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One-Minute Preceptor to Improve Bedside Teaching: a Cluster Randomized Trial in Residents

One-Minute Preceptor to Improve Bedside Teaching: a Cluster Randomized Trial in Residents

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251129006
Enrollment
450
Registered
2025-11-29
Start date
2025-10-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Services Research Clinical Teaching

Interventions

One-Minute Preceptor training: 90-min workshop + pocket card + coaching + fidelity checklist.,Usual bedside teaching
OMP offered after trial completion.
Experimental Behavioral,No Intervention Behavioral
OMP,Control

Sponsors

No Study Secondary Sponsor
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 28 Years

Inclusion criteria

Inclusion criteria: A. Student participants (outcome level): 1. Aged from 18 years at enrollment. 2. Enrolled Year 4-medical students assigned to one of the participating preceptor-led bedside teaching groups during the study period. 3. Able to provide informed consent (and agree to be observed/assessed via mini-CEX). B. Preceptor clusters (randomized units): 1. Resident physicians serving as bedside teaching preceptors in participating departments. 2. Will supervise approximately 15 students during the study period. 3. Agree not to cross over to teach students in the opposite trial arm during the trial period. 4. Able to attend OMP training and permit fidelity observation (checklist) if allocated to the intervention.

Exclusion criteria

Exclusion criteria: A. Student participants: 1. Prior exposure to formal OMP-based teaching within the past 6 months in the same department. 2. Not expected to remain on the rotation long enough to be assessed (e.g., planned absence >2 weeks or early withdrawal). 3. Declines or withdraws informed consent.Severe communication barrier that precludes valid assessment (e.g., language barrier without support). B. Preceptor clusters: 1. Formal OMP training within the past 12 months (to avoid contamination), or role as an OMP trainer for other faculty during the study period. 2. Planned cross-coverage that would result in teaching students from both arms during the trial period. 3. Anticipated extended leave making fidelity and outcome assessments infeasible.

Design outcomes

Primary

MeasureTime frame
Student mini-CEX total score and Time Frame 8 - 12 weeks Mini-CEX score

Secondary

MeasureTime frame
OMP microskills 8 - 12 weeks OMP checklist

Countries

Vietnam

Contacts

Public ContactQuang Ngo

Can Tho University of Medicine and Pharmacy

ncquang@ctump.edu.vn0789565090

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026