- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05502588
Effects of Forest Bathing in Vancouver, B.C. Parks
Effects of Forest Bathing and Environmental Factors on Individual Health Responses in Vancouver, B.C. Parks
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The primary research aim is to investigate the relationship between biotic and abiotic factors in a sample of Vancouver, B.C. forested parks and specific health-related outcomes after forest bathing interventions. Forest bathing programs are a promising therapeutic method for enhancing heart rate and blood pressure functions and an effective psychological relaxation strategy. This study will investigate changes in autonomic nervous system activity and mood states after a 60-90 minute forest bathing program in four Vancouver, B.C. parks. Approximately 100 adult participants will be recruited for the study and participate in four sessions over one year. Physiological responses, pulse rate, systolic and diastolic blood pressure, and psychological indices will be measured before and after each session.
The health effects of forest-based interventions will vary due to environmental factors such as weather, temperature, humidity, light, and participants' psychological and physiological states. We are taking measurements pre- and post-treatment to detect any change in response during each session and seasonally.
Primary endpoint is to determine if the guided walk provides greater enhanced heart rate and blood pressure functions and an effective psychological relaxation strategy over the self-guided walk.
Secondary endpoints: 1) to determine if participants living in neighborhoods with below average street trees receive greater benefits than participants that live in neighborhoods with average or above average street trees, 2) assess changes within the same individuals over time 3) if there are different outcomes seasonally 4) if there are different outcomes between study sites.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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B.C.
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Maple Ridge, B.C., Canada
- Malcolm Knapp Research Forest
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Vancouver, B.C., Canada
- Jericho Beach Park
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Vancouver, B.C., Canada
- Pacific Spirit Regional Park
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Vancouver, B.C., Canada
- Stanley Park
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adults (19+) that are residents of Vancouver, B.C.
- Spend time on a trail in a Vancouver park for at least 60 minutes per month
- Willing to refrain from tobacco products, alcohol, caffeine, marijuana, and psilocybin for at least two hours prior to arriving at the study site and during the forest bathing sessions
Exclusion Criteria:
- Must be able to move along a barrier-free trail independently
- Non-residents (e.g. tourists)
- Children (under 19 years of age)
- Participants with pets
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Self-Guided Forest Bathing
Forest Bathing intervention without a guide and basic navigational instructions, explanation of forest bathing, and time to return.
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Participants will participate in two, 60-90 minute self-guided forest bathing sessions over the course of a year in one of four Vancouver, B.C. park trails and be given prompts to consciously use their five senses in the forest.
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Experimental: Guided Forest Bathing
Forest Bathing intervention led by a certified Forest Therapy guide.
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Participants will participate in two, 60-90 minute guided forest bathing sessions over the course of a year in one of four Vancouver, B.C. park trails.
They will be invited by a certified forest therapy guide to consciously use their five senses in the forest.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Abbreviated Profile of Mood States (POMS) - Change
Time Frame: Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
|
Abbreviated Profile of Mood States (POMS) are routinely used by forest bathing researchers because psychologists regard it as rendering an accurate measure of mood states.
The goal is to determine if spending time in a forest environment affects a psychological response.
Abbreviated POMS contains 40 questions.
Each answer is scored on a Likert Scale with values of 0, 1, 2, 3, and 4. Lower total scores indicated low mood problems, and conversely, a higher score may indicate a high mood problem.
POMS will determine a baseline level of specific moods for a participant at the onset of the research trial and at the beginning and end of each forest bathing session.
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Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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Cardiovascular reactivity - Heart Rate - Change
Time Frame: Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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Cardiovascular reactivity will be measured by participants taking heart rate before and after each forest bathing session.. Three measurements will be taken at 30-second intervals.
The mean of the final two measurements taken for each interval will be used for statistical analysis.
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Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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Cardiovascular reactivity - Blood Pressure (Diastolic) - Change
Time Frame: Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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Cardiovascular reactivity will be measured by participants taking diastolic blood pressure before and after each forest bathing session.. Three measurements will be taken at 30-second intervals.
The mean of the final two measurements taken for each interval will be used for statistical analysis.
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Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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|
Cardiovascular reactivity - Blood Pressure (Systolic) - Change
Time Frame: Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
|
Cardiovascular reactivity will be measured by participants taking systolic blood pressure before and after each forest bathing session.
Three measurements will be taken at 30-second intervals.
The mean of the final two measurements taken for each interval will be used for statistical analysis.
|
Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Connectedness to Nature Scale (CNS) - Change
Time Frame: Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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Connectedness to Nature Scale (CNS) is a scale designed to measure an individual's affective, experiential connection to nature.
It was created based on the argument that for people to participate in environmental issues they need to feel part of the natural world.
Another argument is that aspects of our urban or modern lifestyle relate to our nature connectedness and overall life satisfaction.
The scale contains 13 items.
It is a simple scale question with some reverse coded items Participants responded on a 5-point scale, where 1=strongly disagree and 5=strongly agree.
CNS will determine a baseline level of nature relatedness and subjective well-being at the onset of the research trial and at the beginning and end of each forest bathing session.
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Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
|
|
Satisfaction With Life Scale (SWLS) - Change
Time Frame: Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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The Satisfaction With Life Scale (SWLS) is a short 5-item instrument designed to measure global cognitive judgments of satisfaction with one's life.
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Participants are tested before and after each forest bathing session and invited to attend four sessions during the study. Assessments for each session are included until the study ends. Forest bathing sessions will be held in 2022.
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- H22-00216
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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