Participation to Life of Children With Cerebral Palsy

Cerebral Palsy Clinical Trial

— PLCC  

Official title:

The Investigation of Necessity, Participation to Life of Children With Cerebral Palsy and Their Families

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03191695
• Other study ID #: 116S359-1
• Status: Recruiting
• Start date: February 1, 2018
• Est. completion date: January 2020

Study information

• Verified date: August 2018
• Source: Hacettepe University
• Contact: Mintaze KEREM GÜNEL
• Phone: +905327164221
• Email: mintaze[@]yahoo.com
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Cerebral Palsy (CP) defined as a group of permanent impairments that is originating from non-progressive disorders that develop in the immature brain. CP leads activity limitations of movement and posture development. Motor problems in CP are usually accompanied by sensory and perceptual disorders, cognitive disorders, communication and behavioral disorders, epilepsy, and secondary musculoskeletal system problems. The first 20 years of life is characterized by rapid growth and specific changes in physical, social, and psychological development. Social participation and independence of children and youth are related to the changes in this period. Participation can be identified as being involved in life situations and it reflects the social aspect of functionality. The problems which can be come across in life situations are identified as participation limitation. In literature, no adequate study has investigated the functional inadequacy, activity and participation of children with CP; this project has been planned in order to specify the importance in rehabilitation interventions more detailed. This project aims to specify whether the functional levels correspond to the activity and participation limitations of children with CP living in Ankara city center and determine the effects of their functional status on activity, participation and quality of life. This investigation will be pioneer in indicating the activity and participation limitations of children with CP. According to the results, these limitations will be overcome and the quality of life of children with CP will be increased. The CP follow-up database in Ankara will be specified so their physical activity and participation levels will be followed periodically and CP profile will be determined in Ankara.

Description:

Cerebral Palsy (CP) defined as a group of permanent impairments that is originating from non-progressive disorders that develop in the immature brain. CP leads activity limitations of movement and posture development.The first 20 years of life is characterized by rapid growth and specific changes in physical, social, and psychological development. Social participation and independence of children and youth are related to the changes in this period. Participation can be identified as being involved in life situations and it reflects the social aspect of functionality. The problems which can be come across in life situations are identified as participation limitation. In the past, the impairment seen in child was concentrated and child was the passive receptor of treatment. Today, this view is changed and child is the active participant of the treatment of disability. The aim of treatment is identified as increasing the quality of life by supporting the activity and participation according to the priorities of the child and the parent.

In literature, no adequate study has investigated the functional inadequacy, activity and participation of children with CP; this project has been planned in order to specify the importance in rehabilitation interventions more detailed. This project aims to specify whether the functional levels correspond to the activity and participation limitations of children with CP living in Ankara city center and determine the effects of their functional status on activity, participation and quality of life. This investigation will be pioneer in indicating the activity and participation limitations of children with CP. According to the results, these limitations will be overcome and the quality of life of children with CP will be increased. The CP follow-up database in Ankara will be specified so their physical activity and participation levels will be followed periodically and CP profile will be determined in Ankara. Moreover, the results of this study will be shared with the Ministry of National Education, the Ministry of Family and Social Policies, and the Ministry of Health and this will bring a different viewpoint to the community-based rehabilitation services in Turkey. Furthermore, this study will be expected to motivate countrywide investigations.

In the project, Gross Motor Function Classification System (GMFCS) for the severity of the disability of people with CP, The Measure of Processes of Care (MPOC) for their care process, the Pediatric Outcomes Date Collection (PODCI) Instrument and Pediatric Quality of Life Questionnaire and The Child Health Quality (CHQ PF-50) for their health-related quality of life, the Manual Ability Classification System (MACS) for the manual abilities and the Communication Function Classification System (CFCS) for the communication skill and the Life Habits Questionnaire (LIFE-H) for the participation level and Impact on Family Scale (IPFAM) for family impact will be used and the outcomes will be analyzed by adequate statistical methods. It is intended to be discussed the findings of the project in national and international platforms.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 500
• Est. completion date: January 2020
• Est. primary completion date: October 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 18 Years

Eligibility

Inclusion Criteria:

• To be diagnosed as cerebral palsy

Exclusion Criteria:

• Children whose family didn't accept to participate to study

Related Conditions & MeSH terms

• Cerebral Palsy
• Paralysis

Intervention

Other:
• Assessment via questionnaire
All the children will be assessed via assessment questionnaires.

Locations

Country	Name	City	State
Turkey	Hacettepe University	Ankara

Sponsors (3)

Lead Sponsor	Collaborator
Hacettepe University	Cumhuriyet University, The Scientific and Technological Research Council of Turkey

Country where clinical trial is conducted

Turkey, 

References & Publications (4)

Berg M, Jahnsen R, Frøslie KF, Hussain A. Reliability of the Pediatric Evaluation of Disability Inventory (PEDI). Phys Occup Ther Pediatr. 2004;24(3):61-77. — View Citation

Bodkin AW, Robinson C, Perales FP. Reliability and validity of the gross motor function classification system for cerebral palsy. Pediatr Phys Ther. 2003 Winter;15(4):247-52. — View Citation

Damiano DL, Gilgannon MD, Abel MF. Responsiveness and uniqueness of the pediatric outcomes data collection instrument compared to the gross motor function measure for measuring orthopaedic and neurosurgical outcomes in cerebral palsy. J Pediatr Orthop. 2005 Sep-Oct;25(5):641-5. — View Citation

Himuro N, Kozuka N, Mori M. Measurement of family-centred care: translation, adaptation and validation of the Measure of Processes of Care (MPOC-56 and -20) for use in Japan. Child Care Health Dev. 2013 May;39(3):358-65. doi: 10.1111/j.1365-2214.2012.01371.x. Epub 2012 Feb 28. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Life Habits Questionnaire (LIFE-H)	Assessing of the participation level of children	At baseline
Secondary	Gross Motor Function Classification System (GMFCS)	Assessing severity of the disability of children	At baseline
Secondary	Pediatric Outcomes Date Collection (PODCI) (Questionnaire)	Assessing health-related quality of life of children by parent proxy questionnaire	At baseline
Secondary	Manual Ability Classification System (MACS)	Assessing the manual abilities	At baseline
Secondary	Communication Function Classification System (CFCS)	Assessing communication skill	At baseline
Secondary	The Child Health Quality (CHQ PF-50)	Assessing health-related quality of life	At baseline
Secondary	Pediatric Quality of Life Questionnaire (PedsQL)	Assessing health-related quality of life	At baseline
Secondary	The Measure of Processes of Care (MPOC) (Questionnaire)	Assessing health care process of children by parent proxy questionnaire	At baseline
Secondary	Impact on Family Scale (IPFAM)	Assessing family impact	At baseline
Secondary	Pediatric Evaluation of Disability Inventory	Assessing disability	At baseline