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

A

Ahmed Alshimy

Status

Completed

Conditions

Hemiparesis

Treatments

Other: Dual task training in the form of cognitive - motor task
Other: Conventional physiotherapy rehabilitation program
Other: Modified Constraint Induced Movement therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06457022
P.T.REC/012/005007

Details and patient eligibility

About

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.

Full 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.

Enrollment

45 patients

Sex

All

Ages

55 to 65 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

45 participants in 3 patient groups

Group A
Experimental group
Description:
Receiving modified constraint induced movement therapy , for 30 minutes , in addition to conventional physiotherapy program for the other 30 minutes.
Treatment:
Other: Conventional physiotherapy rehabilitation program
Other: Modified Constraint Induced Movement therapy
Group B
Experimental group
Description:
Receiving dual task training (Cognitive-Motor) for 30 minutes, in addition to conventional physiotherapy program for the other 30 minutes.
Treatment:
Other: Conventional physiotherapy rehabilitation program
Other: Dual task training in the form of cognitive - motor task
Group C
Other group
Description:
Receiving only conventional physiotherapy program for 60 minutes.
Treatment:
Other: Conventional physiotherapy rehabilitation program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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