Growth, Dietary Intakes and Feeding Behaviors of Children With Cerebral Palsy Who Have Chewing Disorders
NCT ID: NCT02777645
Last Updated: 2016-05-19
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
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COMPLETED
85 participants
OBSERVATIONAL
2016-03-31
2016-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Study group
Study group(n=50) included CP children with chewing disorder. Growth, feeding evaluation will be done.
Growth, feeding evaluation
Z-scores of the nutritional indicators were calculated. The dietary assessment was performed by using the 24-hour recall method. The Behavioural Paediatrics Feeding Assessment Scale (BPFAS) was used to assess both frequencies of negative feeding behaviours and parents' problematic perceptions
Control group
Control group(n=35)= healthy children without chewing disorder Growth, feeding evaluation will be done.
Growth, feeding evaluation
Z-scores of the nutritional indicators were calculated. The dietary assessment was performed by using the 24-hour recall method. The Behavioural Paediatrics Feeding Assessment Scale (BPFAS) was used to assess both frequencies of negative feeding behaviours and parents' problematic perceptions
Interventions
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Growth, feeding evaluation
Z-scores of the nutritional indicators were calculated. The dietary assessment was performed by using the 24-hour recall method. The Behavioural Paediatrics Feeding Assessment Scale (BPFAS) was used to assess both frequencies of negative feeding behaviours and parents' problematic perceptions
Eligibility Criteria
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Inclusion Criteria
* Children with cerebral palsy
* Having complaints about chewing function
* Do not manage solid food intake
* Above the age of 18 months Control group
* Healthy children
* No complaints about chewing function
* Can manage solid food intake
* Above the age of 18 months
Exclusion Criteria
* Requiring tube feeding or taking any oral nutritional supplements
* Using any medicine and/or oral appliances that could affect the chewing performance
24 Months
61 Months
ALL
No
Sponsors
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Hacettepe University
OTHER
Responsible Party
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SELEN SEREL ARSLAN
PT, PhD
Principal Investigators
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Selen SEREL ARSLAN, PhD
Role: PRINCIPAL_INVESTIGATOR
Hacettepe University
Locations
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Hacetttepe University
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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ArslanSerel1
Identifier Type: -
Identifier Source: org_study_id
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