Effects of Dynamic Compression Garments in Children With CP
NCT ID: NCT05592236
Last Updated: 2023-03-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
34 participants
INTERVENTIONAL
2023-06-15
2023-12-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Kinesiologic Taping on Trunk Control and Balance in Children With Cerebral Palsy
NCT07188961
Kinesio Taping in Cerebral Palsy Upper Extremity Functionality
NCT04529486
Dynamic Orthotic Garment in Diplegic Cerebral Palsy
NCT05271149
Effects of Using Dynamic Elastomeric Fabric Orthoses
NCT04272398
Effect of Multidimensional Trunk Training in Children With Cerebral Palsy
NCT07034872
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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
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
Standard therapy
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
Standard therapy
Standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
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
Standard therapy
Standard therapy twice a week (1 session of 45 minutes) for a total of 6 weeks
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
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
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
4 Years
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Istanbul University - Cerrahpasa
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ayse Zengin Alpozgen
Assist. Prof
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
004
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.