Comparative Effects of Meditation, Nature Exposure, and Digital Activities on Physiological and Perceived Stress
1 other identifier
interventional
100
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 5, 2025
CompletedFirst Submitted
Initial submission to the registry
June 18, 2026
CompletedFirst Posted
Study publicly available on registry
June 29, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2026
CompletedJune 29, 2026
June 1, 2026
8 months
June 18, 2026
June 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in perceived stress.
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).
Secondary Outcomes (5)
Change in anxiety levels
Baseline and immediately after the single intervention session (same day).
Change in salivary cortisol concentrations
Baseline and immediately after the single intervention session (same day).
Change in salivary DHEA concentrations
Baseline and immediately after the single intervention session (same day).
Correlation between trait mindfulness and physiological stress responses
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
Baseline and immediately after the single intervention session (same day).
Study Arms (4)
Experimental
EXPERIMENTALParticipants 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.
No Intervention
NO INTERVENTIONParticipants 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.
Forest bathing
ACTIVE COMPARATORThe 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
Scrolling
ACTIVE COMPARATORScrolling 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.
Interventions
The intervention consists of 1 in person session of mindfulness of 20 minutes.
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.
Strolling consisted of a slow, relaxed walk in a natural environment without specific mindfulness or sensory-awareness instructions.
Eligibility Criteria
You may qualify if:
- Understanding of the Italian language
You may not qualify if:
- Presence of severe mental disorders and/or significant medical conditions
- Endocrine or metabolic disorders
- Substance dependence
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Pavialead
- University of Padovacollaborator
Study Sites (1)
Cascina Cravino Via Bassi 21
Pavia, Italia, 27100, Italy
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The Outcome Assessor and Data Analyst are blinded to group allocation. Participants are not informed of their assigned condition prior to allocation; however, blinding is not feasible after the intervention begins because the nature of the assigned activity becomes apparent. Personnel delivering the interventions are aware of group assignment but are not involved in outcome assessment or data analysis
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 18, 2026
First Posted
June 29, 2026
Study Start
November 5, 2025
Primary Completion
June 30, 2026
Study Completion
July 1, 2026
Last Updated
June 29, 2026
Record last verified: 2026-06