- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05276245
Nature-based Intervention to Enhance Well-being
March 2, 2022 updated by: Hou Wai Kai, Education University of Hong Kong
Testing a New Protocol of Nature-based Intervention to Enhance Well-being: A Randomized Control Trial
The aim of the present study is to investigate the effectiveness of a nature-based intervention on adaptive psychological functioning.
We compared a structured protocol with a high level of nature engagement and involvement of multiple sensory processes with a waitlist control group.
We expected that participants in the structured protocol of nature contact will report higher levels of mental health and more positive work-related functioning immediately and three months after the interventions.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This study aims to test the associations of nature contact with multiple dimensions of psychological functioning.
A total of 90 university employees were randomly assigned to spend their lunch breaks on a (1) 30-minute structured protocol of nature contact and a (2) control group for 10 consecutive weekdays.
Psychological distress, psychological well-being, and work-related psychological outcomes were assessed at baseline (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
Study Type
Interventional
Enrollment (Actual)
90
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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-
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Hong Kong, China
- The Education University of Hong Kong
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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 and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18 years or older
- Cantonese speaking
- Full-time employment of The Education University of Hong Kong
Exclusion Criteria:
- NA
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: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Program Group
This structured protocol was a 10-day nature-based program with high level of nature engagement and involvement of multiple sensory processes.
The program was held in lunch breaks between 12:00 noon and 2:00 p.m.
Each session consisted of 30 minutes in the Eco Garden of The Education University of Hong Kong.
Activities of this program included walking, ecological photography, sketching butterflies, planting vegetables, drinking herbal tea, observing birds, and taking a nap in nature.
Each activity corresponded to specific sensory pathways.
For example, butterfly sketching is focused on the use of visual sense, whereas drinking herbal tea involved sense of taste, smell, and touch.
Trainers with master's degrees in environmental education and rich experience in guiding ecological tours provided instructions and guidance to participants during the activities.
Participants were also asked to pay attention to their surroundings and focus on their five senses during participation.
|
This structured protocol was a 10-day nature-based program with high level of nature engagement and involvement of multiple sensory processes.
The program was held in lunch breaks between 12:00 noon and 2:00 p.m.
Each session consisted of 30 minutes in the Eco Garden of The Education University of Hong Kong.
Activities of this program included walking, ecological photography, sketching butterflies, planting vegetables, drinking herbal tea, observing birds, and taking a nap in nature.
Each activity corresponded to specific sensory pathways.
For example, butterfly sketching is focused on the use of visual sense, whereas drinking herbal tea involved sense of taste, smell, and touch.
Trainers with master's degrees in environmental education and rich experience in guiding ecological tours provided instructions and guidance to participants during the activities.
Participants were also asked to pay attention to their surroundings and focus on their five senses during participation.
|
|
NO_INTERVENTION: Waitlist control group
Participants who were randomly assigned to the waitlist control group were instructed to spend their usual half-hour lunch break in the office for consecutive 10 weekdays.
Also, the waitlist control group was told to wait for at least three months before they took part in the structured protocol of nature contact.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline (T1) anxiety symptoms to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
The Chinese version of the 7-item Generalized Anxiety Disorder (GAD-7) was used to measure anxiety symptoms at all time points.
Participants rated each item on a 4-point scale ranging from 0 (not at all) to 3 (nearly every day) based on their experience in the past two weeks.
Higher scores indicated greater severity of anxiety symptoms (range = 0-21).
|
Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
|
Change from baseline (T1) depressive symptoms to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
Depressive symptoms were measured using the Chinese version of the Patient Health Questionnaire-9 (PHQ-9) at T1, T2, and T3, respectively.
Participants rated each item on a 4-point scale as in GAD-7.
Higher scores indicate the greatest severity of the depressive symptoms (range 0-27).
|
Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
|
Change from baseline (T1) perceived stress to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
Perceived stress was assessed at all time points using the Chinese version of the 10-item Perceived Stress Scale (PSS-10).
Participants reported their subjective stress in the past two weeks on a 5-point scale (0 = never, 4 = very often).
Total scores ranged from 0 to 40, with higher scores indicating higher levels of perceived stress.
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Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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Change from baseline (T1) subjective well-being to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
The WHO-Five Well-being Index (WHO-5) consisted of five positively worded items.
Participants were asked to report the presence of the five positive mental states in the past 2 weeks on a 6-point scale ranging from 0 (at no time) to 5 (all of the time).
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Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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Change from baseline (T1) satisfaction with life to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
Satisfaction with Life Scale (SWLS) was used to assess participants' well-being with regard to satisfaction and fulfillment of their current state on a 4-point scale (1 = strongly disagree, 4 = strongly agree).
The five items were summed, with higher scores indicating higher life satisfaction (range = 5-20).
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Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
|
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Change from baseline (T1) positive affect to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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The 10-item positive affect subscale of Chinese Affect Scale (CAS-PA) assessed frequency of positive emotional experience in the past 2 weeks on a 5-point scale (0 = not at all, 4 = all the time).
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Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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Change from baseline (T1) burnout to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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Burnout was measured using the Chinese version of the 14-item Maslach Burnout Inventory-General Survey (MBI-GS) at all time points.
Participants rated how often they had different experiences of burnout in the past two weeks on a 7-point scale (0 = never, 6 = always).
The scale consisted of five questions on emotional exhaustion, four on cynicism, and five on professional efficacy.
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Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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Change from baseline (T1) work engagement to post intervention (T2) and follow up (T3)
Time Frame: Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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The Chinese version of the 17-item Utrecht Work Engagement Scale (UWES) was used to assess vigor, dedication, and absorption at work at all time points.
Participants indicated the frequency of these experiences at work in the past two weeks on a 7-point scale (0 = never, 6 = always).
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Before the intervention (T1), the day after the 10-day intervention (T2), and three months after the intervention (T3).
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Wai Kai Hou, PhD, The Education University of Hong Kong
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)
December 9, 2019
Primary Completion (ACTUAL)
June 30, 2021
Study Completion (ACTUAL)
June 30, 2021
Study Registration Dates
First Submitted
February 22, 2022
First Submitted That Met QC Criteria
March 2, 2022
First Posted (ACTUAL)
March 11, 2022
Study Record Updates
Last Update Posted (ACTUAL)
March 11, 2022
Last Update Submitted That Met QC Criteria
March 2, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 04465
- 2019-2020-0191 (OTHER: Human Research Ethics Committee)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data (IPD) will be available on request.
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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