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Stroke Rehabilitation Utilizing Therapeutical Methods Designed for Nature Environments

Outpatient Stroke Rehabilitation Supported by Nature Interventions

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06633146
Enrollment
40
Registered
2024-10-09
Start date
2024-06-01
Completion date
2027-12-31
Last updated
2025-02-28

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

Conditions

Depression, Anxiety, Loneliness, Post Traumatic Stress Disorder, Stress, Psychological, Stroke

Keywords

stroke, rehabilitation, social support, cognitive functions, activity

Brief summary

Outpatient participants with a recent stroke diagnoses receive complimentary rehabilitation. The nature interventions include ergo- and physiotherapeutic and neurocognitive tasks with the support of an psychotherapeutic frame designed to be performed in a nature environment.

Detailed description

Patients with an acute stroke are recruited to the study when signing out from the acute hospital care services. The patients are selected randomly into two groups: intervention and control groups in proportions 1:1. During the four-week study period the partipants in the control group are encouraged to maintain light physical activity 1 to 3 times per week with or without company. The research worker contacts the participants every week. In the nature group the research worker organises individual nature visits in the nearby nature twice a week and encourages the participants to go outdoors with a close-one once a week. All interventional contacts in the nature group are performed in a ecopsychotherapeutical frame consisting of ergo- and physiotherapeutic and neurocognitive tasks.

Interventions

BEHAVIORALTherapies in nature

Therapeutic tasks in nature specifically designed for the study

Sponsors

University of Helsinki
CollaboratorOTHER
University of Jyvaskyla
CollaboratorOTHER
Tampere University
CollaboratorOTHER
Joint Authority for Päijät-Häme Social and Health Care
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

randomised controlled study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Acute stroke

Exclusion criteria

* Traumatic intracranial bleeding without stroke * A malign, aggressive disease * Severe aphasia or incapable of independent decision making

Design outcomes

Primary

MeasureTime frameDescription
The effect of nature interventions on PROMIS questionnaire4 weeksSelf-assessed quality of life assessed by a PROMIS (patient-reported outcomes measurement information system) questionnaire. Time points measured wk 0 and wk 4, efficacy evaluated on the basis of the difference between these time points. An increase in the obtained score is considered a positive effect.

Secondary

MeasureTime frameDescription
The effect of nature interventions on moods assessed by GAD74 weeksEvaluation of anxiety scales by a GAD7 (generalised anxiety disorder 7) interview, the score of the questionnaire (0-21 points) is evaluated wk 0 and wk 4. A decrease in the total score is considered as a positive effect on moods.
The effect of nature-based intervention on neurocognitive functions in COMET questionnaire4 wkAssessment of the efficacy of nature-based neuropsychological tasks on neurocognitive functions by a cognitive test COMET (cognitive method) -questionnaire. The total score is evaluated wk0 and wk4. An increase in the total score is considered a positive effect.

Other

MeasureTime frameDescription
The effect of nature interventions on functional ability assessed by a validated questionnaire WHODAS4 weeksSelf-assessed functional ability in everyday life with a validated questionnaire WHODAS (WHO disability assessment scale). The total scores are evaluated wk0 and wk4. An increase in the total score is considered a positive effect.
The effect of nature interventions on microbiome4 weeksMicrobiological analyses from skin flake and stool samples
The effect of nature interventions on the activity of autonomic nervous system4 weeksThe evaluation of the state of the autonomic nervous system by heart rate variability by a portable device.

Countries

Finland

Contacts

Primary ContactHanna Haveri, MD PhD
hanna.haveri@paijatha.fi+358 3 81911
Backup ContactMarja Mikkelsson, Prof
marja.mikkelsson@paijatha.fi+358 3 81911

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026