Cargando…

Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa

BACKGROUND: Limited research has been conducted on explanations and understandings of biobanking for future genomic research in African contexts with low literacy and limited healthcare access. We report on the findings of a sub-study on participant understanding embedded in a multi-disease communit...

Descripción completa

Detalles Bibliográficos
Autores principales: Luthuli, Manono, Ngwenya, Nothando, Gumede, Dumsani, Gunda, Resign, Gareta, Dickman, Koole, Olivier, Siedner, Mark J., Wong, Emily B., Seeley, Janet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014601/
https://www.ncbi.nlm.nih.gov/pubmed/35436913
http://dx.doi.org/10.1186/s12910-022-00782-z
_version_ 1784688218648608768
author Luthuli, Manono
Ngwenya, Nothando
Gumede, Dumsani
Gunda, Resign
Gareta, Dickman
Koole, Olivier
Siedner, Mark J.
Wong, Emily B.
Seeley, Janet
author_facet Luthuli, Manono
Ngwenya, Nothando
Gumede, Dumsani
Gunda, Resign
Gareta, Dickman
Koole, Olivier
Siedner, Mark J.
Wong, Emily B.
Seeley, Janet
author_sort Luthuli, Manono
collection PubMed
description BACKGROUND: Limited research has been conducted on explanations and understandings of biobanking for future genomic research in African contexts with low literacy and limited healthcare access. We report on the findings of a sub-study on participant understanding embedded in a multi-disease community health screening and biobank platform study known as ‘Vukuzazi’ in rural KwaZulu-Natal, South Africa. METHODS: Semi-structured interviews were conducted with research participants who had been invited to take part in the Vukuzazi study, including both participants and non-participants, and research staff that worked on the study. The interviews were transcribed, and themes were identified from the interview transcripts, manually coded, and thematically analysed. RESULTS: Thirty-nine individuals were interviewed. We found that the research team explained biobanking and future genomic research by describing how hereditary characteristics create similarities among individuals. However, recollection and understanding of this explanation seven months after participation was variable. The large volume of information about the Vukuzazi study objectives and procedures presented a challenge to participant recall. By the time of interviews, some participants recalled rudimentary facts about the genetic aspects of the study, but many expressed little to no interest in genetics and biobanking. CONCLUSION: Participant’s understanding of information related to genetics and biobanking provided during the consent process is affected by the volume of information as well as participant’s interest (or lack thereof) in the subject matter being discussed. We recommend that future studies undertaking biobanking and genomic research treat explanations of this kind of research to participants as an on-going process of communication between researchers, participants and the community and that explanatory imagery and video graphic storytelling should be incorporated into theses explanations as these have previously been found to facilitate understanding among those with low literacy levels. Studies should also avoid having broader research objectives as this can divert participant’s interest and therefore understanding of why their samples are being collected. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-022-00782-z.
format Online
Article
Text
id pubmed-9014601
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-90146012022-04-19 Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa Luthuli, Manono Ngwenya, Nothando Gumede, Dumsani Gunda, Resign Gareta, Dickman Koole, Olivier Siedner, Mark J. Wong, Emily B. Seeley, Janet BMC Med Ethics Research BACKGROUND: Limited research has been conducted on explanations and understandings of biobanking for future genomic research in African contexts with low literacy and limited healthcare access. We report on the findings of a sub-study on participant understanding embedded in a multi-disease community health screening and biobank platform study known as ‘Vukuzazi’ in rural KwaZulu-Natal, South Africa. METHODS: Semi-structured interviews were conducted with research participants who had been invited to take part in the Vukuzazi study, including both participants and non-participants, and research staff that worked on the study. The interviews were transcribed, and themes were identified from the interview transcripts, manually coded, and thematically analysed. RESULTS: Thirty-nine individuals were interviewed. We found that the research team explained biobanking and future genomic research by describing how hereditary characteristics create similarities among individuals. However, recollection and understanding of this explanation seven months after participation was variable. The large volume of information about the Vukuzazi study objectives and procedures presented a challenge to participant recall. By the time of interviews, some participants recalled rudimentary facts about the genetic aspects of the study, but many expressed little to no interest in genetics and biobanking. CONCLUSION: Participant’s understanding of information related to genetics and biobanking provided during the consent process is affected by the volume of information as well as participant’s interest (or lack thereof) in the subject matter being discussed. We recommend that future studies undertaking biobanking and genomic research treat explanations of this kind of research to participants as an on-going process of communication between researchers, participants and the community and that explanatory imagery and video graphic storytelling should be incorporated into theses explanations as these have previously been found to facilitate understanding among those with low literacy levels. Studies should also avoid having broader research objectives as this can divert participant’s interest and therefore understanding of why their samples are being collected. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-022-00782-z. BioMed Central 2022-04-18 /pmc/articles/PMC9014601/ /pubmed/35436913 http://dx.doi.org/10.1186/s12910-022-00782-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Luthuli, Manono
Ngwenya, Nothando
Gumede, Dumsani
Gunda, Resign
Gareta, Dickman
Koole, Olivier
Siedner, Mark J.
Wong, Emily B.
Seeley, Janet
Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa
title Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa
title_full Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa
title_fullStr Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa
title_full_unstemmed Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa
title_short Participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural South Africa
title_sort participant recall and understandings of information on biobanking and future genomic research: experiences from a multi-disease community-based health screening and biobank platform in rural south africa
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014601/
https://www.ncbi.nlm.nih.gov/pubmed/35436913
http://dx.doi.org/10.1186/s12910-022-00782-z
work_keys_str_mv AT luthulimanono participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT ngwenyanothando participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT gumededumsani participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT gundaresign participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT garetadickman participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT kooleolivier participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT siednermarkj participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT wongemilyb participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica
AT seeleyjanet participantrecallandunderstandingsofinformationonbiobankingandfuturegenomicresearchexperiencesfromamultidiseasecommunitybasedhealthscreeningandbiobankplatforminruralsouthafrica