- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04111796
Nature-based Solutions for Work-related Stress
Nature-based Solutions for Work-related Stress: an Intervention Study
Although exposure to nature has restorative effects on human health, beneficial effects of nature-based interventions in the working environment have been underexplored. The investigators aim to conduct a randomised controlled pilot study.
During workhours one group participates in a nature-based program, the other group is a control group. The investigators test stress-related parameters including cortisol levels, wellbeing and stress, and neurocognition.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Michelle Plusquin
- Phone Number: 003211268289
- Email: michelle.plusquin@uhasselt.be
Study Locations
-
-
Limburg
-
Hasselt, Limburg, Belgium, 3590
- Recruiting
- Province of Limburg
-
Contact:
- Diana Clementa
- Phone Number: 003211268289
- Email: diana.clemente@uhasselt.be
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- work at province of Limburg speak dutch
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: group in nature
they participate in nature based-program during work hours
|
participation in nature activities: 30 min stress management in nature and group activity (walking, cycling)
|
No Intervention: control group
they participate don't in nature based-program during work hours and perform their normal work schedule
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Neurocognition: selective attention
Time Frame: 5 minutes
|
computerised tests (stroop test).
The scale is mean reaction time and is used as a continuous variable.
|
5 minutes
|
Neurocognition: short-term memory
Time Frame: 10 minutes
|
computerised tests (Digit Span Test).
The scale is number of digits and is used as a continuous variable.
|
10 minutes
|
Neurocognition:visual information processing speed
Time Frame: 5 minutes
|
computerised tests (Digit Symbol test).
The scale is number of digits and is used as a continuous variable.
|
5 minutes
|
Neurocognition: visual information processing speed
Time Frame: 5 minutes
|
computerised tests (Pattern Comparison test ).
The scale is reaction time and is used as a continuous variable.
|
5 minutes
|
stress levels
Time Frame: 5 minutes
|
Assessed by salivary cortisol levels.
Scale is µg/dl and used as a continuous variable.
|
5 minutes
|
stress levels
Time Frame: 10 minutes
|
Assessed by questionnaires (burnout assessment tool).
Scores are used as continuous variable.
Lower scores represent lower risk of burnout, higher scores represent higher risk of burnout.
The score is constructed from questions concerning exhaustion, mental distance, emotional disorder and cognitive disorder.
|
10 minutes
|
stress levels
Time Frame: 3 weeks
|
Assessed by smartwatch (algorithm including hart rate and movement).
Values are used as continuous variable
|
3 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Michelle Plusquin, Hasselt University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
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 (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
- Nature_health
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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