Clinical trial · Observational
Sexual Orientation and Gender Identity (SOGI) Data Collection Program Implementation and Evaluation
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Sexual and gender minority (SGM) individuals experience significant cancer-related health disparities across the cancer continuum. The overall goal of this proposal is to assess multi-level barriers associated with sexual orientation and gender identity (SOGI) data collection in the health record as well as implementation factors including feasibility, acceptability, and data completeness. The results of this study will make a significant impact by making SOGI data available for research, addressing barriers to SOGI data collection in a large comprehensive cancer center, and informing compassionate cancer care for SGM people.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer Surveillance | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cancer Center Care Environment | Other | — | UNRESOLVED |
| Patient SOGI Self-Report | Other | — | UNRESOLVED |
| SOGI Resource for Clinical Care Education (SORCE) | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- SOGI Data Collection Intervention
- description
- This single arm is an educational intervention for clinicians. After consent, they provide baseline survey fata, then the training intervention, then a post assessment.
- interventionNames
- Other: Patient SOGI Self-Report
- Other: SOGI Resource for Clinical Care Education (SORCE)
- Other: Cancer Center Care Environment
Primary outcomes (21)
- measure
- Sexual Orientation Documentation
- timeFrame
- Baseline (prior to intervention)
- description
- This variable is observed from the electronic health record (EHR) and reported in aggregate form. The investigators will record and analyze the count (number of patients with sexual orientation documented), percent of patient records containing this documentation out of the total number of patient records, and completeness of variable fields (count and percent).
- measure
- Sexual Orientation Documentation
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: Aim 1 * Community group members that represent sex and gender minority (SGM) people * Cisgender/ heterosexual patients and family members * Ambulatory clinic provider and staff responsible for collecting sexual orientation and gender identity (SOGI) data * Age ≥18 years at the time of signing the informed consent form * Able to adhere to the study visit schedule and other protocol requirements * Able to provide informed consent * Able to read and speak English Aim 2 * Ambulatory clinic providers and staff responsible for collecting sexual orientation and gender identity (SOGI) data * Age ≥18 years at the time of signing the informed consent form * Able to adhere to the study visit schedule and other protocol requirements * Able to provide informed consent * Able to read and speak English Exclusion Criteria 1. Language or technology barriers that limit data collection 2. Insufficient evidence of meeting inclusion criteria
References
Publications (0)
Data not yet available