- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07720947
Smartphone-based Nature Noticing Intervention
July 19, 2026 updated by: EUN YEONG CHOE, The Chinese University of Hong Kong, Shenzhen
Smartphone-based Nature Noticing Intervention for Cultivating Social Connectedness
We used a mixed-methods approach involving a RCT study followed by focus group discussions to obtain a more integrative understanding of the effects of a 10-week nature-noticing intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Initially, 127 students were recruited from a Hong Kong secondary school.
Half of the students (n = 63) were randomly assigned to a 10-week intervention by the school teacher; the students' preferences did not affect the assignments.
They were asked to take pictures of nearby nature and share the photos, along with their reflections on what they noticed, in the group chat twice a week for 10 weeks.
The other half of the students (n = 64) were not assigned any tasks and served as the control group.
Two participants who did not complete the baseline questionnaire were excluded.
This resulted in 125 (98.4%) participants who were included in the analysis.
Power analysis indicated that the minimum sample size of 54 participants was required for this study, with an alpha level of 0.05, a power of 0.95, and a small-to-medium effect of f(v) = 0.25.
The students who more proactively engaged in the 10-week nature photo-taking and sharing were invited to the focus group discussion after the intervention.
These participants shared their emotions and thoughts in detail, along with a wider variety of photographic topics, indicating more in-depth observations of their nearby nature.
A total of nine participants took part in the discussion.
Study Type
Interventional
Enrollment (Actual)
127
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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Hong Kong, Hong Kong
- The Hong Kong Polytechnic University
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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
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion criteria:
- Hong Kong secondary school students
- 15-17 years
Exclusion criteria:
- Students receiving intensive psychiatric treatment
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: No-treatment control group
Group who was not assigned any tasks
|
|
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Experimental: A 10-week nature-noticing intervention
Group who asked to take pictures of nearby nature and share their thoughts on the group chat twice a week for 10 weeks
|
Participants were asked to notice nearby nature (i.e.
'anywhere with some nature'), to take a photo when they noticed a specific object or scene in nature evoked a strong emotion in them, and to write down thoughts and emotions twice a week for 10 weeks.
Participants were further instructed that and upload it to the group chat along with a brief description of the emotions that were evoked.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prosocial behaviour
Time Frame: Baseline and 10 weeks
|
Participants' prosocial behaviour was measured using a subscale of the Strengths and Difficulties Questionnaire (SDQ).
In the SDQ, prosocial behaviour is associated with individuals' ability to relate well with their peers and engage in actions that benefit those around them.
Five items are measured on a 3-point Likert scale, ranging from 1 (not true) to 3 (certainly true).
Higher scores indicate greater degrees of prosocial behaviour.
|
Baseline and 10 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Connectedness
Time Frame: Baseline and 10 weeks
|
Social Connectedness Scale - Revised (SCS-R) measures the degree to which youth feel connected to others in their social environment.
The SCS-R contains 20 items (10 positive and 10 negative) measured on a 6-point Likert scale, ranging from 1 (strongly disagree) to 6 (strongly agree).
The negatively worded items are reverse-scored, summed with the positive items and divided by 20 to obtain a total score.
Higher scores indicated a greater sense of belonging, closeness and support.
|
Baseline and 10 weeks
|
|
Empathy
Time Frame: Baseline and 10 weeks
|
Interpersonal Reactivity Index (B-IRI) measures the degree to which individuals can empathise with others.
Among the four sub-scales, empathic concern and perspective-taking were used to obtain the total IRI score [28].
The eight items were measured on a 5-point Likert scale, ranging from 1 (does not describe me well) to 5 (describes me very well).
Higher scores indicate a greater sense of empathy.
|
Baseline and 10 weeks
|
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Loneliness
Time Frame: Baseline and 10 weeks
|
The UCLA Loneliness Scale (ULS-8) measures the severity of respondents' feelings of loneliness.
The scale contains eight items measured on a 4-point Likert scale, ranging from 1 (never) to 4 (often).
Higher scores indicate a greater sense of loneliness.
|
Baseline and 10 weeks
|
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Self-esteem
Time Frame: Baseline and 10 weeks
|
The Rosenberg Self-Esteem Scale (RSES) measures respondents' self-esteem.
The RSES contains 10 items, which are measured on a 4-point Likert scale, ranging from 1 (strongly disagree) to 4 (strongly agree).
|
Baseline and 10 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Eun Yeong Choe, PhD, The Chinese University of Hong Kong, Shenzhen
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)
January 10, 2025
Primary Completion (Actual)
June 20, 2025
Study Completion (Actual)
December 20, 2025
Study Registration Dates
First Submitted
July 14, 2026
First Submitted That Met QC Criteria
July 19, 2026
First Posted (Actual)
July 22, 2026
Study Record Updates
Last Update Posted (Actual)
July 22, 2026
Last Update Submitted That Met QC Criteria
July 19, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CUHKShenzhen_3
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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