4.6 Article

Randomized study of remote telehealth genetic services versus usual care in oncology practices without genetic counselors

Journal

CANCER MEDICINE
Volume 10, Issue 13, Pages 4532-4541

Publisher

WILEY
DOI: 10.1002/cam4.3968

Keywords

alternative service delivery; cancer genetics; cancer predisposition syndromes; genetics; genetic counseling; genetic testing; telegenetics; telehealth; telemedicine

Categories

Funding

  1. Basser Center

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The study found that telehealth can increase the uptake of genetic counseling and testing at oncology practices without genetic counselors, potentially improving the identification of genetic carriers and cancer prevention outcomes.
Purpose To examine the benefit of telehealth over current delivery options in oncology practices without genetic counselors. Methods Participants meeting cancer genetic testing guidelines were recruited to this multi-center, randomized trial comparing uptake of genetic services with remote services (telephone or videoconference) to usual care in six predominantly community practices without genetic counselors. The primary outcome was the composite uptake of genetic counseling or testing. Secondary outcomes compare telephone versus videoconference services. Results 147 participants enrolled and 119 were randomized. Eighty percent of participants in the telehealth arm had genetic services as compared to 16% in the usual care arm (OR 30.52, p < 0.001). Five genetic mutation carriers (6.7%) were identified in the telehealth arm, compared to none in the usual care arm. In secondary analyses, factors associated with uptake were lower anxiety (6.77 vs. 8.07, p = 0.04) and lower depression (3.38 vs. 5.06, p = 0.04) among those who had genetic services. There were no significant differences in change in cognitive or affective outcomes immediately post-counseling and at 6 and 12 months between telephone and videoconference arms. Conclusion Telehealth increases uptake of genetic counseling and testing at oncology practices without genetic counselors and could significantly improve identification of genetic carriers and cancer prevention outcomes.

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