Evaluating in Person Curriculum for Educating Obstetrical Residents on Better Caring for 2 Spirit Metis Patients Using and AI Assisted OSCE.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Manitoba

About this trial

Two-Spirit (2S) Métis individuals often encounter significant barriers and discrimination in healthcare settings. This multisite randomized controlled feasibility trial evaluates a novel artificial intelligence (AI)-assisted Objective Structured Clinical Examination (OSCE) designed to assess and improve Obstetrics and Gynecology (Ob/Gyn) residents' competencies in delivering culturally safe, trauma-informed, and identity-affirming care to 2S Métis patients.

Up to 90 Ob/Gyn residents across three Canadian academic sites (University of Alberta, University of Manitoba, and University of Saskatchewan) will be randomized 1:1 to complete either a 2S Métis Academic Half Day paired with AI-assisted OSCE evaluation or standard institutional anti-racism training with AI-assisted OSCE evaluation. The primary focus is to evaluate study feasibility (recruitment, retention, and delivery fidelity) and resident performance on clinical communication, trauma-informed care, and cultural humility evaluated using a 2S Métis co-developed scoring rubric.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Current enrollment in an accredited Obstetrics and Gynecology residency program at one of the participating institutions (University of Alberta, University of Manitoba, or University of Saskatchewan). * Postgraduate Year 1 through 5 (PGY1-PGY5). * Fluency in English to ensure comprehension of AI-based encounters. * Willingness and ability to participate fully in both the Academic Half Day and AI-assisted OSCE assessments. * Provision of informed consent.

Disqualifiers

Prior participation (within 12 months) in Two-Spirit (2S) Métis-specific or similar cultural safety OSCEs or workshops. * Residents not enrolled in participating Ob/Gyn residency programs.

Trial design

Design model

Parallel

Treatments tested in this trial

  • 2S Métis Cultural Safety Academic Half Day &AI-OSCE

    Behavioral

    Ob/GYN residents participate in a dedicated 2S Métis Academic Half Day covering trauma-informed care and cultural humility, followed by a simulated OSCE encounter using an AI-assisted standardized patient and co-developed scoring rubric.

  • Standard Institutional Cultural Safety Training&AI-OSCE

    Behavioral

    Ob/Gyn residents undergo standard institutional anti-racism/Indigenous cultural safety training, followed by the same AI-assisted 2S Métis OSCE evaluation.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: 2S Metis Cultural Safety Training +AI OSCEExperimental treatment 1 intervention
Group B: Standard Anti-Racism Training+AI OSCEActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Study Feasibility Metrics

Feasibility evaluated by participant recruitment rate (target of 90 Ob/Gyn residents across 3 sites), study retention/completion rate, and intervention delivery fidelity across all participating institutions.

Time frame
Up to 12 months
2

Resident Clinical Communication and Cultural Safety Performance Score

Objective Structured Clinical Examination (OSCE) performance score assessing clinical communication, trauma-informed care, and cultural humility evaluated using the co-developed 2S Métis scoring rubric (scored by blinded raters).

Time frame
Immediately post-intervention

Secondary outcomes

Other outcomes

Sponsors and contacts

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University of Manitoba

Lead sponsor

University of Alberta

Collaborator

University of Saskatchewan

Collaborator

University Health Network, Toronto

Collaborator

McMaster University

Collaborator

Canadian Institutes of Health Research (CIHR)

Collaborator

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