- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04813393
Compliance of Parents of Children With Cerebral Palsy to Home Program Questionnaire (CoPoCPHP)
March 24, 2021 updated by: Mintaze Kerem Gunel, Hacettepe University
Psychometric Properties of Compliance of Parents of Children With Cerebral Palsy to Home Program Questionnaire
This study aims to evaluate the psychometric properties of the Compliance of Parents of Children with Cerebral Palsy to Home Program Assesment Questionnaire (CPHP-Q), a caregiver-report for adherence and frequency of home program implementation of parents of children with Cerebral Palsy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
225
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ankara, Turkey
- Hacettepe University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
2 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Participants in the current study were parents of chlidren with 2 to 18 years and recruited at Hecettepe Univercity Physical Therapy and Rehabilitation Faculty Cerebral Palsy and Pediatric Rehabilitation Unit.
Description
Inclusion Criteria:
- having a child with CP 2 to 18 years,
- being a primary caregiver,
- understanding of Turkish without an interpreter, and Turkish literacy,
Exclusion Criteria:
- having any chronic illness or disability to prevent the home program,
- haven't applied home program before.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Family-Based
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Compliance of Parents of Children with Cerebral Palsy to Home Program Assesment Questionnaire Group
The CPHP-Q was administered as a caregiver-report questionnaire.
It aims to measure home program adherence of parents of children with CP.
Parents applied this instrument in the study.
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To evaluate psychometric the properties of the Compliance of Parents of Children with Cerebral Palsy to Home Program Assesment Questionnaire (CPHP-Q), a caregiver-report for adherence and frequency of home program implementation of parents of children with Cerebral Palsy.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compliance of Parents of Children with Cerebral Palsy to Home Program Assesment Questionnaire (CPHP-Q)
Time Frame: At baseline
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The CPHP-Q was administered as a caregiver-report questionnaire.
It aims to measure home program adherence of parents of children with CP.
İt consist of 22 items.
The highest score 110, the lowest score 22.
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At baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Assessment of Life Habits for Children questionnaire (LIFE-H)
Time Frame: At baseline
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The questionnaire was designed and validated to assess the social participation of children with disabilities.
It consists of 11 category: nutrition, physical fitness, personal care, mobility, interpersonal communication, social roles, education, recreational activities, responsibilities, housing, and social life.
Each Life-H item is ranked on a 0 to 9 scale for accomplishment, where a score of 0 represents "not accomplished" and a score of 9 equals "no difficulty and no assistance."
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At baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Mutlu Hayran, PhD, Hacettepe Univercity
- Study Chair: Meltem Şengelen, PhD, Hacettepe Univercity
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2020
Primary Completion (Actual)
September 1, 2020
Study Completion (Actual)
September 10, 2020
Study Registration Dates
First Submitted
March 21, 2021
First Submitted That Met QC Criteria
March 21, 2021
First Posted (Actual)
March 24, 2021
Study Record Updates
Last Update Posted (Actual)
March 29, 2021
Last Update Submitted That Met QC Criteria
March 24, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO: 20/357
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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