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Effects of the Intervention Clinical Forrest Therapy on Geriatric Patients

Effects of the Intervention Clinical Forrest Therapy on Geriatric Patients

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
DRKS
Registry ID
DRKS00034199
Enrollment
50
Registered
2025-05-15
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Improving the well-being of geriatric patients

Interventions

Group 1: Study type: observational study, monocentric Study arms: intervention only no randomization no blinding Forest therapy programme Implementation specifically adapted to geriatr
information on forest therapy adapted to the target group - Station 2: Exercise for physical activation (joint mobilisation in the form of circular movements) and to become aware of all the senses, -
discovering the microcosm of the forest with the help of magnifying glasses - Station 5: Soundscape
exercise to consciously perceive the forest sounds - Station 6: Relaxation exercise for mindfulness and further deceleration. - Conclusion and farewell at the end point (= starting point) Survey on

Sponsors

Klinik Wartenberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
70 Years to No maximum

Inclusion criteria

Inclusion criteria: Consenting, clinically stable geriatric patients who are at least wheelchair-mobile (definition according to DGG)

Exclusion criteria

Exclusion criteria: Lack of capacity to consent/ moderate to severe dementia

Design outcomes

Primary

MeasureTime frame
Feasibility and safety Survey on the primary endpoint: Assessment of the intervention in terms of feasibility and safety by forest therapist +1 day after the intervention by patient +1 day after the intervention Vital signs monitoring Measurement parameters: HR/RR/SO2 at the time points 0 before intervention 1 after 100% intervention time 3h after start of intervention

Secondary

MeasureTime frame
Gaining indications of possible positive effects of experiencing nature on mood Survey on the secondary endpoint Quality of life assessment using ASTS -2 to -1 day(s) before intervention 0 Day of intervention (2h after intervention) +1 day after the intervention +7 days after the intervention Vital signs monitoring Measurement parameters: HR/RR/SO2 at the time points 0 before intervention 1 after 100% intervention time 3h after start of intervention

Countries

Germany

Contacts

Public ContactSaskia Rupp

Klinik Wartenberg

s.rupp@klinik-wartenberg.de00498762/91-500

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026