NCT04310358

Brief Summary

This study is designed to:

  1. 1.Create 4 short PLMs aimed at improving visual estimation of LVEF on TTE images.
  2. 2.Design a study to determine if these online PLMs can be used to increase the ability of medical students to estimate LVEF on TTE images and create long term retention of this skill.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2023

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 10, 2020

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 17, 2020

Completed
2.9 years until next milestone

Study Start

First participant enrolled

February 20, 2023

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 7, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 7, 2024

Completed
Last Updated

March 20, 2024

Status Verified

March 1, 2024

Enrollment Period

12 months

First QC Date

March 10, 2020

Last Update Submit

March 19, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Impact of the spaced online 4 short PLMs on the ability to correctly visually estimate LVEF during a remote post-test (1 month).

    The mean absolute deviation of the participants' visual estimations from the validated answer (expert estimate) will be used as a measure of the precision of the estimations.

    Change between baseline (pre-test) and remote post-test (1 month)

Secondary Outcomes (3)

  • Impact of the online perceptual modules on the ability to correctly estimate LVEF during an immediate post-test (module validation).

    Change between baseline (pre-test) and immediately after the fourth PLM online session.

  • The progression (improvement of performance) of the participants' ability to correctly assess LVEF throughout the completion of the 4 modules.

    At the end of the fourth online session, on an average of 15 to up to 30 days.

  • The fluency (time to answer) of each participant as they progress through the study protocol.

    At baseline (pretest), immediately after the fourth PLM online session and on remote post-test (1 month).

Study Arms (2)

PLM group 1

EXPERIMENTAL

Participants will do a pretest (Test 1), the 4 short PLMs, an immediate post-test (Test 2) and a remote post-test (Test 1).

Other: 4 short PLMs group 1

PLM group 2

EXPERIMENTAL

Participants will do a pretest (Test 2), the 4 short PLMs, an immediate post-test (Test 1) and a remote post-test (Test 2).

Other: 4 short PLMs group 2

Interventions

Participants will take the 4 short PLMs on the visual estimation of LVEF. They will also take a pretest, an immediate post-test and a remote post-test at 1 month. Test 1 (pre-test), Test 2 (immediate post-test), Test 1 (remote post-test)

PLM group 1

Participants will take the 4 short PLMs on the visual estimation of LVEF. They will also take a pretest, an immediate post-test and a remote post-test at 1 month. Test 2 (pre-test), Test 1 (immediate post-test), Test 2 (remote post-test)

PLM group 2

Eligibility Criteria

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

You may qualify if:

  • Third- or fourth-year medical students
  • Access to a computer with high speed internet (no smartphone or tablet since the images would be too small)

You may not qualify if:

  • Previous formal echocardiographic training (transthoracic, transesophageal or FOCUS echocardiography)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier de l'Université de Montréal (CHUM)

Montreal, Quebec, H2X 3E4, Canada

Location

Study Officials

  • Chantal Mercier-Laporte, MD, FRCPC

    Centre hospitalier de l'Université de Montréal (CHUM)

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Prospective, randomized, open label study.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 10, 2020

First Posted

March 17, 2020

Study Start

February 20, 2023

Primary Completion

February 7, 2024

Study Completion

February 7, 2024

Last Updated

March 20, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

Locations