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Comparative Effects of Meditation, Nature Exposure, and Digital Activities on Physiological and Perceived Stress

2026年8月7日 更新者:Teresa Fazia、University of Pavia

Comparative Effects of Meditation, Nature Exposure, Digital Scrolling, and Reading on Physiological and Perceived Stress: A Non-Randomized Controlled Study

The present study aims to compare the effects of meditation, nature exposure, digital scrolling, and reading on physiological and perceived stress. Participants will undergo a baseline assessment including the Five Facet Mindfulness Questionnaire (FFMQ), a visual analogue scale (VAS) for anxiety, and salivary cortisol collection at 8:30 a.m, prior to cortisol peak. Participants will then engage in one of four activities: guided meditation, a walk in a forest environment, digital scrolling on a smartphone, or reading a neutral text. Following the activity, salivary cortisol will be collected again and anxiety will be reassessed using the VAS. The study will evaluate changes in cortisol levels, perceived stress and perceived anxiety across the four conditions and explore the potential moderating role of baseline mindfulness traits.

The central research question of this study is whether different experiential conditions elicit distinct psychophysiological responses, as reflected by changes in perceived stressm salivary cortisol and perceived anxiety and therefore this investigation could improve the understanding of how different experiential contexts influence short-term stress regulation.

研究概览

详细说明

Stress is a global phenomenon. Chronic exposure to stress is associated with adverse physical and mental health outcomes, including cardiovascular disease, anxiety, depression, sleep disturbances, and impaired cognitive functioning. Consequently, identifying accessible and effective strategies for stress reduction has become a major public health priority. To explore new ways of managing it is of crucial relevance, therefore the effects of meditation, nature exposure, digital scrolling, and neutral reading on physiological and perceived stress will be investigated.

Participants will be allocated to one of 5 intervention groups: (1) guided meditation, (2) guided meditaiton (3) forest walking, (4) smartphone scrolling, or (5) reading a neutral text.

All study procedures will take place in the morning to account for the circadian rhythm of cortisol secretion. At baseline, participants will complete demographic and study-related assessments, including the Five Facet Mindfulness Questionnaire (FFMQ) and a VAS measuring current stress and anxiety levels. A baseline saliva sample for cortisol determination will be collected at 8:45 a.m., shortly before the expected morning cortisol peak.

Participants will then engage in their assigned activity. The 2 meditation groups will complete a 20-minute guided meditation session using two different meditation techniques. The forest exposure group will undertake a 20-minute walk in a forest environment. The digital activity group will spend 20 minutes scrolling on a smartphone, while the control group will spend 20 minutes reading a neutral text. The duration of the intervention will be standardized across all groups.

Immediately following completion of the assigned activity, participants will undergo a second assessment at approximately 9:00 a.m. A post-intervention saliva sample will be collected for cortisol analysis, and participants will again complete the VAS for anxiety and stress. Salivary Cortisol and DHEA levels will be evaluated at 4 time points the above already mentioned two, and in the evening and before sleeep.

The primary objective of the study is to compare changes in perceived stress. Secondary objectives include evaluating changes in cortisool levels, DHEA, perceived anxiety and exploring the relationship between baseline mindfulness traits, as measured by the FFMQ, and physiological and psychological responses to the interventions.

The study aims to provide preliminary evidence regarding the immediate effects of contemplative practice, exposure to natural environments, and digital engagement on stress-related outcomes in healthy adult participants

研究类型

介入性

注册 (实际的)

100

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Italia
      • Pavia、Italia、意大利、27100
        • Cascina Cravino Via Bassi 21

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

描述

Inclusion Criteria:

  • Understanding of the Italian language

Exclusion Criteria:

  • Presence of severe mental disorders and/or significant medical conditions
  • Endocrine or metabolic disorders
  • Substance dependence

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Experimental
Participants in this groups will undergo a mindfulness based intervention. The meditation tecniques will differ one from the other for focused breathing, body relaxation, emotional awareness and acceptance exercises. The intervention consists of 1 in person session of 20 minutes.
The intervention consists of 1 in person session of mindfulness of 20 minutes.
无干预:No Intervention
Participants in this group will not receive any psychophysiological interventions during the study. This group serve as a passiva control group to evaluate the effectivness of the mindfulness-based intervention by comparing pre and post intervention measures.
有源比较器:Forest bathing
The forest bathing group will act as a an active control group. Forest bathing is known to exert psyhophysiological effects on the stress response system, allowing to evaluate different stress management techniques
Participants engaged in guided forest immersion including mindful walking, sensory awareness, meditation, and nature-based contemplative activities.The intervention consists of 1 in person session of 20 minutes.
有源比较器:Scrolling
Scrolling group will act as an active control group to evaluate the absence of the positive psychophysiological stress response. The intervention consists of 1 in person session of 20 minutes.
Strolling consisted of a slow, relaxed walk in a natural environment without specific mindfulness or sensory-awareness instructions.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in perceived stress.
大体时间:Baseline and immediately after the single intervention session (same day).
Change in perceived stress measured using a Visual Analog Scale for Stress (VAS-Stress), ranging from 0 to 100, where 0 indicates no perceived stress and 100 indicates the highest level of perceived stress imaginable. The outcome will be calculated as the difference between post-intervention and pre-intervention scores. Negative values indicate a reduction in perceived stress following the intervention.
Baseline and immediately after the single intervention session (same day).

次要结果测量

结果测量
措施说明
大体时间
Change in anxiety levels
大体时间:Baseline and immediately after the single intervention session (same day).
Change in anxiety levels measured using a Visual Analog Scale for Anxiety (VAS-Anxiety), ranging from 0 to 100, where 0 indicates no anxiety and 100 indicates the highest level of anxiety imaginable. The outcome will be calculated as the difference between post-intervention and pre-intervention scores. Negative values indicate a reduction in anxiety following the intervention.
Baseline and immediately after the single intervention session (same day).
Change in salivary cortisol concentrations
大体时间:Baseline and immediately after the single intervention session (same day).
Change in salivary cortisol concentration (nmol/L) measured from saliva samples collected immediately before and immediately after the intervention session. The outcome will be calculated as the difference between post-intervention and pre-intervention cortisol concentrations
Baseline and immediately after the single intervention session (same day).
Change in salivary DHEA concentrations
大体时间:Baseline and immediately after the single intervention session (same day).
Change in salivary dehydroepiandrosterone (DHEA) concentration (pg/mL) measured from saliva samples collected immediately before and immediately after the intervention session. The outcome will be calculated as the difference between post-intervention and pre-intervention DHEA concentrations
Baseline and immediately after the single intervention session (same day).
Correlation between trait mindfulness and physiological stress responses
大体时间:Baseline and immediately after the single intervention session (same day).
Correlation between trait mindfulness (measured by Five Facet Mindfulness Questionnaire total score) and change in salivary cortisol concentration
Baseline and immediately after the single intervention session (same day).
- Correlations among psychological and biological outcome measures, including VAS-Stress, VAS-Anxiety, cortisol, and DHEA
大体时间:Baseline and immediately after the single intervention session (same day).
Baseline and immediately after the single intervention session (same day).

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年11月5日

初级完成 (实际的)

2026年6月30日

研究完成 (实际的)

2026年7月30日

研究注册日期

首次提交

2026年6月18日

首先提交符合 QC 标准的

2026年6月24日

首次发布 (实际的)

2026年6月29日

研究记录更新

最后更新发布 (实际的)

2026年8月12日

上次提交的符合 QC 标准的更新

2026年8月7日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • Lum_1

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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