TY - JOUR
T1 - Outcomes of Counseling after Education about Carrier Results
T2 - A Randomized Controlled Trial
AU - Lewis, Katie L.
AU - Umstead, Kendall L.
AU - Johnston, Jennifer J.
AU - Miller, Ilana M.
AU - Thompson, Lydia J.
AU - Fishler, Kristen P.
AU - Biesecker, Leslie G.
AU - Biesecker, Barbara B.
N1 - Funding Information:
This study was funded by the National Human Genome Research Institute Intramural Research Program grants HG200317-13, HG200387-04, and HG200359-09. The authors thank the following individuals for their contributions: Cristofer Price and Niraj Trivedi for statistical consultation; Gillian Hooker for input into study design and constructs assessed in ClinSeq; Ashlee Hulbert and John Patton for assistance in the laboratory; William Fix for assistance with piloting the study; William Klein and Paul Han for contributions to the constructs assessed in ClinSeq; David Ng for his participation on the panel that assigned pathogenicity to the variants returned in this study; and Julia Fekecs, Mark T. Fredriksen, Gretchen Gibney, Anh-Dao T. Nguyen, and Tyra G. Wolfsberg for developing the web platform graphics and providing input on and programming the web platform and counseling letters used to return results. L.G.B. receives royalties from Genentech Inc., is an unpaid advisor to Illumina Inc., and received honoraria from Wiley-Blackwell Inc.
Funding Information:
This study was funded by the National Human Genome Research Institute Intramural Research Program grants HG200317-13 , HG200387-04 , and HG200359-09 . The authors thank the following individuals for their contributions: Cristofer Price and Niraj Trivedi for statistical consultation; Gillian Hooker for input into study design and constructs assessed in ClinSeq; Ashlee Hulbert and John Patton for assistance in the laboratory; William Fix for assistance with piloting the study; William Klein and Paul Han for contributions to the constructs assessed in ClinSeq; David Ng for his participation on the panel that assigned pathogenicity to the variants returned in this study; and Julia Fekecs, Mark T. Fredriksen, Gretchen Gibney, Anh-Dao T. Nguyen, and Tyra G. Wolfsberg for developing the web platform graphics and providing input on and programming the web platform and counseling letters used to return results. L.G.B. receives royalties from Genentech Inc., is an unpaid advisor to Illumina Inc., and received honoraria from Wiley-Blackwell Inc.
Publisher Copyright:
© 2018
PY - 2018/4/5
Y1 - 2018/4/5
N2 - In-person education and counseling for all people receiving genetic results is the predominant model of disclosure but is challenged by the growing volume of low-impact results generated by sequencing. Evidence suggests that web-based tools may be as effective as in-person counseling at educating individuals about their low-impact results. However, the effects of counseling have not been assessed. To evaluate its utility, carrier results were returned to 459 post-reproductive participants from the ClinSeq cohort within a randomized controlled trial. Participants received education and were randomized to receive counseling or not. Primary outcomes included risk worry, test-related positive experiences, attitudes, and decisional conflict. Secondary outcomes were satisfaction, preferences, and counseling value. There were no differences between participants who received counseling and those who did not in the primary outcomes. Participants who received counseling were more satisfied than those who did not (x¯ = 10.2 and 9.5, respectively, p < 0.002, range: 3–12), although overall satisfaction was high. Most participants (92%) randomized to counseling preferred it and valued it because it provided validation of their reactions and an opportunity for interpersonal interaction. Web-based tools address the challenge of returning low-impact results, and these data provide empiric evidence that counseling, although preferred and satisfying, is not critical to achieving desired outcomes.
AB - In-person education and counseling for all people receiving genetic results is the predominant model of disclosure but is challenged by the growing volume of low-impact results generated by sequencing. Evidence suggests that web-based tools may be as effective as in-person counseling at educating individuals about their low-impact results. However, the effects of counseling have not been assessed. To evaluate its utility, carrier results were returned to 459 post-reproductive participants from the ClinSeq cohort within a randomized controlled trial. Participants received education and were randomized to receive counseling or not. Primary outcomes included risk worry, test-related positive experiences, attitudes, and decisional conflict. Secondary outcomes were satisfaction, preferences, and counseling value. There were no differences between participants who received counseling and those who did not in the primary outcomes. Participants who received counseling were more satisfied than those who did not (x¯ = 10.2 and 9.5, respectively, p < 0.002, range: 3–12), although overall satisfaction was high. Most participants (92%) randomized to counseling preferred it and valued it because it provided validation of their reactions and an opportunity for interpersonal interaction. Web-based tools address the challenge of returning low-impact results, and these data provide empiric evidence that counseling, although preferred and satisfying, is not critical to achieving desired outcomes.
KW - genetic carrier screening
KW - genetic counseling
KW - outcomes research
KW - randomized controlled trial
KW - whole-exome sequencing
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UR - http://www.scopus.com/inward/citedby.url?scp=85042632836&partnerID=8YFLogxK
U2 - 10.1016/j.ajhg.2018.02.009
DO - 10.1016/j.ajhg.2018.02.009
M3 - Article
C2 - 29526281
AN - SCOPUS:85042632836
SN - 0002-9297
VL - 102
SP - 540
EP - 546
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 4
ER -