Optimising informed consent for participants in a randomised controlled trial in rural Uganda: a comparative prospective cohort mixed-methods study-Reference-Cited by-同舟云学术

Optimising informed consent for participants in a randomised controlled trial in rural Uganda: a comparative prospective cohort mixed-methods study

Published:2018-12 Issue:1 Volume:19 Page:
ISSN:1745-6215
Container-title:Trials
language:en
Short-container-title:Trials

Author:

Ditai J.^ORCID,Kanyago J.,Nambozo M. R.,Odeke N. M.,Abeso J.,Dusabe-Richards J.,Olupot-Olupot P.,Carrol E. D.,Medina-Lara A.,Gladstone M.,Storr J.,Faragher B.,Weeks A. D.

Funder

Medical Research Council

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Medicine (miscellaneous)

Link

http://link.springer.com/content/pdf/10.1186/s13063-018-3030-8.pdf

Reference28 articles.

1. Uganda National Council for Science and Technology (UNCST). National Guidelines for Research involving Humans as Research Participants, no. July. Kampala: UNCST; 2014.

2. World Medical Association. World Medical Association Declaration of Helsinki Ethical Principles for Medical Research Involving Human Subjects. JAMA. 2013;310(20):2191–4.

3. Okello G, et al. Challenges for consent and community engagement in the conduct of cluster randomized trial among school children in low-income settings: experiences from Kenya. Trials. 2013;14(1):142.

4. Williams BF, French JK, White HD. Informed consent during the clinical emergency of acute myocardial infarction (HER0-2 consent substudy): a prospective observational study. Lancet. 2003;361(9361):918–22.

5. Joffe S, Cook EF, Cleary D, Clark JW, Weeks JC. Quality of Informed Consent: a New Measure of Understanding Among Research Subjects. J Natl Cancer Inst. 2001;93(2):139-47.

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