
More Information
| Study ID Numbers: | E2116 |
| First Received: | March 14, 2001 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00013481 |
| Health Authority: | United States: Federal Government |
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