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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04111796
Other study ID # Nature_health
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2019
Est. completion date November 1, 2019

Study information

Verified date October 2019
Source Hasselt University
Contact Michelle Plusquin
Phone 003211268289
Email michelle.plusquin@uhasselt.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date November 1, 2019
Est. primary completion date November 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- work at province of Limburg speak dutch

Exclusion Criteria:

-

Study Design


Related Conditions & MeSH terms


Intervention

Other:
nature based solution for stress reduction
participation in nature activities: 30 min stress management in nature and group activity (walking, cycling)

Locations

Country Name City State
Belgium Province of Limburg Hasselt Limburg

Sponsors (1)

Lead Sponsor Collaborator
Hasselt University

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neurocognition: selective attention computerised tests (stroop test). The scale is mean reaction time and is used as a continuous variable. 5 minutes
Primary Neurocognition: short-term memory computerised tests (Digit Span Test). The scale is number of digits and is used as a continuous variable. 10 minutes
Primary Neurocognition:visual information processing speed computerised tests (Digit Symbol test). The scale is number of digits and is used as a continuous variable. 5 minutes
Primary Neurocognition: visual information processing speed computerised tests (Pattern Comparison test ). The scale is reaction time and is used as a continuous variable. 5 minutes
Primary stress levels Assessed by salivary cortisol levels. Scale is µg/dl and used as a continuous variable. 5 minutes
Primary stress levels 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
Primary stress levels Assessed by smartwatch (algorithm including hart rate and movement). Values are used as continuous variable 3 weeks
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