- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05020977
Physical Actitvity and Blood Pressure Among Ambulance Personnel During Work and Leisure
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The work environment for ambulance personnel consists of several factors that might have negative effect on health, for example shift work, long working hours, stress and physical demanding work. Associations between these work-related factors and increased risk of disease, for example cardiovascular- and musculoskeletal disease, have been observed in several studies. However, few studies have specifically been focusing on ambulance personnel.
There is lack of knowledge regarding how work environment factors affect physical activity during work and leisure time among ambulance personnel. Further, the knowledge about blood pressure during work and leisure time is limited for this group.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Jonkoping, Sweden, 551 11
- Jonkoping University, School of Health and Welfare
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Employed in the ambulance organisation at the time for data collection
Exclusion Criteria:
- Managers and administrative personnel in the ambulance organisation
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Blood pressure
Time Frame: 48 hours
|
Ambulatory blood pressure, Objectively measured
|
48 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physical activity
Time Frame: 7 days
|
Objectively measured with accelerometry
|
7 days
|
Recovery
Time Frame: baseline, pre-intervention/procedure/surgery
|
Self-reported
|
baseline, pre-intervention/procedure/surgery
|
Health
Time Frame: baseline, pre-intervention/procedure/surgery
|
Subjective overall health
|
baseline, pre-intervention/procedure/surgery
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Eleonor I Fransson, PhD, Jönköping University
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
Other Study ID Numbers
- JU 2020/4878-51
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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