ArticleJournal of the National Comprehensive Cancer Network : JNCCN2025
Implementing MyChart-Driven Sexual Orientation and Gender Identity Data Collection at Three Comprehensive Cancer Center Clinics.
Article in Journal of the National Comprehensive Cancer Network : JNCCN, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Barriers to Care Among LGBT Cancer Survivors: An Analysis of the All of Us Research Program.Cancers · 2026Article
- Social Determinants of Health in Cardio Oncology, from Evidence To Action: Translating Concepts into Clinical Practice Through Implementation Science.Current treatment options in oncology · 2025Review
- Mode of Patient Sexual Orientation and Gender Identity Disclosure and Receipt of Tailored Cancer Resources.JAMA network open · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
backgroundAlthough systematic collection of sexual orientation and gender identity (SOGI) data is essential for identifying and addressing disparities-and has been associated with improved survivorship outcomes-its implementation in oncology care remains limited. Recognizing clinic time and staff barriers, we piloted a multicomponent implementation strategy centered on collecting SOGI data through an online patient portal and evaluated its feasibility, acceptability, and effectiveness. PATIENTS AND
methodsThis SOGI strategy, previously developed with input from national stakeholders, included (1) assignment of SOGI questions to all patients via MyChart, with follow-up in clinic as needed; (2) staff training for SOGI understanding, patient respect, and safety; (3) a script for asking patients about their SOGI; and (4) a clinic champion. We piloted the strategy at 3 outpatient adult cancer clinics for a total of 6 months. We conducted an evaluation that included preimplementation clinic staff surveys, patient surveys and interviews (after patients were asked about their SOGI), and postimplementation staff surveys and interviews. We evaluated SOGI collection rates for the study period using EPIC Clarity data.
resultsSOGI data were collected from 71% (n=1,410) of patients, and 94% of responses were collected on MyChart before clinic. The training helped 40% of surveyed staff (n=4) feel more comfortable asking about SOGI; however, staff interviewed (n=6) reported not attending the entire training. This likely contributed to their reported fear of patient reactions and lack of understanding that they were expected to ensure SOGI was documented for all patients. Of the 98 patient survey respondents (33% response rate), 69% reported that it was important for their provider to know their SOGI. In interviews (n=17), patients described MyChart as an acceptable and private method for collecting SOGI information.
conclusionsThe MyChart-driven strategy for SOGI data collection was efficient, effective, feasible, and acceptable for collecting this information from most patients. Future work will focus on refining and reformatting staff training to ensure respectful SPGI data collection and on capturing information from patients who did not previously respond.
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