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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05570461
Other study ID # KMU/IPMR/MS/22
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 4, 2022
Est. completion date September 25, 2023

Study information

Verified date October 2022
Source NCS University System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This RCT will also help the clinicians to provide the best treatment to their patients for better outcomes. The objective of the study is to determine the efficacy of Modified Constraint-induced movement therapy on the Upper Limb function of Sub-acute stroke patients in Peshawar Pakistan. Alternative Hypothesis: There will be a difference in the means of Modified Constraint-induced movement therapyand traditional physical therapy on the upper limb function of subacute stroke patients.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 46
Est. completion date September 25, 2023
Est. primary completion date August 12, 2023
Accepts healthy volunteers No
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: - 1. Age 30 to 60 years - 2. Both female & male will be included. - 3. Cognitive and lingual ability to communicate with the research staff. - 4. A minimum of 10 degrees of active finger extension and 20 degrees of active wrist extension(16). - 5. A history of a single stroke resulting in a hemiparesis Exclusion Criteria: - 1. Recurrent stroke during the training period. - 2. Neurological or orthopedic disorders prohibiting the use of the paretic arm. - 3. Patients who doesn't show willingness to participate in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Modified Constraint-Induced Movement Therapy
Experimental group will receive Modified Constraint-Induced Movement Therapyand traditional physical therapy to the impaired upper limb based on the repetitive training of functional activities and behavioral shaping and a task-oriented approach, while the unaffected arm of subjects in the mCIMT group will be constrained by wearing a mitten during the treatment session and for 3 hours/day outside the therapy hours, 6(six) days/week for two weeks by an experienced Physical therapist.The time duration for Group A will be 40 minutes.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
NCS University System

Outcome

Type Measure Description Time frame Safety issue
Primary Wolf Motor function test Use mainly for post-stroke patients with impaired upper limb motor ability. The purpose of this test is to enumerate upper limb motor ability through a series of functional tasks. The WMFT is an instrument with high internal consistency, interrater reliability and test-retest reliability. The quality of movement during the task is measured by functional ability scale, a 6-point ordinal scale, where 0 = does not attempt with the impaired arm and 5 = arm movement appear to be normal.
Higher the value higher will be the normal function.
4weeks
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