- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04321213
In-hospital Healthcare Professionals' Attitudes and Their Experience in Performing Cardiopulmonary Resuscitation.
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
Conditions
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Mora, Sweden, 79285
- Region of Dalarna
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Västmanland
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Västerås, Västmanland, Sweden, 72189
- Region of Västmanland
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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:
- In-hospital healthcare professionals.
- Patient contact
Exclusion Criteria:
- Absent during the survey
- Parental leave
- Leave of absence
- Sick leave.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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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.
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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In-hospital healthcare professionals' attitudes towards CPR.
Time Frame: one month
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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.
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one month
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In-hospital healthcare professionals' experience in performing CPR.
Time Frame: one month
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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.
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one month
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Does experience in performing CPR have an effect on attitudes towards CPR
Time Frame: two months
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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.
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two months
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Anneli Strömsöe, PhD, Dalarna County Council
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
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)?
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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