Background:The concept of‘experimental public’has been recently applied to publics involved in clinical trials.This term could also be applied to publics involved in longitudinal research such as health and demograp...Background:The concept of‘experimental public’has been recently applied to publics involved in clinical trials.This term could also be applied to publics involved in longitudinal research such as health and demographic surveillance systems.The ethics of practice and public engagement with these experimental publics are of key importance and include issues of informed consent,confidentiality,collection of body tissue samples and fair local benefit.Methods:Individual(n=11)and focus group(n=5)qualitative semi-structured interviews were conducted with 56 local leaders and service providers regarding their views about research activities in a longitudinal health research study site run by the MRC/Wits Rural Public Health and Health Transitions Research Unit(Agincourt)in rural South Africa.Deductive and inductive thematic analysis was undertaken using NVivo software to identify the emergent themes.Results:There was an understanding of the usefulness of collecting demographic data,but reasons for gathering other contextual data such as on food security,as well as the reasons for collection of blood was less clear.While appreciation was expressed for feedback of individual results such as blood pressure levels during home-based data collection,there were requests for more results from biomarkers,and for these to be given at home,rather than at the clinic.There were reports of indirect refusals,and offers by leaders to assist in reducing refusal rates.There were concerns about confidentiality,especially in the publication of results.Some leaders would have liked to receive more individual level data for planning of services,although they understood this would breach confidentiality.Service providers were concerned about the withdrawal of some services post intervention trials.Conclusions:This experimental public has,over time,developed a nuanced understanding of the reasons for research and the procedures undertaken.Discussions concerning fair benefit ranged from requests for more individual clinically-relevant results for participants,to understanding how research results could assist in planning of public health services at local and national levels.The concerns illustrate the complexity of the ethics of practice which has implications for policy,practice and governance for those working in longitudinal health research sites globally.展开更多
基金supported by the University of the Witwatersrand,the South African Medical Research Council,the South African National Research Foundation through their Community Engagement Funding Instrument(grant 93,314)the EU Marie Curie Improving Population Health Through Research Exchanges’(IPHTRE)grantthe Wellcome Trust(grants 058893/Z/99/A,069683/Z/02/Z,085477/Z/08/Z,085477/B/08/Z).
文摘Background:The concept of‘experimental public’has been recently applied to publics involved in clinical trials.This term could also be applied to publics involved in longitudinal research such as health and demographic surveillance systems.The ethics of practice and public engagement with these experimental publics are of key importance and include issues of informed consent,confidentiality,collection of body tissue samples and fair local benefit.Methods:Individual(n=11)and focus group(n=5)qualitative semi-structured interviews were conducted with 56 local leaders and service providers regarding their views about research activities in a longitudinal health research study site run by the MRC/Wits Rural Public Health and Health Transitions Research Unit(Agincourt)in rural South Africa.Deductive and inductive thematic analysis was undertaken using NVivo software to identify the emergent themes.Results:There was an understanding of the usefulness of collecting demographic data,but reasons for gathering other contextual data such as on food security,as well as the reasons for collection of blood was less clear.While appreciation was expressed for feedback of individual results such as blood pressure levels during home-based data collection,there were requests for more results from biomarkers,and for these to be given at home,rather than at the clinic.There were reports of indirect refusals,and offers by leaders to assist in reducing refusal rates.There were concerns about confidentiality,especially in the publication of results.Some leaders would have liked to receive more individual level data for planning of services,although they understood this would breach confidentiality.Service providers were concerned about the withdrawal of some services post intervention trials.Conclusions:This experimental public has,over time,developed a nuanced understanding of the reasons for research and the procedures undertaken.Discussions concerning fair benefit ranged from requests for more individual clinically-relevant results for participants,to understanding how research results could assist in planning of public health services at local and national levels.The concerns illustrate the complexity of the ethics of practice which has implications for policy,practice and governance for those working in longitudinal health research sites globally.
