- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01741220
Resilience and Mentoring in German-speaking Intensive Care Providers and Anesthesiologists (REMEDIA)
April 4, 2015 updated by: Helmar Bornemann-Cimenti, MD DMedSci, Medical University of Graz
The aim of this study is to identify factors influencing work engagement and wellbeing in German-speaking intensive-care providers and anesthesiologists.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
92
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
-
-
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Graz, Austria, 8036
- Medical Univeristy Graz
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Innsbruck, Austria, 6020
- Innsbruck Medical University
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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 to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
German-speaking intensive-care providers and anesthetists
Description
Inclusion Criteria:
- resident or staff anesthetist
- since more than 6 months working for the same institution
Exclusion Criteria:
- no informed-consent
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
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
---|
anesthetists
German-speaking intensive-care providers and anesthetists
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Utrecht Work Engagement Scale
Time Frame: 4 weeks
|
4 weeks
|
Positive and negative affective scale
Time Frame: 4 weeks
|
4 weeks
|
Psychological Well-Being questionnaire
Time Frame: 4 weeks
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Acceptance and Action Questionnaire
Time Frame: 4 weeks
|
4 weeks
|
Experience Questionnaire
Time Frame: 4 weeks
|
4 weeks
|
Dutch Workaholism Scale
Time Frame: 4 weeks
|
4 weeks
|
Multidimensional Perfectionism Scale
Time Frame: 4 weeks
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Horst Mitmansgruber, MSc, PhD, Medical University Innsbruck
- Study Director: Helmar Bornemann-Cimenti, MD, DMedSci, Medical University of Graz
- Study Chair: Andreas Sandner-Kiesling, MD, Medical University of Graz
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
February 1, 2015
Primary Completion (Actual)
March 1, 2015
Study Completion (Actual)
March 1, 2015
Study Registration Dates
First Submitted
November 27, 2012
First Submitted That Met QC Criteria
November 30, 2012
First Posted (Estimate)
December 4, 2012
Study Record Updates
Last Update Posted (Estimate)
April 7, 2015
Last Update Submitted That Met QC Criteria
April 4, 2015
Last Verified
April 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- REMEDIA
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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