Assessment of Nutritional Status Using Mid-Upper Arm Circumference Z-Score in Children With Cerebral Palsy

January 10, 2026 updated by: Hülya Kayılıoğlu, Muğla Sıtkı Koçman University

Assessment of Nutritional Status in Children With Cerebral Palsy

Children with cerebral palsy are at increased risk of malnutrition due to motor impairment, feeding difficulties, and chronic health problems. Accurate assessment of nutritional status in this population can be challenging, particularly when standard anthropometric measurements are difficult to obtain.

This observational study aims to evaluate nutritional status in children with cerebral palsy using the mid-upper arm circumference Z-score (MUACZ) and to examine its relationship with functional severity levels. Anthropometric measurements and clinical data will be collected during routine outpatient visits. Nutritional status will be classified using predefined reference standards, and associations with motor and feeding function classifications will be analyzed.

The findings of this study are expected to contribute to a better understanding of practical approaches for nutritional assessment in children with cerebral palsy across different ages and functional levels.

Study Overview

Status

Completed

Detailed Description

Cerebral palsy is a non-progressive neurodevelopmental condition frequently associated with motor dysfunction, feeding difficulties, and impaired growth. Malnutrition remains a common and clinically important comorbidity in children with cerebral palsy and is associated with adverse health outcomes, including increased susceptibility to infections, reduced muscle strength, and diminished quality of life. Despite its clinical relevance, accurate nutritional assessment in this population is often complicated by postural limitations, contractures, and difficulties in obtaining reliable weight and height measurements.

This cross-sectional, observational study is designed to assess nutritional status in children with cerebral palsy using anthropometric indicators, with a particular focus on the mid-upper arm circumference Z-score (MUACZ). MUACZ is derived from age- and sex-adjusted reference standards and can be obtained with minimal equipment, making it potentially suitable for use across a wide range of functional severity levels.

The study will include pediatric patients with a confirmed diagnosis of cerebral palsy who attend routine follow-up visits at a tertiary care center. Anthropometric measurements, including mid-upper arm circumference, body mass index-for-age, and height-for-age Z-scores, will be recorded according to standardized procedures. Functional severity will be classified using the Gross Motor Function Classification System (GMFCS) and the Eating and Drinking Ability Classification System (EDACS).

Nutritional status will be categorized based on predefined Z-score thresholds. Statistical analyses will examine the distribution of nutritional status across functional severity levels and evaluate the performance of MUACZ in identifying undernutrition using established cutoff values. All analyses will be conducted using appropriate statistical software, and the study will adhere to relevant ethical standards, with informed consent obtained from parents or legal guardians.

This study does not involve any intervention or alteration of standard clinical care. Data are collected solely for observational and analytical purposes.

Study Type

Observational

Enrollment (Actual)

84

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

    • Muğla
      • Menteşe, Muğla, Turkey (Türkiye), 48000
        • Muğla Sıtkı Koçman Research and Training Hospital

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

  • Child
  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

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.

Description

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)

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

Cohorts and Interventions

Group / Cohort
Cerebral Palsy

This observational study includes a single cohort of pediatric patients with a confirmed diagnosis of cerebral palsy. Participants are enrolled during routine outpatient follow-up visits at a tertiary care center.

Within the cohort, participants are categorized according to nutritional status based on predefined anthropometric criteria and according to functional severity using established classification systems. No separate control group is included. Comparisons are performed within the cohort across nutritional status categories and functional severity levels to evaluate distributions and associations.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of undernutrition in children with cerebral palsy
Time Frame: At study enrollment (single assessment during routine outpatient visit).
Undernutrition status will be determined using predefined anthropometric Z-score criteria. Undernutrition is defined as the presence of wasting (body mass index-for-age Z-score ≤ -2) and/or stunting (height-for-age Z-score ≤ -2), based on standardized growth references.
At study enrollment (single assessment during routine outpatient visit).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Distribution of nutritional status across functional severity levels
Time Frame: At study enrollment.
The distribution of undernutrition will be evaluated across functional severity categories as defined by the Gross Motor Function Classification System (GMFCS) and the Eating and Drinking Ability Classification System (EDACS).
At study enrollment.
Association between MUACZ and functional severity classifications
Time Frame: At study enrollment.
The relationship between mid-upper arm circumference Z-score (MUACZ) values and functional severity levels (GMFCS and EDACS) will be analyzed using appropriate statistical methods.
At study enrollment.
Performance of MUACZ in identifying undernutrition
Time Frame: At study enrollment.
The ability of MUACZ to identify undernutrition will be evaluated using receiver operating characteristic analysis with a predefined cutoff value (≤ -2).
At study enrollment.

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)

October 1, 2023

Primary Completion (Actual)

January 30, 2025

Study Completion (Actual)

January 30, 2025

Study Registration Dates

First Submitted

January 10, 2026

First Submitted That Met QC Criteria

January 10, 2026

First Posted (Actual)

January 20, 2026

Study Record Updates

Last Update Posted (Actual)

January 20, 2026

Last Update Submitted That Met QC Criteria

January 10, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified individual participant data underlying the results reported in this study, including demographic variables, anthropometric measurements, and functional classification data.

IPD Sharing Time Frame

Beginning 6 months after publication of the primary results and ending 5 years following publication.

IPD Sharing Access Criteria

Individual participant data will be made available to qualified researchers upon reasonable request. Requests will be reviewed by the corresponding author and require approval from the relevant institutional and/or ethics committees, where applicable. Data will be shared in de-identified form to protect participant privacy, and access may require a data use agreement specifying the intended use of the data.

IPD Sharing Supporting Information Type

  • ANALYTIC_CODE

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.

Clinical Trials on Cerebral Palsy (CP)

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