Overview
Research examines camps, social relationships, illness-specific quality of life, and parent–child perspectives in celiac disease. The work connects psychological measurement with practical questions about support for young people and families.
Research approach
Camp evaluation · Dyadic measurement.
This project overview explains the research direction; it does not present unpublished estimates or participant-level data.
Related publications
How to make gluten-free friends: A quasi-experimental study on the psychosocial benefits of celiac camps
Shani, M. & Böttcher, M.
British Journal of Health Psychology, 30(4), e70027
The potential benefits of camps for children and adolescents with celiac disease on social support, illness acceptance, and health-related quality of life
Shani, M., Kraft, L., Müller, M., & Boehnke, K.
Journal of Health Psychology, 27(7), 1635–1645
Structural validation and dyadic child-parent measurement invariance of the celiac disease quality of life questionnaire
Meyer, S., & Shani, M.
European Journal of Gastroenterology & Hepatology, 34(1), 39–47 · Shared first authorship
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For collaboration or thesis research related to this project, contact the lab.