- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05489835
Work-Health-Life-Balance - Mental Resilience, Stability & Healthy Nutrition
Work-Health-Life-Balance 4.0 - Mental Resilience, Stability & Healthy Nutrition in a New Work Reality
New working environments (digitalization, flexibilization) can lead to increased levels of stress. A balanced work-life balance is therefore important in order to prevent negative effects of stress on mental health.
This study investigates,
- how stress, recovery, nutritional behavior, resilience and sleep behavior are related to the changed working conditions.
- how standardized nutritional training affects individual body composition (measured using Bioelectrical Impedance Analyses, BIA), stress perception, burn-out symptoms and sleep.
Study Overview
Status
Intervention / Treatment
Detailed Description
The ways of working must adapt to the challenges and opportunities of the digital world. Work 4.0 describes the process of change in the working environment in the digital age. Adapting to rapidly changing and sometimes uncertain living and working conditions in times of digitization, dislocated working (including "home office") and altered work processes demands a considerable effort of resources from numerous employees. Previously established work environments and behaviors are being evaluated and adapted to the new circumstances and requirements.
Such times of change often cause uncertainty and result in increased stress levels. Stress, in turn, leads to a variety of symptoms in many areas of life and work, which can limit the ability to work. As a result, successful adaptation to the challenges of the new work reality of Work 4.0 can fail.
Research Questions:
This study investigates,
- how stress, recovery, nutritional behavior, resilience and sleep behavior are related to the changed working conditions and central characteristics of work 4.0.
- how standardized nutritional training based on the Austrian Food Pyramid affects individual body composition (measured using Bioelectrical Impedance Analyses, BIA), stress perception, burn-out symptoms and sleep.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Andreas Baranyi, M.D.
- Phone Number: 0043-316-385-86241
- Email: an.baranyi@medunigraz.at
Study Contact Backup
- Name: Melanie Schweinzer
- Email: melanie.schweinzer@medunigraz.at
Study Locations
-
-
Styria
-
Graz, Styria, Austria, 8036
- Recruiting
- Medical University of Graz
-
Contact:
- Andreas Baranyi, Prof. MD
- Phone Number: +4331638586241
- Email: an.baranyi@medunigraz.at
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- employees in austrian companies affected by digitalization
- Informed consent
Exclusion Criteria:
- no informed consent
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Employees
Employees in Austrian companies affected by digitalization
|
Nutritional counseling
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress
Time Frame: 3 months
|
Stress-Erholungsfragebogen (RESTQ); minimum value: 0, maximum value: 294; High scores reflect high subjective stress.
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sleep
Time Frame: 3 months
|
Insomnis severity index: minimum value: 0, maximum value: 28; High scores reflect the presence of sleeping disorders
|
3 months
|
|
Body mass index
Time Frame: 3 months
|
Body mass index (BMI); BMI= body weight / (body height)²
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Andreas Baranyi, M.D., Medical University of Graz, Auenbruggerplatz 31, 8036 Graz, Austria
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- EK 34-147 ex 21/22
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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