RBR-83pwm3
Recruiting
未知
The effect of the aerobic exercise associated to the constraint-induced movement therapy in chronic hemiparetic individuals: a randomized clinical trial
niversidade Federal de São Carlos0 sitesMay 7, 2018
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Chronic hemiparetic individuals post Stroke
- Sponsor
- niversidade Federal de São Carlos
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Chronic Hemiparetic individuals (more than 6 months) what the vascular accident involved the same hemisphere with lesions restricted to the middle and anterior vascular, report of the imaging test; 18 and 80 years; present a minimum active movement of 45° of shoulder flexion and abduction, 20° of elbow extension, 10° of wrist extension, 10° of abduction or extension of the thumb, and 10° extension in at least two fingers (metacarpophalangeal and interphalangeal joints) and thumb; present asymmetry in the use of the upper limbs with score 2\.5 in the Motor Activity Log (MAL) Quantity Scale; ability to remain in a seated position without support for the trunk and/or of the arms for one minute
Exclusion Criteria
- •Individuals with cognitive deficits; smokers; alcohol; users of illicit drugs; with structural abnormalities in the cardiovascular and respiratory systems, uncorrected auditory and visual deficits, abnormalities on the electrocardiogram such as ischemic changes, arrhythmias, conduction disorders at rest and/or during the clinical exercise test; diseases or osteomiarticular alterations that affect the data collection or generate pain during the activities; obese (Body Mass Index more than 28 kg/ m2\); diabetes mellitus and uncontrolled hypertension; comprehension aphasia; apraxia; stroke bilateral or acute or subacute stroke (less than 6 months) or transient vascular accident and other the central and peripheral nervous system diseases; who are participating in other experimental or rehabilitation studies; who have had botulinum toxin application in the last three months prior to evaluation will be not included
Outcomes
Primary Outcomes
Not specified
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