Effects of Dynamic Compression Garments in Children With CP

NCT ID: NCT05592236

Last Updated: 2023-03-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-15

Study Completion Date

2023-12-15

Brief Summary

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In recent years, it is seen that dynamic compression garments are used to increase body stability and to provide tone regulation. Dynamic compression garments are used to apply pressure to specific muscles or muscle groups. Different studies have drawn attention to the effect of dynamic compression garments on postural control and proximal stability. Researchers observed that upper extremity functions and fine motor skills improved with the use of clothing, and they associated this with improved proximal stability. In light of this information, the aim of this study is; To investigate the effects of dynamic compression garments applied in addition to traditional treatment on posture, trunk control, and upper extremity functions during sitting in children with hemiparetic CP.

Detailed Description

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Cerebral palsy (CP) is a group of permanent neurodevelopmental disorders in the development of movement and posture, non-progressive, resulting in activity limitations, resulting from an injury to the developing brain. Children with CP who have problems in sensorimotor coordination due to decreased muscle strength and impaired sensory processing experience postural control problems. In hemiparetic CP, deterioration in the upper extremities affects children's daily living activities such as eating, dressing, undressing, combing hair, brushing teeth, self-care skills, functional independence, and quality of life. Since the trunk plays a very important role in postural control and extremity functions, providing trunk stability and thus effective use of the extremities is one of the important goals of physiotherapy.

Conditions

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Cerebral Palsy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Study group

Dynamic compression garments for 2 hours a day in addition to standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks

Group Type EXPERIMENTAL

Dynamic compression garments

Intervention Type OTHER

Dynamic compression garments for 2 hours a day in addition to standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks

Standard therapy

Intervention Type OTHER

Standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks

Control Group

Standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks

Group Type ACTIVE_COMPARATOR

Standard therapy

Intervention Type OTHER

Standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks

Interventions

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Dynamic compression garments

Dynamic compression garments for 2 hours a day in addition to standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks

Intervention Type OTHER

Standard therapy

Standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Being diagnosed with congenital spastic hemiparetic cerebral palsy,
2. To be between the ages of 4-18
3. To be at the level of I, II or III according to the Manual Ability Classification System
4. Having sufficient communication skills
5. The willingness of the family and the child to be included in the study

Exclusion Criteria

1. The family's refusal to participate in the study
2. Botulinum toxin application to the upper extremity or having undergone upper extremity surgery in the last 6 months
3. Having behavioral and communication problems that hinder the practices to be carried out within the scope of the study
4. Having an epileptic seizure
Minimum Eligible Age

4 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role lead

Responsible Party

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Ayse Zengin Alpozgen

Assist. Prof

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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004

Identifier Type: -

Identifier Source: org_study_id

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