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April 15, 2026ChildrenOpen Access

Psychosocial Impact of Celiac Disease on Primary Caregivers of Children in Jordan: A Cross-Sectional Study

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Authors

AAAla’a Al-Dala’ienNANedal AlnawaisehPAProfessor Khitam Al-Refu

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Overview

Cross-sectional study investigates psychosocial impact on caregivers of pediatric celiac disease patients, indicating significant burden requires attention.

Key Points

  • This study aims to explore the psychosocial impact on caregivers of children with celiac disease in Jordan and its correlation with various factors.
  • Cross-sectional design conducted from September to December 2025.
  • Participants were Jordanian caregivers of pediatric celiac disease patients with confirmed diagnosis.
  • Utilized Arabic version of the Celiac Disease Parent/Caregiver Quality of Life Questionnaire (CDPCA-QoL) to assess psychosocial outcome.
  • Performed descriptive and inferential analyses including t-tests, ANOVA, correlation, and multiple linear regression.
  • 198 caregivers participated with a mean age of 39.5 years; 85.9% were female.
  • Overall psychosocial burden was moderate to moderately high, with parental worries scoring highest.
  • Younger age, lower education, and lower income correlated with greater psychosocial burden (p < 0.05).
  • Caring for multiple affected children heightened emotional and social strain, while longer disease duration was linked to lower parental worry.

Cite This Study

Al-Dala’ien et al. (2026) studied this question.

synapsesocial.com/papers/69df2ba0e4eeef8a2a6b08cahttps://doi.org/10.3390/children13040533
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Also Consider

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