Effects of Constraints Induced Movement Therapy Versus Mirror Therapy in Children With Hemiplegic Cerebral Palsy

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05659355
Collaborator
(none)
18
1
2
13
1.4

Study Details

Study Description

Brief Summary

The aim of this study is to find Effects of constraints induced movement therapy (CIMT) versus mirror therapy (MT) on hand dexterity and grip strength in children with hemiplegic cerebral palsy.

Condition or Disease Intervention/Treatment Phase
  • Other: Constraint Induced Movement Therapy (CIMT)
  • Other: Mirror Therapy (MT)
N/A

Detailed Description

Although quite number of research has been done on effects of CIMT and mirror therapy but most of the studies included stroke population. There was no literature on comparative effect of both CIMT and Mirror therapy in children with hemiplegic cerebral palsy. This study will be covering specifically cerebral palsy children to have better treatment techniques to be introduced in therapeutic programs of hemiplegic cerebral palsy children.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
18 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Constraints Induced Movement Therapy Versus Mirror Therapy on Hand Dexterity and Grip Strength in Children With Hemiplegic Cerebral Palsy
Actual Study Start Date :
Jan 15, 2022
Anticipated Primary Completion Date :
Feb 1, 2023
Anticipated Study Completion Date :
Feb 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment Group

Constraint Induced Movement Therapy

Other: Constraint Induced Movement Therapy (CIMT)
I will apply CIMT on effected hand to observe the hand dexterity and grip strength
Other Names:
  • CIMT
  • Experimental: Control Group

    Mirror Therapy

    Other: Mirror Therapy (MT)
    I will apply Mirror Therapy on effected hand to obeserve the hand dexterity and grip strength

    Outcome Measures

    Primary Outcome Measures

    1. 9 Hole pegboard test: [3 months]

      The 9 hole peg test is a standardized quantitative assessment used to measure finger dexterity in patients with various neurological diagnosis.

    2. Haptic (Tactile) Recognition Test: [3 months]

      it's a quantitative measure of haptic (tactile) object recognition design to test one's ability to recognize everyday objects across seven sensory attributes using 14 sets of objects. Haptic recognition of everyday objects is quite fast and highly accurate with 96% correctly named: 68% in less than 3 s and 94% within 5 sec.

    3. Hand Dynamometer: [3 months]

      Hand Dynamometer: Hand dynamometer is an evaluation tool that is used to measure isometric grip force. . Once the grip position is adjusted, the user holds the handle and squeezes the handle

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    9 Years to 14 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Children of age range 9-14 year

    • Children with diagnosed hemiplegic cerebral palsy

    • Children who can perform active extension of affected wrist and more than

    • two fingers at an angle of more than 10 degrees

    • Active abduction of affected thumb at an angle of 10 degrees

    • Children who can respond to simple communication-

    Exclusion Criteria:
    • Children with uncontrolled seizures

    • Botulinum toxin injections or orthopedic surgery in the upper or lower

    • extremities within the previous 12 months or planned within the study period

    • Children with depression who were unable to cooperate in treatment

    • Children who are unable to perform active task training

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mobility Quest Lahore Punjab Pakistan 54000

    Sponsors and Collaborators

    • Riphah International University

    Investigators

    • Principal Investigator: Shabana Ashraf, Riphah International University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Riphah International University
    ClinicalTrials.gov Identifier:
    NCT05659355
    Other Study ID Numbers:
    • REC/RCR&AHS/22/0730
    First Posted:
    Dec 21, 2022
    Last Update Posted:
    Jan 5, 2023
    Last Verified:
    Jan 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Riphah International University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 5, 2023