Finding With Nature: A Study Testing Nature-Based Support for Family Caregivers Aged 65 and Over (FWN)

September 15, 2026 updated by: Julija Chichaeva, JAMK University Of Applied Sciences

Finding With Nature: A Nature-Based Intervention for the Well-Being of Family Caregivers Aged 65 and Over: Protocol for a Randomised Controlled Trial

This research project investigates the effects of a nature-based programme (Finding with Nature, FWN), on psychological well-being, functioning, and nature connectedness among older adults (65 and older) who provide care for their close one in Finland. The FWN programme combines nature exposure, physical activity, and Acceptance and Commitment Therapy (ACT) methods. The effects of the FWN programme are studied in a randomised controlled trial. The psychological well-being, functioning, and nature connectedness are investigated with self-report measures and analysed with quantitative methods. The results provide knowledge about the ability of nature-based, low-threshold methods to support older adults (65+) who provide care for their close one.

Study Overview

Detailed Description

An intervention study in randomised control trial design will be conducted with a target sample of 350 participants living in Central Finland. After receiving information about the research and providing a written consent, participants answer a question of caregiver burden and indicate whether they would prefer to participate in the Finding with Nature (FWN) programme in face-to-face group meetings or individually via an interactive online platform. After that, the participants are randomly allocated to intervention and control groups which are balanced according to the caregiver burden. The participants in the intervention group will be offered a 6-week FWN programme either in a face-to-face group or individually online, according to their own preference. In the face-to-face group implementation, the FWN programme will be carried out by a trained facilitator with meetings once a week. In the online implementation, the FWN programme will be completed individually at their own pace via an interactive online platform. In both implementation formats, participants will complete independent tasks and have the opportunity to share their experiences with peers.

At the core of the FWN programme are facilitated nature-based, low-threshold exercises in six theme areas of the FWN programme (one theme for each week): 1) Introduction, personal situation, and starting points for change; 2) personally meaningful matters and values; 3) acceptance of emotions and confronting barriers; 4) listening to the body, meaningful movement, and natural settings; 5) mindfulness skills and everyday choices; and (6) self-concept, self-compassion, and self-awareness.

Participants respond to surveys at three measurement points: a pre-measurement at the start of the programme, a post-measurement at the end of the programme, and a follow-up measurement three months after the end of the programme. The participants in the intervention group are compared to the participants in the control group who continue life as usual and only respond to online surveys at three measurement points (pre-, post- and follow-up measurements). The control group participants are offered a opportunity to participate in face-to-face group meetings or the online implementation of the FWN programme after the follow-up measurement.

This research is funded by the Health Promotion Grant (Ministry of Social Affairs and Health, STM, va-thl-2025-1-80).

Study Type

Interventional

Enrollment (Estimated)

350

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age 65 years and older
  • Providing care for a close one, formally or informally
  • Able to communicate adequately in Finnish
  • Willingness to commit to a 6-week intervention programme

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Finding with Nature intervention
Participants aged ≥65 years who are informal/family caregivers and living in Central Finland. Participants randomized to this arm will take part in a 6-week structured intervention program.
A 6-week nature-based program integrating physical activity in nature and Acceptance and Commitment Therapy (ACT) methods to promote well-being, functioning, and nature connectedness. Delivered either in face-to-face groups or via an online platform, including guided sessions, independent exercises, informational content, and opportunities for peer support.
No Intervention: No intervention
Participants aged ≥65 years who are informal/family caregivers and living in Central Finland. Participants randomized to this arm will continue their usual daily life without the study intervention during the 6-week follow-up period. After the follow-up, they will be offered the opportunity to participate in the intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychological well-being: the Short Warwick-Edinburgh Mental Well-being Scale (SWEMWBS)
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
7-item scale, range 7-35; higher scores indicate better mental well-being.
Pre-intervention, immediately post-intervention, and 3-month follow-up.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Caregivers' perceived coping as caregivers: COPE Index
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
COPE Index evaluates the caregiver's subjective experience of strain, support, and quality of the caregiving relationship. 15-item scale, range 15-75; higher scores indicate greater caregiving burden.
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Functioning: the WHO Disability Assessment Schedule 2.0 (WHODAS 2.0)
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
A standardized assessment of functioning across multiple life domains. 12-item scale, range 0-48; higher scores indicate greater disability (worse functioning).
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Adult Social Care Outcomes Toolkit (ASCOT) SCT4
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
Measure designed specifically for informal caregivers, focusing on social care-related quality of life. 8-item scale; higher scores indicate better social care-related quality of life.
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Self-rated health: a single validated item
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Connectedness to nature: short version of Connectedness to Nature Scale (CNS)
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
Short version of the Connectedness to Nature Scale (CNS), 7-item scale, range 7-35; higher scores indicate greater connectedness to nature.
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Connectedness to nature and nature-related experiences: the Holistic Nature Experience measure
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
16-item scale, range 16-96; higher scores indicate more positive nature-related experiences.
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Psychological flexibility: Comprehensive Assessment of ACT Processes (CompACT-10)
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
10-item scale, range 0-60; higher scores indicate greater psychological flexibility
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Anxiety: Generalized Anxiety Disorder 7-item Scale (GAD-7)
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
7-item scale, range 0-21; higher scores indicate greater anxiety symptoms
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Physical activity: International physical activity questionnaire -short form (IPAQ-SF)
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
International Physical Activity Questionnaire - Short Form (IPAQ-SF), 7-item questionnaire. Total physical activity is expressed as MET-minutes per week. The minimum value is 0 MET-minutes/week, with no fixed maximum value. Higher scores indicate higher levels of physical activity.
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Restorative experiences: the Restoration Outcome Scale (ROS)
Time Frame: Immediately before and after each of the six weekly intervention sessions during the 6-week intervention period.
6-item scale, range 6-42; higher scores indicate greater restorative experiences
Immediately before and after each of the six weekly intervention sessions during the 6-week intervention period.
Life-space mobility: the Life-Space Assessment (LSA)
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
Capture the spatial extent and frequency of participants' mobility in daily life, assessing mobility over the previous 4 weeks, range 0-120; higher scores indicate greater life-space mobility
Pre-intervention, immediately post-intervention, and 3-month follow-up.
Engagement with natural and green environments
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
Assessed through questions on frequency, purpose, and patterns of nature visits.
Pre-intervention, immediately post-intervention, and 3-month follow-up.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Caregiver characteristics
Time Frame: Pre-intervention, immediately post-intervention, and 3-month follow-up.
Information is collected on the care recipient, duration of caregiving, formal caregiver status, and use of support services.
Pre-intervention, immediately post-intervention, and 3-month follow-up.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Julija Chichaeva, MHS, JAMK University Of Applied Sciences

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 7, 2026

Primary Completion (Estimated)

March 1, 2028

Study Completion (Estimated)

March 1, 2028

Study Registration Dates

First Submitted

September 3, 2026

First Submitted That Met QC Criteria

September 15, 2026

First Posted (Actual)

September 16, 2026

Study Record Updates

Last Update Posted (Actual)

September 16, 2026

Last Update Submitted That Met QC Criteria

September 15, 2026

Last Verified

September 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Anonymised quantitative data will be archived, where applicable, in the Finnish Social Science Data Archive (FSD).

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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