Psychophysiological Effects of Green Exercise in Outdoor Green vs. Indoor Control
GREEN-OI
Psychophysiological Restorative Effects of Green Exercise: A Randomized Controlled Trial
1 other identifier
interventional
80
1 country
1
Brief Summary
Core Purpose: Researchers want to learn if walking in an outdoor green environment helps people recover from mental tiredness and stress better than walking indoors. This study investigates how a 30-minute walk in an outdoor green setting affects the mind and body compared to a 30-minute walk on a treadmill in a room without windows. The Study Process: The study included 80 healthy young adults between the ages of 18 and 35. Researchers randomly split the participants into two groups.
- 1.The Outdoor Green group: Participants walked for 30 minutes on a path in an outdoor green environment.
- 2.The Indoor Control group: This group walked for 30 minutes on a treadmill in a windowless room.
- 3.Information Harvesting: Researchers used a new tool called the Nature Sensory Sensitivity Index (NSSI). This measures how well participants notice and "capture" sensory details from their surroundings, like the sounds of birds or the textures of plants.
- 4.Restorative Feelings: Using the Perceived Restorativeness Scale (PRS), participants reported if they felt the environment helped them "get away" from daily stress and if the setting was interesting or beautiful.
- 5.Overall Mood Changes (POMS TMD): Researchers used the Profile of Mood States (POMS) to calculate a Total Mood Disturbance (TMD) score. This helps show if participants feel less tense, angry, or tired, and more energetic after the walk.
- 6.Connection to Nature (NR): Researchers measured each participant's Nature Relatedness (NR). This describes how much a person naturally feels connected to the natural world, which may influence how much they benefit from the green walk.
- 7.Attention and Thinking: Participants performed a "Digit Span Task" (repeating sequences of numbers) to test if their focus improved.
- 8.Physical Stress: The study used objective markers, including salivary cortisol (a stress hormone) and heart rate variability (a measure of how the nervous system relaxes).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 15, 2025
CompletedFirst Submitted
Initial submission to the registry
January 23, 2026
CompletedFirst Posted
Study publicly available on registry
January 30, 2026
CompletedJanuary 30, 2026
January 1, 2026
2 months
January 23, 2026
January 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Profile of Mood States - Total Mood Disturbance (ΔTMD)
The POMS TMD is a self-report scale consisting of 6 subscales: Tension, Depression, Anger, Fatigue, Confusion, and Vigor. Each item is rated on a 5-point scale (0 = Not at all to 4 = Extremely). The TMD score is calculated as: (Tension + Depression + Anger + Fatigue + Confusion) - Vigor. The final outcome (ΔTMD) is the difference between the post-intervention TMD score and the pre-intervention (baseline) TMD score \[ΔTMD = TMD (Post) - TMD (Pre)\]. TMD scores range from -120 to 120. A larger negative ΔTMD value indicates a greater reduction in negative emotions and more significant psychological restoration.
From Baseline (Pre-test) to 30 minutes post-intervention (Post-test)
Secondary Outcomes (5)
Nature Relatedness (NR)
Baseline (T0, before intervention)
Nature Sensory Sensitivity Index (NSSI)
Immediately after the 10-minute intervention (T1)
Change in Perceived Restorativeness Scale (ΔPRS)
From Baseline (T0) to Immediately after the 10-minute intervention (T1)
Change in Total Digit Span Score (ΔDigit Span)
From Baseline (T0) to immediately after the 30-minute intervention (T2)
Change in Self-Esteem (ΔSelf-Esteem)
From Baseline (T0) to immediately after the 30-minute intervention (T2)
Other Outcomes (2)
Change in Heart Rate (ΔHR)
From Baseline (T0) to immediately after the 30-minute intervention (T2)
Change in Salivary Cortisol (ΔCortisol)
From Baseline (T0) to immediately after the 30-minute intervention (T2)
Study Arms (2)
Outdoor Green Group
EXPERIMENTALParticipants in this arm perform a standardized 30-minute walk at a moderate pace along a pre-defined route in an outdoor green enviroment. This arm focuses on the effects of exposure to natural environmental stimuli.
Indoor Control Group
ACTIVE COMPARATORParticipants walk on a treadmill at a fixed moderate speed (4.0-5.5 km/h) with a 1% incline. This specific incline is used to compensate for the lack of air resistance indoors and to more accurately match the physiological energy expenditure of outdoor ground walking.
Interventions
Participants perform a supervised 30-minute walk at a moderate pace (4.0-5.5 km/h) along a pre-defined 2.5 km loop trail within a suburban forest park. The environment is characterized by high canopy cover (\>60%) and diverse natural vegetation. To ensure consistency, all sessions are conducted under stable weather conditions (Temperature: 20-26°C; Humidity: 40-60%). Participants walk individually to prevent social interaction, ensuring the restorative experience is derived solely from the individual-nature interaction.
Participants perform a 30-minute walk on a treadmill in a windowless indoor laboratory. To ensure consistency with the outdoor environment, the laboratory is climate-controlled with a temperature range of 20-26°C and humidity of 40-60%. The treadmill is set to a fixed moderate speed (4.0-5.5 km/h) with a 1% incline. The 1% incline is specifically applied to compensate for the lack of air resistance indoors and to accurately match the physiological energy expenditure and biomechanical demands of outdoor ground walking. The laboratory walls are neutral-colored to eliminate visual nature stimuli.
Eligibility Criteria
You may qualify if:
- Healthy adults aged 18 to 30 years.
- University students or individuals with equivalent educational background.
- Normal or corrected-to-normal vision and hearing.
- Willingness to comply with all study procedures and sign the informed consent form.
You may not qualify if:
- Physical Health: History of cardiovascular disease, respiratory illness, or chronic pain that may affect Heart Rate Variability (HRV).
- Mental Health: Diagnosis of clinical depression, anxiety disorders, or other psychiatric conditions.
- Substance Use: Current smokers or individuals with a history of alcohol or drug abuse.
- Medication: Recent use of any medications that affect the autonomic nervous system or endocrine function (e.g., steroids, beta-blockers, or hormonal medications) within the past month.
- Cognitive/Physical Impairment: Any disability that prevents walking for 30 minutes or completing the Digit Span cognitive task.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Lincoln University Collegelead
- Wuhan Technical Universitycollaborator
Study Sites (1)
Wuhan Technical University
Wuhan, Hubei, 430074, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Sheng Yan
Wuhan Technical University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Doctoral Researcher
Study Record Dates
First Submitted
January 23, 2026
First Posted
January 30, 2026
Study Start
March 1, 2025
Primary Completion
May 1, 2025
Study Completion
December 15, 2025
Last Updated
January 30, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share
There is no plan to share individual participant data to protect the privacy of the participants and ensure data security.