Nature-based Solutions for Work-related Stress

October 1, 2019 updated by: Michelle Plusquin, Hasselt University

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

Unknown

Detailed Description

Participants of the intervention group follow a 30-minute stress management course in nature followed by a nature-based activity of 1.5 hours, twice a week for 3 consecutive weeks. The investigators measure neurocognition via neurocognitive tests, emotional status via burnout assessment tool and well-being questionnaires, and asses stress levels via salivary cortisol and smartwatches.

Study Type

Interventional

Enrollment (Anticipated)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Limburg
      • Hasselt, Limburg, Belgium, 3590

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

Description

Inclusion Criteria:

  • work at province of Limburg speak dutch

Exclusion Criteria:

-

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

  • 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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Michelle Plusquin, Hasselt University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (Actual)

August 1, 2019

Primary Completion (Anticipated)

November 1, 2019

Study Completion (Anticipated)

November 1, 2019

Study Registration Dates

First Submitted

September 27, 2019

First Submitted That Met QC Criteria

September 30, 2019

First Posted (Actual)

October 1, 2019

Study Record Updates

Last Update Posted (Actual)

October 3, 2019

Last Update Submitted That Met QC Criteria

October 1, 2019

Last Verified

October 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • Nature_health

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

Data will only be shared with postdoctoral researcher involved in this project in our research group. Data is pseudonymised .

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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