Effects of Home-based Neurostimulation Associated With Motor Training in Chronic Stroke Patients
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Purpose
Objective: To investigate effects of home-based somatosensory stimulation associated with motor training on improvement in performance of the paretic upper extremity in patients in the chronic phase after stroke.
| Condition | Intervention | Phase |
|---|---|---|
|
Stroke |
Device: Relief band (Somatosensory stimulation) Device: Placebo stimulation |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Effects of Home-based Neurostimulation Associated With Motor Training in Chronic Stroke Patients |
- the improvement in upper extremity performance assessed using Jebsen-Taylor test [ Time Frame: Treatment lasted four weeks. Measures were performed before the treatment, immediately after the treatment and four months after the end of the treatment ] [ Designated as safety issue: Yes ]
- Compliance with the interventions, assessed through a daily written log, and oral reports of the patients [ Time Frame: immediately after the treatment ] [ Designated as safety issue: Yes ]
- Adverse events [ Time Frame: at end of treatment ] [ Designated as safety issue: Yes ]
| Enrollment: | 20 |
| Study Start Date: | December 2007 |
| Study Completion Date: | November 2009 |
| Primary Completion Date: | September 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Somatosensory stimulation
Active group
|
Device: Relief band (Somatosensory stimulation)
Electrical median nerve stimulation
Other Name: Relief band
|
|
Placebo Comparator: Control group
Placebo stimulation
|
Device: Placebo stimulation
Placebo stimulation
Other Name: no stimulation
|
Detailed Description:
Design: Double-blind, randomized, controlled clinical trial. Setting: Home-based rehabilitation. Subjects: Patients in the chronic phase (> 6 months) after stroke. Interventions: Patients will be randomized to an active and a control group. In both groups, treatments will be performed at home, daily, over four weeks. Patients in the active group will be instructed to use a device that provides somatosensory stimulation in the form of electrical stimulation of the median nerve for two hours. Patients in the control group will also be instructed to use the device for two hours, and sham stimulation will be administered. In both groups, patients will be instructed to train activities with the paretic hand immediately after nerve stimulation.
Main measures: The primary outcome will be improvement in performance of the paretic hand evaluated by the Jebsen-Taylor test at end of treatment and four months after end of treatment, compared to baseline. Secondary outcomes were: 1) Compliance with the interventions, assessed through a daily written log, and oral reports of the patients; 2) safety profile of the interventions.
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- age 18-80 years;
- single ischemic or hemorrhagic stroke in a cerebral hemisphere, documented by computed tomography (CT) or magnetic resonance imaging (MRI);
- stroke onset at least six months before;
- hand paresis with preserved ability to perform all tasks of the Jebsen-Taylor Test (JTT).
Exclusion Criteria:
- previous strokes;
- epilepsy and other neurological conditions;
- proprioceptive or tactile anesthesia;
- shoulder or hand pain;
- severe joint deformity;
- severe chronic disease;
- inability to give provide informed consent due to severe aphasia or cognitive impairment;
- left handedness before the stroke.
Contacts and Locations| Brazil | |
| University of São Paulo/General Hospital | |
| São Paulo, SP, Brazil, 55 | |
| Principal Investigator: | Adriana Conforto, MD PhD | Hospital das Clínicas/FMUSP |
More Information
No publications provided
| Responsible Party: | Adriana Bastos Conforto/ Staff neurologist, Hospital das Clinicas/University of Sao Paulo, Hospital das Clinicas/University of Sao Paulo |
| ClinicalTrials.gov Identifier: | NCT01034150 History of Changes |
| Other Study ID Numbers: | 1309-06, 477916/06-6 |
| Study First Received: | December 11, 2009 |
| Last Updated: | December 16, 2009 |
| Health Authority: | Brazil: Ethics Committee |
Additional relevant MeSH terms:
|
Stroke Cerebral Infarction Cerebrovascular Disorders Brain Diseases Central Nervous System Diseases |
Nervous System Diseases Vascular Diseases Cardiovascular Diseases Brain Infarction Brain Ischemia |
ClinicalTrials.gov processed this record on May 16, 2013