- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05213663
Investıgatıon Of The Awareness Of The Parents Of Cerebral Palsy Children (CP)
September 10, 2022 updated by: Hatice Adiguzel, Kahramanmaras Sutcu Imam University
Investıgatıon Of The Awareness Of The Parents Of The Cerebral Palsy Children About The Disease, Physiotherapy And Rehabilitation
Parents of Cerebral Palsy (CP) children participate in treatments, education services and general medical check-ups; They have many responsibilities such as the use of drugs, devices, educational materials.
Therefore, involving parents of CP children in the rehabilitation process provides a stronger rehabilitation service for their children.
In the studies, it was stated that the active participation of the parents in the physiotherapy and rehabilitation process increases the success rate of the treatment and the participation of the parents plays a key role for the success of the physiotherapy and rehabilitation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Cerebral Palsy (CP) children have a different clinical picture that includes many diseases.
Abnormal muscle tone, insufficiency of postural control, weakness of muscle strength, abnormal behavior patterns and sensory problems are common symptoms, especially motor impairment can be in these children.
These symptoms cause orthopedic problems, deformity and developmental delay over time.
Motor disorders may be accompanied by various problems such as cognitive disorders, sensory, speech, cognitive, communication and behavioral problems, epilepsy and secondary musculoskeletal system problems.
Functional skills such as independent sitting, standing, walking, balance, coordination, and fine motor skills are affected in these children due to different damage of neuronal system.
This negatively affects the independence of activity in the child's daily life.
CP children's treatment; It is carried out by a multidisciplinary team of specialists, such as specialist physicians, physiotherapists, psychologists, social counselors, child neurologists, orthopedists, vision-hearing specialists, pediatricians, occupational therapists, special educators, orthotics technicians, and with the participation of parents.
The most important element of the rehabilitation team is the parents.
In the postnatal period, parents are the primary responsible persons for the care of the child.
This responsibility increases even more in the child with CP.
The motor activity loss and movement disorder that develops in a child increase the functional dependency of the child in his daily life and cause him to need more support.
All family members are somehow involved in the health services provided to these children.
Parents are constantly involved in the life of the CP children and become aware of their child's abilities and needs.
Parents of children participate in treatments, education services and general medical check-ups; They have many responsibilities such as the use of drugs, devices, educational materials.
Therefore, involving parents of children in the rehabilitation process provides a stronger rehabilitation service for their children.
In the studies, it was stated that the active participation of the parents in the physiotherapy and rehabilitation process increases the success rate of the treatment and the participation of the parents plays a key role for the success of the physiotherapy and rehabilitation.
Parental support contributes to health and well-being and influences the success of long-term rehabilitation.
With the increasing importance of family-centered practices in recent years, parents have started to take an active part in rehabilitation studies by continuing the practices in the clinic at home and in the community.
It is an increasingly important view that parents play an important role in the lives of CP children.
The acceptance of family-oriented care and the emergence of new theories on motor development have affected the treatment approach to these children, and the practices have become more family and function-centered rather than child-centered.
The aim of this study is to investigate the awareness of parents of CP children about the disease, sports and physiotherapy and rehabilitation.
Study Type
Observational
Enrollment (Actual)
80
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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Kahramanmaras, Turkey, 46100
- Kahramanmaras Sutcu Imam 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
4 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
The universe of the research will consist of the parents of children with cerebral palsy who can be reached, who receive active treatment in special education and rehabilitation centers.
Description
Inclusion Criteria:
- Being the parents of children with cerebral palsy between the ages of 4-18
- Volunteering to participate in the study
- Having communication skills to answer the questions in the personal information form and the evaluation form.
Exclusion Criteria:
• Having any psychiatric diagnosis of parents
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 |
---|---|
1/parents of the Cerebral Palsy children
parents of the children with cerebral palsy will be evaluated about the awereness of their children's disease, physical and social activities and physiotherapy and rehabilitation.
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To examine the awareness of parents of Cerebral Palsy children about the disease, physiotherapy and rehabilitation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
1/The awareness of parents of children with Cerebral Palsy (CP) about the disease, physiotherapy and rehabilitation
Time Frame: first day of assessment
|
The awareness of parents of children with Cerebral Palsy (CP) about the disease, physiotherapy and rehabilitation will be assessed with a 50-question questionnaire prepared by the researcher.
|
first day of assessment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Demographic information of parents
Time Frame: first day of assessment
|
Demographic information of parents will be recorded (age, gender, height, body weight).
|
first day of assessment
|
Demographic information of the children
Time Frame: first day of assessment
|
Demographic information of the children will be recorded (age, gender, height, body weight,physiotherapy and rehabilitation years, diagnosis duration of the disease).
|
first day of assessment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
January 1, 2022
Primary Completion (Actual)
February 15, 2022
Study Completion (Actual)
February 28, 2022
Study Registration Dates
First Submitted
January 15, 2022
First Submitted That Met QC Criteria
January 15, 2022
First Posted (Actual)
January 28, 2022
Study Record Updates
Last Update Posted (Actual)
September 14, 2022
Last Update Submitted That Met QC Criteria
September 10, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KSUFTR
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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