Central University of Finance and Economics, Beijing, Beijing 100875
Beijing, Beijing Municipality, China
NCT Number: NCT06950801
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.
This study is active but is not currently recruiting participants.
Notify MeAll sexes
Interventional
Not applicable
Beijing, Beijing Municipality, China
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Students are randomly assigned to the Outdoor Horticultural Therapy group, where they will receive outdoor horticultural therapy for eight weeks
Students are randomly assigned to the indoor horticultural therapy group, where they will receive indoor horticultural therapy for 8 weeks
Students were randomly assigned to general group groups to participate in an 8-week mental health group activity
Time frame: From enrollment to 2 weeks after the completion of the 8-week treatment Edit Copy Outcome
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
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
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
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
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
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
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
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
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
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
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
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.
Ye Zhiyin
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06571435
Behavior, Healthy
Istanbul, Ataşehir, Turkey (Türkiye)
View Trial DetailsNCT07513207
Healthy
Biberach, Germany
View Trial DetailsNCT05180981
Healthy
Boston, Massachusetts, United States
View Trial DetailsNCT07649941
Healthy
Biberach, Germany
View Trial Details