Investigating people's attitudes towards participating in longitudinal health research: an intersectionality-informed perspective

被引:5
作者
Merz, Sibille [1 ]
Jaehn, Philipp [1 ,2 ]
Pischon, Tobias [3 ,4 ,5 ,6 ,7 ]
Fischer, Beate [8 ]
Wirkner, Kerstin [9 ]
Rach, Stefan [10 ]
Guenther, Kathrin [10 ]
Obi, Nadia
Holmberg, Christine [1 ,2 ]
AdvanceGender Study Grp
机构
[1] Brandenburg Med Sch Theodor Fontane, Inst Social Med & Epidemiol, Hochstr 15, D-14770 Brandenburg, Germany
[2] Univ Potsdam, Joint Fac Brandenburg Univ Technol Cottbus Senften, Fac Hlth Sci, Brandenburg Med Sch, Fehrbelliner Str 38, D-16816 Neuruppin, Germany
[3] Max Delbrueck Ctr Mol Med Helmholtz Assoc MDC, Mol Epidemiol Res Grp, Robert Rossle Str 10, D-13125 Berlin, Germany
[4] Max Delbrueck Ctr Mol Med Helmholtz Assoc MDC, Biobank Technol Platform, RobertRossl-Str 10, D-13125 Berlin, Germany
[5] Charite Univ Med Berlin, Core Facil Biobank, Berlin Inst Hlth, Anna Louisa Karsch Str 2, D-10178 Berlin, Germany
[6] Charite Univ Med Berlin, Freie Univ Berlin, Charitepl 1, D-10117 Berlin, Germany
[7] Humboldt Univ, Charitepl 1, D-10117 Berlin, Germany
[8] Univ Regensburg, Dept Epidemiol & Prevent Med, Franz Josef Strauss Allee 11, D-93053 Regensburg, Germany
[9] LIFE Leipzig Res Ctr Civilizat Dis, D-04103 Leipzig, Germany
[10] BIPS, Leibniz Inst Prevent Res & Epidemiol, Martinistr 52, D-20251 Hamburg, Germany
关键词
SURVEY NONRESPONSE; PUBLIC-HEALTH; BIOBANK; CONSENT; COHORT; INFORMATION; RECRUITMENT; MINORITIES; INSIGHTS; DECISION;
D O I
10.1186/s12939-022-01807-0
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Increasing evidence suggests that participation proportions in longitudinal health research vary according to sex/gender, age, social class, or migration status. Intersectionality scholarship purports that such social categories cannot be understood in isolation and makes visible the co-dependent nature of the social determinants of health and illness. This paper uses an intersectionality-informed approach in order to expand the understanding of why people participate in health research, and the impact of intersecting social structures and experiences on these attitudes.Methods A sample of 80 respondents who had previously either accepted or declined an invitation to participate in the German National Cohort (NAKO) participated in our interview study. Interviews were semi-structured and contained both narrative elements and more structured probes. Data analysis proceeded in two steps: first, the entire data set was analysed thematically (separately for participants and non-participants); second, key themes were compared across self-reported sex/gender, age group and migration status to identify differences and commonalities.Results Respondents' attitudes towards study participation can be categorised into four themes: wanting to make a contribution, seeking personalised health information, excitement and feeling chosen, and seeking social recognition. Besides citing logistical challenges, non-participants narrated adverse experiences with or attitudes towards science and the healthcare system that deterred them from participating. A range of social experiences and cultural value systems shaped such attitudes; in particular, this includes the cultural authority of science as an arbiter of social questions, transgressing social categories and experiences of marginalisation. Care responsibilities, predominantly borne by female respondents, also impacted upon the decision to take part in NAKO.Discussion Our findings suggest that for participants, health research constitutes a site of distinction in the sense of making a difference and being distinct or distinguishable, whereas non-participants inhabited an orientation towards science that reflected their subjective marginalisation through science. No clear relationship can thereby be presumed between social location and a particular attitude towards study participation; rather, such attitudes transgress and challenge categorical boundaries. This challenges the understanding of particular populations as more or less disadvantaged, or as more or less inclined to participate in health research.
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页数:18
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