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Comparison of Constraint Induced Movement Therapy and Mirror Therapy

R

Riphah International University

Status

Completed

Conditions

Hemiplegic Cerebral Palsy

Treatments

Other: Mirror therapy
Other: Constraint Induced Movement Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06294444
REC/RCR&AHS/23/0741

Details and patient eligibility

About

Hemiplegia in infants and children is a type of Cerebral Palsy that results from damage to the part (hemisphere) of the brain that controls muscle movements. This damage may occur before, during or shortly after birth. The term hemiplegia means that the paralysis is on one vertical half of the body. The aim of this study will be the to know the effect of mCIMT with and without mirror therapy on upper limb function in children with hemiplegic cerebral palsy. A randomized control trial will be conducted at Sheikh Zayed Hospital, RYK through convenience sampling technique on 30 patients which will be allocated through simple random sampling through sealed opaque enveloped into group A and group B. Group A will be treated with mCIMT and Group B will be treated with mCIMT and mirror therapy. Outcome measure will be conducted through pain and disability questionnaire after 6 weeks. Data will be analyzed using SPSS software version 21. After assessing normality of data by Shapiro - wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups. mCIMT with and without mirror therapy will be applied in patients with hemiplegic cerebral palsy to see the effect on upper limb function.

Full description

Patients who will meet the inclusion criteria will be recruited by convenience sampling technique and allocated to groups by simple randomization process by sealed opaque enveloped labeled as 0 for Group A and 1 for Group B.

After taking consent from the patients parents with hemiplegic CP of both genders will be randomized into two equal groups. Patients from physical therapy department will be assessed with CHEQ and Melbourne Assessment of the Unilateral Upper Limb Function (MAULF) and the Functional Hand Grip Test (FHGT) . At start of study, a formal educational session, lasting about 30 min will be given by physiotherapist.

Group A: This group patients will be treated with mCIMT, the forced use of the affected arm by restraining the unaffected arm, with a sling or a hand splint, during dedicated exercise sections or usual ADLs (90% of waking hours).Massed practice (eight hours of exercise) of the affected arm through a shaping method, where shaping involves a commonly operant conditioning method in which a behavioural objective (in this case 'movement') is approached in small steps of progressively increasing difficulty. The participant is rewarded with enthusiastic approval for improvement, but never blamed or punished for failure. This therapy will be given 4hrs daily for 6 weeks. The results will be based upon pre and post evaluation.

Group B: These patients will be treated with mCIMT and mirror therapy. Children were taught repetitive symmetrical upper limbs exercises: with modelling-clay in each hand to elicit bilateral thumb-finger pinch and grasping. They performed these during a 15-minute daily routine at home with mCIMT (forced use of arm and massed practice 4hrs of exercise of affected arm). This combination of therapy will be given for 6 weeks. The results will be seen through pre and post evaluation.

Enrollment

30 patients

Sex

All

Ages

6 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Medically diagnosed with Hemiplegic CP
  • Age ranges btween3-12 years
  • Hemiplegic CP with motor disability
  • No major contractures of upper limb muscle
  • Both genders were included
  • Able to follow command
  • No orthopedic surgery during the previous six months(8)

Exclusion criteria

  • Functional limb
  • Patients with contracture
  • Patient with sensory,cognitive and perceptual disorders
  • Patient with seizures
  • Patient with orthopedic surgery

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Constraint induced Movement Therapy
Experimental group
Description:
Group of 15 members will be given constraint induced movement therapy for 6 weeks.
Treatment:
Other: Constraint Induced Movement Therapy
Mirror therapy group
Experimental group
Description:
Group of 15 members will be given modified constraint induced movement therapy with mirror theray for 6 weeks.
Treatment:
Other: Mirror therapy

Trial contacts and locations

2

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Central trial contact

Muhammad Asif Javed, MS; Imran Amjad, PhD

Data sourced from clinicaltrials.gov

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