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investigation of electrical stimulation induced changes in nerves and muscles in individuals with post stroke paralysis

Not yet recruiting
Conditions
Hemiplegia, unspecified,
Registration Number
CTRI/2024/02/062279
Lead Sponsor
PDUNIPPD
Brief Summary

**the main purpose of our study is to examine the Functional Electrical Stimulation (FES) induced effects in the neuromuscular tissues (nerves and muscles); functional activities, muscle firing and spasticity in the post stroke hemiparetic individuals. The second purpose of our study is to correlate the FES induced effects in the neuromuscular tissues with the functional activities, muscle firing and spasticity in the upper extremity of post stroke hemiparetic individuals.**

**Alternate:**Functional Electrical Stimulation Produces Significant effects in Neuromuscular tissues and Functional Activities in post stroke hemiparetic individuals

**Null Hypothesis:** There is no significant effect of Functional Electrical Stimulation in

Neuromuscular tissues and Functional Activities in post stroke hemiparetic individuals

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
57
Inclusion Criteria
  • Ipsilateral Hemiparesis following stroke either ischemic or hemorrhagic Three months to one year of the stroke.
  • Hemiparesis having grade 1+ to 3 on Modified Ashworth Scale of Biceps Brachi, wrist flexors and finger flexors Individuals of the both the gender age group between 40 years and 60 years Both male and females Individual willing to participate voluntarily in the study.
Exclusion Criteria
  • Bilateral Hemiparesis Hemiparesis following reason or caused other than stroke such as head injury, multiple sclerosis.
  • Any previous history of stroke History of Brain or spinal cord tumor, injury or surgery Stroke patients having other co morbidities such as Alzemer,s disease, Parkinson’s disease, and dementia that preclude their participation in the study.
  • Participants having severre spasticity and contracture in the elbow, hand and fingers.
  • Individual with uncontrolled hypertension Individual with any systemic illness Individual with hypersensitivity or hypersensitivity disorders and Participants not able to follow the instructions and having difficulty in comprehension.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ELECTROMYOGRAPHY AND NERVE CONDUCTION VELOCITY STUDIESFirst outcome baseline assessment will be done at first visit before starting the intervention. | Second outcome assessment will be done at the end of fourth week of the study
Secondary Outcome Measures
NameTimeMethod
Fugal-Meyer Upper Extremity functional scale and modified Ashworth scalefour weeks

Trial Locations

Locations (1)

Pandit Deendayal Upadhyaya National Institute for the Persons with Physical Disabilities

🇮🇳

Delhi, DELHI, India

Pandit Deendayal Upadhyaya National Institute for the Persons with Physical Disabilities
🇮🇳Delhi, DELHI, India
ROSHAN LAL MEENA
Principal investigator
9811368079
roshan7leo@yahoo.com

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