Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
768 participants
OBSERVATIONAL
2018-01-01
2024-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Obstetric Life Support, a Curriculum to Effectively Resuscitate Pregnant Patients Experiencing Cardiac Arrest.
NCT05355519
Sex-unique Disparities in Survival and Resuscitation After Out-of-hospital Cardiac Arrest - a Danish Analysis
NCT05583084
Environmental and Behavioral Risk Factors for Childhood Drowning
NCT00341289
Dispatcher-Assisted CPR: Low-Dose, High-Frequency Simulation-Based Training
NCT04085692
Use of an Observer Tool to Improve Learning Outcomes for Cardiac Arrest Management
NCT05187299
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Passed in situ assessment
This group passed their in situ assessment (summative assessment)
In situ simulation assessment
Unannounced in situ simulation assessment during working hours
Failed in situ assessment
This group failed their in situ assessment (summative assessment)
In situ simulation assessment
Unannounced in situ simulation assessment during working hours
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
In situ simulation assessment
Unannounced in situ simulation assessment during working hours
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Dublets
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Prehospital Center, Region Zealand
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Niklas Breindahl
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Helle C Christensen, Ass. Prof.
Role: STUDY_DIRECTOR
Prehospital Center, Region Zealand
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Prehospital Center
Næstved, Region Sjælland, Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
DROWN_INSITU
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.