- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04914572
Therapeutic Rainforest Study in Generating Positive Energy Among Undergraduate Students
July 28, 2023 updated by: Goh Yong-Shian, National University of Singapore
Using Therapeutic Rainforest Mindful Walking in Generating Positive Mental Well-being Among Undergraduate Students
This study looked into how therapeutic forest walking will impact the well-being of undergraduate students at the National University of Singapore.
A three-arm randomized control trial on 108 participants is being planned for this study.
The primary aim of this study is to assess the feasibility and primary effect of the Therapeutic Rainforest Walking in generating positive energy among undergraduate students project in enhancing the quality of life, physical, mental, and psycho-social well-being among University students.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
81
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 Locations
-
-
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Singapore, Singapore
- Alice Lee Centre for Nursing Studies
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-
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
18 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Current NUS undergraduate students
- No self-reported physical mobility issue
- No self-reported existing mental health conditions
- Enjoys nature
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: Other
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Therapeutic rainforest & MIndful walking
The first arm uses mindful walking through a 2km forest trail in Singapore.
All Interventional and Control arms will conduct their walk between 8 am to 11 am for five occasions weekly.
At the T1, participants will attend a Zoom orientation session to familiarize themselves with the route.
During this session, participants will need to answer the self-report questionnaire and provide the first saliva sample for the baseline measurement.
In T2, a pre-intervention and post-intervention saliva sample will be taken before the walk.
This will follow by T3 the following week.
At T4, participants will attend a 60 mins reflection session and answer the self-report questionnaire.
On T5 and T6, the participants will continue with the therapeutic rainforest mindfulness walk.
On T7, a pre-intervention and post-intervention saliva sample will be taken.
On T8, participants will attend a 60 mins reflection session and answer the self-report questionnaire.
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A two-kilometer trail curated by the National Parks Board, Singapore.
The walk will be led by Mindfulness Practitioner who volunteered to be guides for this study.
|
Experimental: Therapeutic rainforest walk
The second arm of the intervention includes walking through a guided forest trail suggested by NParks Board.
The collection of samples and answering of the self-report questionnaire will follow the same sequence as the 1st arm of the 3-arm RCT.
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A two-kilometer trail curated by the National Parks Board, Singapore.
The walk will be led by volunteer guides recruited by the research team.
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Active Comparator: Campus green walk
The control for this study includes guided casual walking around the campus green trial conducted at the same intervals as per the interventions.
The collection of samples and answering of the self-report questionnaire will also follow the same sequence as the 1 arm of the 3-arm RCT.
|
A two-kilometer trail curated by the Office of Facility Management, NUS.
The walk will be led by volunteer guides recruited by the research team.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Perceived Stress Scale 4 (PSS-4)
Time Frame: 8 weeks
|
4 items, Likert scale (0-lowest, 4-highest) Scoring higher in the scale would translate to higher perceived stress.
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8 weeks
|
Generalised Anxiety Disorder Scale (GAD-7)
Time Frame: 8 weeks
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7 items, Likert scale (0-lowest, 3-highest) Scoring higher in the scale would translate to higher anxiety level.
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8 weeks
|
English Brief Resilience Scale (BRS)
Time Frame: 8 weeks
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6 items, Likert scale (1-lowest, 5-highest) Scoring higher in the scale would translate to higher resilience.
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8 weeks
|
Saliva Cortisol
Time Frame: 8 weeks
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Measured using Passive drool method
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8 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yong Shian Goh, PhD, National University of Singapore
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)
August 31, 2021
Primary Completion (Actual)
March 31, 2023
Study Completion (Actual)
March 31, 2023
Study Registration Dates
First Submitted
June 1, 2021
First Submitted That Met QC Criteria
June 1, 2021
First Posted (Actual)
June 4, 2021
Study Record Updates
Last Update Posted (Actual)
August 1, 2023
Last Update Submitted That Met QC Criteria
July 28, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MindtheGap200
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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