- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04716530
The Changing Panorama in Risk Factors of Cerebral Palsy
The Changing Panorama in Risk Factors of Cerebral Palsy: A Single National Tertiary Center Experience
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study will be carried of scanning the database of 296 individuals with cerebral palsy followed in the university pediatric rehabilitation clinic. Cerebral palsy risk factors and demographic information will be obtained from the database.
Cerebral palsy subtypes classified according to The Surveillance for Cerebral Palsy in Europe (SCPE) classification into four groups: spastic (unilateral and bilateral), dyskinetic (dystonic and choreoathetoic), ataxic/hypotonic, non-classifiable. Cerebral palsy risk factors will be primarily divided into 4 as preconceptional, antenatal, intrapartum and neonatal risk factors. Then, risk factors in the data will be distributed to the appropriate risk factor group.
The data will be classified according to date of birth, divided into 3 groups: those born before 2000, those born between 2000-2010, and those born after 2010. Changes in cerebral palsy risk factors will be investigated at 10-year intervals.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Istanbul, Turkey, 34732
- Recruiting
- Istanbul Medeniyet University Faculty of Medicine, Physical Medicine and Rehabilitation Department
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Sub-Investigator:
- Afitap Icagasioglu, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- cerebral palsy patients
Exclusion Criteria:
- missing data on the cerebral palsy database
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
born before 2000
No patient treatment is associated with the study.
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No intervention is associated with the study.
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born between 2000-2010
No patient treatment is associated with the study.
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No intervention is associated with the study.
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born after 2010
No patient treatment is associated with the study.
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No intervention is associated with the study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Define the risk factors of cerebral palsy
Time Frame: 1 month
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Risk factors of cerebral palsy questioned as preconceptional, antenatal, intrapartum and neonatal.
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1 month
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Define the change in the risk factors among age groups
Time Frame: 1 month
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The difference in cerebral palsy risk factors in age groups measured by chi-square statistics (born before 2000/ born between 2000-2010/ born after 2010)
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1 month
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Istanbul MU CP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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