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Exempting low-risk health and medical research from ethics reviews: comparing Australia, the United Kingdom, the United States and the Netherlands.
Scott, Anna Mae; Kolstoe, Simon; Ploem, M C Corrette; Hammatt, Zoë; Glasziou, Paul.
Afiliação
  • Scott AM; Institute for Evidence-Based Healthcare, Bond University, 14 University Drive, Robina, QLD, 4226, Australia. ascott@bond.edu.au.
  • Kolstoe S; University of Portsmouth, Portsmouth, UK.
  • Ploem MCC; Amsterdam University Medical Centre, Amsterdam, The Netherlands.
  • Hammatt Z; Z Consulting LLC, Denver, USA.
  • Glasziou P; John A. Burns School of Medicine, University of Hawaii, Honolulu, USA.
Health Res Policy Syst ; 18(1): 11, 2020 Jan 28.
Article em En | MEDLINE | ID: mdl-31992320
BACKGROUND: Disproportionate regulation of health and medical research contributes to research waste. Better understanding of exemptions of research from ethics review in different jurisdictions may help to guide modification of review processes and reduce research waste. Our aim was to identify examples of low-risk human health and medical research exempt from ethics reviews in Australia, the United Kingdom, the United States and the Netherlands. METHODS: We examined documents providing national guidance on research ethics in each country, including those authored by the National Health and Medical Research Council (Australia), National Health Service (United Kingdom), the Office for Human Research Protections (United States) and the Central Committee on Research Involving Humans (the Netherlands). Examples and types of research projects exempt from ethics reviews were identified, and similar examples and types were grouped together. RESULTS: Nine categories of research were exempt from ethics reviews across the four countries; these were existing data or specimen, questionnaire or survey, interview, post-marketing study, evaluation of public benefit or service programme, randomised controlled trials, research with staff in their professional role, audit and service evaluation, and other exemptions. Existing non-identifiable data and specimens were exempt in all countries. Four categories - evaluation of public benefit or service programme, randomised controlled trials, research with staff in their professional role, and audit and service evaluation - were exempted by one country each. The remaining categories were exempted by two or three countries. CONCLUSIONS: Examples and types of research exempt from research ethics reviews varied considerably. Given the considerable costs and burdens on researchers and ethics committees, it would be worthwhile to develop and provide clearer guidance on exemptions, illustrated with examples, with transparent underpinning rationales.
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Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Comitês de Ética em Pesquisa / Pesquisa Biomédica / Pesquisa sobre Serviços de Saúde Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Humans País como assunto: America do norte / Europa / Oceania Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Comitês de Ética em Pesquisa / Pesquisa Biomédica / Pesquisa sobre Serviços de Saúde Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Humans País como assunto: America do norte / Europa / Oceania Idioma: En Ano de publicação: 2020 Tipo de documento: Article