NCT05562128

Brief Summary

In recent years, nature and forest therapy has increasingly become the focus of medical research. Recent scientific findings indicate overall positive effects of nature and forest therapy on physical and mental health. In Asia and Australia, it has already been implemented as a public health concept of prevention and health promotion. The aim of the project is to replicate the experience gained in Asia over the last three decades on the physical and psychological effects of nature/forest therapy in the context of the German forest and to investigate it further scientifically.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

First Submitted

Initial submission to the registry

September 28, 2022

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 30, 2022

Completed
10 days until next milestone

Study Start

First participant enrolled

October 10, 2022

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2025

Completed
Last Updated

May 31, 2025

Status Verified

December 1, 2024

Enrollment Period

2.6 years

First QC Date

September 28, 2022

Last Update Submit

May 27, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Profile of Mood States (POMS)

    Change from baseline POMS score at 3 months

Secondary Outcomes (11)

  • Profile of Mood States (POMS)

    Baseline, day 1, day 3, 1 week, 3 months

  • Perceived Benefits of Nature Questionnaire (PBNQ)

    Baseline, 1 week, 3 months

  • Subjective Vitality Scale state (SVS-G state)

    Baseline, day 1, day 3, 1 week, 3 months

  • Complaint List (B-LR)

    Baseline, 1 week, 3 months

  • Perceive Stress Questionaire (PSQ)

    Baseline, day 1, day 3, 1 week, 3 months

  • +6 more secondary outcomes

Other Outcomes (2)

  • Heart Rate Variability (HRV)

    Baseline, 1 week

  • Qualitative interviews

    1 week and 8 weeks after inclusion

Study Arms (3)

Active forest therapy

EXPERIMENTAL
Behavioral: Active forest therapy

Passive forest therapy

ACTIVE COMPARATOR
Behavioral: Passive forest therapy

Waiting list

NO INTERVENTION

Interventions

Participants take part in a two-hour active clinical forest therapy in Berlin-Wannsee on two days (with a break day in between). In this setting, a trained clinical forest therapist teaches exercises on the perception of nature and the connection between nature and health.

Active forest therapy

Participants take part in a two-hour passive clinical forest therapy in Berlin-Wannsee over two days (with a break day in between). In this setting, a trained clinical forest therapist will guide participants to various locations in the forest where participants can stay and let nature have its effect on them.

Passive forest therapy

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \- Ability to Consent

You may not qualify if:

  • Serious acute or chronic illness
  • Immobility or limitation of mobility due to orthopedic, neurologic, or other medical causes
  • Participation in another study
  • Serious mental illness
  • Pregnancy and lactation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Charité Hochschulambulanz für Naturheilkunde am Immanuel Krankenhaus

Berlin, State of Berlin, 14109, Germany

RECRUITING

MeSH Terms

Conditions

Disease

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 28, 2022

First Posted

September 30, 2022

Study Start

October 10, 2022

Primary Completion

June 1, 2025

Study Completion

August 1, 2025

Last Updated

May 31, 2025

Record last verified: 2024-12

Locations