CClinicalTrials.gg
Status unknownNCT05592236Updated Mar 21, 2023

Effects of Dynamic Compression Garments in Children With CP

An interventional study of Dynamic compression garments and Standard therapy in Cerebral Palsy, sponsored by Istanbul University - Cerrahpasa. Status unknown. Open to participants aged 4 Years to 18 Years. Per ClinicalTrials.gov, last updated 2023-03-21.

Sponsored by Istanbul University - Cerrahpasa · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
4 Years to 18 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

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Conditions studied

  • Cerebral Palsy

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Keywords

  • cerebral palsy
  • dynamic compression
  • postural control
  • trunk control
  • upper extremity function
03

In context

Cerebral Palsy

1,853 studies on the registry are indexed under Cerebral Palsy; 435 are open to participants now.

This study's planned enrollment of 34 is close to the median of 33 across 1,368 interventional studies indexed under Cerebral Palsy.

Browse Cerebral Palsy studies →

Lead sponsor

Istanbul University - Cerrahpasa is the lead sponsor of 680 studies on the registry; 208 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
4 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
34 participants (estimated)

Study arms

  • Experimental
    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

    Other: Dynamic compression garments · Other: Standard therapy

  • Active comparator
    Control Group

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

    Other: Standard therapy

Interventions

  • OtherDynamic 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

  • OtherStandard therapy

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

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What researchers measure

Primary outcomes

  1. Manual Ability Classification System

    Individuals' manual dexterity will be classified according to Manual Ability Classification System before treatment. Manual Ability Classification System is a 5-level classification system developed to classify how children with cerebral palsy aged 4-18 use their hands while holding objects during activities of daily living.

    Time frame: 8 weeks

  2. Sitting Assessment Scale

    It is a standard video-based observation tool designed for the assessment of sitting in children with cerebra palsy. The scale consists of five items: head control, trunk control, foot control, arm functions and hand functions and is evaluated as follows: 1= none; 2= weak; 3= reasonable; 4 = good. Minimum and maximum scores range from 5 to 20.

    Time frame: 8 weeks

  3. The Trunk Control Measurement Scale

    The Trunk Control Measurement Scale measures two key components of trunk control during functional activities. For this reason, the scale consists of two parts: Static Sitting Balance and Dynamic Sitting Balance. The scale consists of 15 items in total. While the total score of the scale varies between 0-58 points, higher scores indicate a better performance.

    Time frame: 8 weeks

  4. Quality of Upper Extremity Skills Test

    It is a test that evaluates the quality of movement and manual skills of children with cerebral palsy. It deals with how the child does the activity. It consists of 7 parts. The evaluator scores the test by observing how the child performs the desired movements. The increase in the score obtained from the test indicates the increase in the quality of upper extremity skills.

    Time frame: 8 weeks

  5. ABILHAND-Kids: a measure of manual ability

    ABILHAND-Kids is a 21-item scale that evaluates bilateral hand use in activities of daily living in children with cerebral palsy. Each sub-item evaluates the difficulty level of children while performing the activity at three levels as impossible, difficult and easy.

    Time frame: 8 weeks

  6. Shriners Hospital Upper Extremity Evaluation

    It is an upper extremity movement and function assessment tool based on video observation for children aged 3-18 years. It consists of 3 sub-sections: positional dynamic analysis, spontaneous functional analysis and catch-release function.

    Time frame: 8 weeks

  7. The Pediatric Evaluation of Disability Inventory

    It is a scale used to evaluate changes in performance, functional skills and functional skills in children. It consists of 3 subsections. These; "Functional skills", "Caregiver level of help" and "Adaptations". Each division consists of the areas of self-care, mobility and social function. Functional skills subsection will be used in accordance with the purpose of our study.

    Time frame: 8 weeks

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 21, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05592236
Lead sponsor
Istanbul University - Cerrahpasa
Responsible party
Ayse Zengin Alpozgen (Assist. Prof, Istanbul University - Cerrahpasa) — Principal investigator
First posted
Oct 24, 2022
Start date
Jun 15, 2023 (estimated)
Primary completion
Nov 15, 2023 (estimated)
Completion
Dec 15, 2023 (estimated)
Last update
Mar 21, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2023. You cannot join it, but the record below documents what was studied.

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