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Effects of Forest Therapy Program on Stress and Cognitive Function in Older Adults: Focusing on Salivary Cortisol and Cognitive Screening Test

Effects of Forest Therapy Program on Stress and Cognitive Function in Older Adults: Focusing on Salivary Cortisol and Cognitive Screening Test

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011753
Enrollment
120
Registered
2026-03-20
Start date
2026-03-30
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : The experimental group receives a community-based forest therapy program (6080 Village Forest Friends) once per week for 8 weeks (8 sessions total, 120 minutes per session). Each session

Sponsors

Apple Tree Medical Foundation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Adults aged 55 years or older 2.Currently enrolled or scheduled to enroll in the community-based forest therapy program (6080 Village Forest Friends) (experimental group), or community-dwelling adults of the same age range who do not participate in the program (control group) 3.Willing and able to provide saliva samples, gargle solution samples, complete the cognitive function test (MMSE-K), and answer questionnaires 4.Agreeable to the secondary use of anonymized data and residual biological specimens for future research 5.Provided written informed consent for both the study participation consent form and the human-derived materials research consent form

Exclusion criteria

Exclusion criteria: 1. Use of antibiotics (oral or injectable) within the past 1 week 2. Participation in another clinical study within the past 1 month 3. Currently taking systemic corticosteroid medications (may interfere with salivary cortisol measurement) 4. Presence of acute oral infection 5. Diagnosed with dementia 6. Deemed ineligible for study participation by the investigator

Design outcomes

Primary

MeasureTime frame
Change in salivary cortisol concentration Salivary cortisol levels (nmol/L) measured by enzyme-linked immunosorbent assay (ELISA) as a physiological biomarker of stress. The primary outcome is the change in salivary cortisol concentration from baseline to post-intervention.

Secondary

MeasureTime frame
Change in cognitive function score (MMSE-K) Cognitive function assessed using the Mini-Mental State Examination-Korean version (MMSE-K). The outcome is the change in total score from baseline to post-intervention.

Countries

Korea, Republic of

Contacts

Public ContactMu Yeol Cho

Apple Tree Medical Foundation

whanduf@appleden.com+82-70-4601-5479

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Apr 3, 2026