{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T03:29:13Z","timestamp":1790998153250,"version":"4.1.0"},"reference-count":55,"publisher":"American Medical Association (AMA)","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec>\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Cascade genetic testing (CGT) is a key strategy for cancer prevention in families with hereditary breast and ovarian cancer syndrome (HBOC) and Lynch syndrome (LS), yet uptake among at-risk relatives remains persistently low, particularly in medically underserved populations where structural and informational barriers limit access to genetic services.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To evaluate the feasibility and preliminary effects of IGNITE-TX (Identifying Individuals for Genetic Testing and Treatment), a scalable, bilingual, navigator-supported digital intervention designed to increase CGT uptake among at-risk relatives of individuals with HBOC or LS.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>In this 2\u2009\u00d7\u20092 factorial pilot randomized clinical trial, probands with HBOC or LS self-enrolled online from October 1, 2023, to February 15, 2025, after recruitment through clinical, laboratory, and community pathways across the US and invited their at-risk relatives to participate. Families were cluster-randomized to 4 study arms (1:1:1:1); outcomes were assessed at 6 months.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interventions<\/jats:title>\n                    <jats:p>Usual care with standard printed materials (arm 1); no-cost telegenetic counseling and testing, self-initiated by the at-risk relative (arm 2); IGNITE-TX, comprising proactive family genetic navigator support and access to a bilingual digital education and decision-support platform (arm 3); or IGNITE-TX plus no-cost telegenetic counseling and testing with navigator-assisted access (arm 4).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Feasibility outcomes were enrollment and survey completion at baseline and 6 months. Secondary outcomes were CGT completion among at-risk relatives, informed decision-making, and readiness along the genetic testing pathway.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In this pilot randomized clinical trial, 60 probands (median age, 46.5 [range, 20-83] years; 59 female [98.3%]) and 144 at-risk relatives (median age, 39 [range, 18-87] years; 71 female [49.3%]) were enrolled. Among at-risk relatives, 99 (68.8%) reported at least 1 structural barrier to care. A total of 58 probands (97.2%) and 117 at-risk relatives (81.3%) completed the 6-month survey. Among at-risk relatives, 1 of 29 (3.4%) completed CGT in arm 1, 8 of 39 (20.5%) in arm 2, 17 of 30 (56.7%) in arm 3, and 36 of 46 (78.3%) in arm 4. Compared with non\u2013IGNITE-TX arms, at-risk relatives in IGNITE-TX arms showed greater CGT completion (odds ratio, 26.9; 95% CI, 2.4-59.5), informed decision-making (48 of 60 [80.0%] vs 8 of 57 [14.0%];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001), and readiness to pursue CGT (action stage: 53 of 61 [86.9%] vs 9 of 55 [16.4%];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this pilot randomized clinical trial, IGNITE-TX was feasible to deliver in a community-recruited cohort with structural barriers to care and was associated with higher CGT completion and improved informed decision-making and readiness compared with non\u2013IGNITE-TX arms. These findings support further evaluation of IGNITE-TX as a scalable navigation model for equitable hereditary cancer care.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Trial Registration<\/jats:title>\n                    <jats:p>\n                      ClinicalTrials.gov Identifier:\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/clinicaltrials.gov\/study\/NCT05677048\">NCT05677048<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2026.30668","type":"journal-article","created":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T15:30:28Z","timestamp":1787844628000},"page":"e2630668","source":"Crossref","is-referenced-by-count":1,"title":["A Multilevel Intervention to Identify Individuals for Genetic Testing and 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