- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05249296
The Impact of Green Spaces on the General Well-being and Stress of Students
The Impact of Green Spaces on the General Well-being and Stress of Students: an Intervention Study
The number of students with psychological problems is on the rise, due to a combination of increasing performance pressure, high expectations, difficulties handling stress, social pressure, and studying. Spending time in a green space has been shown to have positive effects on the mental and general health. This project aims to alleviate the symptoms of mental fatigue and stress related disorders such as burn out in students by offering a nature-based activity.
Participants are asked to take a thirty-minute walk in a nature-based area for five consecutive days, followed by a control period (regular schedule of the participant) for five days, or vice versa. The investigators test stress-related parameters including concentration tests, cognitive tests, cortisol levels, and cardiovascular measurements.
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: +3211268289
- Email: michelle.plusquin@uhasselt.be
Study Contact Backup
- Name: Tim Nawrot
- Phone Number: +3211268382
- Email: tim.nawrot@uhasselt.be
Study Locations
-
-
Limburg
-
Hasselt, Limburg, Belgium, 3590
- Recruiting
- Hasselt University
-
Contact:
- Kenneth Vanbrabant
- Phone Number: +32493714758
- Email: Kenneth.vanbrabant@uhasselt.be
-
Contact:
- Rossella Alfano
- Phone Number: +3211268529
- Email: rossella.alfano@uhasselt.be
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Student of Hasselt university or university college PXL and dutch speaking
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1: intervention/control group
Phase 1: Two weeks of green space intervention Phase 2: One week wash out period Resume daily activities Phase 3: Two weeks of 'daily activities' Regular, daily activities are resumed by the participants Phase 4: One week wash out period Resume daily activities Between each phase, detailed questionnaires, neurocognitive tests and cardiovascular measurements are taken from the participants. |
participation in nature activities: daily 30 min walking in nature
|
|
Experimental: Group 2: control/intervention group
Phase 1: Two weeks of 'daily activities' Regular, daily activities are resumed by the participants Phase 2: One week wash out period Resume daily activities Phase 3: Two weeks of green space intervention Phase 4: One week wash out period Resume daily activities Between each phase, detailed questionnaires, neurocognitive tests and cardiovascular measurements are taken from the participants. |
participation in nature activities: daily 30 min walking in nature
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
General health
Time Frame: 5 minutes
|
An questionnaire is used to collect sociodemographic data and life-style factors, including movement data and health of the participant
|
5 minutes
|
|
Stress levels
Time Frame: 10 minutes
|
Assessed via questionnaires (the burn out assessment tool (score 1-5) and general health questionnaire (score 0-12) and Five Item Well Being Index (score 0-100).
Scores are used as continuous variables.
Lower scores represent a lower risk of burn out, higher scores represent a higher risk of burnout.
The score is constructed from questions concerning exhaustion, mental distance, emotional disorder(s), and cognitive disorder(s).
|
10 minutes
|
|
cortisol level (stress levels)
Time Frame: 5 minutes
|
Assessed by salivary cortisol levels.
Scale is µg/dl and used as a continuous variable.
|
5 minutes
|
|
visual memory
Time Frame: 5 minutes
|
Computerized tests (eye-tracking test).
The scale is pupil size, spontaneous blinking rate and eye movements and is used as a continuous variable.
|
5 minutes
|
|
selective attention
Time Frame: 5 minutes
|
Computerized tests (stroop test).
The scale is mean reaction time and is used as a continuous variable.
|
5 minutes
|
|
short-term memory
Time Frame: 10minutes
|
Computerized tests (Digit Span Test).
The scale is number of digits and is used as a continuous variable.
|
10minutes
|
|
visual information processing speed
Time Frame: 5 minutes
|
Computerized tests (Digit Symbol Test).
The scale is number of digits and is used as a continuous variable.
|
5 minutes
|
|
visual information processing speed
Time Frame: 5 minutes
|
Computerized tests (Pattern Comparison test).
The scale is reaction time and is used as a continuous variable.
|
5 minutes
|
|
Heart rate variability
Time Frame: 30 minutes
|
The heart rate is monitored throughout the entire baseline and follow-up visit through a small patch attached to the participant's skin.
The results is used as a continuous variable in milliseconds (ms).
|
30 minutes
|
|
Blood pressure
Time Frame: 5 minutes
|
Blood pressure is measured through an automated system.
The results is used as a continuous variable in mmHg.
|
5 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Michelle Plusquin, Hasselt University
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
Keywords
Other Study ID Numbers
- Nature_Stress
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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