Grant Number:	1R01CA211625-01 Interpret this number
Primary Investigator:	Kinney, Anita
Organization:	University Of New Mexico Health Scis Ctr
Project Title:	Comparative Effectiveness of Interventions to Increase Guideline-Based Genetic Counseling in Ethnically and Geographically Diverse Cancer Survivors
Fiscal Year:	2017

Genetic counseling or Cancer Genetic Risk Assessment (CGRA) for hereditary breast and ovarian cancer (HBOC) is an evidence-based precision medicine strategy that facilitates informed decision making about effective health management options. Identification of individuals at increased risk of HBOC is crucial for cancer survivors and their families to benefit from biomedical advances in cancer prevention, early detection, treatment and survivorship. Although national guidelines for CGRA and genetic testing have been available for two decades, only one-third or less of high-risk women have accessed these services. The optimal risk assessment strategy starts with an individual with an HBOC-related cancer. Widespread dissemination and adoption of national guidelines for informed decision-making and promoting CGRA is needed to achieve a population-level reduction in cancer morbidity, mortality and disparities. Thus, it is important to promote access to CGRA, particularly in medically underserved populations. The proposed Genetic Risk Assessment for Cancer Education and Empowerment (GRACE) Project seeks to address this important translational gap by developing and implementing strategies to promote guideline-based care in the Rocky Mountain region where there are distinguishable disparities in CGRA utilization by ethnicity and geography. Remarkably, few intervention studies have been conducted to address the regional and national translational gap in CGRA utilization for these diverse populations, underscoring our study's high impact and innovative public health intervention delivery approach. The GRACE Project is guided by evidenced-based behavior change counseling strategies to promote risk-based care delivery and reduce disparities that consider individual, cultural, social and system-level factors. The study's primary aim is to test the comparative effectiveness of mailed targeted print (TP) vs. TP plus a telephone-based tailored counseling and navigation intervention (TCN) vs. usual care (UC) to increase guideline-based CGRA for HBOC. We will oversample Hispanics and rural dwellers and enroll 1206 high-risk female cancer survivors. Women will be recruited through the Colorado and New Mexico cancer registries and meet the criteria for a CGRA referral. Enrollees will be randomized to one of 3 study arms and complete baseline, 1-month, 6-month and 12-month surveys. Specific aims are to: 1) compare the effectiveness of a targeted intervention (TP) vs. a tailored (TPC) intervention vs. usual care (UC) on CGRA utilization 6 months (primary outcome) after the intervention and at 12 months, after removal of key access barriers; 2) compare the effectiveness of the interventions on genetic testing utilization; 3) examine potential underlying theoretical mediating and moderating mechanisms that will further specify and elucidate significant intervention effects; and 4) compare the cost effectiveness of the interventions vs. usual care, for utilization of CGRA services. If effective, either or both interventions have the potential to reach a large number of high-risk families and reduce disparities through broad dissemination.




Randomized trial promoting cancer genetic risk assessment when genetic counseling cost removed: 1-year follow-up.
Authors: An J. , McDougall J. , Lin Y. , Lu S.E. , Walters S.T. , Heidt E. , Stroup A. , Paddock L. , Grumet S. , Toppmeyer D. , et al. .
Source: Jnci Cancer Spectrum, 2024-03-15 00:00:00.0; , .
EPub date: 2024-03-15 00:00:00.0.
PMID: 38490263
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Identifying Mediators of Intervention Effects Within a Randomized Controlled Trial to Motivate Cancer Genetic Risk Assessment Among Breast and Ovarian Cancer Survivors.
Authors: An J. , Lu S.E. , McDougall J. , Walters S.T. , Lin Y. , Heidt E. , Stroup A. , Paddock L. , Grumet S. , Toppmeyer D. , et al. .
Source: Annals Of Behavioral Medicine : A Publication Of The Society Of Behavioral Medicine, 2023-09-02 00:00:00.0; , .
EPub date: 2023-09-02 00:00:00.0.
PMID: 37658805
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Improving Uptake of Cancer Genetic Risk Assessment in a Remote Tailored Risk Communication and Navigation Intervention: Large Effect Size but Room to Grow.
Authors: Kinney A.Y. , Walters S.T. , Lin Y. , Lu S.E. , Kim A. , Ani J. , Heidt E. , Le Compte C.J.G. , O'Malley D. , Stroup A. , et al. .
Source: Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology, 2023-02-14 00:00:00.0; , p. JCO2200751.
EPub date: 2023-02-14 00:00:00.0.
PMID: 36787512
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Understanding cancer genetic risk assessment motivations in a remote tailored risk communication and navigation intervention randomized controlled trial.
Authors: Le Compte C.G. , Lu S.E. , Ani J. , McDougall J. , Walters S.T. , Toppmeyer D. , Boyce T.W. , Stroup A. , Paddock L. , Grumet S. , et al. .
Source: Health Psychology And Behavioral Medicine, 2022; 10(1), p. 1190-1215.
EPub date: 2022-12-09 00:00:00.0.
PMID: 36518606
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Promoting guideline-based cancer genetic risk assessment for hereditary breast and ovarian cancer in ethnically and geographically diverse cancer survivors: Rationale and design of a 3-arm randomized controlled trial.
Authors: Kinney A.Y. , Howell R. , Ruckman R. , McDougall J.A. , Boyce T.W. , Vicuña B. , Lee J.H. , Guest D.D. , Rycroft R. , Valverde P.A. , et al. .
Source: Contemporary Clinical Trials, 2018 Oct; 73, p. 123-135.
EPub date: 2018-09-18 00:00:00.0.
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