Efficiency of Pulsed Electromagnetic Field & Neuromuscular Electrical Stimulation on Hemiplegic Shoulder Pai
Not Applicable
Completed
- Conditions
- Health Condition 1: I69- Sequelae of cerebrovascular disease
- Registration Number
- CTRI/2023/06/054354
- Lead Sponsor
- Guru Jambheshwar University of Science and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 62
Inclusion Criteria
1.Duration of stroke more than 6 months
2.Patient with unilateral hemiplegia
3.Score on Visual Analogue Scale (VAS) more than 4
4.Patient with 1-3 degree of spasticity according to Modified Ashworth Scale (MAS)
Exclusion Criteria
1.Had history of traumatic shoulder injury
2.Uncontrolled seizures
3.Severe arrhythmia
4.History of tuberculosis/ infection in the shoulder
5.Patient with severe spasm or contracture of upper limb
6.Severe cognitive impairment
7.Cardiac pacemaker
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analogue Scale (VAS) <br/ ><br>Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up)
- Secondary Outcome Measures
Name Time Method Active Range of Motion (AROM)Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up);Fugl-Meyer Assessment-Upper Extremity(FMA-UE) <br/ ><br>Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up);Modified Ashworth Scale(MAS)Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up);Passive Range of Motion(PROM)Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up)