Effectiveness of Modified Constraint-Induced Movement Therapy Versus Mirror Therapy in Spastic Hemiplegic Cerebral Palsy Children
A Randomized Controlled Trial to Compare the Effectiveness of Modified Constraint-Induced Movement Therapy Versus Mirror Therapy on Grip Strength, Manual Dexterity, and Spasticity in Children With Spastic Hemiplegic Cerebral Palsy
1 other identifier
interventional
42
1 country
1
Brief Summary
This randomized controlled trial was conducted to compare the effectiveness of Modified Constraint-Induced Movement Therapy (MCIMT) and Mirror Therapy in improving upper limb function among children with spastic hemiplegic cerebral palsy. Upper limb dysfunction, including reduced grip strength, impaired manual dexterity, and increased spasticity, limits functional independence and participation in daily activities in these children. Although both interventions are widely used in pediatric rehabilitation, direct comparative evidence remains limited. A total of 42 children aged 5-9 years diagnosed with spastic hemiplegic cerebral palsy were recruited from Akbar Kare Institute and Comprehensive Physical Rehabilitation Center, Peshawar. Participants were selected through convenience sampling and randomly allocated into two equal groups using the sealed envelope method. Group A received Modified Constraint-Induced Movement Therapy, while Group B received Mirror Therapy. Both groups received treatment for 30 minutes per session, five sessions per week, for six consecutive weeks. Grip strength was assessed using the Hand-Held Dynamometer, manual dexterity using the Box and Block Test, and spasticity using the Modified Ashworth Scale. The findings of this study provide evidence regarding the comparative effectiveness of these two rehabilitation approaches and may assist clinicians in selecting the most appropriate intervention for improving upper limb function in children with spastic hemiplegic cerebral palsy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 3, 2026
CompletedFirst Submitted
Initial submission to the registry
July 31, 2026
CompletedFirst Posted
Study publicly available on registry
August 5, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
August 5, 2026
June 1, 2026
6 months
July 31, 2026
July 31, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Grip Strength
Instrument: Hand-Held Dynamometer
Assessment Time: Baseline and 6 Weeks
Secondary Outcomes (2)
Manual Dexterity
Assessment Time: Baseline and 6 Weeks
Spasticity
Assessment Time: Baseline and 6 Weeks
Study Arms (2)
Modified Constraint-Induced Movement Therapy (MCIMT)
EXPERIMENTALParticipants received MCIMT for 30 minutes per session, five sessions per week for six weeks, together with conventional physiotherapy.
Mirror Therapy
ACTIVE COMPARATORParticipants received Mirror Therapy for 30 minutes per session, five sessions per week for six weeks, together with conventional physiotherapy.
Interventions
Participants received MCIMT for 30 minutes per session, five sessions per week for six weeks, together with conventional physiotherapy.
Participants received Mirror Therapy for 30 minutes per session, five sessions per week for six weeks, together with conventional physiotherapy.
Eligibility Criteria
You may qualify if:
- Children aged 5-9 years.
- Male and female participants.
- Diagnosed with spastic hemiplegic cerebral palsy.
- Modified Ashworth Scale Grade 1 or 1+.
- Able to understand and follow verbal commands.
You may not qualify if:
- Severe fixed hand deformity.
- Cognitive impairment.
- Severe visual impairment.
- Uncontrolled seizures.
- Previous upper limb surgery.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ibadat International University
Islamabad, 4700, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant professor
Study Record Dates
First Submitted
July 31, 2026
First Posted
August 5, 2026
Study Start
March 3, 2026
Primary Completion (Estimated)
August 30, 2026
Study Completion (Estimated)
September 30, 2026
Last Updated
August 5, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share