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NCT Number: NCT07673653

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

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cascina Cravino Via Bassi 21

Pavia, Italia, 27100, Italy

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Mindfulness-based Intervention

Behavioral

The intervention consists of 1 in person session of mindfulness of 20 minutes.

Forest bathing

Behavioral

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.

Scrolling

Behavioral

Strolling consisted of a slow, relaxed walk in a natural environment without specific mindfulness or sensory-awareness instructions.

Primary outcomes

  1. Change in perceived stress.

    Time frame: 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.

Secondary outcomes

  1. Change in anxiety levels

    Time frame: 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.

  2. Change in salivary cortisol concentrations

    Time frame: 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

  3. Change in salivary DHEA concentrations

    Time frame: 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

  4. Correlation between trait mindfulness and physiological stress responses

    Time frame: 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

  5. - Correlations among psychological and biological outcome measures, including VAS-Stress, VAS-Anxiety, cortisol, and DHEA

    Time frame: Baseline and immediately after the single intervention session (same day).

Sponsors and collaborators

Lead sponsor

University of Pavia

Other

Collaborators

  • University of Padova

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 29, 2026
Registry last updated
Jun 29, 2026

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.

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