Evaluation of an Online Application for Point of Care Ultrasound Training in General Internal Medicine Residents

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorKantonsspital Baden

About this trial

This study compares Point of Care Ultrasound (POCUS) training in two hospitals, one that uses an online application for supervision and one that does not use the application. The goal of this trial is to learn if POCUS supervision using the online application is associated with improved POCUS skills in residents in General Internal Medicine (GIM). The main question it aims to answer is:

\- Do POCUS skills improve more during 6 months in GIM residents supervised using the application than in GIM residents who do not use the application?

Further questions the study aims to answer are:

* Do residents using the application perform more POCUS exams during 6 months than residents not using the application? * Are residents using the application more satisfied with their POCUS training than residents not using the application?

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

General Internal Medicine resident employed at one of the study sites for at least 2 months

Probably or definitely interested in achieving POCUS certification (mandatory for the General Internal Medicine specialisation in Switzerland)

Basic ultrasound course completed (Basic course Abdominal ultrasound or Emergency ultrasound)

Will spend at least 3 months within a rotation where POCUS training is offered during the 6 months after baseline assessment

Disqualifiers

Definitely or probably not interested in achieving POCUS certification

Has already performed more than 80 supervised and more than 160 total POCUS exams

Will end employment at the study site less than 7 months after baseline assessment

Trial population

General internal medicine residents at two hospitals in Switzerland

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

56 Participants
are grouped into 2 trial groups
Group A: POCUS supervision using application
Group B: Usual POCUS supervision

Trial outcomes

Primary outcomes

1

Change from baseline in POCUS skills

POCUS skills will be evaluated on healthy volunteers by video-recorded OSCE

Time frame
Post-test 6 months (+/- 2 weeks) from pre-test

Secondary outcomes

1

Number of POCUS exams performed

In the cohort using the application, the number is automatically recorded. The usual supervision cohort will manually record the number of exams.

Time frame
During 6 months after baseline assessment (pre-test)
2

Number of supervised POCUS exams performed

In the cohort using the application, the number is automatically recorded. The usual supervision cohort will manually record the number of exams.

Time frame
During 6 months after baseline assessment (pre-test)
3

Number of directly supervised POCUS exams performed

Direct supervision means that the supervisor is present during the exam. In the cohort using the application, the number is automatically recorded. The usual supervision cohort will manually record the number of exams.

Time frame
During 6 months after baseline assessment (pre-test)
4

Change in satisfaction and engagement with POCUS training

Measured with a survey

Time frame
Follow-up assessment 6 months (+/- 2 weeks) after baseline assessment

Other outcomes

1

Usefulness of the online application

Assessed with a survey, only in the cohort using the application

Time frame
6 months (+/- 2 weeks) after baseline assessment
2

Change from baseline in POCUS skills within the individual cohorts

Evaluating how POCUS skills evolve during 6 months in each of the individual study arms.

Time frame
Post-test 6 month (+/- 2 weeks) from pre-test

Sponsors and contacts

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Kantonsspital Baden

Lead sponsor

Spital Limmattal Schlieren

Collaborator

This trial is not recruiting at the moment. You can still explore other options: