The Impact of Green Spaces on the General Well-being and Stress of Students

February 18, 2022 updated by: Michelle Plusquin, Hasselt University

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

Detailed Description

This project aims study the effectiveness of nature-based solutions on the prevention of stress-related symptoms due to high study pressure in students. A nature-based physical activity is recommended once a day to prevent stress build-up and positively influence the cardiovascular system. Participants are randomized into two groups: the first group of participants are asked to walk a nature-based route near the University campus for thirty minutes per day for two weeks (phase 1). After each activity-based phase, a washout period of one week is implemented to avoid carry-over of results (phase 2 and 4). In the third phase, the participants are asked to resume their daily activities for two weeks (control). The second group undergo the same phases but reversed: participants start with two weeks of their usual daily activities, followed by two weeks of nature-based activity. After each phase, the investigators measure neurocognition through neurocognitive tests, the emotional status through detailed questionnaires and assess stress levels through cardiovascular measurements, including salivary cortisol levels of saliva collected upon awakening, 30 min after waking and at 8 pm.

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 Contact Backup

Study Locations

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

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Student of Hasselt university or university college PXL and dutch speaking

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: 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

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

Investigators

  • Principal Investigator: Michelle Plusquin, Hasselt University

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)

February 10, 2020

Primary Completion (Anticipated)

December 30, 2022

Study Completion (Anticipated)

December 31, 2022

Study Registration Dates

First Submitted

April 2, 2020

First Submitted That Met QC Criteria

February 18, 2022

First Posted (Actual)

February 21, 2022

Study Record Updates

Last Update Posted (Actual)

February 21, 2022

Last Update Submitted That Met QC Criteria

February 18, 2022

Last Verified

February 1, 2022

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)?

No

IPD Plan Description

Data is pseudonymized. Data will then only be shared with the predoctoral researchers involved in this project, within our research group.

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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