期刊论文详细信息
Trials
Challenges for consent and community engagement in the conduct of cluster randomized trial among school children in low income settings: experiences from Kenya
Simon J Brooker2  Sassy Molyneux9  Matthew CH Jukes1  Katherine E Halliday2  Margaret M Dubeck7  Kevin Kinyua6  Juddy Kengo3  Carlos Mcharo3  Sarah N Ndegwa4  Maureen Bonareri4  Caroline Jones5  George Okello8 
[1] Graduate School of Education, Harvard University, Cambridge, MA, USA;Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK;Health and Literacy Intervention Project, Ukunda, Kenya;Malaria Public Health & Epidemiology Group, Kenya Medical Research Institute-Wellcome Trust Collaborative Programme, Nairobi, Kenya;Department of Public Health & Primary Care, University of Oxford, Oxford, UK;Ministry of Public Health and Sanitation, District Medical Officer of Health, Msambweni, Kenya;Department of Teacher Education, College of Charleston, Charleston, SC, USA;Health Systems Department, Kenya Medical Research Institute-Wellcome Trust Collaborative Programme, Kilifi, Kenya;Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK
关键词: Kenya;    School-based research;    Community engagement;    Consent;    Cluster-randomized trial;    Malaria;   
Others  :  1093981
DOI  :  10.1186/1745-6215-14-142
 received in 2012-10-09, accepted in 2013-04-18,  发布年份 2013
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【 摘 要 】

Background

There are a number of practical and ethical issues raised in school-based health research, particularly those related to obtaining consent from parents and assent from children. One approach to developing, strengthening, and supporting appropriate consent and assent processes is through community engagement. To date, much of the literature on community engagement in biomedical research has concentrated on community- or hospital-based research, with little documentation, if any, of community engagement in school-based health research. In this paper we discuss our experiences of consent, assent and community engagement in implementing a large school-based cluster randomized trial in rural Kenya.

Methods

Data collected as part of a qualitative study investigating the acceptability of the main trial, focus group discussions with field staff, observations of practice and authors’ experiences are used to: 1) highlight the challenges faced in obtaining assent/consent; and 2) strategies taken to try to both protect participant rights (including to refuse and to withdraw) and ensure the success of the trial.

Results

Early meetings with national, district and local level stakeholders were important in establishing their co-operation and support for the project. Despite this support, both practical and ethical challenges were encountered during consenting and assenting procedures. Our strategy for addressing these challenges focused on improving communication and understanding of the trial, and maintaining dialogue with all the relevant stakeholders throughout the study period.

Conclusions

A range of stakeholders within and beyond schools play a key role in school based health trials. Community entry and information dissemination strategies need careful planning from the outset, and with on-going consultation and feedback mechanisms established in order to identify and address concerns as they arise. We believe our experiences, and the ethical and practical issues and dilemmas encountered, will be of interest for others planning to conduct school-based research in Africa.

Trial registration

National Institute of Health NCT00878007

【 授权许可】

   
2013 Okello et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Bundy D: Rethinking School Health: A Key component of Education for All. Washington, DC: World Bank; 2011.
  • [2]Brooker S, Kolaczinski JH, Gitonga CW, Noo AM, Snow RW: The use of schools for malaria surveillance and programme evaluation in Africa. Malar J 2009, 8:231. BioMed Central Full Text
  • [3]Coyne I: Research with children and young people: the issue of parental (proxy) consent. Children Soc 2010, 24:227-237.
  • [4]Council for International Organizations of Medical Sciences (CIOMS): International Ethical Guidelines for Biomedical Research Involving Human Subjects. Geneva: CIOMS; 2002.
  • [5]Molyneux S, Wassenaar DR, Peshu N, Marsh K: ‘Even if they ask you to stand by a tree all day, you will have to do it (laughter)!’: community voices on the notion and practice of informed consent for biomedical research in developing countries. SocSci Med 2005, 61:443-454.
  • [6]Molyneux S, Peshu N, Marsh K: Understanding of informed consent in a low-income setting: three case studies from the Kenyan coast. Soc Sci Med 2004, 59:2547-2559.
  • [7]Kamuya D, Marsh V, Molyneux S: What we learned about voluntariness and consent: incorporating “background situations” and understanding into analyses. Am J Bioeth 2011, 11:31-33.
  • [8]Marsh V, Kamuya D, Rowab Y, Gikonyo C, Molyneux S: Beginning community engagement at a busy biomedical research programme: experiences from the KEMRI CGMRC-Wellcome Trust Research Programme, Kilifi, Kenya. Soc Sci Med 2008, 67:721-733.
  • [9]Kerr C, Robinson E, Stevens A, Braunholtz D, Edwards S, Lilford R: Randomisation in trials: do potential trial participants understand it and find it acceptable? J Med Ethics 2004, 30:80-84.
  • [10]Donovan JL: Random allocation or allocation at random? Patients’ perspectives of participation in a randomised controlled trial. Br Med J 1998, 317:1177-1180.
  • [11]Robinson E, Kerr CEP, Stevens AJ, Lilford RJ, Braunholtz DA, Edwards SJ, Beck SR, Rowley MG: Lay public’s understanding of equipoise and randomisation in randomised controlled trials. Health Technol Assess 2005, 9:1-192.
  • [12]O’Lonergan T, Zodrow JJ: Pediatric assent: subject protection issues among adolescent females enrolled in research. J Law Med Ethics 2006, 34:451-459.
  • [13]Lott JP: Module three: vulnerable/special participant populations. Dev World Bioeth 2005, 5:30-54.
  • [14]Tessa J, Hope T, Savulescu J, Stein A, Pollard AJ: Children’s consent and paediatric research: is it appropriate for healthy children to be the decision-makers in clinical research? Arch Dis Child 2009, 93:379-383.
  • [15]Broome ME, Stieglitz KA: The consent process and children. Res Nurs Health 1992, 15:147-152.
  • [16]Tindana P, Singh JA, Tracy SC, Upshur REG, Daar AS, Singer PA, Frohlich J, Lavery JV: Grand challenges in global health: community engagement in research in developing countries. PLoS Med 2007, 4:e273.
  • [17]Lavery J, Tindana PO, Scott TW, Harrington LC, Ramsey JM, Ytuarte-Nunez C, James AA: Towards a framework for community engagement in global health research. Trends Parasitol 2010, 26:279-283.
  • [18]Tindana P, Rozmovits L, Boulanger RF, Bandewar SVS, Aborigo RA, Hodgson AVO, Kolopack P, Lavery JV: Aligning community engagement with traditional authority structures in global health research: a case study from northern Ghana. Am J Public Health 2011, 101:1857-1867.
  • [19]Lang T, Gould J, Seidlein Von L, Lusingu JP, Mshamu S, Ismael S, Liheluka E, Kamuya D, Mwachiro D, Olotu A, Njuguna P, Bejon P, Marsh V, Molyneux C: Approaching the community about screening children for a multicentre malaria vaccine trial. Int Health 2012, 4:47-54.
  • [20]Nyika A, Chilengi R, Ishengoma D, Mtenga S, Thera MA, Sissoko MS, Lusingu J, Tiono AB, Doumbo O, Sirima SB, Lemnge M, Kilama WL: Engaging diverse communities participating in clinical trials: case examples from across Africa. Malar J 2010, 9:86. BioMed Central Full Text
  • [21]Brooker S, Okello G, Njagi K, Dubeck MM, Halliday EK, Inyega H, Jukes MCH: Improving educational achievement and anaemia of school children: design of a cluster randomised trial of school-based malaria prevention and enhanced literacy instruction in Kenya. Trials 2010, 11:93. BioMed Central Full Text
  • [22]Halliday E, Karanja P, Turner EL, Okello G, Njagi K, Dubeck MM, Allen E, Jukes MCH, Brooker S: Plasmodium falciparum, anaemia and cognitive and educational performance among school children in an area of moderate malaria transmission: baseline results of a cluster randomised controlled trial on the coast of Kenya. Trop Med Int Health 2012, 17:532-549.
  • [23]Okello G, Ndegwa SN, Halliday KE, Hanson K, Brooker SJ, Jones C: Local perceptions of intermittent screening and treatment for malaria in school children on the south coast of Kenya. Malar J 2012, 11:185. BioMed Central Full Text
  • [24]David M: Children and school-based research: ‘informed consent’ or ‘educated consent’? British Educational Research Journal 2001, 27:347-365.
  • [25]Snowdon C, Garcia J, Elbourne D: Making sense of randomization; responses of parents of critically ill babies to random allocation of treatment in a clinical trial. Soc Sci Med 1997, 45:1337-1355.
  • [26]Featherstone K, Donovan JL: “Why don’t they just tell me straight, why allocate it?” The struggle to make sense of participating in a randomised controlled trial. Soc Sci Med 2002, 55:709-719.
  • [27]Weijer C, Grimshaw JM, Taljaard M, Binik A, Boruch R, Brehaut JC, Donner A, Eccles MP, Gallo A, McRae AD, Saginur R, Zwarenstein M: Ethical issues posed by cluster randomized trials in health research. Trials 2011, 12:100. BioMed Central Full Text
  • [28]McRae J, Weijer C, Binik A, White A, Grimshaw JM, Boruch R, Brehaut JC, Donner A, Eccles MP, Saginur R, Zwarenstein M, Taljaard M: Who is the research subject in cluster randomized trials in health research? Trials 2011, 12:183. BioMed Central Full Text
  • [29]Gallo A, Weijer C, White A, Grimshaw JM, Boruch R, Brehaut JC, Donner A, Eccles MP, McRae AD, Saginur R, Zwarenstein M, Taljaard M: What is the role and authority of gatekeepers in cluster randomized trials in health research? Trials 2012, 13:116. BioMed Central Full Text
  • [30]Kamuya D, Theobald S, Munyoki P, Koech D, Geissler W, Molyneux S: Evolving friendships and shifting ethical dilemmas: fieldworkers’ experiences in a short term community based study in Kenya. Dev World Bioeth 2013, 13:1-9.
  • [31]McRae A, Weijer C, Binik A, Grimshaw JM, Boruch R, Brehaut JC, Donner A, Eccles MP, Saginur R, White A, Taljaard M: When is informed consent required in cluster randomized trials in health research? Trials 2011, 12:202. BioMed Central Full Text
  • [32]Weijer C, Grimshaw JM, Eccles MP, McRae AD, White A, Brehaut JC, Taljaard M: The Ottawa statement on the ethical design and conduct of cluster randomized trials. PLoS Med 2012, 9:e1001346.
  • [33]Alibali M, Nathan MJ: Conducting research in schools: a practical guide. J Cogn Dev 2010, 11:397-407.
  • [34]Ross JG, Sundberg EC, Flint KH: Informed consent in school health research: why, how, and making it easy. J Sch Health 1999, 69:171-176.
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