Cargando…
Assent, parental consent and reconsent for health research in Africa: thematic analysis of national guidelines and lessons from the SickleInAfrica registry
The enrolment of children and adolescents in health research requires that attention to be paid to specific assent and consent requirements such as the age range for seeking assent; conditions for parental consent (and waivers); the age group required to provide written assent; content of assent for...
Autores principales: | Munung, Nchangwi Syntia, Nembaware, Victoria, Osei-Tutu, Lawrence, Treadwell, Marsha, Chide, Okocha Emmanuel, Bukini, Daima, Tutuba, Hilda, Wonkam, Ambroise |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730625/ https://www.ncbi.nlm.nih.gov/pubmed/36482457 http://dx.doi.org/10.1186/s12910-022-00843-3 |
Ejemplares similares
-
Establishing a Multi-Country Sickle Cell Disease Registry in Africa: Ethical Considerations
por: Munung, Nchangwi Syntia, et al.
Publicado: (2019) -
Patient-centric research in the time of COVID-19: conducting ethical COVID-19 research in Africa
por: Nembaware, Victoria, et al.
Publicado: (2020) -
Adolescent Assent and Reconsent for Biobanking: Recent Developments and Emerging Ethical Issues
por: Kasperbauer, T. J., et al.
Publicado: (2021) -
Knowledge and Challenges Associated With Hearing Impairment in Affected Individuals From Cameroon (Sub-Saharan Africa)
por: Wonkam-Tingang, Edmond, et al.
Publicado: (2021) -
Development of multi-level standards of care recommendations for sickle cell disease: Experience from SickleInAfrica
por: Paintsil, Vivian, et al.
Publicado: (2023)