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Perspectives on returning individual and aggregate genomic research results to study participants and communities in Kenya: a qualitative study.
Kisiangani, Isaac; Mohamed, Shukri F; Kyobutungi, Catherine; Tindana, Paulina; Ghansah, Anita; Ramsay, Michele; Asiki, Gershim.
  • Kisiangani I; African Population and Health Research Center (APHRC), P.O. Box 10787, Nairobi, 00100, Kenya. ikisiangani@aphrc.org.
  • Mohamed SF; African Population and Health Research Center (APHRC), P.O. Box 10787, Nairobi, 00100, Kenya.
  • Kyobutungi C; African Population and Health Research Center (APHRC), P.O. Box 10787, Nairobi, 00100, Kenya.
  • Tindana P; School of Public Health, College of Health Sciences, University of Ghana, Legon, Ghana.
  • Ghansah A; Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
  • Ramsay M; Sydney Brenner Institute for Molecular Bioscience, The University of Witwatersrand, The Mount, 9 Jubilee Rd, Parktown, Johannesburg, 2193, South Africa.
  • Asiki G; African Population and Health Research Center (APHRC), P.O. Box 10787, Nairobi, 00100, Kenya.
BMC Med Ethics ; 23(1): 27, 2022 03 18.
Article en En | MEDLINE | ID: mdl-35300680
BACKGROUND: A fundamental ethical challenge in conducting genomics research is the question of what and how individual level genetic findings and aggregate genomic results should be conveyed to research participants and communities. This is within the context of minimal guidance, policies, and experiences, particularly in Africa. The aim of this study was to explore the perspectives of key stakeholders' on returning genomics research results to participants in Kenya. METHODS: This qualitative study involved focus group discussions (FGDs) and in-depth interviews (IDIs) with 69 stakeholders. The purposively selected participants, included research ethics committee (REC) members (8), community members (44), community resource persons (8), and researchers (9). A semi-structured interview guide was used to facilitate discussions. Six FGDs and twenty-five (IDIs) were conducted among the different stakeholders. The issues explored in the interviews included: (1) views on returning results, (2) kind of results to be returned, (3) value of returning results to participants, and (4) challenges anticipated in returning results to participants and communities. The interviews were audio-recorded, transcribed verbatim, and coded in Nvivo 12 pro. Thematic and content analysis was conducted. RESULTS: Participants agreed on the importance of returning genomic results either as individual or aggregate results. The most cited reasons for returning of genomic results included recognizing participants' contribution to research, encouraging participation in future research, and increasing the awareness of scientific progress. Other aspects on how genomic research results should be shared included sharing easy to understand results in the shortest time possible and maintaining confidentiality when sharing sensitive results. CONCLUSIONS: This study identified key stakeholders' perspectives on returning genomic results at the individual and community levels in two urban informal settlements of Nairobi. The majority of the participants expect to receive feedback about their genomic results, and it is an obligation for researchers to see how to best fulfil it.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genoma / Comités de Ética en Investigación Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans País como asunto: Africa Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genoma / Comités de Ética en Investigación Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans País como asunto: Africa Idioma: En Año: 2022 Tipo del documento: Article