NCT07675564

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
204

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 9, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 9, 2024

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

June 22, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 30, 2026

Completed
Last Updated

June 30, 2026

Status Verified

June 1, 2026

Enrollment Period

7 months

First QC Date

June 22, 2026

Last Update Submit

June 26, 2026

Conditions

Keywords

Transgender PersonsGender IdentityClinical Decision-Making.

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

EXPERIMENTAL

Participants 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.

Behavioral: Clinical Case Scenario

Cisgender Woman Case

EXPERIMENTAL

Participants 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.

Behavioral: Clinical Case Scenario

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.

Cisgender Woman CaseTransgender Woman Case

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Location

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
Model Details: Participants were randomly assigned in a 1:1 ratio to evaluate one of two versions of the same hypothetical dental clinical case. The cases were identical regarding clinical findings, photographs, complaints, and treatment alternatives, differing only in the patient's gender identity. One group evaluated a case involving a transgender woman, while the other evaluated a case involving a cisgender woman. Treatment recommendations were compared between groups to assess whether patient gender identity influenced clinical decision-making.
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.

Locations