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A Study on the Intervention Effect of Therapeutic Horticulture Based on the Healing System on Non-suicidal Self-injury in Adolescent Patients With Depression

NCT07115381 · tracked via the Priya Life Science China tracker
Sponsor
Lei Huang
Phase
Not applicable
Started
2026-02
Last updated
2025-12-30

Condition(s) studied

Depression

Investigational drug(s) / intervention(s)

Therapeutic HorticultureRoutine treatment and nursing

Therapeutic Horticulture: Therapeutic Horticulture uses plant cultivation and related gardening activities as the medium of action, allowing patients to participate in gardening activities such as planting, maintenance, and harvesting of plants.

Routine treatment and nursing: The conventional treatment mainly involves the use of antidepressant drugs, supplemented by physical therapy, psychological therapy, and rehabilitation training, etc. The routine care includes admission introduction, health education (manifestations, hazards, treatment methods of depression and non-suicidal self-harm, as well as the importance of following medical advice for treatment), medication guidance, discharge guidance, and psychological care, etc.

Study summary

Non-suicidal self-harm is a serious issue. Adolescents with depression are among the high-risk groups for non-suicidal self-harm behavior. Therapeutic gardening uses plant cultivation and corresponding gardening activities as the medium of action, allowing patients to obtain therapeutic benefits by participating in gardening activities such as planting, maintaining, and harvesting plants. Therefore, this study will apply therapeutic gardening based on the healing system to adolescents with depression who have non-suicidal self-harm behavior, in order to improve their non-suicidal self-harm behavior, negative emotions, emotional expression disorders, self-efficacy, sleep quality, and loneliness.

Eligibility

Sex
ALL
Min age
12 Years
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * It meets the diagnostic criteria for moderate to severe depression in the Fifth Edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5). * It meets the diagnostic criteria for non-suicidal self-harm in the Fifth Edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5). * The patients and their guardians gave informed consent and voluntarily participated in this study. * Have normal reading comprehension ability, language communication ability and writing ability. Exclusion Criteria: * Include mental disorders such as mental retardation, autism spectrum disorder, stereotyped movement disorder with self-harm, etc. * Have had or currently have central nervous system diseases, endocrine system diseases, and other serious physical disorders. * Are currently receiving or have received any form of systematic horticultural therapy within the past 3 months. * Have allergic reactions to pollen, soil, or other substances that may be encountered during the intervention process. * Have a risk of suicide and suicidal behavior.

Primary outcome measure(s)

  • The level and frequency of non-suicidal self-injury — Day 1 and Day 14
    The adolescent self-harm questionnaire was used to measure.This questionnaire is a self-assessment form, consisting of 19 items. Among them, the frequency of non-suicidal self-injury behavior is scored using the Likert 4-point scale: "0 times" is scored 0 points, "1 time" is scored 1 point, "2-4 times" is scored 2 points, and "5 times or more" is scored 3 points. The degree of physical harm caused is scored using the Likert 5-point scale: "No" is scored 0 points, "Mild" is scored 1 point, "Moderate" is scored 2 points, "Severe" is scored 3 points, and "Extremely severe" is scored 4 points. NSSI equivalence is equal to the product of the NSSI frequency score and the NSSI severity score. The higher the score, the more severe the condition.

Trial sites (1)

FacilityCityRegionStatus
The Affiliated Brain Hospital, Guangzhou Medical University Guangzhou China
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07115381 on ClinicalTrials.gov ↗ ← All trials in China