The Effect of a Contemplative Nature-based Intervention on Spiritual Well-being
1 other identifier
interventional
41
1 country
1
Brief Summary
The goal of this randomized control trial is to test if contemplating in nature could benefit spiritual well-being in general adults. The main question it aims to answer is: Does a 2-week contemplative nature intervention improve spiritual well-being? Participants in the intervention condition will walk for 10 minutes and then choose a nice spot to sit for 10 minutes. During these minutes they will be asked to be silently present and observe trees, plants, flowers, or other aspects of nature and contemplate their connectedness to nature and their own awareness. Then walk back 10 minutes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2024
Shorter than P25 for not_applicable
1 active site
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
April 5, 2024
CompletedFirst Posted
Study publicly available on registry
April 15, 2024
CompletedStudy Start
First participant enrolled
May 10, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 4, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 4, 2024
CompletedSeptember 22, 2025
September 1, 2025
4 months
April 5, 2024
September 16, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Spiritual well-being assessed by Spiritual Attitude and Involvement List Short Form (SAIL-SF)
On a 6-point Likert scale ranging from 1 (not at all) to 6 (to a very high degree), respondents rate in how far they think specific statements about spiritual well-being apply to themselves. Higher scores indicate higher scores of spiritual well-being.
Change from baseline to post-intervention at 2 weeks.
Spiritual well-being assessed by Spiritual Attitude and Involvement List Short Form (SAIL-SF)
On a 6-point Likert scale ranging from 1 (not at all) to 6 (to a very high degree), respondents rate in how far they think specific statements about spiritual well-being apply to themselves. Higher scores indicate higher scores of spiritual well-being.
Change from Baseline to Short-term follow-up at 1 month.
Spiritual well-being assessed by Spiritual Attitude and Involvement List Short Form (SAIL-SF)
On a 6-point Likert scale ranging from 1 (not at all) to 6 (to a very high degree), respondents rate in how far they think specific statements about spiritual well-being apply to themselves. Higher scores indicate higher scores of spiritual well-being.
Change from baseline to longer-term follow-up at 3 months.
Spiritual well-being assessed by Daily Spiritual Experience Scale (DSES)
The non-theistic items from DSES will be used. Ranging from 1 (multiple times a day) to 6 (never). The item responses were reverse coded prior to analysis so that larger values would reflect a higher level of daily spiritual experiences.
Change from baseline to post-intervention at 2 weeks.
Spiritual well-being assessed by Daily Spiritual Experience Scale (DSES)
The non-theistic items from DSES will be used. Ranging from 1 (multiple times a day) to 6 (never). The item responses were reverse coded prior to analysis so that larger values would reflect a higher level of daily spiritual experiences.
Change from baseline to short-term follow-up at 1 month.
Spiritual well-being assessed by Daily Spiritual Experience Scale (DSES)
The non-theistic items from DSES will be used. Ranging from 1 (multiple times a day) to 6 (never). The item responses were reverse coded prior to analysis so that larger values would reflect a higher level of daily spiritual experiences.
Change from baseline to longer-term follow-up at 3 months.
Other Outcomes (18)
Client satisfaction of intervention condition assessed by Client Satisfaction Questionnaire (CSQ-8)
From post-intervention to short-term follow-up at 1 month.
Client satisfaction of active control condition assessed by Client Satisfaction Questionnaire (CSQ-8)
From post-intervention to short-term follow-up at 1 month.
Client satisfaction of passive control condition assessed by Client Satisfaction Questionnaire (CSQ-8)
From post-intervention to longer term follow-up at 3 months.
- +15 more other outcomes
Study Arms (1)
Contemplative nature intervention
EXPERIMENTALParticipants will spend 30 minutes in nature per day for 10 times over 14 days. Participants will walk for 10 minutes and then choose a nice spot to sit for 10 minutes. During these minutes they will be asked to be silently present and observe trees, plants, flowers, or other aspects of nature and contemplate their connectedness to nature and their own awareness. Then walk back 10 minutes.
Interventions
Participants will spend 30 minutes in nature per day for 10 times over 14 days. Each time, participants will walk for 10 minutes and then choose a nice spot to sit for 10 minutes. During these minutes they will be asked to be silently present and observe trees, plants, flowers or other aspects of nature and contemplate their connectedness to nature and their own awareness. Then walk back 10 minutes.
Eligibility Criteria
You may qualify if:
- is 18 years or older;
- has access to a nearby natural environment for walking and sitting activities such as a forest, park, or walking area;
- possesses the physical ability to walk for half an hour;
- has access to a computer or tablet with a stable internet connection and an email address;
- is willing to commit half an hour to engage in nature walks 10 times over 14 days.
You may not qualify if:
- \- NA.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Twente
Enschede, Overijssel, 7522NB, Netherlands
Study Officials
- PRINCIPAL INVESTIGATOR
Ernst Bohlmeijer, Prof. Dr.
University of Twente
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 5, 2024
First Posted
April 15, 2024
Study Start
May 10, 2024
Primary Completion
September 4, 2024
Study Completion
September 4, 2024
Last Updated
September 22, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share