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Intervention Arm for Gender Affirming Communication Skills

N/A
Waitlist Available
Research Sponsored by SIMmersion, LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up phase ii, months 17-22
Awards & highlights

Study Summary

Simulated Conversation Training for Mental Healthcare Providers to Improve Care for Transgender and Gender Nonconforming Individuals

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~phase ii, months 17-22
This trial's timeline: 3 weeks for screening, Varies for treatment, and phase ii, months 17-22 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Knowledge Assessment
Standardized Patient Checklist
Training Experience Questionnaire

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention ArmExperimental Treatment1 Intervention
The educational intervention will be TTACS, the training program with simulated roleplays. Each participant will be asked to schedule 10 hours of time to utilize the simulation. In order to ensure all participants adhere to the minimum intervention requirements, each will be asked to schedule training time with a member of the research team. Participants will attend an initial training session where each participant will receive a short orientation about the product and its capabilities. Participants will attend an initial training session at one of two sites Psychology Department at Towson University or SIMmersion's office in Columbia, MD based on participant preference. Subsequent training sessions may be completed at Towson, SIMmersion or can be completed individually. Participants will receive confirmation emails the day before a scheduled session and a phone call to reschedule any missed sessions.
Group II: Contro ArmActive Control1 Intervention
Students randomized to the control group will be given an electronic copy of the Guidelines for Psychological Practice with Transgender and Gender Non-Conforming People (APA, 2015) and asked to take notes in the pdf document. The amount of time students spend on the document and note-taking will be recorded and notes will be analyzed for content. As an incentive, the participants in the control group will be given access to TTACS after they complete the post-intervention assessment.

Find a Location

Who is running the clinical trial?

SIMmersion, LLCLead Sponsor
7 Previous Clinical Trials
914 Total Patients Enrolled
Towson UniversityOTHER
8 Previous Clinical Trials
382 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Simulated Conversation Training for Mental Healthcare Providers to Improve Care for Transgender and Gender Nonconforming Individuals
2019. "Simulated Conversation Training for Mental Healthcare Providers to Improve Care for Transgender and Gender Nonconforming Individuals". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04820088.
All > Mental Health > Transgender
~20 spots leftby Apr 2025
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