Effect of Constraint-Induced Movement Therapy Combined with Neuromuscular Electrical Stimulation on Upper Extremity Function in Chronic Stroke Survivors

Not Applicable

• Conditions: pper Extremity Dysfunction in Chronic Stroke Survivors; Upper Extremity Dysfunction in Chronic Stroke Survivors; Physical Medicine / Rehabilitation - Physiotherapy; Stroke - Haemorrhagic; Stroke - Ischaemic

• Registration Number: ACTRN12624000564550
• Lead Sponsor: niversiti Kebangsaan Malaysia (UKM)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-05-05
• Last Update Posted: 29 July 2024

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

1. Stroke survivors (ischemic or hemorrhagic), last subacute stroke (4-6) months; and chronic stroke more than 6 months post-onset.
2. A score of greater than or equal to 3 on the upper arm item of the Motor Assessment Scale (MAS).
3. A score of greater than or equal to 26 on the Montreal Cognitive Assessment (MoCA).
4. A grade of less than or equal to 2 on the Modified Ashworth Scale for upper extremity and lower extremity.
5. No history of upper extremity injuries.

Exclusion Criteria

1. A greater than or equal to 2 of sensory loss on the sensory item of the National Institutes of Health Stroke Scale (NIHSS).
2. Patients with pacemakers or tumors.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Perceived Motor Function[Motor Activity Log (MAL) At baseline and the end of the intervention (4 weeks post-commencement of the intervention),];Motor Impairment[Motor function subscale of the upper limb Fugl-Meyer (FM) assessment At baseline and the end of the intervention (4 weeks post-commencement of the intervention),];Motor Function[Wolf Motor Function Test (WMFT) At baseline and the end of the intervention (4 weeks post-commencement of the intervention),]

Secondary Outcome Measures

Name	Time	Method
Upper Limb Self-efficacy[Upper Limb Self-Efficacy Test (UPSET) At baseline and the end of the intervention (4 weeks post-commencement of the intervention),]