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Active, not recruitingNCT06950801Updated Apr 30, 2025

Comparing the Effects of Indoor vs. Outdoor Horticultural Therapy on College Students

An interventional study of outdoor-horticultural therapy and indoor-Horticultural Therapy group in Healthy, sponsored by Ye Zhiyin. Active, not recruiting at 1 site in China. Per ClinicalTrials.gov, last updated 2025-04-30.

Sponsored by Ye Zhiyin · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by May 2026, 4 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Sex
All
01

Study summary

This study used a randomised controlled trial to investigate the effects of different forms of horticultural group interventions on college students' depression, anxiety and subjective well-being, and the internal mechanisms of the effects.

Participants are required to complete the following tasks:

Attend one indoor/outdoor group gardening activity per week, lasting 2 hours each session, for a total of 8 weeks.

Complete psychological scale assessments at five time points: before the activity begins, at 4 weeks after the start, upon completion of the activity, and at 1 week and 2 weeks after completion.

02

Conditions studied

  • Healthy
03

In context

Lead sponsor

Ye Zhiyin is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • University students

Exclusion criteria

Exclusion Criteria:

  • Diagnosed with a mental disorder
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    outdoor-horticultural

    The participants in outdoor horticultural therapy engaged in weekly horticultural therapy activities outdoors for a total duration of eight weeks.

    Behavioral: outdoor-horticultural therapy

  • Experimental
    indoor-Horticultural

    The participants in indoor horticultural therapy engaged in therapeutic gardening activities indoors once a week for a total duration of eight weeks.

    Behavioral: indoor-Horticultural Therapy group

  • Placebo comparator
    General Psychological Group

    Participants in the control group attended weekly psychological group sessions (without horticultural elements) for a total duration of eight weeks.

    Behavioral: General Psychological Group Counselling Team

  • No intervention
    Blank control group

    These participants did not engage in any psychological activities; they only regularly took part in questionnaire completion.

Interventions

  • Behavioraloutdoor-horticultural therapy

    Students are randomly assigned to the Outdoor Horticultural Therapy group, where they will receive outdoor horticultural therapy for eight weeks

  • Behavioralindoor-Horticultural Therapy group

    Students are randomly assigned to the indoor horticultural therapy group, where they will receive indoor horticultural therapy for 8 weeks

  • BehavioralGeneral Psychological Group Counselling Team

    Students were randomly assigned to general group groups to participate in an 8-week mental health group activity

06

What researchers measure

Primary outcomes

  1. Depression

    The Patient Health Questionnaire 9-item (PHQ-9): This scale consists of 9 items, each rated on a 4-point Likert scale, with higher scores indicating more severe depressive symptoms in the subject.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment Edit Copy Outcome

  2. Anxiety

    Generalized Anxiety Disorder 7-item Scale (GAD-7): This scale consists of 7 items, each rated on a 4-point Likert scale, with higher scores indicating more severe anxiety symptoms in the subjects.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  3. Positive And Negative Affective

    Positive and Negative Affect Schedule (PANAS): This scale consists of 20 items, including 10 positive affect items and 10 negative affect items, with each item rated on a Likert five-point scale. Higher scores on the positive affect items indicate higher levels of positive affect in the participants, while higher scores on the negative affect items indicate higher levels of negative affect in the participants.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  4. Life satisfaction

    The Satisfaction With Life Scale (SWLS): This scale consists of 5 items, each rated on a 7-point Likert scale, with higher scores indicating greater life satisfaction among participants.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

Secondary outcomes

  1. Resilience

    The Connor-Davidson Resilience Scale (CD-RISC): The scale consists of 25 items divided into three dimensions-tenacity, self-reliance, and optimism. Each item is rated on a Likert five-point scale. Higher scores indicate greater psychological resilience in the subjects.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  2. Loneliness

    UCLA Loneliness Scale: This scale consists of 8 items, each rated on a 5-point Likert scale, with higher scores indicating stronger feelings of loneliness in the subjects.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  3. Sense of control

    Sense of Mastery Scale (SMS): This scale consists of 7 items, each using a 5-point Likert scale, with higher scores indicating a stronger sense of mastery in the subjects.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  4. Avoidance

    The Brief Experiential Avoidance Questionnaire (BEAQ) was initially simplified and revised by Gámez et al. based on the Multidimensional Experiential Avoidance Questionnaire to assess content related to experiential avoidance. Cao et al. conducted a Chinese version revision in 2021. The questionnaire consists of 15 items, with the cognitive avoidance dimension containing 8 items and the behavioral avoidance dimension containing 7 items, all rated on a 6-point scale from "Strongly Disagree" to "Strongly Agree."

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  5. Self-concept

    Sense of Mastery Scale, SMS. This scale consists of 12 items, with each item rated on a five-point Likert scale. Higher scores indicate a clearer self-concept among the participants.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  6. meaning in life

    The Meaning in Life Questionnaire (MLQ): This scale consists of 10 items with two dimensions: Presence of Meaning (MLQ-P) and Search for Meaning (MLQ-S). Each item adopts a 7-point Likert scale, with higher scores indicating that participants experience a stronger sense of meaning in life.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  7. Grit

    The Grit Scale consists of 12 items with two dimensions: the Effort dimension and the Interest Consistency dimension. Each item is rated on a five-point Likert scale, with higher scores indicating that participants perceive themselves as more perseverant.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

  8. nature connection

    The Nature Connection Scale, which consists of 14 items, employs a 5-point Likert scale for each item, with higher scores indicating that participants perceive themselves as more closely connected to nature.

    Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment

07

Study locations

1 site
  • Central University of Finance and Economics, Beijing, Beijing 100875
    Beijing, Beijing, China
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06950801
Lead sponsor
Ye Zhiyin
Responsible party
Ye Zhiyin (Teaching assistant, Central University of Finance and Economics, China) — Sponsor-investigator
First posted
Apr 30, 2025
Start date
Mar 20, 2025
Primary completion
May 30, 2026 (estimated)
Completion
Jun 1, 2026 (estimated)
Last update
Apr 30, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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