Impact of Gender Identity on Dentists' Clinical Decision-Making
GID-CDM
Does Gender Identity Influence Dentists' Clinical Decision-Making? A Randomized Study
1 other identifier
interventional
204
1 country
1
Brief Summary
This randomized study evaluated whether patient gender identity influences dentists' clinical decision-making. Dentists in southern Brazil were randomly assigned to receive one of two versions of the same hypothetical dental clinical case. The cases were identical except for the patient's gender identity, which was presented as either a transgender woman or a cisgender woman. Participants selected treatment options for anterior and posterior teeth and completed questionnaires regarding professional characteristics and knowledge about transgender health. The primary objective was to determine whether patient gender identity influenced treatment recommendations. Differences in clinical decision-making between groups were analyzed using regression models.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 12, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 9, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 9, 2024
CompletedFirst Submitted
Initial submission to the registry
June 22, 2026
CompletedFirst Posted
Study publicly available on registry
June 30, 2026
CompletedJune 30, 2026
June 1, 2026
7 months
June 22, 2026
June 26, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Treatment Recommendation for Posterior Tooth
Treatment recommendation for tooth 26 based on the assigned clinical case. Available options included endodontic treatment followed by direct composite restoration, endodontic treatment followed by indirect ceramic restoration, or extraction.
Immediately after questionnaire completion
Treatment Recommendation for Anterior Tooth
Treatment recommendation for tooth 11 based on the assigned clinical case. Available options included no intervention, repair of the composite restoration, replacement of the restoration, direct composite veneer, or indirect ceramic veneer.
Immediately after questionnaire completion
Study Arms (2)
Transgender Woman Case
EXPERIMENTALParticipants evaluated a hypothetical dental clinical case in which the patient was identified as a transgender woman. Clinical information, complaints, and treatment options were identical to the comparison arm.
Cisgender Woman Case
EXPERIMENTALParticipants evaluated a hypothetical dental clinical case in which the patient was identified as a cisgender woman. Clinical information, complaints, and treatment options were identical to the comparison arm.
Interventions
Participants were randomly assigned to evaluate one of two versions of a hypothetical dental clinical case. The cases contained identical clinical information, photographs, complaints, and treatment options, differing only in the patient's gender identity. One version described a transgender woman and the other described a cisgender woman. Participants selected treatment recommendations based on the assigned scenario.
Eligibility Criteria
You may qualify if:
- Professionally active dentists.
- Able and willing to provide informed consent.
- Practicing dentistry during the data collection period.
You may not qualify if:
- Dentists not actively practicing during the data collection period.
- Dentists who participated in the pilot study.
- Individuals who declined participation or did not provide informed consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Universidade Federal de Santa Maria
Santa Maria, Rio Grande do Sul, 97501-650, Brazil
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- Participants were blinded to the primary objective of the study and were unaware that patient gender identity was the variable of interest. The informed consent form was modified to avoid revealing the specific focus of the research. In addition, the statistician responsible for data analysis remained blinded to group allocation throughout the analytical process.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Graduate Researcher
Study Record Dates
First Submitted
June 22, 2026
First Posted
June 30, 2026
Study Start
September 12, 2023
Primary Completion
April 9, 2024
Study Completion
April 9, 2024
Last Updated
June 30, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be made publicly available because the study collected information from individual professionals under conditions of confidentiality and anonymity. Data sharing may be restricted by ethical and institutional requirements.