Stroke Clinical Trial
Official title:
Skeletal Muscle Plasticity As An Indicator of Functional Performance Post-Stroke
| Verified date | February 2020 |
| Source | VA Office of Research and Development |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Hemiparesis, strictly defined as (muscular) weakness affecting one side of the body, is seen in three-quarters of individuals following stroke. Weakness in this population results from both neural and muscular factors which include, respectively, the ability to activate skeletal muscle as well as the force generating capacity of the muscle. The overall goal is to improve walking in persons post-stroke by training subjects with an intervention that specifically targets existing neural and muscular impairments, thereby facilitating locomotor recovery.
| Status | Completed |
| Enrollment | 56 |
| Est. completion date | May 31, 2019 |
| Est. primary completion date | September 29, 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 50 Years to 70 Years |
| Eligibility |
Inclusion Criteria: - age 50-70, - stroke within the past 6 to 24 months, - residual paresis in the lower extremity (Fugl-Meyer Lower Extremity motor score <34), - ability to walk without assistance and without an ankle foot orthotic (AFO) on the treadmill 30 seconds at speeds ranging from 0.3 - 0.8 m/s, and - provision of informed consent. - In addition, all subjects who meet criteria for the training portion must complete an exercise tolerance test and be cleared for participation by the study cardiologist. Exclusion Criteria: - Unable to ambulate at least 150 feet prior to stroke, or experienced intermittent claudication while walking; - rating on Modified Ashworth Scale 3 at the knee or ankle; - limited lower extremity range of motion of the knee (passive flexion Range of Motion [ROM] < 90); hip (inability to achieve neutral 0 hip extension); or ankle (inability to achieve 0 of active dorsiflexion); - history of congestive heart failure, unstable cardiac arrhythmias, hypertrophic cardiomyopathy, severe aortic stenosis, angina or dyspnea at rest or during activities of daily living (ADLs); - History of chronic obstructive pulmonary disease (COPD) or oxygen dependence; - Preexisting neurological disorders, dementia or previous stroke; - History of major head trauma; - Legal blindness or severe visual impairment; - history of significant psychiatric illness - Life expectancy <1 yr., - Severe arthritis or other problems that limit passive ROM; - post-stroke depression (PHQ-9 10), - History of deep vein thrombosis (DVT) or pulmonary embolism within 6 months; - Uncontrolled diabetes with recent diabetic coma, or frequent insulin reactions; - Severe hypertension with systolic >200 mmHg and diastolic >110 mmHg at rest; - Previous or current enrollment in a trial to enhance motor recovery; - Presence of non-magnetic resonance (MR) compatible implants, pregnancy or severe claustrophobia. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Ralph H. Johnson VA Medical Center, Charleston, SC | Charleston | South Carolina |
| Lead Sponsor | Collaborator |
|---|---|
| VA Office of Research and Development |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Gait Speed | The speed the subject chooses to walk when instructed to walk at their "comfortable speed" | 8 weeks | |
| Secondary | Muscle Strength | The strength of the paretic lower leg muscles will be measured by asking the participants to contract their muscles as forcefully as possible. Testing will be conducted on a specialized machine called an isokinetic dynamometer. This testing is designed to assess the ability to generate muscle power. Before testing the participants will be asked to perform 5 minutes of low intensity cycling. Strength testing will include movements at the hip, knee and ankle in both legs. | 8 weeks |
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