Gender-Affirming Hormone Therapy Research Enrollment Form

Streamline Your Gender-Affirming Care Research with Paperform

Conducting ethical, participant-centered research on gender-affirming hormone therapy requires clear communication, thorough consent processes, and seamless coordination across medical and mental health providers. This Gender-Affirming Hormone Therapy Research Enrollment Form is designed specifically for healthcare researchers, academic institutions, and clinical research organizations conducting studies on hormone therapy outcomes, safety protocols, and quality of life improvements.

Why This Template Works for Research Teams

This template guides potential participants through every stage of the enrollment process—from eligibility screening and informed consent to baseline health data collection and support service coordination. The structured format ensures you capture all necessary information for IRB compliance while creating a respectful, affirming experience for participants.

With built-in conditional logic, the form adapts based on participant responses, showing only relevant questions about hormone therapy history, baseline lab requirements, and mental health support needs. This reduces form fatigue while ensuring you collect complete data sets for your research protocol.

Built for Healthcare Research Workflows

Whether you're a university research team, clinical trial coordinator, or healthcare provider conducting outcomes research, this form handles the complexity of participant onboarding. Collect demographics, medical history, current hormone use, consent for baseline labs, agreement to dose titration protocols, and mental health support preferences—all in one professional, LGBTQ+-affirming interface.

Automate what comes next with Stepper: Once a participant submits their enrollment form, use Stepper to automatically notify your research coordinator, schedule baseline appointments, send lab requisitions to your diagnostic partner, and trigger welcome emails with study timelines and support resources. Keep your IRB-approved protocols on track without manual data entry.

Professional, Secure, and Participant-Centered

Paperform's flexible design lets you match your institution's branding while maintaining the professional tone required for research enrollment. Every submission is securely stored with SOC 2 Type II compliance, and you can export data directly to your research database or statistical analysis tools.

Trusted by research institutions and healthcare organizations worldwide, this template helps you conduct rigorous, ethical research while centering the dignity and autonomy of transgender and gender-diverse participants.