- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03721666
Medical Dispatchers' Perception of Visual Information in Real Out-of-hospital Cardiac Arrest
October 25, 2018 updated by: Gitte Linderoth, Emergency Medical Services, Capital Region, Denmark
Medical Dispatchers' Perception of Visual Information in Real Out-of-hospital Cardiac Arrest: A Qualitative Interview Study
Dispatcher-assisted cardiopulmonary resuscitation is a complex, nonvisual procedure that is challenging for the dispatcher.
The aim was to explore the medical dispatchers' perception of bystanders' responses and dispatchers' reflections about the added value of visual information in out-of-hospital cardiac arrests (OHCA) situations.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Ten individual interviews with medical dispatchers who had previously handled an emergency call concerning OHCA captured on closed-circuit television (CCTV) were conducted.
First, the medical dispatcher listened to the emergency call and described their perception of the scenario.
Afterward, the CCTV recording was shown to the dispatcher, who was then interviewed.
The interviews were videotaped, and the audio files were transcribed verbatim.
Thematic content analysis was conducted.
Study Type
Observational
Enrollment (Actual)
10
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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Emergency Medical dispatchers
Description
Inclusion Criteria:
- Emergency Medical dispatchers who had previously handled an emergency call concerning OHCA captured on closed-circuit television (CCTV)
Exclusion Criteria:
- None
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The added value of visual information to the medical dispatcher in out-of-hospital cardiac arrests (OHCA) situations.
Time Frame: One hour interview with earch of the emergency medical dispathers
|
We applied a qualitative research methodology using thematic analysis with an explorative and inductive approach.
The first author followed Braun and Clarke's six-step analytical approach, which has the following steps: familiarising with data, generating initial codes, searching for themes, reviewing themes, defining and naming themes, and producing the report.
Codes and themes were organised using Nvivo10 software (QSR International Pty Ltd, Australia).
Analysis continued until saturation; that is, when information became redundant.
|
One hour interview with earch of the emergency medical dispathers
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Freddy K. Lippert, Emergency Medical Services, Capital Region, Denmark
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)
February 1, 2015
Primary Completion (ACTUAL)
June 1, 2015
Study Completion (ACTUAL)
January 1, 2017
Study Registration Dates
First Submitted
October 23, 2018
First Submitted That Met QC Criteria
October 25, 2018
First Posted (ACTUAL)
October 26, 2018
Study Record Updates
Last Update Posted (ACTUAL)
October 26, 2018
Last Update Submitted That Met QC Criteria
October 25, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- F-15035-02-GL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
If other researchers want the themes and transcriptions it can be arranged.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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.