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Recruiting NCT06390332

NCT06390332 Centering Gender Affirming Resources in Higher Education

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Clinical Trial Summary
NCT ID NCT06390332
Status Recruiting
Phase
Sponsor University of Pittsburgh
Condition Sexual Violence
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2024-12-11
Primary Completion 2026-05

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Giving Information for Trauma Support and Safety (GIFTSS) TrainingCentering gender Affirming Resources in higher Education (CARE) Learning Modules

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2024-12-11 with a primary completion date of 2026-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Centering gender Affirming Resources in higher Education (CARE) project is nested within the parent study "Reducing Alcohol Involved Sexual violence in higher Education" (RAISE; R01 AA023260; NCT05185440). CARE is a pilot cluster-randomized trial that centers trans and gender diverse (TGD) students who are at elevated risk for SV and hazardous drinking. CARE tests a novel college health and counseling center (CHC) training program designed to improve provider knowledge about TGD individuals, increase their self-efficacy and use of trans-inclusive practices. This includes an evaluation of the feasibility, acceptability, appropriateness, and usability of CARE's training intervention for college health and counseling center providers. This research will produce the first rigorously evaluated TGD-focused CHC provider training which has the potential to increase the accessibility of CHC's for TGD university students- ultimately lowering rates of alcohol use and SV among this disproportionately impacted population.

Eligibility Criteria

Inclusion Criteria: * Those who are seeing undergraduate students at health and counseling appointments as a provider. * Providers may include counselors, clinicians, nurses, health educators, medical assistants, social workers, advocates, and administrators. Exclusion Criteria: * A college health or counseling center provider that does not interface with students. * A college health or counseling center provider not participating in the RAISE study.

Contact & Investigator

Central Contact

Regina Futcher, MSW

✉ futcherr2@upmc.edu

📞 757-272-3783

Principal Investigator

Elizabeth Miller, PhD

PRINCIPAL INVESTIGATOR

Principal Investigator

Frequently Asked Questions

Who can join the NCT06390332 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Sexual Violence. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06390332 currently recruiting?

Yes, NCT06390332 is actively recruiting participants. Contact the research team at futcherr2@upmc.edu for enrollment information.

Where is the NCT06390332 trial being conducted?

This trial is being conducted at Pittsburgh, United States.

Who is sponsoring the NCT06390332 clinical trial?

NCT06390332 is sponsored by University of Pittsburgh. The principal investigator is Elizabeth Miller, PhD at Principal Investigator. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology