- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04478786
Ambulance Crews' Experiences of Using a Mechanical Chest Compression Device.
What Are Ambulance Crews' Experiences of Using a Mechanical Chest Compression Device for Out-of-hospital Resuscitation? A Constructivist Qualitative Study Utilising Online Focus Groups
Should a person have a cardiac arrest (where their heart stops beating) they require treatment of cardiopulmonary resuscitation (CPR). This includes providing chest compressions. Traditionally these compressions are provided by hand but mechanical chest compression devices (MCCD) have been investigated for use in out of hospital resuscitation attempts.
Research trials recruiting human participants have concluded recently. They all found no difference in survival outcomes when MCCD and manual compressions were compared.
Despite this, the latest expert review on MCCD suggests that MCCD can be a reasonable alternative to high quality manual compressions when these cannot be provided. MCCD continue to be used by Specialists in the local ambulance service and historically by those recruiting patients to a national multi centre trial of MCCD. There is another, as yet under-investigated element, and that is of ambulance crews' experiences of using such devices. Therefore it is a reasonable topic to investigate.
Study Overview
Detailed Description
This study will invite local United Kingdom (UK) National Health Service (NHS) operational ambulance crews to participate in a 1-2 hour online focus group discussion (a collective group discussion) about their experiences of using MCCD. The participants will be any operational ambulance crew member, employed by the local ambulance Trust and who had experience of using any type of MCCD. The focus groups will be audio recorded; participants will be aware of this when they choose to participate.
The aim of this research is to collect and report ambulance crews' experiences of using mechanical chest compression devices for out of hospital resuscitation attempts.
Ultimately there may of course be benefits for patients by exploring whether MCCD play a part in out of hospital resuscitations. Funding has been offered by a manufacturer one of the types of MCCD; they have had no involvement in the design or analysis of the study.
Once transcribed, the data will be analysed manually. The content of each focus group will be coded and then each participants' individual responses will be coded, first using open coding, then focused coding to identify emergent themes, before concluding with the categories that have been identified. The constant comparison method of data analysis will be used.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Newcastle Upon Tyne, United Kingdom, NE15 8NY
- North East Ambulance Service NHS Foundation Trust
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- aged 18 or over
- an employee of the local ambulance service
- employed as an operational ambulance crew member, irrespective of title
- to have experienced an out of hospital resuscitation where MCCD was used, irrespective of the type of device or their level of involvement.
Exclusion Criteria:
- not an employee of the local ambulance service
- have no experience of using a mechanical chest compression device at an out of hospital resuscitation
- the participant is unwilling to provide consent to participate
- the participant is unwilling to provide consent to be audio recorded.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Focus Groups 1-4
An anticipated 3-8 participants who meet the inclusion criteria of being aged 18 or over, a employee of the local ambulance service, are employed as an operational ambulance crew member, irrespective of title and to have had experienced an out of hospital resuscitation where MCCD was used, irrespective of the type of device or their level of involvement, and who also volunteer and agree to take part in the online focus group.
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There is no intervention.
This is a qualitative piece of work only.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Collect and report ambulance crews' experiences of using MCCDs for out-of-hospital resuscitation attempts.
Time Frame: 2 hours
|
The transcribed discussions will be coded and then themes emerging from the data identified and developed.
To do this I will use a constant comparison method of analysis.
The presence or lack of consensus and reinforcement on certain topics will also be observed for.
|
2 hours
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Does the use of MCCDs have any effect on, or facilitate, the team leader role at an out-of-hospital resuscitation attempt
Time Frame: 2 hours
|
The transcribed discussions will be coded and then themes emerging from the data identified and developed.
To do this I will use a constant comparison method of analysis.
The presence or lack of consensus and reinforcement on certain topics will also be observed for.
|
2 hours
|
|
Does providing mechanical versus manual chest compressions have an effect on how ambulance crews feel physically and emotionally after an out-of-hospital resuscitation attempt.
Time Frame: 2 hours
|
The transcribed discussions will be coded and then themes emerging from the data identified and developed.
To do this I will use a constant comparison method of analysis.
The presence or lack of consensus and reinforcement on certain topics will also be observed for.
|
2 hours
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Richelle Duffy, PhD, Northumbria University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 18018/275607
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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