- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05274581
General Practitioners' POCUS Competence Following Structured Training
Evaluating Scanning Competence Following a Structured POCUS Training Program for General Practitioners - A Hybrid Effectiveness-implementation Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Type of study:
This is a hybrid effectiveness-implementation study . The investigators will test the effectiveness of a new type of point-of-care ultrasound course, tailored to meet the educational needs of office-based general practitioners, in a real-world setting while gathering information on its delivery and the implementation of the intervention.
Setting:
This study will be conducted in office-based general practice in Denmark with the educational sessions taking place at an ultrasound educational facility.
The intervention:
The ultrasound course consists of three teaching seminars over three months, a curriculum of 10 point-of-care ultrasound (POCUS) applications, an online learning platform providing educational support before, during and after the teaching sessions.
The online platform includes instruction videos demonstrating the performance of POCUS, suggestions for additional literature, flashcards training the recognition of pathology, participant assignments to support the development of skills, self-quizzes to focus attention of learning outcomes and specific actioncards for each of the 10 POCUS applications framing the examinations in the clinical context. In addition, the online platform gives participants access to webinars and communication with other participants and teachers. A detailed description of the educational elements in the ultrasound course can be found in the attached study protocol.
Data collection:
The primary outcomes are the Objective Structured Assessment of Ultrasound Skills (OSAUS) score scored three (outcome 1) and six months (outcome 2) after baseline.
The OSAUS assessment tool has been developed and validated as a generic tool for assessing scanning competence. The OSAUS scale consists of seven items: 'indication for the examination', 'applied knowledge of ultrasound equipment', 'image optimization', 'systematic examination', 'interpretation of images', 'documentation of the examination' and 'medical decision-making' and each item is rated using a provided five-point Likert-scale with descriptions of performance ranging from very poor (score = 1) to excellent (score = 5). All items are weighted equally, as high inter-item correlation have been found previously. Hence, for each scanning modality a total score from 7 to 35 points may be achieved.
On the third teaching seminar (three months after baseline) and again six months after baseline, participants will have their scanning competence assessed by external experts. These experts are blinded to the participants previous experience and learning process.
The experts will assess the participants by asking the following questions:
- In which clinical scenarios would you perform this POCUS examination (Item 1 in the OSAUS)
The experts will ask participants to demonstrate the POCUS examination (for maximum five minutes) to assess the following:
- Applied knowledge of the ultrasound equipment (Item 2 in the OSAUS)
- Image optimazation (Item 3 in the OSAUS)
- Systematic examination (Item 4 in the OSAUS)
- Interpretation of images (Item 5 in the OSAUS)
The experts will present the participants with two picture of common pathology and ask the participants the following questions:
- How would you interpret these ultrasound findings? (Item 5 in the OSAUS)
- If you were to describe this examination in the medical record, what would you write? (Item 6 in the OSAUS)
- What would you do if you found it? (Item 7 in the OSAUS) The OSAUS score will also be used for secondary outcomes S1, S2 and S3)
Immediately before each competence assessment by experts, participants will be asked to fill out a questionnaire where they declare whether or not they have POCUS scanning competence within this scanning modality to perform the scan un-supervised in general practice (outcomes 6 and 7). The expert assessor are blinded to this declaration.
In addition, the following process-related outcomes will be collected:
The GPs keep a log book of all scans they perform. The number of scans of the 10 POCUS modalities performed during months 1 to 3 and month 4 to 6 are summarized (outcome 8).
The GPs will register the number of adverse events and near-miss cases associated with their use of POCUS during months 1 to 6, in a questionnaire specifically designed for this purpose (outcome 9).
The GPs activity on the online platform will be registered during the educational period (months 1-3) (outcome 10).
Background characteristics of participating GPs At baseline the following participant characteristics will be collected: Age (years), gender (M, F, other), previous use of ultrasound (number of months with regular use), previous ultrasound courses of minimum 1 day duration (yes/no), scanner type (low range, mid range, high end), type of practice (collaboration, partnership, solo), location of practice (urban, rural, mixed), number of patients assigned to the practice, number of GPs working in the practice will be presented.
Data analysis:
All statistical analyses will be performed using STATA version 17 (StataCorp, Texas, USA) and analyzed according to a predefined statistical analysis plan, which will be uploaded prior to the data collection for the primary outcome (three months after baseline).
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Camilla A Andersen
- Phone Number: 22482885
- Email: caakjaer@dcm.aau.dk
Study Contact Backup
- Name: Martin B Jensen
- Email: mbj@dcm.aau.dk
Study Locations
-
-
-
Aalborg, Denmark, 9220
- Center for General Practice at Aalborg University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion criteria:
- GP, i.e., be a postgraduate medical doctor with a specialization in general practice.
- Work in office-based general practice in Denmark
- Have access to an ultrasound device in the practice during the study period
Exclusion criteria:
- GPs with a possible conflict of interest (e.g., industry affiliation related to the use of ultrasound)
- No signed informed consent to participate.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Course participants
Course participants er general practitioners who have signed-up to participate in an ultrasound course
|
All participants will receive the educational intervention.
The educations intervention consists of three teaching seminars over three months, a curriculum of 10 point-of-care ultrasound applications, an online learning platform providing educational support before, during and after the teaching sessions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Participants' ultrasound competence score after three months
Time Frame: three months after baseline
|
Participants' ultrasound competence score across ten scanning modalities (The Objective Structured Assessment of Ultrasound Skills (OSAUS)) after the educational period
|
three months after baseline
|
Participants' ultrasound compentence score after six months
Time Frame: six months after baseline
|
Participants' ultrasound competence score across ten scanning modalities (The Objective Structured Assessment of Ultrasound Skills (OSAUS)) six months after baseline
|
six months after baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Participants' ultrasound competence items scores
Time Frame: three months after baseline
|
Participants' total ultrasound competence score (The Objective Structured Assessment of Ultrasound Skills (OSAUS) 7-35) and the item scores (1-5), for each of the ten scanning modalities included in the curriculum.
|
three months after baseline
|
Participants' ultrasound compentence scores above avarage after three months
Time Frame: three months after baseline
|
The proportion of participants, who have an ultrasound competence score (OSAUS score) of three or more, after the educational period, in all of the seven OSAUS items, for each of the ten scanning modalities included in the curriculum
|
three months after baseline
|
Participants' ultrasound compentence scores above avarage after six months
Time Frame: six months after baseline
|
The proportion of participants, who have an ultrasound competence score (OSAUS score) of three or more, in all of the seven OSAUS items, for each of the ten scanning modalities included in the curriculum
|
six months after baseline
|
Participants' self-rated ultrasound compentence after three months
Time Frame: three months after baseline
|
The proportion of participants, who rate themselves to be competent to perform un-supervised POCUS in general practice, after the educational period, for each of the ten scanning modalities included in the curriculum.
|
three months after baseline
|
Participants' self-rated ultrasound compentence after six months
Time Frame: six months after baseline
|
The proportion of participants, who rate themselves to be competent to perform un-supervised POCUS in general practice, six months after baseline, for each of the ten scanning modalities included in the curriculum.
|
six months after baseline
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of performed POCUS examinations
Time Frame: months 1-6 after baseline
|
The number of performed POCUS examinations by each participant in the first six months after introducing POCUS use in general practice
|
months 1-6 after baseline
|
Number of adverse events and near-miss cases
Time Frame: months 1-6 after baseline
|
The number of adverse events and near-miss cases associated with the use of POCUS reported by the participants in the first six months after introducing POCUS use in general practice
|
months 1-6 after baseline
|
Participants' completion of educational elements
Time Frame: months 1-3 after baseline
|
The proportion of participants, who have completed the different educational elements in the educational intervention three months after baseline
|
months 1-3 after baseline
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Camilla A Andersen, Center for General Practice at Aalborg University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ID 242-2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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