In-hospital Healthcare Professionals' Attitudes and Their Experience in Performing Cardiopulmonary Resuscitation.

March 25, 2020 updated by: Jennie Silverplats, Dalarna County Council, Sweden

Attitudes among healthcare professionals can possibly affect the treatment given in cardiac arrest situations. The attitudes of healthcare professionals towards cardiopulmonary resuscitation (CPR) has been poorly studied. The few existing previous international results shows attitudes reported by nurses as hesitation, fear of defibrillation, anxiety and fear of harming the patient.

The aim of this study was to describe the attitudes towards performing cardiopulmonary resuscitation among in-hospital healthcare professionals, furthermore to assess if experience in performing CPR has an effect on attitudes.

Study Overview

Status

Completed

Detailed Description

Data will be collected using questionnaires containing attitude questions. The questionnaires contains questions regarding attitudes towards being required to perform CPR (6 questions), previous experience in performing CPR (time since last performance and number of performances) and attitudes during the latest CPR performance (8 questions). All attitude questions are constructed as multiple choice questions.

Results regarding attitudes towards being required to perform CPR and attitudes during the latest CPR performance will be presented descriptively. To analyse a possible effect of time since CPR performance and number of CPR performances on attitudes during the latest CPR performance logistic regression will be used. Response variables will be "yes" or "no" on 8 specific attitude questions with predictors consisting of time since CPR performance (0-3 months ago, 4-23 months ago and >24 months) and number of CPR performances (1-3 times, 4-10 times and >10 times).

Study Type

Observational

Enrollment (Actual)

3639

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

      • Mora, Sweden, 79285
        • Region of Dalarna
    • Västmanland
      • Västerås, Västmanland, Sweden, 72189
        • Region of Västmanland

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

In-hospital healthcare professionals of all professions at five hospitals in the region of Västmanland and Region of Dalarna, Sweden.

Description

Inclusion Criteria:

  • In-hospital healthcare professionals.
  • Patient contact

Exclusion Criteria:

  • Absent during the survey
  • Parental leave
  • Leave of absence
  • Sick leave.

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
Healthcare professionals in the Region of Västmanland
Healthcare professionals of all professions working in-hospital with patient contact at two hospitals in the Region of Västmanland, Sweden. Data is collected by questionnaires.
Healthcare professionals in the Region of Dalarna
Healthcare professionals of all professions working in-hospital with patient contact at three hospitals in the Region of Dalarna, Sweden. Data is collected by questionnaires.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
In-hospital healthcare professionals' attitudes towards CPR.
Time Frame: one month
14 questions regarding attitudes towards performing CPR will be presented descriptively. Number of respondents answering "yes", "no" and "I don´t know" to each attitude question will be presented.
one month
In-hospital healthcare professionals' experience in performing CPR.
Time Frame: one month
Two questions regarding experience in performing CPR will be presented descriptively. Number of respondents in each response category concerning number of previous CPR performances and time since last CPR performance will be presented.
one month
Does experience in performing CPR have an effect on attitudes towards CPR
Time Frame: two months
The effect of previous experience in CPR on attitudes during a cardiac arrest situation will be analysed using binary logistic regression. Each of the eight questions concerning attitudes during a cardiac arrest situation will serve as a dependent variable with "yes" as the response. Independent variables consists of number of previous CPR performances, time since last CPR performance and workplace. Independent variables associated with the dependent variable at a level of p <0.1 will be included in a multiple model. The model will be adjusted for profession and number of years in profession.
two months

Collaborators and Investigators

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

Investigators

  • Study Director: Anneli Strömsöe, PhD, Dalarna County Council

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)

December 1, 2008

Primary Completion (Actual)

December 30, 2016

Study Completion (Actual)

December 30, 2016

Study Registration Dates

First Submitted

February 21, 2020

First Submitted That Met QC Criteria

March 23, 2020

First Posted (Actual)

March 25, 2020

Study Record Updates

Last Update Posted (Actual)

March 26, 2020

Last Update Submitted That Met QC Criteria

March 25, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2006/201/2 (part 2)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

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