TY - JOUR
T1 - A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research
AU - Biesecker, Barbara B.
AU - Lillie, Sarah E.
AU - Amendola, Laura M.
AU - Donohue, Katherine E.
AU - East, Kelly M.
AU - Foreman, Ann Katherine M.
AU - Gilmore, Marian J.
AU - Greve, Veronica
AU - Liangolou, Billie
AU - O'Daniel, Julianne M.
AU - Odgis, Jacqueline A.
AU - Rego, Shannon
AU - Rolf, Bradley
AU - Scollon, Sarah
AU - Suckiel, Sabrina A.
AU - Zepp, Jamilyn
AU - Joseph, Galen
N1 - Publisher Copyright:
© 2020 National Society of Genetic Counselors
PY - 2021/2
Y1 - 2021/2
N2 - The descriptor ‘usual care’ refers to standard or routine care. Yet, no formal definition exists. The need to define what constitutes usual care arises in clinical research. Often one arm in a trial represents usual care in comparison with a novel intervention. Accordingly, usual care in genetic counseling research appears predominantly in randomized controlled trials. Recent standards for reporting genetic counseling research call for standardization, but do not address usual care. We (1) inventoried all seven studies in the Clinical Sequencing Evidence-Generating Consortium (CSER) about how genetic counseling was conceptualized, conducted, and whether a usual care arm was involved; (2) conducted a review of published randomized control trials in genetic counseling, comparing how researchers describe usual care groups; and (3) reviewed existing professionally endorsed definitions and practice descriptions of genetic counseling. We found wide variation in the content and delivery of usual care. Descriptions frequently detailed the content of usual care, most often noting assessment of genetic risk factors, collecting family histories, and offering testing. A minority included addressing psychological concerns or the risks versus benefits of testing. Descriptions of how care was delivered were vague except for mode and type of clinician, which varied. This significant variation, beyond differences expected among subspecialties, reduces the validity and generalizability of genetic counseling research. Ideally, research reflects clinical practice so that evidence generated can be used to improve clinical outcomes. To address this objective, we propose a definition of usual care in genetic counseling research that merges common elements from the National Society of Genetic Counselors’ practice definition, the Reciprocal Engagement Model, and the Accreditation Council for Genetic Counselors’ practice-based competencies. Promoting consistent execution of usual care in the design of genetic counseling trials can lead to more consistency in representing clinical care and facilitate the generation of evidence to improve it.
AB - The descriptor ‘usual care’ refers to standard or routine care. Yet, no formal definition exists. The need to define what constitutes usual care arises in clinical research. Often one arm in a trial represents usual care in comparison with a novel intervention. Accordingly, usual care in genetic counseling research appears predominantly in randomized controlled trials. Recent standards for reporting genetic counseling research call for standardization, but do not address usual care. We (1) inventoried all seven studies in the Clinical Sequencing Evidence-Generating Consortium (CSER) about how genetic counseling was conceptualized, conducted, and whether a usual care arm was involved; (2) conducted a review of published randomized control trials in genetic counseling, comparing how researchers describe usual care groups; and (3) reviewed existing professionally endorsed definitions and practice descriptions of genetic counseling. We found wide variation in the content and delivery of usual care. Descriptions frequently detailed the content of usual care, most often noting assessment of genetic risk factors, collecting family histories, and offering testing. A minority included addressing psychological concerns or the risks versus benefits of testing. Descriptions of how care was delivered were vague except for mode and type of clinician, which varied. This significant variation, beyond differences expected among subspecialties, reduces the validity and generalizability of genetic counseling research. Ideally, research reflects clinical practice so that evidence generated can be used to improve clinical outcomes. To address this objective, we propose a definition of usual care in genetic counseling research that merges common elements from the National Society of Genetic Counselors’ practice definition, the Reciprocal Engagement Model, and the Accreditation Council for Genetic Counselors’ practice-based competencies. Promoting consistent execution of usual care in the design of genetic counseling trials can lead to more consistency in representing clinical care and facilitate the generation of evidence to improve it.
KW - genetic counseling interventions
KW - genetic counseling research
KW - randomized controlled trials
KW - usual care
UR - http://www.scopus.com/inward/record.url?scp=85097051347&partnerID=8YFLogxK
U2 - 10.1002/jgc4.1363
DO - 10.1002/jgc4.1363
M3 - Article
C2 - 33278053
AN - SCOPUS:85097051347
SN - 1059-7700
VL - 30
SP - 42
EP - 50
JO - Journal of Genetic Counseling
JF - Journal of Genetic Counseling
IS - 1
ER -