- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06548243
Act with Nature: Promoting Planetary Well-being (AWN)
Act with Nature (AWN): Promoting Well-being and Pro-environmental Behaviour Among Working-age Adults During the Era of Environmental Crises
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
An intervention study with a randomised control trial design will be conducted among a sample of 158 working age participants in various locations in Finland. After receiving information about the research and signing the study consent, participants are randomly allocated to intervention and control groups. The participants in the intervention group will be offered a 12-week, nature-based, Act with Nature (AWN) programme. The programme will be carried out online with individual coaching and independent tasks for each week. Participants share experiences during workshops that are facilitated in nature environment, either in-person or online.
Throughout the AWN programme, nature-based exercises are facilitated in which participants are encouraged to recognise the significance of physical environment and social support in coping with environment-related emotions, nature connectedness and wellbeing. AWN programme is facilitated by a trained health care professional.
The AWN has three separate stages (4 weeks each): Stage 1: nature connectedness, environmental self-regulation and confidence in the group; Stage 2: environmental-related emotions, psychological flexibility and coping strategies; Stage 3: experimenting with change alternatives and affirming positive change in environmental behaviour.
Participants respond to online surveys at five measurement points: a pre-measurement at the start of the programme, two measurements during the programme (at 4 and 8 weeks 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 (nature-based AWN programme) 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). Coping with environment-related emotions, comprehensive nature experience, nature connectedness, environmental emotions and personal environmental goals are investigated as mediators to explain changes in well-being and pro-environmental behaviour.
This research is funded by the Research Council of Finland (Project Numbers: 350971 and 350964).
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Jyväskylä, Finland, 40100
- Institute of Rehabilitation, JAMK University of Applied Sciences
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Tampere, Finland, 33100
- Tampere University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Working age adults
- Able to communicate adequately in Finnish in order to participate
- Willingness to commit to a 12-week intervention programme
Study Plan
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: Act with Nature Programme
A nature-based programme to promote well-being and pro-environmental behaviour.
The programme is facilitated by a trained health care professional.
|
The participants in the intervention group are offered a 12-week nature-based programme, which includes independent exercises and information on an online learning environment, as well as online or in-person group meetings.
|
|
No Intervention: Control group
The participants in the control group continue life as usual.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Emotional wellbeing
Time Frame: 6 months
|
Health related quality of life (RAND): emotional wellbeing dimension, the scores range from 1 to 6 and some items are recoded.
Higher total score refers to better emotional wellbeing.
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6 months
|
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Mental wellbeing
Time Frame: 6 months
|
Short Warwick-Edinburgh Mental Well-being Scale (SWEMWBS), the scores range from 1 to 5, a higher scores refers to better mental wellbeing.
|
6 months
|
|
Pro-environmental behaviour
Time Frame: 6 months
|
Self-report scale of the frequency of pro-environmental actions.
Items refering to pro-environmental actions during one month are responded on a scale ranging from 1 to 5. Items refering to pro-environmental actions during the past year are responded on a scale 1 (yes) and 2 (no).
Some items are recoded and all items include an option for "doesn't apply to me".
A higher total score refers to more self-reported pro-environmental behaviour.
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6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Behavioural Willingness
Time Frame: 6 months
|
Willingness to act pro-environmentally, the scores range from 1 to 4. A higher score refers to more willingness to act pro-environmentally.
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6 months
|
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Affect regulation
Time Frame: 6 months
|
Measure of Affect Regulation Styles (MARS), the scores range from 1 to 6 and all items include an option for "doesn't apply to me".
A higher score refers to a higher efficiency in affect regulation styles.
|
6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Katriina Hyvönen, PhD, JAMK University Of Applied Sciences
Publications and helpful links
General Publications
- Korpela, K., Hyvönen, K., Ratcliffe, E., Salonen, K., & Paakkolanvaara, J.-V. (2023, Jan 30). Act with Nature (AWN): Promoting well-being and pro-environmental behaviour among working-age adults during the era of environmental crises. https://doi.org/10.17605/OSF.IO/69QVW
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- JAMKUAS_AWN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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