Effects of Classic and Modified CIMT on Quality of Life of Children With Hemiplegic CP

Health Education Research Foundation (HERF)

Status: Completed

Conditions: Hemiplegic Cerebral Palsy

Treatments: Other: modified constraint induced movement therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT06021899

YIRS/007

Details and patient eligibility

About

The purpose of this research is to see the effect of classic constraint-induced movement therapy and its modified form on quality of life of children with hemiplegic cerebral palsy. Randomized controlled trials with 2-3 weeks follow-up. The sample size is 40. The subjects are divided in two groups, 20 subjects in classical CIMT group and 20 in modified CIMT group. Study duration is of 6 months. Sampling technique applied will be purposive non probability sampling technique. Only 4-12 years individual with hemiplegic cerebral palsy are included. Tools used in the study are Cerebral palsy (quality of life) and Kid Screen 27.

Full description

Both CCIMT and MCIMT are effective treatments to improve quality of life of children with CP. However conflicting evidence is present on which one of these is more effective and no final conclusion can be made to date. This study intends to add to the literature and contribute in reaching final conclusion about the superiority of either intervention. The purpose of this study was to see the psychosocial effect (quality of life) of CIMT and its modified form on HCP

Enrollment: 40 patients

Sex: All

Ages: 4 to 12 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 4 to 12 years CP with unilateral, bilateral or severely asymmetrical impairment Manual Ability Classification System(MACS) I, II or III Wrist extension capacity at least 20°; fingers with 10° of complete flexion Children able to follow Command

Exclusion criteria

• Children also having disabilities other than Cerebral palsy Contractures that significantly limit functional arm use. Children with MR

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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40 participants in 2 patient groups

Classic CIMT group

Active Comparator group

Description:

Total session of 6 hours a day, 5 days per week for 3 weeks to Classic CIMT groups will be given.

Treatment:

Other: modified constraint induced movement therapy

mCIMT group

Experimental group

Description:

Session of 6 hours a day, 5 session per week for first 2 weeks (CIMT), session of 2 hours a day, 5 days per week for last 1 week (BIT) to modified CIMT group will be given.

Treatment:

Other: modified constraint induced movement therapy