Arm circumference may help spot malnutrition in kids with cerebral palsy
NCT ID NCT07351695
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study involved 84 children with cerebral palsy to see if measuring mid-upper arm circumference can help assess their nutritional status. Standard height and weight measurements are often hard to get in these children due to motor and feeding difficulties. The researchers compared arm measurements to standard growth charts and linked them to the children's motor and feeding abilities. The goal is to find a practical way to identify malnutrition early in this vulnerable group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to better, simpler ways to check for malnutrition in children with cerebral palsy, helping doctors provide more targeted nutritional support.
- What could go wrong
- This is an observational study, not a treatment trial. It only measures current nutrition status and does not test any intervention, so it cannot directly improve health outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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84 people
The number who actually took part.
- Started
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Oct 2023
- Finished
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Jan 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of children and adolescents with a confirmed diagnosis of cerebral palsy who are followed at a tertiary referral center. Participants are recruited during routine outpatient follow-up visits and represent a wide spectrum of motor and feeding functional severity. The population includes patients across all levels of gross motor function and eating and drinking ability, allowing evaluation of nutritional status across varying degrees of functional impairment. Anthropometric and clinical data are collected as part of standard care, without any modification to routine clinical management. This population reflects a real-world clinical setting in which nutritional assessment is routinely performed in children with cerebral palsy, including those with severe motor and feeding limitations.
- Ages
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18 months to 18 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Children and adolescents with a confirmed diagnosis of cerebral palsy * Age between 18 months and 18 years at the time of assessment * Attendance at routine outpatient follow-up at the study center during the study period * Availability of anthropometric measurements required for nutritional assessment * Availability of functional classification using the Gross Motor Function Classification System (GMFCS) and/or the Eating and Drinking Ability Classification System (EDACS) * Written informed consent obtained from a parent or legal guardian Exclusion Criteria * Presence of acute illness or infection at the time of assessment that could interfere with anthropometric measurements * Known genetic syndromes or metabolic disorders affecting growth independently of cerebral palsy * Incomplete clinical or anthropometric data preventing classification of nutritional status * Previous major surgery or hospitalization within a period that could significantly influence nutritional measurements (as determined by the treating clinician)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Muğla Sıtkı Koçman Research and Training Hospital
Menteşe, Muğla, 48000, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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