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临床试验/NCT04139421
NCT04139421Unknown不适用

Effects of Shinrin-Yoku (Forest Bathing) on Psychological Well-being in Urban or Rural Green Space: A Pilot Randomized Controlled Trial

Chinese University of Hong Kong2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2019年11月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
30
试验地点
2
主要终点
Change in the Profile of Mood States-Short Form

研究概览

简要总结

This study will examine the effects of Shinrin-Yoku (forest bathing) as an intervention for enhancing psychological well-being in Chinese population. The main component of Shinrin-Yoku is the use of 5 senses in various activities, which typically includes forest walking, meditation, yoga etc. While Shinrin-Yoku has been widely recognized in Japan as a means of preventative health and stress management, it is still a new concept in some countries. In the existing literature, there is increasing evidence demonstrating the efficacy of Shinrin-Yoku for improving for health promotion. However, there is very limited research examining the effectiveness of Shinrin-Yoku in different types of natural environment and the sustainability of its effects.

详细描述

This study will be a pilot randomized controlled trial on the effects of Shinrin-Yoku (forest bathing) as an intervention for enhancing psychological well-being in Chinese population. Prior to all study procedures, an online informed consent (with phone support) will be obtained from potential participants. Around 30 eligible participants will be randomly assigned to either the natural forest group or the urban green area group in a ratio of 1:1.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

盲法说明

Deception will be necessary prior to and during the study to achieve blinding of participants for the prevention of expectation bias.

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hong Kong residents
  • Aged from 18 to 65
  • Cantonese language fluency
  • a willingness to provide informed consent and comply with the trial protocol.

排除标准

  • Have suicidal ideation
  • Using medication or psychotherapy for depression
  • Experiencing Depression, Anxiety and Stress
  • Having unsafe conditions and are not recommended for physical activity by physicians
  • Have major psychiatric, medical or neurocognitive disorders that make participation infeasible based on the research team's judgment.

结局指标

主要结局

Change in the Profile of Mood States-Short Form

时间窗: Pre-, post-intervention and 1-month post-intervention

The POMS-SF is a 30-item scale that measures six different dimensions of mood swings over a period of time. These include: Tension or Anxiety, Anger or Hostility, Vigor or Activity, Fatigue or Inertia, Depression or Dejection, Confusion or Bewilderment. A five-point scale ranging from "not at all" to "extremely" is administered by experimenters to patients to assess their mood states.

次要结局

  • Change in Insomnia Severity Index(Up to 1 month after the intervention)
  • Change in Brief Resilience Scale(Up to 1 month after the intervention)
  • Change in Depression Anxiety Stress Scales-21(Up to 1 month after the intervention)
  • Change in Nature-relatedness Scale-6(Up to 1 month after the intervention)
  • Change in Subjective Vitality Scales - State Version(Up to 1 month after the intervention)
  • Change in Self-Compassion Scale-Short Form(Up to 1 month after the intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Fiona YY Ho

Assistant Professor

Chinese University of Hong Kong

研究点 (2)

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