Caregiver decision-making on pediatric research participation in congenital heart disease in western China: a qualitative study

BackgroundHigh-quality pediatric clinical research depends on effective and ethically robust recruitment, yet participation can be difficult for families of children with congenital heart disease (CHD), particularly in resource-constrained and culturally diverse settings. In western China, long-dist...

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Autors principals:	Mou Peng, Yuxin Ding, Zexi Li, Shuran Shao, Yaru Cui, Li Zhao, Yimin Hua, Kaiyu Zhou, Chuan Wang, Jinhui Li, Chunyi Yan
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2026-06-01
Col·lecció:	Frontiers in Public Health
Matèries:	caregivers clinical research participation congenital heart disease informed consent therapeutic misconception western China
Accés en línia:	https://www.frontiersin.org/articles/10.3389/fpubh.2026.1843389/full
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