Improving The Breast Cancer Care Delivery Model for Sex and Gender Minority Survivors, Intended for SGM Study

N/ACompletedNCT06205394

Ohio State University Comprehensive Cancer Center28 enrolled

Overview

This study evaluates Improving the Breast Cancer Care Delivery Model for Sex and Gender Minority (INTENDED for SGM) in identifying the patient, support person and provider barriers to quality care in SGM breast/chest cancer survivors.

PRIMARY OBJECTIVE: I. To determine the important ways the iCanDecide breast cancer decision aid needs revised for SGM people, and how best to integrate a culturally-relevant tool into clinical practice. OUTLINE: This is an observational study. AIM 1: Interview transcripts from SANGRIA study utilized to explore the values, preferences and key considerations for breast cancer treatment decision making in SGM individuals. AIM 2: Patients are assigned to 1 of 2 groups. GROUP 1: Cancer survivors participate in a focus group on study. GROUP 2: Breast cancer clinicians undergo a semi-structured interview on study.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Breast Carcinoma

Interventions

Non-Interventional StudyOTHER

Non-interventional study

Eligibility

Sex: ALLHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * SURVIVORS: * Self-identify as a member of the sex and gender minority community or partner with an individual of the same sex or gender * Must be a breast cancer survivor, in active treatment or completed active treatment in the last 10 years (not including hormone therapy) * Be over age 18 * English-speaking * Received care in the US BREAST ONCOLOGY CLINICIANS: Physicians, advanced practice providers, nurses, psychologists and social workers will be eligible if they: * Provide care and/or surgical decision support to individuals diagnosed with early stage breast cancer in the US * Are English-speaking

Locations (1)

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

Outcomes

Primary Outcomes

Survivor participant feedback, opinions, and preferences for breast cancer care

Data is verbally reported and collected in focus groups

Time frame: At completion of study up to 2 years

Clinician participant reports of experiences, opinions, and knowledge of caring for LGBTQ+ people

Data is verbally reported and collected in interviews

Time frame: At completion of study up to 2 years

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.