Digital Informed Consent/Assent in Clinical Trials Among Pregnant Women, Minors, and Adults: Multicountry Cross-Sectional Evaluation of Comprehension and Satisfaction

The primary aim of this study is to assess participants’ comprehension of and satisfaction with eIC materials tailored to their specific needs. The secondary objectives are to identify demographic predictors of comprehension, evaluate the cross-cultural applicability of materials, and explore format...

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Detalles Bibliográficos
Autores: Fons-Martinez, Jaime, Murciano-Gamborino, Carlos, Vergara- Hernandez, Carlos, Ferrer Albero, Cristina, Díez Domingo, Javier
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universidad Católica de Valencia San Vicente Mártir
Repositorio:RIUCV. Repositorio de la Universidad Católica de Valencia San Vicente Mártir
Idioma:inglés
OAI Identifier:oai:riucv.ucv.es:20.500.12466/6749
Acceso en línea:https://hdl.handle.net/20.500.12466/6749
Access Level:acceso abierto
Palabra clave:Informed consent
eConsent
Clinical trials
Comprehension
Pregnant women
Adults
Participant satisfaction
Demographic factors
eHealth
Electronic consent materials
Pregnant
Women
Minor
Youth
Adolescent
Teenager
Older adult
Electronic informed consent
Digital informed consent
Statistical analysis
32 Ciencias Médicas
Descripción
Sumario:The primary aim of this study is to assess participants’ comprehension of and satisfaction with eIC materials tailored to their specific needs. The secondary objectives are to identify demographic predictors of comprehension, evaluate the cross-cultural applicability of materials, and explore format preferences.

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