Evidence map›Paper›PMID 40616077›Full record

ArticleBMC medical ethics2025

How participation in deliberative engagement affects awareness of, and attitudes towards, genomics research and data sharing: evidence from rural Ghana.

Irene Honam Tsey, Pamela Emefa Selormey, John Ganle, Patricia Akweongo, Paulina Tindana

Abstract read
In one paragraph

Article in BMC medical ethics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Irene Honam TseyDepartment of Health Policy, Planning and Management, School of Public Health, College of Health Sciences, University of Ghana, Accra, Ghana. itsey@uhas.edu.gh.
Pamela Emefa SelormeyDepartment of Health Policy, Planning and Management, School of Public Health, College of Health Sciences, University of Ghana, Accra, Ghana.
John GanleDepartment of Population, Family and Reproductive Health, School of Public Health, College of Health Sciences, University of Ghana, Accra, Ghana.
Patricia AkweongoDepartment of Health Policy, Planning and Management, School of Public Health, College of Health Sciences, University of Ghana, Accra, Ghana.
Paulina TindanaDepartment of Health Policy, Planning and Management, School of Public Health, College of Health Sciences, University of Ghana, Accra, Ghana.

Funding

Project-005U54HG010275 · NHGRI · NOGUCHI MEMORIAL INSTITUTE / MEDICAL RES · PI GHANSAH, ANITA, TINDANA, PAULINA · 2018 to 2021
$1.7M
National Institute of Health (NIH), United States No. 5U54HG010275NHGRI NIH HHS U54 HG010275
6 · The paper itself

Abstract

backgroundDeliberative engagement offers an opportunity for communities to provide informed opinions on complex ethical, legal, and social issues in genomic research and biobanking. However, its use is limited, particularly in resource-constrained settings like Ghana. This study examines the influence of deliberative engagement on participants’ awareness of genomic research and attitudes towards data sharing.

methodsThis research forms part of a larger mixed-methods study exploring deliberative methods for community engagement in genomics research in Ghana. Using a quasi-experimental one-group pretest-posttest design, 66 participants completed a baseline survey assessing awareness of genomic research and attitudes toward data sharing. Following this, a deliberative workshop was conducted with facilitated discussions. Post-engagement surveys measured changes in awareness and attitudes, and Fisher’s exact test was used to assess statistical significance.

resultsRespondents (aged 47–67 years; mean 57, SD 4.2) were predominantly male (65%), with 18% having no formal education. Significant improvements were observed in participants’ awareness of genomic research (51–90%, p = 0.001) and confidence in consent processes ensuring privacy and confidentiality. Other variables, including willingness to share samples and trust in data governance, showed no significant change.

conclusionsThis study demonstrates that deliberative engagement could enhance awareness of genomic research and offers a promising approach to informing, educating, and fostering dialogue on complex ethical issues in genomic research and biobanking, particularly in resource-limited settings. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

AttitudeAwarenessCommunity ParticipationGenetic ResearchGenomicsHealth Knowledge, Attitudes, PracticeInformation DisseminationAgedBiological Specimen BanksConfidentialityFemaleGhanaHumansInformed ConsentMaleMiddle AgedBiobankingData sharingDeliberative engagementGenomic researchGhana

Identifiers

PMID40616077
PMCPMC12231673

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.