Breast Cancer Clinical Trial

Family History Study on Cancer Risk

Summary

This study aims to identify the optimal method to recognize, risk stratify, and provide follow-up care for individuals at risk of hereditary cancer. The study team will conduct a Hybrid Type II comparative effectiveness-implementation trial, with a mixed methods component and process/formative evaluations for stakeholder engagement. The study team will evaluate three methods for identifying and risk-stratifying individuals at risk of hereditary cancer and providing post-risk stratification longitudinal care.

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Full Description

The study team proposes a randomized, Hybrid Type II comparative effectiveness-implementation trial, with a mixed methods component and process/formative evaluations for stakeholder engagement. The study team will evaluate three methods for identifying and risk-stratifying individuals at risk of hereditary cancer and providing post-risk stratification longitudinal care.

Hypothesis: The study hypothesis is that Comparator 3 will identify more people at high risk of hereditary cancers and result in more screening behaviors, greater resource use, increased distress, higher perceived risk of cancer and higher satisfaction.

Long term objective: At study end, the study will show: 1) each comparator's strengths and weaknesses, 2) patient preferences, clinical outcomes, and compliance with each step from history collection to screening test completion, 3) the resources needed for each strategy, and 4) the contextual factors that impact their sustainability, dissemination and implementation. Study findings have high potential for generalizability because: 1) The multidisciplinary stakeholder team will help to minimize barriers to dissemination and implementation of the investigator's findings in other research settings; 2) Study results are independent of study setting; 3) The tested methods of family history assessment can occur remotely via paper or electronic interfaces; 4) The care coordination method has successful precedent in other disciplines and can be delivered remotely; 5) A process and formative evaluation with a diverse stakeholder team will inform sustainability, dissemination, and implementation, and result in an implementation guide; 6) The results will be relevant for both family history-based and direct-genetic testing strategies for population screening for hereditary cancer; 7) The results will inform population screening for any disease with hereditary risk.

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Eligibility Criteria

Inclusion Criteria:

Adult patients with ≥2 years of prior membership, ≥1 clinical visit in prior two years, and a listed email are eligible
Patients must also have received healthcare services during the past 2 years at Kaiser Permanente Northern California (KPNC) sampling sites

Exclusion Criteria:

Patients outside the targeted geographic area
Patients who cannot speak or read English (given some survey instruments are validated only in English)
Kaiser Permanente Northern California members in the no-contact database for research studies

Study is for people with:

Breast Cancer

Estimated Enrollment:

18000

Study ID:

NCT04145388

Recruitment Status:

Recruiting

Sponsor:

Kaiser Permanente

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There is 1 Location for this study

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Division of Research, Kaiser Permanente Northern California
Oakland California, 94612, United States More Info
Laura B Amsden, MSW, MPH
Contact
510-891-3870
[email protected]
Cecilia Doan, MPH
Contact
510-891-3710
[email protected]

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Study is for people with:

Breast Cancer

Estimated Enrollment:

18000

Study ID:

NCT04145388

Recruitment Status:

Recruiting

Sponsor:


Kaiser Permanente

How clear is this clinincal trial information?

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