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Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa
BACKGROUND: South Africa is likely to be the first country in the world to host an adolescent HIV vaccine trial. Adolescents may be enrolled in late 2007. In the development and review of adolescent HIV vaccine trial protocols there are many complexities to consider, and much work to be done if thes...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1878488/ https://www.ncbi.nlm.nih.gov/pubmed/17498316 http://dx.doi.org/10.1186/1472-6939-8-5 |
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author | Slack, Catherine Strode, Ann Fleischer, Theodore Gray, Glenda Ranchod, Chitra |
author_facet | Slack, Catherine Strode, Ann Fleischer, Theodore Gray, Glenda Ranchod, Chitra |
author_sort | Slack, Catherine |
collection | PubMed |
description | BACKGROUND: South Africa is likely to be the first country in the world to host an adolescent HIV vaccine trial. Adolescents may be enrolled in late 2007. In the development and review of adolescent HIV vaccine trial protocols there are many complexities to consider, and much work to be done if these important trials are to become a reality. DISCUSSION: This article sets out essential requirements for the lawful conduct of adolescent research in South Africa including compliance with consent requirements, child protection laws, and processes for the ethical and regulatory approval of research. SUMMARY: This article outlines likely complexities for researchers and research ethics committees, including determining that trial interventions meet current risk standards for child research. Explicit recommendations are made for role-players in other jurisdictions who may also be planning such trials. This article concludes with concrete steps for implementing these important trials in South Africa and other jurisdictions, including planning for consent processes; delineating privacy rights; compiling information necessary for ethics committees to assess risks to child participants; training trial site staff to recognize when disclosures trig mandatory reporting response; networking among relevant ethics commitees; and lobbying the National Regulatory Authority for guidance. |
format | Text |
id | pubmed-1878488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18784882007-05-29 Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa Slack, Catherine Strode, Ann Fleischer, Theodore Gray, Glenda Ranchod, Chitra BMC Med Ethics Debate BACKGROUND: South Africa is likely to be the first country in the world to host an adolescent HIV vaccine trial. Adolescents may be enrolled in late 2007. In the development and review of adolescent HIV vaccine trial protocols there are many complexities to consider, and much work to be done if these important trials are to become a reality. DISCUSSION: This article sets out essential requirements for the lawful conduct of adolescent research in South Africa including compliance with consent requirements, child protection laws, and processes for the ethical and regulatory approval of research. SUMMARY: This article outlines likely complexities for researchers and research ethics committees, including determining that trial interventions meet current risk standards for child research. Explicit recommendations are made for role-players in other jurisdictions who may also be planning such trials. This article concludes with concrete steps for implementing these important trials in South Africa and other jurisdictions, including planning for consent processes; delineating privacy rights; compiling information necessary for ethics committees to assess risks to child participants; training trial site staff to recognize when disclosures trig mandatory reporting response; networking among relevant ethics commitees; and lobbying the National Regulatory Authority for guidance. BioMed Central 2007-05-13 /pmc/articles/PMC1878488/ /pubmed/17498316 http://dx.doi.org/10.1186/1472-6939-8-5 Text en Copyright © 2007 Slack et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Debate Slack, Catherine Strode, Ann Fleischer, Theodore Gray, Glenda Ranchod, Chitra Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa |
title | Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa |
title_full | Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa |
title_fullStr | Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa |
title_full_unstemmed | Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa |
title_short | Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa |
title_sort | enrolling adolescents in hiv vaccine trials: reflections on legal complexities from south africa |
topic | Debate |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1878488/ https://www.ncbi.nlm.nih.gov/pubmed/17498316 http://dx.doi.org/10.1186/1472-6939-8-5 |
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