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Understanding Perceived Access and Receipt of Gender-affirming Treatments Among Transgender Veterans

Understanding Perceived Access and Receipt of Gender-affirming Treatments Among Transgender Veterans

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06615401
Enrollment
986
Registered
2024-09-26
Start date
2024-10-01
Completion date
2025-01-18
Last updated
2026-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gender Dysphoria

Keywords

transgender, gender dysphoria, gender-affirming treatment

Brief summary

Transgender Veterans (trans Vets) frequently experience gender dysphoria or distress related to discord between their gender identity and birth sex. Gender-affirming treatments (GATs) are medically necessary treatments to reduce gender dysphoria. However, not much is known about the barriers and facilitators that influence GAT access and receipt in VA and VA Community Care (CC), among trans Vets who desire GATs. The goals of this mixed-methods study are to determine which GATs trans Vets receive and in which setting, identify barriers and facilitators associated with desired GAT receipt in VA and CC, examine association of GAT receipt, specifically mental healthcare and hormone therapy, with mental health and suicide risk and understand trans Vet experiences related to receipt and desire for mental healthcare and hormone therapy in VA and CC.

Detailed description

Background: Transgender people experience discord between their gender identity and birth sex, defined as gender dysphoria. Gender-affirming treatments (GATs) are medically necessary treatments to reduce gender dysphoria. However, among transgender Veterans (trans Vets) who desire GATs, not much is known about barriers and facilitators to accessing and receiving GATs in VA and VA Community Care (CC). To ensure effective and equitable GAT access for trans Vets, it is critical to understand: \[1\] GATs trans Vets receive and where they receive them, \[2\] barriers, including social determinants of health (SDOH) barriers that are highly prevalent among trans Vets, and facilitators associated with desired GAT receipt in VA and CC, \[3\] association of GAT receipt, specifically mental healthcare and hormone therapy with mental health and suicide risk , and \[4\] experiences related to receipt of mental healthcare and hormone therapy in VA and CC . Significance: This study addresses the 2022 HSR&D priority areas of Access to Care, Health Equity/SDOH, MISSION Act, and research gap of underserved LGBTQ+ Veterans. It is also a high priority for our operational partners in VA LGBTQ+ Health Program, Pharmacy Benefits Management, Office of Integrated Veteran Care, and Office of Mental Health and Suicide Prevention. Knowledge gained from this study will ensure that GAT delivery in the VA is patient-centered and is responsive to the lived realities and needs of trans Vets. Innovation and Impact: This study will be the first to characterize the GATs received in VA and/or CC to understand how VA and CC are balanced in terms of delivering GATs. This study will also provide novel data on trans Vet experiences related to GAT access in CC and on services and resources used by trans Vets to address barriers that influence GAT access. Specific Aims: We propose a sequential explanatory mixed method study whose aims are to: Aim 1. Characterize the GATs received by trans Vets in VA and/or CC (VA/CC) Aim 2. Identify barriers and facilitators associated with desired GAT receipt in VA and CC Aim 3a: Explore association of mental healthcare and hormone with mental health and suicide risk. Aim 3b. Understand trans Vet experiences related to mental healthcare and hormone therapy in VA and CC. Methodology: Database Aim 1: We will expand our VA cohort of 9,608 trans Vets (IIR 17-238) from 2006-18 to the data available at the time of funding. We will add CC data to determine the types of GATs received by trans Vets in VA and/or CC. Survey Aim 2: We will survey a national sample of trans Vets identified from Aim 1. Among trans Vets who desire GATs, we will determine SDOH barriers, other barriers, and facilitators associated with desired GAT receipt. Among trans Vets who did not desire GATs, we will determine reasons for not wanting GATs. Aim 3a: Existing survey data from the Aim 2 and linked survey-VA Corporate Data Warehouse will allow robust examination of associations between clinical factors (e.g. co-morbidities), non-clinical factors (e.g. demographics), mental health outcomes (e.g. depression), and suicide risk (e.g. suicide ideation) based on receipt/non-receipt of treatment (mental healthcare, hormone therapy). Aim 3b. Using Aim 2 survey free text responses, we will construct themes related to the experience of trans Vets for mental healthcare and hormone therapy in VA and CC. Next Steps/Implementation: The proposed study will provide key insights related to the health of trans Vets, while adhering to the new guidance provided within the Forms, Publications, Guidance and Documents Action Team business rules released in April 2025.

Interventions

None listed

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* All veterans with documentation of gender identity disorder diagnoses * Self-reported gender identity as transgender and relevant transgender-related health factor

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Receipt of Gender Affirming TreatmentAbout 3.5 monthsThrough a national survey, the investigators will identify receipt of gender-affirming treatment in VA and VA Community Care among transgender and gender diverse Veterans.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORGuneet K. Jasuja, PhD

VA Bedford HealthCare System, Bedford, MA

Baseline characteristics

Characteristic
Age, Customized
Categorical Age
30 - 39
297 Participants
Age, Customized
Categorical Age
40 - 49
158 Participants
Age, Customized
Categorical Age
50 - 59
127 Participants
Age, Customized
Categorical Age
60 - 69
91 Participants
Age, Customized
Categorical Age
70 and over
51 Participants
Age, Customized
Categorical Age
Missing
63 Participants
Age, Customized
Categorical Age
Under 30
199 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Asian
21 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Black/African American
37 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Hispanic/Latino (Any Race)
89 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Missing
76 Participants
Race/Ethnicity, Customized
Race/Ethnicity
More than one race
71 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Other
25 Participants
Race/Ethnicity, Customized
Race/Ethnicity
White
667 Participants
Sex/Gender, Customized
Gender Identity
Missing
20 Participants
Sex/Gender, Customized
Gender Identity
More than one Gender Identity
122 Participants
Sex/Gender, Customized
Gender Identity
Non-Binary and/or Gender Diverse
191 Participants
Sex/Gender, Customized
Gender Identity
Trans Man/Trans Masculine/Male
164 Participants
Sex/Gender, Customized
Gender Identity
Trans Woman/Trans Feminine/Female
489 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
2 / 986
other
Total, other adverse events
0 / 986
serious
Total, serious adverse events
0 / 986

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026