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Social BehaviourNCT07720947

Smartphone-based Nature Noticing Intervention

A study testing Nature-noticing intervention in people with Social Behaviour, run by The Chinese University of Hong Kong, Shenzhen at 1 site in Hong Kong.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 15 to 17 yearsHealthy volunteers can take part
Conditions the study is for
Social Behaviour
What is being tested?
Nature-noticing intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
127 participants
Where
1 siteHong Kong
Study dates
10 Jan 2025to 20 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 17 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Hong Kong secondary school students
  • 15-17 years

Who cannot join

  • Students receiving intensive psychiatric treatment

Trial locations and contacts

1 site in 1 country.

Hong Kong1 site
  • The Hong Kong Polytechnic University

    Hong Kong

Other trials in Hong Kong

About this study

Official title: 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.

Read the 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.

Being tested
Nature-noticing intervention
Keywords
prosocial behaviour, social connectedness, adolescent
Medical subject headings
Social Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nature-noticing interventionBehavioural

    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.

Study groups in NCT07720947
Study groupRoleWhat they receive
No-treatment control groupNo interventionGroup who was not assigned any tasks
A 10-week nature-noticing interventionExperimentalGroup who asked to take pictures of nearby nature and share their thoughts on the group chat twice a week for 10 weeks
Receives: Behavioral: Nature-noticing intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prosocial behaviour

    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.

    Measured: Baseline and 10 weeks

Secondary outcomes (4)
  1. Social Connectedness

    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.

    Measured: Baseline and 10 weeks

  2. Empathy

    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.

    Measured: Baseline and 10 weeks

  3. Loneliness

    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.

    Measured: Baseline and 10 weeks

  4. Self-esteem

    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).

    Measured: Baseline and 10 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jul 2026
  2. Study start10 Jan 2025
  3. Primary completion20 Jun 2025
  4. Study completion20 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
127 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07720947
Sponsor's protocol ID
CUHKShenzhen_3
Status last verified
Jul 2026
First submitted
14 Jul 2026
Last updated
22 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Nature-noticing intervention in people with Social Behaviour, run by The Chinese University of Hong Kong, Shenzhen at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prosocial behaviour (time frame: Baseline and 10 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jul 2026; AzTrials last refreshed its copy on 27 Oct 2026.

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