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DrowningDROWN_INSITUNCT06320197

In Situ Simulation Training in Lifeguard Organisations

An observational study of Drowning and Drowning, Near, run by Prehospital Center, Region Zealand at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This retrospective study will analyse a dataset consisting of 919 in situ simulation assessments collected between 2018 and 2023 in a Danish nationwide surf lifeguard organisation. The primary objective is to estimate the pass/fail ratio of in situ simulation assessments. Read more about this study

Who is it for?
Any age
What is being tested?
In situ simulation assessment
How many people
768 participants
Where
1 siteDenmark
Study dates
1 Jan 2018to 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
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: The participants from this study are all trained in the nationwide Danish lifeguard organisation according to the International Life Saving Federations standards.

Who may be able to join

  • All in situ assessments in the nationwide Danish lifeguard organisation from 2018 to 2023.

Who cannot join

  • Blank entries
  • Dublets

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Prehospital Center

    Næstved, Region Sjælland, 4700

Other trials in Denmark

About this study

Official title: In Situ Simulation Training in Lifeguard Organisations: a Danish Retrospective Study From 2018-2023

This retrospective study will analyse a dataset consisting of 919 in situ simulation assessments collected between 2018 and 2023 in a Danish nationwide surf lifeguard organisation. The primary objective is to estimate the pass/fail ratio of in situ simulation assessments. The secondary objective is to analyse risk factors associated with a failed assessment. These results may guide future efforts to improve the Danish surf lifeguard training program.

Read the detailed description

Background: Once weekly on all lifeguard-supervised beaches during the summer holiday period, a lifeguard instructor sneaks undetected into the primary surveillance zone between the flags and raises a hand to indicate a drowning scenario. This is called in situ simulation and is used to assess Danish surf lifeguards' rescue and medical skills. It is an unannounced test occurring during working hours, followed by feedback and training with the lifeguard instructors. Previous data indicate that approximately 1 in 5 lifeguards fail the in situ assessment. Analysing data from in situ simulation assessments may pinpoint areas for future improvement.

Objectives: The primary objective is to estimate the pass/fail ratio of in situ simulation assessments. The secondary objective is to analyse risk factors associated with a failed assessment. These results may guide future efforts to improve the Danish surf lifeguard training program.

Methods: This retrospective study will analyse a dataset consisting of 919 in situ simulation assessments collected between 2018 and 2023 in a Danish nationwide surf lifeguard organisation. Data on the local conditions (e.g., wave height, time of the day, and the number of beach visitors) and the in situ evaluation (pass/fail) were extracted directly from the predefined variables. Data on failure reasons were extracted through manual validation of the semi-structured free text fields by four independent observers. Any discrepancies were resolved by a senior member of the research group.

Being tested
In situ simulation assessment
Keywords
In situ simulation, Simulation, Drowning, Lifeguard, Lifesaver
Medical subject headings
Drowning, Near Drowning

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • In situ simulation assessmentOther

    Unannounced in situ simulation assessment during working hours

Study groups in NCT06320197
Study groupRoleWhat they receive
Passed in situ assessmentThis group passed their in situ assessment (summative assessment)
Receives: Other: In situ simulation assessment
Failed in situ assessmentThis group failed their in situ assessment (summative assessment)
Receives: Other: In situ simulation assessment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pass/fail ratio of in situ simulation assessments

    To estimate the pass/fail ratio of in situ simulation assessments.

    Measured: All in situ assessments from 2018-2023 will be included in this analysis.

Secondary outcomes (1)
  1. Risk factors associated with a failed assessment

    To analyse risk factors associated with a failed assessment

    Measured: All in situ assessments from 2018-2023 will be included in this analysis.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Mar 2024
  2. Study start1 Jan 2018
  3. Primary completion31 Dec 2023
  4. Study completion31 Dec 2024

Resources

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
Retrospective
Enrolment
768 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06320197
Sponsor's protocol ID
DROWN_INSITU
Acronym
DROWN_INSITU
Status last verified
Jun 2025
First submitted
13 Mar 2024
Last updated
4 Jun 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data will be available from the corresponding author upon reasonable request.

Questions about this trial

What is this clinical trial studying?

An observational study of Drowning and Drowning, Near, run by Prehospital Center, Region Zealand at 1 site in Denmark.

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 2 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: finished, as of the sponsor's last update on 4 Jun 2025. 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 Denmark. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Pass/fail ratio of in situ simulation assessments (time frame: All in situ assessments from 2018-2023 will be included in this analysis.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 4 Jun 2025.

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