Point-of-care UltrasoundNCT04396925
Point-of-care Ultrasonography in Norwegian General Practice
An observational study of Point-of-care Ultrasound and General Practice, run by University of Oslo at 1 site in Norway.
Trial summary
The scope of this study is to explore how general practitioners (GPs) use Point-of-Care Ultrasonography (POCUS) in Norway. Thirty GPs will register information each time they use POCUS during a three-month period. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Point-of-care Ultrasound, General Practice, Family Medicine
- What is being tested?
- Point-of care Ultrasonography
- How many people
- 30 participants
- Where
- 1 siteNorway
- Study dates
- 1 Dec 2022to 31 Dec 2024
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: General practitioners who use point-of-care ultrasonography as a part of clinical practice. Out-of-hours scanning excluded
Who may be able to join
- General practitioners who use point-of-care ultrasound in day time general practice
Who cannot join
- Conflict of interest, e.g. if the GP is part of the research group or if the GP has direct financial interest in selling US devices.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Point-of-care Ultrasonography in Norwegian General Practice and Self-perceived Use in Diagnostics - a Prospective Observational Study
The scope of this study is to explore how general practitioners (GPs) use Point-of-Care Ultrasonography (POCUS) in Norway. Thirty GPs will register information each time they use POCUS during a three-month period. Acquired information include the purpose of the scan, which organ is scanned, frequencies of POCUS and changes in diagnosis, plan, and treatment after the scan.
This is a strict observational study without any intervention.
Read the detailed description
The scope of this prospective, observational study is to explore how general practitioners (GPs) use Point-of-care Ultrasonography (POCUS) in their daily practice and whether or not POCUS affects the diagnostic process. A similar study has previously by the university of Aalborg, Denmark with Clinical Trials ID NCT03375333. A part of this project is to assess the external validity of their questionaire.
POCUS use will be explored through reports of indication, frequency, consumed time both in total and the the scan, changes in diagnosis and further follow-up by the following questions:
What is the purpose of the planned scan? Which organ(s) do the GPs plan to scan? What is(are) the tentative diagnosis(-es) that warrants the use of POCUS? How would the GP follow-up the patient, if scanning was not possible? Would treatment be initiated? What kind of treatment?
The GP will register the precise time before and after the scan to assess how much time the use of POCUS adds to the consultation. The time spent scanning will also be registered to explore how much time is spent undressing/dressing the patient and booting the ultrasound device.
Which organ(s) was(were) scanned? How often are the GPs able to display the relevant structure(s) with POCUS? How confident are the GPs in their assessments? Did the scan alter the tentative diagnosis? What are the new diagnosis(es)? Did the scan alter the plan for further examination(s)? Did the scan alter the plan for further treatment?
The effect on the diagnostic process will be investigated through the reported change(s) in the tentative diagnosis after the use of POCUS. The GPs' confidence in the scans will also be evaluated. The aims are to describe:
Do POCUS change the GPs' tentative diagnosis? Do POCUS increase the confidence of the GPs' tentative diagnosis? What is the relationship between the experience of GPs' confidence and the change in the tentative diagnoses? Is there a relationship between change from symptom diagnoses to disease diagnoses? What was the relationship between scanned organs and the GPs' confidence in the tentative diagnosis? What was the effect on the treatment of patients?
This will be explored through changes in the planned follow-up or need for further treatment for the patient. The aims are to describe:
Did POCUS change the GPs' plan for further examinations of the patient Did POCUS change the planned treatment for the patient
Study setting:
Norwegian day-time general practice
Interventions:
This study do not involve any new interventions. The GPs involved in this study already use POCUS as at part of their clinical practices.
Sample size Norway has approximately 4700 GPs. A recent study states that 30% of Norwegian GPs used POCUS in 2016. Most of these GPs scans less than one monthly. Duration of registration is three months. Of the entire GP population, 30 GPs will be included in this study. If the participating GPs scan twice weekly on average, the aim is to achieve 720 scans.
Recruitment
Participating GPs:
GPs using POCUS will be recruited through the continuous post-graduate small-group education, ultrasonography networks, participation in conferences, through teaching sessions, and through contacts via the Norwegian association for ultrasonography in general practice.
Participating patients:
No direct patient data will be used, only the assumed diagnosis and changes to these.
There are no restrictions made regarding age or gender.
Base-line assessment of GPs The will not be an assessment of the GPs' skills in the use of POCUS. Any GP is allowed to scan regardless of formal skills
Data collection A questionnaire is made for both electronic and manual registration. SurveyXact is the online database used for electronic registration. The questionnaire includes a time log to ensure the before and after registration. Several pilot tests have been and will be performed both in the research group and with GPs using POCUS to ensure comprehension, feasibility and compliance.
The GPs will be asked to access a questionnaire in SurveyXact each time they use their ultrasound device during their daily work. The GPs can access the questionnaire via mobile phone, iPad or computer, using a unique link (respondent link) allocated each participating GP. A key file, connecting each participating GP with the respondent link in SurveyXact (link), will be safely stored at the Research Unit for General Practice in Aalborg.
Questions before scanning are the following:
GP ID number What is the main reason to use POCUS in this patient? (Rule-in/Rule-out, Explore, Scan a known condition, Screening or Other) Which organs/positions is expected to be scanned? (organs on list) What is the main tentative diagnosis for this patient? (ICPC2 codes) Are there any other possible tentative diagnoses in this case? (ICPC2 codes) What is the overall plan for this patient? (Acute admission to hospital, Subacute referral to hospital, Elective referral hospital, Subacute referral to specialist, Elective referral to specialist, Referral to radiology, Other referral e.g. physiotherapist, Follow-up in the clinic, No plan for follow-up, Other) Which treatment will be initiated at this stage? (medical treatment, referral for treatment, initiated other treatment, None, Other)
Questions after the performed scanned:
Time used on the POCUS examination? (minutes) Which organs/positions were scanned? (organs on list) Was the GP able to produce ultrasound images of the relevant structures of (inserted text) ? (yes, no - please specify) What did the GP find? (Certain positive findings, Uncertain positive findings, Certain negative findings, Uncertain negative findings, Incidental findings - please specify in free text) Before POCUS the following tentative diagnoses were registered (inserted text) Has this changed? (yes but the ICPC-2 code is unchanged, Yes both diagnosis and ICPC-2 code have changed, no) What is the tentative diagnosis for this patient now? (ICPC-2 codes) Are there any other possible tentative diagnoses for this patient (please specify)? (ICPC-2 codes) How is the GPs confidence in their main tentative diagnosis, after POCUS? (Highly increased confidence, More confident, unchanged confidence, Less confident, Highly reduced confidence) Before POCUS the following plan was registered (inserted text) for the patient. Has this plan changed? (yes, no) What is the overall plan for this patient, now? (Acute admission to hospital, Subacute referral to hospital, Elective referral hospital, Subacute referral to specialist, Elective referral to specialist, Referral to radiology, Other referral e.g. physiotherapist, Follow-up in the clinic, No plan for follow-up, Other) Before POCUS the following treatment was registered (inserted text) for the patient. Has the treatment changed? (yes, no) Which treatment will be initiated at this stage? (medical treatment, referral for treatment, initiated other treatment, None, Other)
Statistics The data will be analyzed using descriptive statistics. Multivariate regression analysis will be used to analyze whether traits of the GP affect the results of the scans.
Research ethics approval
The study has an approval from the Norwegian Center for Research Data.
As this study is an observational study, and does not include any intervention, approval by the Norwegian Regional Committee for medical and Health Research Ethics was granted.
Protocol amendments will be declared and all editions. Any changes to the protocol will be saved.
- Being tested
- Point-of care Ultrasonography
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Point-of care UltrasonographyOther
GPs using POCUS and how it affects clinical judgement
What is being measured
The primary outcome is the main question the study is designed to answer.
How general practitioners use POCUS in their daily practice
The GPs' indications for the use of point-of-care ultrasound (POCUS) will be described through the number and type of scans performed, and through frequencies of the tentative diagnoses that warrant the use of POCUS. The frequency of each POCUS examination (numerator) will be compared to all performed scans (denominator). The GPs will register the time used for the POCUS examination. By the before and after registration of the organs intended to scan and the organ actually scanned, the extent of modification of tentative diagnosis, plan for further examination and/or treatment.
Measured: 2024
Secondary outcomes (2)
How GPs evaluate their confidence
The GPs state a tentative diagnosis as one main and other possible diagnoses before the use of POCUS. After the scan, the GPs will see their tentative diagnosis prior to the scan. The GPs are asked if these diagnoses have changed. Has the diagnosis changed, they will be asked to specify this. The tentative diagnosis is registered as ICPC-2 codes. The GPs assess their confidence in the tentative diagnoses after the use of POCUS: Increased confidence, more confident, unchanged confidence, less confident, reduced confidence. To test the reliability of the GPs' declaration of confidence, we examine if an increased confidence is correlated to specific organs scanned (Q2.2), a reduction in the total number of diagnoses (Q1.3, Q1.4, Q2.6 and Q2.7), or a change from symptom diagnosis to disease diagnosis.
Measured: 2024
Characteristics of the physician that influence the effect of POCUS
The effect on changes in tentative diagnoses, diagnostic confidence and plan for patients including treatment. We aim to describe:
- Does the gender of the GP affect any of these outcomes?
- Do the years of clinical experience affect any of these changes?
- Do the years of POCUS experience affect any of these changes?
- Are there geographical variations in the performed scans?
Measured: 2024
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 May 2020
- Study start1 Dec 2022
- Primary completion31 Dec 2023
- Study completion31 Dec 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Point-of-care UltrasoundStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Oslo
- Sponsor type
- University, hospital or other
- Collaborators
- Aalborg University
- Responsible party
- Principal investigator, Mette Brekke, University of Oslo
- Investigators
- Mette Brekke, Professor, Study chair, University of Oslo, Department of General PracticeHans-Christian Myklestul, M.D., Principal investigator, University of Oslo, Department of General PracticeTrygve Skonnord, PhD, Study director, University of Oslo, Department of General Practice
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04396925
- Sponsor's protocol ID
- 521500-710890-413601
- Status last verified
- May 2024
- First submitted
- 15 May 2020
- Last updated
- 6 May 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The data registered are available for the cooperating researchers at the university in Aalborg Denmark. The purpose of further analyses is to compare the external validity of the questionnaire.
Publications
Aakjaer Andersen C, Brodersen J, Davidsen AS, Graumann O, Jensen MBB. Use and impact of point-of-care ultrasonography in general practice: a prospective observational study. BMJ Open. 2020 Sep 17;10(9):e037664. doi: 10.1136/bmjopen-2020-037664.
PubMed 32948563
Study at a glance
From the registry record, last updated by the sponsor on 6 May 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Point-of-care Ultrasonography in Norwegian General Practice and Self-perceived Use in Diagnostics - a Prospective Observational Study
- ClinicalTrials.gov ID
- NCT04396925
- Acronym / sponsor ID
- 521500-710890-413601
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 30 participants (actual)
- Lead sponsor
- University of OsloUniversity, hospital or other
- Collaborators
- Aalborg University
- Study start
- 1 Dec 2022 (actual)
- Primary completion
- 31 Dec 2023 (actual)
- Study completion
- 31 Dec 2024 (estimated)
- First posted
- 21 May 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The scope of this study is to explore how general practitioners (GPs) use Point-of-Care Ultrasonography (POCUS) in Norway. Thirty GPs will register information each time they use POCUS during a three-month period. Acquired information include the purpose of the scan, which organ is scanned, frequencies of POCUS and changes in diagnosis, plan, and treatment after the scan.
This is a strict observational study without any intervention.
Detailed description
The scope of this prospective, observational study is to explore how general practitioners (GPs) use Point-of-care Ultrasonography (POCUS) in their daily practice and whether or not POCUS affects the diagnostic process. A similar study has previously by the university of Aalborg, Denmark with Clinical Trials ID NCT03375333. A part of this project is to assess the external validity of their questionaire.
POCUS use will be explored through reports of indication, frequency, consumed time both in total and the the scan, changes in diagnosis and further follow-up by the following questions:
What is the purpose of the planned scan? Which organ(s) do the GPs plan to scan? What is(are) the tentative diagnosis(-es) that warrants the use of POCUS? How would the GP follow-up the patient, if scanning was not possible? Would treatment be initiated? What kind of treatment?
The GP will register the precise time before and after the scan to assess how much time the use of POCUS adds to the consultation. The time spent scanning will also be registered to explore how much time is spent undressing/dressing the patient and booting the ultrasound device.
Which organ(s) was(were) scanned? How often are the GPs able to display the relevant structure(s) with POCUS? How confident are the GPs in their assessments? Did the scan alter the tentative diagnosis? What are the new diagnosis(es)? Did the scan alter the plan for further examination(s)? Did the scan alter the plan for further treatment?
The effect on the diagnostic process will be investigated through the reported change(s) in the tentative diagnosis after the use of POCUS. The GPs' confidence in the scans will also be evaluated. The aims are to describe:
Do POCUS change the GPs' tentative diagnosis? Do POCUS increase the confidence of the GPs' tentative diagnosis? What is the relationship between the experience of GPs' confidence and the change in the tentative diagnoses? Is there a relationship between change from symptom diagnoses to disease diagnoses? What was the relationship between scanned organs and the GPs' confidence in the tentative diagnosis? What was the effect on the treatment of patients?
This will be explored through changes in the planned follow-up or need for further treatment for the patient. The aims are to describe:
Did POCUS change the GPs' plan for further examinations of the patient Did POCUS change the planned treatment for the patient
Study setting:
Norwegian day-time general practice
Interventions:
This study do not involve any new interventions. The GPs involved in this study already use POCUS as at part of their clinical practices.
Sample size Norway has approximately 4700 GPs. A recent study states that 30% of Norwegian GPs used POCUS in 2016. Most of these GPs scans less than one monthly. Duration of registration is three months. Of the entire GP population, 30 GPs will be included in this study. If the participating GPs scan twice weekly on average, the aim is to achieve 720 scans.
Recruitment
Participating GPs:
GPs using POCUS will be recruited through the continuous post-graduate small-group education, ultrasonography networks, participation in conferences, through teaching sessions, and through contacts via the Norwegian association for ultrasonography in general practice.
Participating patients:
No direct patient data will be used, only the assumed diagnosis and changes to these.
There are no restrictions made regarding age or gender.
Base-line assessment of GPs The will not be an assessment of the GPs' skills in the use of POCUS. Any GP is allowed to scan regardless of formal skills
Data collection A questionnaire is made for both electronic and manual registration. SurveyXact is the online database used for electronic registration. The questionnaire includes a time log to ensure the before and after registration. Several pilot tests have been and will be performed both in the research group and with GPs using POCUS to ensure comprehension, feasibility and compliance.
The GPs will be asked to access a questionnaire in SurveyXact each time they use their ultrasound device during their daily work. The GPs can access the questionnaire via mobile phone, iPad or computer, using a unique link (respondent link) allocated each participating GP. A key file, connecting each participating GP with the respondent link in SurveyXact (link), will be safely stored at the Research Unit for General Practice in Aalborg.
Questions before scanning are the following:
GP ID number What is the main reason to use POCUS in this patient? (Rule-in/Rule-out, Explore, Scan a known condition, Screening or Other) Which organs/positions is expected to be scanned? (organs on list) What is the main tentative diagnosis for this patient? (ICPC2 codes) Are there any other possible tentative diagnoses in this case? (ICPC2 codes) What is the overall plan for this patient? (Acute admission to hospital, Subacute referral to hospital, Elective referral hospital, Subacute referral to specialist, Elective referral to specialist, Referral to radiology, Other referral e.g. physiotherapist, Follow-up in the clinic, No plan for follow-up, Other) Which treatment will be initiated at this stage? (medical treatment, referral for treatment, initiated other treatment, None, Other)
Questions after the performed scanned:
Time used on the POCUS examination? (minutes) Which organs/positions were scanned? (organs on list) Was the GP able to produce ultrasound images of the relevant structures of (inserted text) ? (yes, no - please specify) What did the GP find? (Certain positive findings, Uncertain positive findings, Certain negative findings, Uncertain negative findings, Incidental findings - please specify in free text) Before POCUS the following tentative diagnoses were registered (inserted text) Has this changed? (yes but the ICPC-2 code is unchanged, Yes both diagnosis and ICPC-2 code have changed, no) What is the tentative diagnosis for this patient now? (ICPC-2 codes) Are there any other possible tentative diagnoses for this patient (please specify)? (ICPC-2 codes) How is the GPs confidence in their main tentative diagnosis, after POCUS? (Highly increased confidence, More confident, unchanged confidence, Less confident, Highly reduced confidence) Before POCUS the following plan was registered (inserted text) for the patient. Has this plan changed? (yes, no) What is the overall plan for this patient, now? (Acute admission to hospital, Subacute referral to hospital, Elective referral hospital, Subacute referral to specialist, Elective referral to specialist, Referral to radiology, Other referral e.g. physiotherapist, Follow-up in the clinic, No plan for follow-up, Other) Before POCUS the following treatment was registered (inserted text) for the patient. Has the treatment changed? (yes, no) Which treatment will be initiated at this stage? (medical treatment, referral for treatment, initiated other treatment, None, Other)
Statistics The data will be analyzed using descriptive statistics. Multivariate regression analysis will be used to analyze whether traits of the GP affect the results of the scans.
Research ethics approval
The study has an approval from the Norwegian Center for Research Data.
As this study is an observational study, and does not include any intervention, approval by the Norwegian Regional Committee for medical and Health Research Ethics was granted.
Protocol amendments will be declared and all editions. Any changes to the protocol will be saved.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- General practitioners who use point-of-care ultrasonography as a part of clinical practice. Out-of-hours scanning excluded
Key inclusion criteria (1 listed)
- General practitioners who use point-of-care ultrasound in day time general practice
Key exclusion criteria (1 listed)
- Conflict of interest, e.g. if the GP is part of the research group or if the GP has direct financial interest in selling US devices.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Point-of care UltrasonographyGPs using POCUS and how it affects clinical judgement | Other | – |
Primary outcome
How general practitioners use POCUS in their daily practice
Time frame: 2024
The GPs' indications for the use of point-of-care ultrasound (POCUS) will be described through the number and type of scans performed, and through frequencies of the tentative diagnoses that warrant the use of POCUS. The frequency of each POCUS examination (numerator) will be compared to all performed scans (denominator). The GPs will register the time used for the POCUS examination. By the before and after registration of the organs intended to scan and the organ actually scanned, the extent of modification of tentative diagnosis, plan for further examination and/or treatment.
2 secondary outcomes
How GPs evaluate their confidence
Time frame: 2024
Characteristics of the physician that influence the effect of POCUS
Time frame: 2024
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 May 2024.
- Results publication: PubMed 32948563Aakjaer Andersen C, Brodersen J, Davidsen AS, Graumann O, Jensen MBB. Use and impact of point-of-care ultrasonography in general practice: a prospective observational study. BMJ Open. 2020 Sep 17;10(9):e037664. doi: 10.1136/bmjopen-2020-037664.
- URL to the study published in BMJ OpenLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. The data registered are available for the cooperating researchers at the university in Aalborg Denmark. The purpose of further analyses is to compare the external validity of the questionnaire.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mette Brekke, Professor study chair
University of Oslo, Department of General Practice
Hans-Christian Myklestul, M.D. principal investigator
University of Oslo, Department of General Practice
Trygve Skonnord, PhD study director
University of Oslo, Department of General Practice
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Point-of-care Ultrasound and General Practice, run by University of Oslo at 1 site in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 6 May 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Norway. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
How general practitioners use POCUS in their daily practice (time frame: 2024). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04396925, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2024.