Uptake of Cancer Genetic Services for Chatbot vs Standard-of-Care Delivery Models

Author:

Kaphingst Kimberly A.12,Kohlmann Wendy K.1,Lorenz Chambers Rachelle3,Bather Jemar R.4,Goodman Melody S.4,Bradshaw Richard L.5,Chavez-Yenter Daniel12,Colonna Sarah V.16,Espinel Whitney F.1,Everett Jessica N.3,Flynn Michael789,Gammon Amanda1,Harris Adrian4,Hess Rachel710,Kaiser-Jackson Lauren1,Lee Sang3,Monahan Rachel311,Schiffman Joshua D.18,Volkmar Molly1,Wetter David W.110,Zhong Lingzi1,Mann Devin M.11,Ginsburg Ophira12,Sigireddi Meenakshi3,Kawamoto Kensaku5,Del Fiol Guilherme5,Buys Saundra S.17

Affiliation:

1. Huntsman Cancer Institute, Salt Lake City, Utah

2. Department of Communication, University of Utah, Salt Lake City

3. Perlmutter Cancer Center, NYU Langone Health, New York

4. School of Global Public Health, New York University, New York

5. Department of Biomedical Informatics, University of Utah, Salt Lake City

6. Veterans Administration Medical Center, Salt Lake City, Utah

7. Department of Internal Medicine, University of Utah, Salt Lake City

8. Department of Pediatrics, University of Utah, Salt Lake City

9. Community Physicians Group, University of Utah Health, Salt Lake City

10. Department of Population Health Sciences, University of Utah, Salt Lake City

11. Department of Population Health, NYU Grossman School of Medicine, New York

12. Center for Global Health, National Cancer Institute, Rockville, Maryland

Abstract

ImportanceIncreasing numbers of unaffected individuals could benefit from genetic evaluation for inherited cancer susceptibility. Automated conversational agents (ie, chatbots) are being developed for cancer genetics contexts; however, randomized comparisons with standard of care (SOC) are needed.ObjectiveTo examine whether chatbot and SOC approaches are equivalent in completion of pretest cancer genetic services and genetic testing.Design, Setting, and ParticipantsThis equivalence trial (Broadening the Reach, Impact, and Delivery of Genetic Services [BRIDGE] randomized clinical trial) was conducted between August 15, 2020, and August 31, 2023, at 2 US health care systems (University of Utah Health and NYU Langone Health). Participants were aged 25 to 60 years, had had a primary care visit in the previous 3 years, were eligible for cancer genetic evaluation, were English or Spanish speaking, had no prior cancer diagnosis other than nonmelanoma skin cancer, had no prior cancer genetic counseling or testing, and had an electronic patient portal account.InterventionParticipants were randomized 1:1 at the patient level to the study groups at each site. In the chatbot intervention group, patients were invited in a patient portal outreach message to complete a pretest genetics education chat. In the enhanced SOC control group, patients were invited to complete an SOC pretest appointment with a certified genetic counselor.Main Outcomes and MeasuresPrimary outcomes were completion of pretest cancer genetic services (ie, pretest genetics education chat or pretest genetic counseling appointment) and completion of genetic testing. Equivalence hypothesis testing was used to compare the study groups.ResultsThis study included 3073 patients (1554 in the chatbot group and 1519 in the enhanced SOC control group). Their mean (SD) age at outreach was 43.8 (9.9) years, and most (2233 of 3063 [72.9%]) were women. A total of 204 patients (7.3%) were Black, 317 (11.4%) were Latinx, and 2094 (75.0%) were White. The estimated percentage point difference for completion of pretest cancer genetic services between groups was 2.0 (95% CI, −1.1 to 5.0). The estimated percentage point difference for completion of genetic testing was −1.3 (95% CI, −3.7 to 1.1). Analyses suggested equivalence in the primary outcomes.Conclusions and RelevanceThe findings of the BRIDGE equivalence trial support the use of chatbot approaches to offer cancer genetic services. Chatbot tools can be a key component of sustainable and scalable population health management strategies to enhance access to cancer genetic services.Trial RegistrationClinicalTrials.gov Identifier: NCT03985852

Publisher

American Medical Association (AMA)

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