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

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

      • Graz, Austria, 8036
        • Medical Univeristy Graz
      • Innsbruck, Austria, 6020
        • Innsbruck Medical University

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.

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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