Health Condition 1: I639- Cerebral infarction, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: To be included for participation in this study process, individuals must (1) possess a verified diagnosis of unilateral ischemic stroke by either CT or magnetic resonance imaging, (2) exhibit stable vital signs and normal levels of consciousness, (3) demonstrate a Brunnstrom recovery stage 1 to 4 for the functionality of the affected upper limb 20, (4) 2-4 months after stroke onset, (5) must give consent to attend in the study.
Exclusion criteria
Exclusion criteria: Subjects will be accounted as disqualified if they (1) have a prior medical history of stroke, including both reversible and hemorrhagic strokes (2) experience severe cognitive impairment, speech or communication difficulties (3) are diagnosed with mental health disorders, (4) implanted cardiac pacemaker, (5) unable to receive treatment for the specific time frame.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hand pain and function - NPRS, Modified Fugl-Meyer Assessment Upper Extremity (FMA-UE)Timepoint: Baseline, After 4 weeks and 8 weeks of intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Manual dexterity and muscle tone - Modified Ashworth Scale, The Box and Blocks Test (BBT)Timepoint: Baseline, After 4 weeks and 8 weeks of intervention | — |
Countries
Bangladesh
Contacts
Jashore University of Science and Technology (JUST), Jashore