TY - JOUR
T1 - “It takes a village”
T2 - multilevel approaches to recruit African Americans and their families for genetic research
AU - Ochs-Balcom, Heather M.
AU - Jandorf, Lina
AU - Wang, Youjin
AU - Johnson, Detric
AU - Meadows Ray, Veronica
AU - Willis, Mattye J.
AU - Erwin, Deborah O.
N1 - Publisher Copyright:
© 2014, Springer-Verlag Berlin Heidelberg.
PY - 2015/1
Y1 - 2015/1
N2 - One barrier to searching for novel mutations in African American families with breast cancer is the challenge of effectively recruiting families—affected and non-affected relatives—into genetic research studies. Using a community-based participatory research (CBPR) orientation, we incorporated several evidence-based approaches through an iterative fashion to recruit for a breast cancer genetic epidemiology study in African Americans. Our combined methods allowed us to successfully recruit 341 African American women (247 with breast cancer and 94 relatives without breast cancer) from 127 families. Twenty-nine percent of participants were recruited through National Witness Project (NWP) sites, 11 % came from in-person encounters by NWP members, 34 % from the Love Army of Women, 24 % from previous epidemiologic studies, and 2 % from a support group. In terms of demographics, our varied recruitment methods/sources yielded samples of African American women that differ in terms of several sociodemographic factors such as education, smoking, and BMI, as well as family size. To successfully recruit African American families into epidemiological research, investigators should include community members in the recruitment processes, be flexible in the adoption of multipronged, iterative methods, and provide clear communication strategies about the underlying benefit to potential participants. Our results enhance our understanding of potential benefits and challenges associated with various recruitment methods. We offer a template for the design of future studies and suggest that generalizability may be better achieved by using multipronged approaches.
AB - One barrier to searching for novel mutations in African American families with breast cancer is the challenge of effectively recruiting families—affected and non-affected relatives—into genetic research studies. Using a community-based participatory research (CBPR) orientation, we incorporated several evidence-based approaches through an iterative fashion to recruit for a breast cancer genetic epidemiology study in African Americans. Our combined methods allowed us to successfully recruit 341 African American women (247 with breast cancer and 94 relatives without breast cancer) from 127 families. Twenty-nine percent of participants were recruited through National Witness Project (NWP) sites, 11 % came from in-person encounters by NWP members, 34 % from the Love Army of Women, 24 % from previous epidemiologic studies, and 2 % from a support group. In terms of demographics, our varied recruitment methods/sources yielded samples of African American women that differ in terms of several sociodemographic factors such as education, smoking, and BMI, as well as family size. To successfully recruit African American families into epidemiological research, investigators should include community members in the recruitment processes, be flexible in the adoption of multipronged, iterative methods, and provide clear communication strategies about the underlying benefit to potential participants. Our results enhance our understanding of potential benefits and challenges associated with various recruitment methods. We offer a template for the design of future studies and suggest that generalizability may be better achieved by using multipronged approaches.
KW - African American
KW - Breast cancer
KW - Community-based participatory research (CBPR)
KW - Genetic epidemiology
UR - https://www.scopus.com/pages/publications/84939874440
U2 - 10.1007/s12687-014-0199-8
DO - 10.1007/s12687-014-0199-8
M3 - Article
AN - SCOPUS:84939874440
SN - 1868-310X
VL - 6
SP - 39
EP - 45
JO - Journal of Community Genetics
JF - Journal of Community Genetics
IS - 1
ER -