In Situ Simulation Training in Lifeguard Organisations (DROWN_INSITU)

June 1, 2025 updated by: Niklas Breindahl, Prehospital Center, Region Zealand

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.

Study Overview

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.

Study Type

Observational

Enrollment (Actual)

768

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Region Zealand
      • Næstved, Region Zealand, Denmark, 4700
        • Prehospital Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

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

Description

Inclusion Criteria:

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

Exclusion Criteria:

  • Blank entries
  • Dublets

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Passed in situ assessment
This group passed their in situ assessment (summative assessment)
Unannounced in situ simulation assessment during working hours
Failed in situ assessment
This group failed their in situ assessment (summative assessment)
Unannounced in situ simulation assessment during working hours

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pass/fail ratio of in situ simulation assessments
Time Frame: All in situ assessments from 2018-2023 will be included in this analysis.
To estimate the pass/fail ratio of in situ simulation assessments.
All in situ assessments from 2018-2023 will be included in this analysis.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Risk factors associated with a failed assessment
Time Frame: All in situ assessments from 2018-2023 will be included in this analysis.
To analyse risk factors associated with a failed assessment
All in situ assessments from 2018-2023 will be included in this analysis.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Helle C Christensen, Ass. Prof., Prehospital Center, Region Zealand

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2018

Primary Completion (Actual)

December 31, 2023

Study Completion (Actual)

December 31, 2024

Study Registration Dates

First Submitted

March 13, 2024

First Submitted That Met QC Criteria

March 13, 2024

First Posted (Actual)

March 20, 2024

Study Record Updates

Last Update Posted (Actual)

June 4, 2025

Last Update Submitted That Met QC Criteria

June 1, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • DROWN_INSITU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Data will be available from the corresponding author upon reasonable request.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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