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CompletedNCT07368231HSP-FORESTUpdated Jan 26, 2026

Forest Therapy and Mindfulness for Highly Sensitive Persons

An interventional study of Forest Therapy + Mindfulness + Psychotherapy and Behavioral: Indoor Sensory Control (Art and Aromatherapy) in Stress (Psychology), Well-Being, Psychological and Mind-Body Therapies, sponsored by IFM International Forest Medicine. Completed at 2 sites in Spain. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-26.

Sponsored by IFM International Forest Medicine · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled May 2025, registered Dec 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
310
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This randomized, multicenter interventional study evaluates a combined forest therapy (shinrin-yoku) and mindfulness-based program in adults with high sensory-processing sensitivity confirmed using a validated instrument. Participants are randomized (1:1) to either a forest-based intervention or an active indoor sensory control condition. The intervention is delivered over approximately 22 weeks according to a predefined protocol, with assessments conducted at baseline and at the end of the intervention.

Read the detailed description

This is a multicenter, randomized, parallel-group interventional study in adults with high sensory-processing sensitivity confirmed using a validated instrument. Participants are randomized 1:1 to one of two study arms at study entry and remain in their assigned group for the duration of the study.

Intervention delivery is standardized across participating sites through facilitator training and a predefined session manual. The experimental arm consists of structured sessions conducted in forest environments and includes guided walking, mindfulness-based practices, and structured sensory awareness activities, with facilitated group reflection. The active comparator arm consists of structured indoor group activities designed to match the experimental arm in duration, group interaction, and facilitator contact, without exposure to forest or outdoor natural environments.

Study procedures and assessment schedules are predefined in the protocol and implemented in accordance with applicable ethical requirements and Good Clinical Practice guidelines.

02

Conditions studied

  • Stress (Psychology)
  • Well-Being, Psychological
  • Mind-Body Therapies
  • Complementary Therapies
  • Mindfulness
  • Preventive Medicine

Keywords

  • Forest Bathing
  • Forest Therapy
  • Shinrin Yoku
  • Mindfulness
  • Forest Medicine
  • Highly Sensitive Person (HSP)
  • Stress reduction
  • Mental Health
03

In context

Psychological Well-Being

967 studies on the registry are indexed under Psychological Well-Being; 501 are open to participants now.

This study's enrollment of 310 is above the median of 116 across 827 interventional studies indexed under Psychological Well-Being.

Browse Psychological Well-Being studies →

Lead sponsor

IFM International Forest Medicine is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age 18 to 65 years
  • High sensory-processing sensitivity confirmed using a validated instrument (e.g., HSPS/Aron scale)
  • Able to perform moderate physical activity (e.g., walking)
  • Able to provide written informed consent

Exclusion criteria

Exclusion Criteria:

  • Severe psychiatric disorder or acute clinical instability
  • Medical condition contraindicating moderate physical activity
  • Use of medications with strong autonomic or neuroendocrine effects (e.g., high-dose systemic corticosteroids; selected beta-blockers)
  • Recent participation in a structured mindfulness or forest-therapy program
  • Pregnancy or unstable medical condition
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
310 participants (actual)

Study arms

  • Experimental
    Forest Therapy + Mindfulness + Psychotherapy

    Participants will undergo an approximately 22-week program with 4.5 hours weekly in forest settings. Sessions include a guided forest walk, mindfulness meditation, structured sensory awareness exercises, facilitated group reflection, and a brief psychotherapeutic component focused on emotional processing and cognitive regulation. Intervention delivery is standardized through facilitator training and a predefined session manual.

    Behavioral: Forest Therapy + Mindfulness + Psychotherapy

  • Active comparator
    Indoor Sensory Control (Art and Aromatherapy)

    Structured indoor sensory-based group sessions delivered weekly over approximately 22 weeks. Sessions are designed to match the experimental intervention in duration, structure, facilitator contact, and social interaction, without exposure to forest or outdoor natural environments. Activities include creative tasks, guided aromatherapy, sensory-focused exercises, and facilitated group discussion according to a predefined protocol.

    Behavioral: Behavioral: Indoor Sensory Control (Art and Aromatherapy)

Interventions

  • BehavioralForest Therapy + Mindfulness + Psychotherapy

    Participants will undergo a approximately 22-week program with 4.5 hours weekly in forest settings. Each session includes: A 2-hour guided walk with scheduled rest/hydration breaks Mindfulness meditation (20-30 minutes) Discussion/reflection segment (\~20 minutes) for participants to express sensations, experiences, or doubts A psychotherapeutic component focused on emotional processing and cognitive regulation Sensory observation (5-10 minutes) of forest stimuli (olfactory, auditory, tactile, visual) Post-session journaling capturing emotional and sensory feedback Monitoring of environmental parameters (temperature, humidity, wind, estimated phytoncide levels) Standardized facilitator training and session protocols to ensure consistency across sites This protocol is distinguished by integrating forest immersion, mindfulness, psychotherapy, and sensory training in a unified intervention tailored for Highly Sensitive Persons (HSP).

  • BehavioralBehavioral: Indoor Sensory Control (Art and Aromatherapy)

    Structured indoor sensory-based group sessions delivered weekly over approximately 22 weeks. Activities include creative tasks, guided aromatherapy, and sensory-focused exercises conducted in indoor, non-forest environments. Sessions are designed to match the experimental intervention in duration, structure, facilitator contact, and social interaction, according to a predefined protocol.

06

What researchers measure

Primary outcomes

  1. Change in Perceived Stress Score (PSS-10) From Baseline to End of Intervention

    Measure the difference in total score on the Perceived Stress Scale (PSS-10) between baseline and the end of the intervention. PSS-10 comprises 10 items scored 0-40, with higher scores indicating greater perceived stress.

    Time frame: Baseline to end of intervention (approximately 22 weeks)

Secondary outcomes

  1. Change in Psychological Well-Being Score (WHO-5) From Baseline to End of Intervention

    Measure the difference in total score on the WHO-5 Well-Being Index between baseline and the end of the intervention. WHO-5 comprises 5 items scored 0-25, with higher scores indicating better well-being.

    Time frame: Baseline to end of intervention (approximately 22 weeks)

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Study locations

2 sites
  • IFM International Forest Medicine
    Ronda, Andalusia 29492, Spain
  • Sessions conducted in natural forest settings within the Serranía de Ronda, specifically the Valle del Genal area
    Ronda, Andalusia 29492, Spain
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References and documents

Publications

  • Sánchez Hdz, Ana I. Forest Therapy and Mindfulness in Highly Sensitive Persons (HSP): Confirmatory Evidence from a Multicenter Randomized Controlled Trial with 6-Month Follow-up. Zenodo. DOI: 10.5281/zenodo.17361382. Available at: https://zenodo.org/records/17361382

Individual participant data

Plan to share: Yes — De-identified individual participant data supporting publications arising from this study will be shared with qualified researchers beginning 6 to 36 months after publication.

Supporting information: Study protocol

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07368231
Lead sponsor
IFM International Forest Medicine
Responsible party
Sponsor
First posted
Jan 26, 2026
Start date
May 1, 2025
Primary completion
Oct 3, 2025
Completion
Oct 3, 2025
Last update
Jan 26, 2026

Study contacts

Ana I Sánchez Hdz
principal investigator · IFM International Forest Medicine

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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