- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07675564
Impact of Gender Identity on Dentists' Clinical Decision-Making (GID-CDM)
Does Gender Identity Influence Dentists' Clinical Decision-Making? A Randomized Study
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.
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
Clinical decision-making in dentistry may be influenced by factors beyond clinical findings, including professional characteristics, personal beliefs, and social perceptions. While disparities related to race and socioeconomic status have been documented in oral health care, little is known about the influence of patient gender identity on dentists' treatment decisions.
This randomized parallel-group study was conducted among practicing dentists in southern Brazil between September 2023 and April 2024. Participants were randomly assigned to evaluate one of two versions of a hypothetical dental clinical case. The clinical information, photographs, complaints, and treatment scenarios were identical in both versions, differing only in the patient's gender identity. In one version, the patient was identified as a transgender woman, while in the other the patient was identified as a cisgender woman.
Participants selected treatment options for an anterior tooth and a posterior tooth and subsequently completed questionnaires addressing sociodemographic characteristics, professional profile, previous experience with transgender patients, and training related to transgender health. The primary outcome was the treatment recommendation provided by the dentist. Recommendations were categorized into conservative and invasive treatment approaches for analysis.
The study aimed to determine whether patient gender identity influences dentists' clinical decision-making and to identify professional characteristics associated with treatment recommendations.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
-
Rio Grande do Sul
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Santa Maria, Rio Grande do Sul, Brasile, 97501-650
- Universidade Federal de Santa Maria
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Professionally active dentists.
- Able and willing to provide informed consent.
- Practicing dentistry during the data collection period.
Exclusion Criteria:
- 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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Ricerca sui servizi sanitari
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Transgender Woman Case
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.
|
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.
|
|
Sperimentale: Cisgender Woman Case
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.
|
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.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Treatment Recommendation for Posterior Tooth
Lasso di tempo: Immediately after questionnaire completion
|
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
Lasso di tempo: Immediately after questionnaire completion
|
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
|
Collaboratori e investigatori
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Altri numeri di identificazione dello studio
- CAEE 55339221.3.0000.5346
Piano per i dati dei singoli partecipanti (IPD)
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Descrizione del piano IPD
Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .