Upper Extremity Selective Voluntary Motor Control in Children With Unilateral Cerebral Palsy
NCT ID: NCT03504787
Last Updated: 2018-04-20
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.
COMPLETED
24 participants
OBSERVATIONAL
2017-04-25
2018-03-25
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 Relationship Between Upper Extremity Functionality, Trunk Control and Balance in Children With Cerebral Palsy
NCT06378723
Effects of Trunk-Focused Rehabilitation on Spinal Mobility, Trunk Control, and Hand Functions in Cerebral Palsy
NCT06781047
Investigation of the Relationship Between Lower and Upper Extremity Selective Motor Control and Sensory Functions in Children With Spastic Cerebral Palsy
NCT05696535
Investigation of the Effect of Constraint Induced Movement Therapy Applied to the Lower Extremity on Lower Extremity Functions in Individuals With Unilateral Cerebral Palsy
NCT06753812
Upper Extremity Function In Cerebral Palsy And Its Association With Balance And Trunk Control
NCT03179124
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.
OTHER
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age between 5 and 18 years,
* ability to follow simple instructions.
Exclusion Criteria
* orthopedic intervention or botulinum toxin injection to the upper extremities in the last 6 months
* orthopedic problems or medical conditions that prevented children from participating in the assessment
6 Years
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Gazi University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ayse Simsek
Research assistant
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Bulent Elbasan
Role: STUDY_CHAIR
Gazi University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Gazı University
Ankara, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
77082166-302.08.01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.