Clinical trial Recruiting at 1 site Interventional

One-Minute Preceptor to improve bedside teaching

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

Run by Can Tho University of Medicine and Pharmacy · NCT07305077 · Data updated 2026-11-12

This project will test whether training resident preceptors in the One-Minute Preceptor method helps fourth-year medical students learn better during bedside teaching.

Quick facts

Study typeInterventional
SexAll
Enrollment450 (estimated)
SponsorCan Tho University of Medicine and Pharmacy
Academic / other
Locations1 site (Can Tho, Province)
StatusRecruiting
StartedAugust 20, 2025
Main results expectedDecember 15, 2025
Study endsApril 10, 2026
Registry record updatedDecember 26, 2025
Trial IDNCT07305077 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Fourth-year medical students at Can Tho Children Hospital assigned to participating resident-led bedside teaching groups who expect to remain on the rotation for 8–12 weeks and can provide informed consent.

Probably not a fit

Students with formal OMP exposure within the past six months, those who do not receive at least two OMP feedback encounters, or those who leave the rotation early are unlikely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This cluster-randomized study assigns 30 resident preceptors at Can Tho Children Hospital to either One-Minute Preceptor (OMP) training or usual teaching, with 15 clusters per arm. Each preceptor will supervise about 15 fourth-year medical students and student-level outcomes will be measured using observed mini-CEX assessments with outcome assessors blinded. Adequate OMP exposure is predefined as at least two structured OMP feedback encounters of five minutes or more delivered across two separate weeks, and fidelity will be monitored. The primary analysis compares student clinical performance between the OMP and control arms accounting for cluster randomization.

Why it matters

Potential benefit: If successful, improved bedside teaching could lead to better clinical examination and decision-making by future doctors, which may improve patient care and safety.

How similar studies have gone: One-Minute Preceptor interventions have improved teaching efficiency and learner satisfaction in prior studies, though evidence for consistent gains in objective clinical performance is mixed.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* A. Student participants (outcome level):

Aged ≥18 years at enrollment.

Enrolled Year 4-medical students assigned to one of the participating preceptor-led bedside teaching groups during the study period.

Expected to attend the rotation for 8-12 weeks (or the site's standard rotation length).

Able to provide informed consent (and agree to be observed/assessed via mini-CEX).

\- B. Preceptor clusters (randomized units):

Resident physicians serving as bedside teaching preceptors in participating departments.

Will supervise approximately 15 students during the study period.

Agree not to cross over to teach students in the opposite trial arm during the trial period.

Able to attend OMP training and permit fidelity observation (checklist) if allocated to the intervention.

Exclusion Criteria:

* A. Student participants:

Prior exposure to formal OMP-based teaching within the past 6 months in the same department.

Not expected to remain on the rotation long enough to be assessed (e.g., planned absence \>2 weeks or early withdrawal).

Declines or withdraws informed consent.

Severe communication barrier that precludes valid assessment (e.g., language barrier without support).

\- B. Preceptor clusters:

Formal OMP training within the past 12 months (to avoid contamination), or role as an OMP trainer for other faculty during the study period.

Planned cross-coverage that would result in teaching students from both arms during the trial period.

Anticipated extended leave making fidelity and outcome assessments infeasible.

Where it's running

  • Can Tho Children Hospital
    Can Tho, Province, Vietnam
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.