Nature-based Contemplation and Spiritual Well-being Among Adults With Moderate Prolonged Grief Symptoms
1 other identifier
interventional
262
1 country
1
Brief Summary
The goal of this randomized controlled trial is to evaluate whether a nature-based contemplation intervention can enhance spiritual well-being and reduce grief symptoms among adults with moderate prolonged grief symptoms. The main questions it aims to answer are: Does a nature-based contemplation intervention improve spiritual well-being compared to an active control condition (noticing nature) and a waitlist control condition? Does a nature-based contemplation intervention reduce grief severity and improve mental well-being, nature connectedness, selflessness, ability to adapt, personal recovery, and elevation compared to control conditions? How do spiritual well-being, ability to adapt, nature connectedness, selflessness, grief reactions, and positive/negative affect change during the intervention period? Researchers will compare a nature-based contemplation intervention to both a noticing-nature active control group and a waitlist control group to isolate mindfulness-specific effects from possible general nature exposure benefits. Participants will: Complete baseline, post-intervention, and follow-up assessments (at one and three months) Engage in either 10 sessions of nature-based contemplation practice or noticing nature activities over a two-week period (intervention and active control groups) Provide daily diary responses about their experiences throughout the 14-day intervention period
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2025
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
March 12, 2025
CompletedStudy Start
First participant enrolled
March 24, 2025
CompletedFirst Posted
Study publicly available on registry
April 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2025
CompletedMay 5, 2026
April 1, 2026
6 months
March 12, 2025
April 28, 2026
Conditions
Outcome Measures
Primary Outcomes (4)
Spiritual well-being measured by Spiritual Attitude and Involvement List-Short Form
Measured using the Spiritual Attitude and Involvement List-Short Form (SAIL-SF; Bohlmeijer et al., 2023). The SAIL-SF measures seven dimensions of spiritual well-being: meaningfulness, trust, acceptance, caring for others, connectedness with nature, transcendent experiences, and spiritual activities. Each dimension is assessed by one item (e.g., "I experience the things I do as meaningful", "I try to take life as it comes"). Items are rated on a 6-point Likert scale ranging from 1 (not at all) to 6 (to a very high degree), with higher scores indicating greater spiritual well-being. The total score is calculated as the mean of all items.
Baseline
Spiritual well-being measured by Spiritual Attitude and Involvement List-Short Form
Measured using the Spiritual Attitude and Involvement List-Short Form (SAIL-SF; Bohlmeijer et al., 2023). The SAIL-SF measures seven dimensions of spiritual well-being: meaningfulness, trust, acceptance, caring for others, connectedness with nature, transcendent experiences, and spiritual activities. Each dimension is assessed by one item (e.g., "I experience the things I do as meaningful", "I try to take life as it comes"). Items are rated on a 6-point Likert scale ranging from 1 (not at all) to 6 (to a very high degree), with higher scores indicating greater spiritual well-being. The total score is calculated as the mean of all items.
1 month after baseline
Spiritual well-being measured by Spiritual Attitude and Involvement List-Short Form
Measured using the Spiritual Attitude and Involvement List-Short Form (SAIL-SF; Bohlmeijer et al., 2023). The SAIL-SF measures seven dimensions of spiritual well-being: meaningfulness, trust, acceptance, caring for others, connectedness with nature, transcendent experiences, and spiritual activities. Each dimension is assessed by one item (e.g., "I experience the things I do as meaningful", "I try to take life as it comes"). Items are rated on a 6-point Likert scale ranging from 1 (not at all) to 6 (to a very high degree), with higher scores indicating greater spiritual well-being. The total score is calculated as the mean of all items.
2 months after baseline
Spiritual well-being measured by Spiritual Attitude and Involvement List-Short Form
Measured using the Spiritual Attitude and Involvement List-Short Form (SAIL-SF; Bohlmeijer et al., 2023). The SAIL-SF measures seven dimensions of spiritual well-being: meaningfulness, trust, acceptance, caring for others, connectedness with nature, transcendent experiences, and spiritual activities. Each dimension is assessed by one item (e.g., "I experience the things I do as meaningful", "I try to take life as it comes"). Items are rated on a 6-point Likert scale ranging from 1 (not at all) to 6 (to a very high degree), with higher scores indicating greater spiritual well-being. The total score is calculated as the mean of all items.
4 months after baseline
Secondary Outcomes (37)
Grief intensity measured by Traumatic Grief Inventory-Self Report Plus
Baseline
Grief intensity measured by Traumatic Grief Inventory-Self Report Plus
1 month after baseline
Grief intensity measured by Traumatic Grief Inventory-Self Report Plus
2 months after baseline
Grief intensity measured by Traumatic Grief Inventory-Self Report Plus
4 months after baseline
Nature connectedness measured by Inclusion of Nature in Self scale
Baseline
- +32 more secondary outcomes
Other Outcomes (7)
Demographic characteristics
Baseline
Loss-related characteristics
Baseline
Previous mindfulness experience
Baseline
- +4 more other outcomes
Study Arms (3)
Nature-based contemplation
EXPERIMENTAL10 minutes walking to a chosen natural location, 10 minutes guided contemplation practice, 10 minutes walking back.
Noticing-nature
ACTIVE COMPARATORwalk in nature for 30 minutes per day and pay attention to how the natural objects/scenes they encounter in their daily surroundings make them feel over the 14-day period.
Waitlist
NO INTERVENTIONInterventions
Participants allocated to the noticing-nature active control group will be instructed to walk in nature for 30 minutes per day and pay attention to how the natural objects/scenes they encounter in their daily surroundings make them feel over the 14-day period.
The intervention consisted of a daily 30-minute self-guided practice structured in three parts: (1) participants first walked mindfully for 10 minutes in a natural environment of their choosing (e.g., local park, forest, garden), (2) upon reaching a suitable location, they engaged in a 10-minute guided contemplative practice, and (3) concluded with a 10-minute mindful walk back.
Eligibility Criteria
You may qualify if:
- Be a family member, spouse, or friend of a person who died at least 6 months prior to study enrollment;
- Be ≥18 years of age;
- Report moderate subclinical grief (score range from 47-70) based on the Traumatic Grief Inventory-Self Report Plus (TGI-SR+, Lenferink, Eisma, et al., 2022);
- Have access to a natural environment suitable for the intervention;
- Be willing and able to move in nature daily (with or without mobility assistance devices) and engage in brief mindfulness practices;
- Have sufficient Dutch language proficiency;
- Have access to Internet and mobile applications.
You may not qualify if:
- Acute suicide risk assessed in the screening step;
- A score lower than 47 or higher than 70 on TGI-SR+;
- Physical limitations that prevent moving outdoors for 30 minutes daily, even with mobility assistance devices.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Twente
Enschede, 7522 NB, Netherlands
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 12, 2025
First Posted
April 1, 2025
Study Start
March 24, 2025
Primary Completion
October 1, 2025
Study Completion
October 1, 2025
Last Updated
May 5, 2026
Record last verified: 2026-04