CClinicalTrials.gg
Status unknownNCT05249296Updated Feb 21, 2022

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

An interventional study of Nature based solution for stress reduction in Stress, Neurocognition and Psychological, sponsored by Hasselt University. Status unknown at 1 site in Belgium. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-02-21.

Sponsored by Hasselt University · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Feb 2022), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Stress
  • Neurocognition
  • Psychological
  • Cardiovascular

Keywords

  • Green space
03

In context

Lead sponsor

Hasselt University is the lead sponsor of 195 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • 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.

    Other: Nature based solution for stress reduction

  • 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.

    Other: Nature based solution for stress reduction

Interventions

  • OtherNature based solution for stress reduction

    participation in nature activities: daily 30 min walking in nature

06

What researchers measure

Primary outcomes

  1. General health

    An questionnaire is used to collect sociodemographic data and life-style factors, including movement data and health of the participant

    Time frame: 5 minutes

  2. Stress levels

    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).

    Time frame: 10 minutes

  3. cortisol level (stress levels)

    Assessed by salivary cortisol levels. Scale is µg/dl and used as a continuous variable.

    Time frame: 5 minutes

  4. visual memory

    Computerized tests (eye-tracking test). The scale is pupil size, spontaneous blinking rate and eye movements and is used as a continuous variable.

    Time frame: 5 minutes

  5. selective attention

    Computerized tests (stroop test). The scale is mean reaction time and is used as a continuous variable.

    Time frame: 5 minutes

  6. short-term memory

    Computerized tests (Digit Span Test). The scale is number of digits and is used as a continuous variable.

    Time frame: 10minutes

  7. visual information processing speed

    Computerized tests (Digit Symbol Test). The scale is number of digits and is used as a continuous variable.

    Time frame: 5 minutes

  8. visual information processing speed

    Computerized tests (Pattern Comparison test). The scale is reaction time and is used as a continuous variable.

    Time frame: 5 minutes

  9. Heart rate variability

    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).

    Time frame: 30 minutes

  10. Blood pressure

    Blood pressure is measured through an automated system. The results is used as a continuous variable in mmHg.

    Time frame: 5 minutes

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — Data is pseudonymized. Data will then only be shared with the predoctoral researchers involved in this project, within our research group.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 21, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05249296
Lead sponsor
Hasselt University
Responsible party
Michelle Plusquin (assistant professor, Hasselt University) — Principal investigator
First posted
Feb 21, 2022
Start date
Feb 10, 2020
Primary completion
Dec 30, 2022 (estimated)
Completion
Dec 31, 2022 (estimated)
Last update
Feb 21, 2022

Study contacts

Michelle Plusquin
Contact
michelle.plusquin@uhasselt.be
+3211268289
Tim Nawrot
Contact
tim.nawrot@uhasselt.be
+3211268382
Michelle Plusquin
principal investigator · Hasselt University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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