Academic Journal
Knowledge of cancer genetics and attitudes about genetic counseling and testing: a randomized trial of the Know Your Risk intervention compared to conventional genetic counseling.
| Τίτλος: | Knowledge of cancer genetics and attitudes about genetic counseling and testing: a randomized trial of the Know Your Risk intervention compared to conventional genetic counseling. |
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| Συγγραφείς: | Katz ML; Division of Health Behavior and Health Promotion, College of Public Health, The Ohio State University, Columbus, OH, USA. mira.katz@osumc.edu.; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA. mira.katz@osumc.edu.; The Ohio State University, Room 212, 3650 Olentangy River Road, Columbus, OH, 43214, USA. mira.katz@osumc.edu., Schnell PM; Division of Biostatistics, College of Public Health, The Ohio State University, Columbus, OH, USA., Reiter PL; Division of Health Behavior and Health Promotion, College of Public Health, The Ohio State University, Columbus, OH, USA.; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA., Senter L; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Aeilts A; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Spears C; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Cooper J; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Brown J; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Shane-Carson KP; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Agnese DM; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.; Department of Surgery, College of Medicine, The Ohio State University, Columbus, OH, USA., Toland AE; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.; Department of Cancer Biology and Genetics, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA., Sweet K; Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.; Division of Human Genetics, Department of Internal Medicine, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA. |
| Πηγή: | Cancer causes & control : CCC [Cancer Causes Control] 2026 Jun 30; Vol. 37 (7). Date of Electronic Publication: 2026 Jun 30. |
| Τύπος έκδοσης: | Journal Article; Randomized Controlled Trial |
| Γλώσσα: | English |
| Στοιχεία περιοδικού: | Publisher: Kluwer Academic Publishers Country of Publication: Netherlands NLM ID: 9100846 Publication Model: Electronic Cited Medium: Internet ISSN: 1573-7225 (Electronic) Linking ISSN: 09575243 NLM ISO Abbreviation: Cancer Causes Control Subsets: MEDLINE |
| Imprint Name(s): | Publication: Dordrecht : Kluwer Academic Publishers Original Publication: Oxford, UK : Rapid Communications of Oxford Ltd., 1990- |
| Ιατρικοί όροι (MeSH): | Genetic Counseling*/methods , Genetic Counseling*/psychology , Genetic Testing*/methods , Breast Neoplasms*/genetics , Breast Neoplasms*/psychology , Breast Neoplasms*/diagnosis , Health Knowledge, Attitudes, Practice*, Humans ; Female ; Middle Aged ; Adult ; Genetic Predisposition to Disease ; Surveys and Questionnaires |
| Περίληψη: | Purpose: To determine if the developed Know Your Risk (KYR) intervention is similar to conventional genetic counseling; we evaluated participants' knowledge of cancer genetics, breast cancer risk perception, attitudes about genetic counseling and testing, and satisfaction with genetic counseling. Methods: Women (n = 866) who screened at elevated risk for breast cancer were randomized to the KYR intervention or conventional genetic counseling (2022-2024). The KYR intervention included a series of online pre-test educational videos, direct access to genetic testing, and patient preference for receiving post-test genetic counseling. Participants completed surveys at baseline and after genetic counseling and testing. Non-inferiority hypothesis testing compared the two participant groups. Results: The mean knowledge score (range 0-12) increased in both study groups from a baseline mean of 6.87 (standard deviation (SD) = 2.46) to 8.66 (SD = 2.16) for the KYR intervention and 8.56 (SD = 2.14) for conventional counseling. Additionally, statistical analyses suggest the non-inferiority of the KYR intervention for participants' accuracy of their breast cancer risk, attitudes about genetic counseling and genetic testing, and satisfaction with genetic counseling compared to participants randomized to conventional genetic counseling. Conclusion: Findings support that the components included in the KYR intervention are non-inferior for cancer genetic knowledge, risk perception, genetic counseling and testing attitudes, and genetic counseling satisfaction among women who screen at elevated risk for breast cancer. By using the combination of components included in the KYR intervention, genetic counseling and genetic testing are more accessible, convenient, and patient-driven. Trial Registration: ClinicalTrials.gov Identifier: NCT05325151. (© 2026. The Author(s).) |
| Competing Interests: | Declarations. Competing interests: The authors declare no competing interests. Ethical approval: This study was performed in line with the principles of the Declaration of Helsinki. The Institutional Review Board at The Ohio State University approved this study. Consent to participate: Informed consent was obtained from all individual participants included in the study. |
| References: | Freedman AN, Graubard BI, Rao SR, McCaskill-Stevens W, Ballard-Barbash R, Gail MH (2003) Estimates of the number of US women who could benefit from tamoxifen for breast cancer chemoprevention. J Natl Cancer Inst 95(7):526–532. https://doi.org/10.1093/jnci/95.7.526. (PMID: 10.1093/jnci/95.7.52612671020) Sabatino SA, Burns RB, Davis RB, Phillips RS, Chen Y, McCarthy EP (2004) Breast carcinoma screening and risk perception among women at increased risk for breast carcinoma: Results from a national survey. Cancer 100(11):2338–2346. https://doi.org/10.1002/cncr.20274. (PMID: 10.1002/cncr.2027415160336) National Comprehensive Cancer Network (2025 March) Genetic/familial high-risk assessment: Breast, ovarian, pancreatic, and prostate. National Comprehensive Cancer Network; https://www.nccn.org/guidelines/guidelines-detail?category=2&id=1545. Collins FS, Varmus H (2015) A new initiative on precision medicine. N Engl J Med 372(9):793–795. https://doi.org/10.1056/NEJMp1500523. (PMID: 10.1056/NEJMp1500523256353475101938) Hoskovec JM, Bennett RL, Carey ME, DaVanzo JE, Dougherty M, Hahn SE et al (2018) Projecting the supply and demand for certified genetic counselors: a workforce study. J Genet Couns 27(1):16–20. https://doi.org/10.1007/s10897-017-0158-8. (PMID: 10.1007/s10897-017-0158-829052810) Buchanan AH, Rahm AK, Williams JL (2016) Alternate service delivery models in cancer genetic counseling: a mini-review. Front Oncol 6:120. https://doi.org/10.3389/fonc.2016.00120. (PMID: 10.3389/fonc.2016.00120272429604865495) Kaphingst KA, Kohlmann WK, Lorenz Chambers R, Bather JR, Goodman MS, Bradshaw RL et al (2024) Uptake of cancer genetic services for chatbot vs standard-of-care delivery models: the BRIDGE randomized clinical trial. JAMA Netw Open 7(9):e2432143. https://doi.org/10.1001/jamanetworkopen.2024.32143. (PMID: 10.1001/jamanetworkopen.2024.321433925015311385050) Sie AS, Spruijt L, van Zelst-Stams WAG, Mensenkamp AR, Ligtenberg MJL, Brunner HG et al (2016) High satisfaction and low distress in breast cancer patients one year after BRCA-mutation testing without prior face-to-face genetic counseling. J Genet Couns 25(3):504–514. https://doi.org/10.1007/s10897-015-9899-4. (PMID: 10.1007/s10897-015-9899-426531312) Tabor HK, Jamal SM, Yu J, Crouch JM, Shankar AG, Dent KM et al (2017) My46: A web-based tool for self-guided management of genomic test results in research and clinical settings. Genet Med 19(4):467–475. https://doi.org/10.1038/gim.2016.133. (PMID: 10.1038/gim.2016.13327632689) Prentice-Dunn S, Rogers RW (1986) Protection motivation theory and preventive health: beyond the health belief model. Health Educ Res 1:153–161. https://doi.org/10.1093/her/1.3.153. (PMID: 10.1093/her/1.3.153) Katz ML, Senter L, Reiter PL, Emerson B, Ennis AC, Shane-Carson KP et al (2023) Development of a web-based, theory-guided narrative intervention for women at elevated risk for breast cancer. Patient Educ Couns 106:163–169. https://doi.org/10.1016/j.pec.2022.10.348. (PMID: 10.1016/j.pec.2022.10.34836333195) Tyrer J, Duffy SW, Cuzick J (2004) A breast cancer prediction model incorporating familial and personal risk factors. Stat Med 23(7):1111–1130. https://doi.org/10.1002/sim.1668. (PMID: 10.1002/sim.166815057881) Morris NS, MacLean CD, Chew LD, Littenberg B (2006) The single item literacy screener: evaluation of a brief instrument to identify limited reading ability. BMC Fam Pract 7:21. https://doi.org/10.1186/1471-2296-7-21. (PMID: 10.1186/1471-2296-7-21165631641435902) Fagerlin A, Zikmund-Fisher BJ, Ubel PA, Jankovic A, Derry HA, Smith DM (2007) Measuring numeracy without a math test: development of the subjective numeracy scale. Med Decis Making 27(5):672–680. https://doi.org/10.1177/0272989X07304449. (PMID: 10.1177/0272989X0730444917641137) Underhill-Blazey M, Stopfer J, Chittenden A, Nayak MM, Lansang K, Lederman R et al (2019) Development and testing of the KnowGene scale to assess general cancer genetic knowledge related to multigene panel testing. Patient Educ Couns 102(8):1558–1564. https://doi.org/10.1016/j.pec.2019.04.014. (PMID: 10.1016/j.pec.2019.04.01431010603) Lerman C, Lustbader E, Rimer B, Daly M, Miller S, Sands C et al (1995) Effects of individualized breast cancer risk counseling: a randomized trial. J Natl Cancer Inst 87(4):286–292. https://doi.org/10.1093/jnci/87.4.286. (PMID: 10.1093/jnci/87.4.2867707420) DeMarco TA, Peshkin BN, Mars BD, Tercyak KP (2004) Patient satisfaction with cancer genetic counseling: a psychometric analysis of the genetic counseling satisfaction scale. J Genet Couns 13(4):293–304. https://doi.org/10.1023/b:jogc.0000035523.96133.bc. (PMID: 10.1023/b:jogc.0000035523.96133.bc197366953551590) Sweet K, Reiter PL, Schnell PM, Senter L, Shane-Carson KP, Aeilts A, Cooper J, Spears C, Brown J, Toland AE, Agnese DM, Katz ML (2023) Genetic counseling and testing for females at elevated risk for breast cancer: protocol for the randomized controlled trial of the Know Your Risk intervention. Contemp Clin Trials 133:107323. https://doi.org/10.1016/j.cct.2023.107323. (PMID: 10.1016/j.cct.2023.1073233766100510591709) Schmidlen T, Sturm AC, Hovick S, Scheinfeldt L, Scott Roberts J, Morr L et al (2018) Operationalizing the reciprocal engagement model of genetic counseling practice: a framework for the scalable delivery of genomic counseling and testing. J Genet Couns 27(5):1111–1129. https://doi.org/10.1007/s10897-018-0230-z. (PMID: 10.1007/s10897-018-0230-z294601106098987) Jiang S, Liberti L, Lebo D (2023) Direct-to-consumer genetic testing: a comprehensive review. Ther Innov Regul Sci 57(6):1190–1198. https://doi.org/10.1007/s43441-023-00567-5. (PMID: 10.1007/s43441-023-00567-537589855) Culver JO, Bertsch NL, Kurz RN, Cheng LL, Pritzlaff M, Rao SK et al (2024) Systematic evidence review and meta-analysis of outcomes associated with cancer genetic counseling. Genet Med 26(1):100980. https://doi.org/10.1016/j.gim.2023.100980. (PMID: 10.1016/j.gim.2023.10098037688462) Matloff ET, Moyer A, Shannon KM, Niendorf KB, Col NF (2006) Healthy women with a family history of breast cancer: impact of a tailored genetic counseling intervention on risk perception, knowledge, and menopausal therapy decision making. J Womens Health (Larchmt) 15(7):843–856. https://doi.org/10.1089/jwh.2006.15.843. (PMID: 10.1089/jwh.2006.15.84316999640) Smerecnik CMR, Mesters I, Verweij E, de Vries NK, de Vries H (2009) A systematic review of the impact of genetic counseling on risk perception accuracy. J Genet Couns 18(3):217–228. https://doi.org/10.1007/s10897-008-9210-z. (PMID: 10.1007/s10897-008-9210-z192913767451018) Fisher BA, Wilkinson L, Valencia A (2016) Women’s interest in a personal breast cancer risk assessment and lifestyle advice at NHS mammography screening. J Public Health (Oxf) 39(1):113–121. https://doi.org/10.1093/pubmed/fdv211. (PMID: 10.1093/pubmed/fdv211) Printz C (2014) Most women have an inaccurate perception of their breast cancer risk. Cancer 120(3):314–315. https://doi.org/10.1002/cncr.28557. (PMID: 10.1002/cncr.2855724452671) Kullo IJ (2025) Clinical use of polygenic risk scores: current status, barriers and future directions. Nat Rev Genet. https://doi.org/10.1038/s41576-025-00900-8. (PMID: 10.1038/s41576-025-00900-841073616) |
| Contributed Indexing: | Keywords: Breast cancer; Female; Genetic counseling; Genetic testing |
| Molecular Sequence: | ClinicalTrials.gov NCT05325151 |
| Entry Date(s): | Date Created: 20260630 Date Completed: 20260630 Latest Revision: 20260726 |
| Update Code: | 20260726 |
| PubMed Central ID: | PMC13319172 |
| DOI: | 10.1007/s10552-026-02207-3 |
| PMID: | 42377622 |
| Βάση Δεδομένων: | MEDLINE |
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