TY - JOUR
T1 - Longitudinal changes in patient distress following interactive decision aid use among BRCA1/2 carriers
T2 - A randomized trial
AU - Hooker, Gillian W.
AU - Leventhal, Kara Grace
AU - DeMarco, Tiffani
AU - Peshkin, Beth N.
AU - Finch, Clinton
AU - Wahl, Erica
AU - Joines, Jessica Rispoli
AU - Brown, Karen
AU - Valdimarsdottir, Heiddis
AU - Schwartz, Marc D.
N1 - Funding Information:
The authors thank Michael Green, Lisa Moss, and Sharon Hecker for their contributions to this research. Institutional review board approval was granted for this study, and all participants provided informed consent. This research was supported by National Cancer Institute grant R01 CA1846 and by the Jess and Mildred Fisher Center for Familial Cancer Research. The authors do not have any financial conflicts to disclose.
PY - 2011/5
Y1 - 2011/5
N2 - Background. Increasingly, women with a strong family history of breast cancer are seeking genetic testing as a starting point to making significant decisions regarding management of their cancer risks. Individuals who are found to be carriers of a BRCA1 or BRCA2 mutation have a substantially elevated risk for breast cancer and are frequently faced with the decision of whether to undergo risk-reducing mastectomy. Objective. In order to provide BRCA1/2 carriers with ongoing decision support for breast cancer risk management, a computer-based interactive decision aid was developed and tested against usual care in a randomized controlled trial. Design. Following genetic counseling, 214 female (aged 21-75 years) BRCA1/2 mutation carriers were randomized to usual care (UC; n = 114) or usual care plus decision aid (DA; n = 100) arms. UC participants received no further intervention; DA participants were sent the CD-ROM-based decision aid to view at home. Main Outcome Measures. The authors measured general distress, cancer-specific distress, and genetic testing-specific distress at 1-, 6-, and 12-month follow-up time points postrandomization. Results. Longitudinal analyses revealed a significant longitudinal impact of the DA on cancer-specific distress (B = 5.67, z = 2.81, P = 0.005), which varied over time (DA group by time; B = -2.19, z = -2.47, P = 0.01), and on genetic testing-specific distress (B = 5.55, z = 2.46, P = 0.01), which also varied over time (DA group by time; B = -2.46, z = -2.51, P = 0.01). Individuals randomized to UC reported significantly decreased distress in the month following randomization, whereas individuals randomized to the DA maintained their postdisclosure distress over the short term. By 12 months, the overall decrease in distress between the 2 groups was similar. Conclusion. This report provides new insight into the long-term longitudinal effects of DAs.
AB - Background. Increasingly, women with a strong family history of breast cancer are seeking genetic testing as a starting point to making significant decisions regarding management of their cancer risks. Individuals who are found to be carriers of a BRCA1 or BRCA2 mutation have a substantially elevated risk for breast cancer and are frequently faced with the decision of whether to undergo risk-reducing mastectomy. Objective. In order to provide BRCA1/2 carriers with ongoing decision support for breast cancer risk management, a computer-based interactive decision aid was developed and tested against usual care in a randomized controlled trial. Design. Following genetic counseling, 214 female (aged 21-75 years) BRCA1/2 mutation carriers were randomized to usual care (UC; n = 114) or usual care plus decision aid (DA; n = 100) arms. UC participants received no further intervention; DA participants were sent the CD-ROM-based decision aid to view at home. Main Outcome Measures. The authors measured general distress, cancer-specific distress, and genetic testing-specific distress at 1-, 6-, and 12-month follow-up time points postrandomization. Results. Longitudinal analyses revealed a significant longitudinal impact of the DA on cancer-specific distress (B = 5.67, z = 2.81, P = 0.005), which varied over time (DA group by time; B = -2.19, z = -2.47, P = 0.01), and on genetic testing-specific distress (B = 5.55, z = 2.46, P = 0.01), which also varied over time (DA group by time; B = -2.46, z = -2.51, P = 0.01). Individuals randomized to UC reported significantly decreased distress in the month following randomization, whereas individuals randomized to the DA maintained their postdisclosure distress over the short term. By 12 months, the overall decrease in distress between the 2 groups was similar. Conclusion. This report provides new insight into the long-term longitudinal effects of DAs.
KW - breast cancer/mammography
KW - genetics
KW - oncology
UR - http://www.scopus.com/inward/record.url?scp=79957592143&partnerID=8YFLogxK
U2 - 10.1177/0272989X10381283
DO - 10.1177/0272989X10381283
M3 - Article
C2 - 20876346
AN - SCOPUS:79957592143
VL - 31
SP - 412
EP - 421
JO - Medical Decision Making
JF - Medical Decision Making
SN - 0272-989X
IS - 3
ER -