â??Effectiveness of Graded Motor Imagery (GMI) on upper limb motor function in patients with subacute stroke â??

Phase 1

Completed

• Conditions: Health Condition 1: I633- Cerebral infarction due to thrombosis of cerebral arteries

• Registration Number: CTRI/2019/01/016966
• Lead Sponsor: Soumya S

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2020-03-19
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 151

Inclusion Criteria

1.Patients between 4 weeks and within 12 months post stroke

2. Patients with first episode of ischemic or hemorrhagic unilateral stroke

3. Patients residing in selected community area registered under pain and palliative society

4. Patients aged between 31- 70.

5. Patients with subacute stroke exhibiting stable, residual motor deficits in their affected limbs

6. Patients with right or left arm paresis

7. Patient with ability to imitate action with their ipsilateral arm

8. Subjects who are able to respond to verbal instructions

9. Patients with MIQ-RS score with ability to do motor imagery

10. Able to sit independently for >30 minutes

11. Patients who had no previous exposure to mirror therapy

Exclusion Criteria

1. Patients with cognitive deficits (Minimental status examination < 24)

2. Patient with co-morbidities, with apraxia or aphasia

3. Patients with other neurological or orthopedic disorders affecting upper extremity motor function

4. Individuals with any musculoskeletal disorders, visual impairment, systemic disease and neurological disorder other than stroke.

5. Non co-operative patients and suffering from psychological problems.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
PPER LIMB MOTOR FUNCTIONTimepoint: UPPER LIMB MOTOR FUNCTION assessed on before intervention, AT 2 WEEKS, AT 4 WEEKS (AFTER INTERVENTION)AND AT 6 WEEKS(FOLLOW UP)

Secondary Outcome Measures

Name	Time	Method
DEPRESSION <br/ ><br>QUALITY OF LIFE <br/ ><br>VISUOSPATIAL NEGLECT <br/ ><br>BODY IMAGETimepoint: BEFORE INTERVENTION, AT 2 WEEKS, AT 4 WEEKS(AFTER INTERVENTION), AT 6 WEEKS( FOLLOW UP)