A clinical interventional study to compare the efficacy of two combined non invasive brain stimulation as motor enhancement therapy for upper extremity in brain attack due to blocked blood vessel cases of more than six months.
Not Applicable
- Conditions
- Health Condition 1: I633- Cerebral infarction due to thrombosis of cerebral arteries
- Registration Number
- CTRI/2019/11/022009
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a)Age between 18year and 70year
b)Cases diagnosed as stroke by MRI/CT scan as non-recurrent chronic MCA ischemic stroke
c)Cases after six months of post stroke
d)Normal as per Montreal Cognitive Assessment
e)Brunnstrom 3-5 stages of recovery
R
Exclusion Criteria
a)Any contraindications for rTMS/tDCS intervention.
b)Any other associated neuropsychiatric disorder
c)Underwent any prior non-invasive brain stimulation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fugl-Meyer Assessment - Upper extremityTimepoint: Baseline, After 10 sessions of treatment, 12 weeks
- Secondary Outcome Measures
Name Time Method Modified Modified Ashworth Scale(MMAS), Somatosensory evoked potential(SSEP), Single Photon Emission Computed Tomography(SPECT), Modified Rankin Scale(mRS) and Stroke Specific Quality of Life Scale (SS-QOL)Timepoint: Baseline, After 10 sessions of treatment, 12 weeks