Conditional trust as a driver of public engagement in Korea’s national project of bio-big data

Public perception of biodata collection reflected a mix of anticipated personal and public benefits, alongside concerns regarding data disclosure. Willingness to participate was influenced more by personal benefits (60.9%) than by public interest (29.9%). While personal incentives such as treatment cost coverage were valued, participation was also driven by a desire to contribute to research and support drug development, reflecting a blend of self-interest and altruistic motivation. Concerns centered on data leakage, with dynamic consent emerging as a key condition of trust, alongside public governance and the right to information. To secure public trust and increase participation in the NPBBD, tailored strategies must be used to balance personal and public benefits with transparent governance, information provision, and consent procedures.

Authors

Institutions

Publication Details

Journal
Frontiers in Genetics
Published
2026-01-04
DOI
https://doi.org/10.3389/fgene.2025.1713598
Primary Topic
Ethics in Clinical Research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Conditional trust as a driver of public engagement in Korea’s national project of bio-big data

Huiwon No, Yul Gyo Jung, Jae Sun Kim, Seung Hyun Kim et al.
Frontiers in Genetics
Ethics in Clinical Research
article

Conditional trust as a driver of public engagement in Korea’s national project of bio-big data

Huiwon No, Yul Gyo Jung, Jae Sun Kim, Seung Hyun Kim, Kwangmo Yang, Sungsoo Lim, Ilhak Lee, Cheyeon Lee, Wonoh Jeong
article en

Abstract

Public perception of biodata collection reflected a mix of anticipated personal and public benefits, alongside concerns regarding data disclosure. Willingness to participate was influenced more by personal benefits (60.9%) than by public interest (29.9%). While personal incentives such as treatment cost coverage were valued, participation was also driven by a desire to contribute to research and support drug development, reflecting a blend of self-interest and altruistic motivation. Concerns centered on data leakage, with dynamic consent emerging as a key condition of trust, alongside public governance and the right to information. To secure public trust and increase participation in the NPBBD, tailored strategies must be used to balance personal and public benefits with transparent governance, information provision, and consent procedures.

Frontiers in GeneticsVol. 16
Yonsei University (KR), Dongguk University (KR), Samsung (South Korea) (KR), Samsung Medical Center (KR), Gallup Korea (KR), Sungkyunkwan University (KR)
National IT Industry Promotion Agency, Korea Health Industry Development Institute, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 97%
Ethics in Clinical Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.