Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care
Abstract Background BRCA1 and BRCA2 mutations confer a substantial breast risk of developing breast cancer to those who carry them. For this reason, the United States Preventative Services Task Force (USPSTF) has recommended that all women be screened in the primary care setting for a family history...
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doaj-8c39046d7c9a4ac38226b8a17474d9b62020-11-24T21:24:39ZengBMCBMC Health Services Research1472-69632018-08-0118111210.1186/s12913-018-3442-xStudy protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary careThomas B. Silverman0Alejandro Vanegas1Awilda Marte2Jennie Mata3Margaret Sin4Juan Carlos Rodriguez Ramirez5Wei-Yann Tsai6Katherine D. Crew7Rita Kukafka8Department of Biomedical Informatics, Columbia UniversityDepartment of Biomedical Informatics, Columbia UniversityDepartment of Medicine, Columbia UniversityDepartment of Medicine, Columbia UniversityDepartment of Biomedical Informatics, Columbia UniversityDepartment of Biomedical Informatics, Columbia UniversityDepartment of Biostatistics, Columbia UniversityDepartment of Medicine, Columbia UniversityDepartment of Biomedical Informatics, Columbia UniversityAbstract Background BRCA1 and BRCA2 mutations confer a substantial breast risk of developing breast cancer to those who carry them. For this reason, the United States Preventative Services Task Force (USPSTF) has recommended that all women be screened in the primary care setting for a family history indicative of a mutation, and women with strong family histories of breast or ovarian cancer be referred to genetic counseling. However, few high-risk women are being routinely screened and fewer are referred to genetic counseling. To address this need we have developed two decision support tools that are integrated into clinical care. Method This study is a cluster randomized controlled trial of high-risk patients and their health care providers. Patient-provider dyads will be randomized to receive either standard education that is supplemented with the patient-facing decision aid, RealRisks, and the provider-facing Breast Cancer Risk Navigation Toolbox (BNAV) or standard education alone. We will assess these tools’ effectiveness in promoting genetic counseling uptake and informed and shared decision making about genetic testing. Discussion If found to be effective, these tools can help integrate genomic risk assessment into primary care and, ultimately, help expand access to risk-appropriate breast cancer prevention options to a broader population of high-risk women. Trial registration This trial is retrospectively registered with ClinicalTrials.gov Identifier: NCT03470402: 20 March 2018.http://link.springer.com/article/10.1186/s12913-018-3442-xBreast Cancer preventionDecision supportRisk communicationGenetic testing |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Thomas B. Silverman Alejandro Vanegas Awilda Marte Jennie Mata Margaret Sin Juan Carlos Rodriguez Ramirez Wei-Yann Tsai Katherine D. Crew Rita Kukafka |
spellingShingle |
Thomas B. Silverman Alejandro Vanegas Awilda Marte Jennie Mata Margaret Sin Juan Carlos Rodriguez Ramirez Wei-Yann Tsai Katherine D. Crew Rita Kukafka Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care BMC Health Services Research Breast Cancer prevention Decision support Risk communication Genetic testing |
author_facet |
Thomas B. Silverman Alejandro Vanegas Awilda Marte Jennie Mata Margaret Sin Juan Carlos Rodriguez Ramirez Wei-Yann Tsai Katherine D. Crew Rita Kukafka |
author_sort |
Thomas B. Silverman |
title |
Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care |
title_short |
Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care |
title_full |
Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care |
title_fullStr |
Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care |
title_full_unstemmed |
Study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing BRCA1/2 genetic counseling referral in primary care |
title_sort |
study protocol: a cluster randomized controlled trial of web-based decision support tools for increasing brca1/2 genetic counseling referral in primary care |
publisher |
BMC |
series |
BMC Health Services Research |
issn |
1472-6963 |
publishDate |
2018-08-01 |
description |
Abstract Background BRCA1 and BRCA2 mutations confer a substantial breast risk of developing breast cancer to those who carry them. For this reason, the United States Preventative Services Task Force (USPSTF) has recommended that all women be screened in the primary care setting for a family history indicative of a mutation, and women with strong family histories of breast or ovarian cancer be referred to genetic counseling. However, few high-risk women are being routinely screened and fewer are referred to genetic counseling. To address this need we have developed two decision support tools that are integrated into clinical care. Method This study is a cluster randomized controlled trial of high-risk patients and their health care providers. Patient-provider dyads will be randomized to receive either standard education that is supplemented with the patient-facing decision aid, RealRisks, and the provider-facing Breast Cancer Risk Navigation Toolbox (BNAV) or standard education alone. We will assess these tools’ effectiveness in promoting genetic counseling uptake and informed and shared decision making about genetic testing. Discussion If found to be effective, these tools can help integrate genomic risk assessment into primary care and, ultimately, help expand access to risk-appropriate breast cancer prevention options to a broader population of high-risk women. Trial registration This trial is retrospectively registered with ClinicalTrials.gov Identifier: NCT03470402: 20 March 2018. |
topic |
Breast Cancer prevention Decision support Risk communication Genetic testing |
url |
http://link.springer.com/article/10.1186/s12913-018-3442-x |
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