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Clinical Trials/NCT06457022
NCT06457022
Completed
Not Applicable

Outcome Measures of Modified Constraint Induced Movement Therapy Versus Dual Task Training on Upper Extremity and Cognitive Functions in Patients With Hemiparesis

Ahmed Alshimy1 site in 1 country45 target enrollmentJune 10, 2024
ConditionsHemiparesis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hemiparesis
Sponsor
Ahmed Alshimy
Enrollment
45
Locations
1
Primary Endpoint
Biodex isokinetic dynamometer
Status
Completed
Last Updated
last year

Overview

Brief Summary

All stroke patients were assessed via isokinetic dynamometer, Montreal cognitive assessment scale (MOCA) and Fugl Myer Upper extremity (FMUE) before and after the treatment program.

Detailed Description

The patients were classified randomly into three equal groups, Study group A (GA) receiving modified constraint induced movement therapy in addition to conventional physical therapy program, Study group B (GB) receiving dual task training in addition to conventional physical therapy program and control group C (GC) receiving only conventional physiotherapy program.

Registry
clinicaltrials.gov
Start Date
June 10, 2024
End Date
July 10, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
Ahmed Alshimy
Responsible Party
Sponsor Investigator
Principal Investigator

Ahmed Alshimy

Lecturer of Physical Therapy for Neurology and it's Surgery

AlRyada University for Science & Technology

Eligibility Criteria

Inclusion Criteria

  • Patients with age range between 55 and 65 years old.
  • The patients were from both genders (males \&females).
  • Patients were of duration of illness between 6 and 12 months.
  • The patients were scoring 1 \&1+ on modified Ashworth scale (mild spasticity).
  • The patients were of good ability to see and hear.
  • Consent form was obtained from all participants to approve the study and follow the commands.
  • All patients were scoring more than 26 on MMSE. All patients were medically stable.

Exclusion Criteria

  • patients with moderate and sever spasticity.
  • patients with cognitive disorder due to other cause rather than spasticity.
  • patients with unstable medical conditions.
  • patients with previous or recurrent stroke.
  • patients with respiratory problems.
  • patients with shoulder dislocation or subluxation or frozen shoulder.
  • patients with uncontrolled hypertension, diabetes mellitus, unstable angina or heart failure.

Outcomes

Primary Outcomes

Biodex isokinetic dynamometer

Time Frame: 4 weeks

Used to assess muscle strength and function

Montreal cognitive assessment

Time Frame: 4 weeks

a quick test that is used to examine mild cognitive impairment and early dementia.

Fugl Myer upper extremity

Time Frame: 4 weeks

a scale used to measure the functional impairment of stroke

Study Sites (1)

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