NCT06904976

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
262

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 12, 2025

Completed
12 days until next milestone

Study Start

First participant enrolled

March 24, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

April 1, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2025

Completed
Last Updated

May 5, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

March 12, 2025

Last Update Submit

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

EXPERIMENTAL

10 minutes walking to a chosen natural location, 10 minutes guided contemplation practice, 10 minutes walking back.

Behavioral: Nature-based contemplation

Noticing-nature

ACTIVE COMPARATOR

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.

Behavioral: Noticing-nature

Waitlist

NO INTERVENTION

Interventions

Noticing-natureBEHAVIORAL

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.

Noticing-nature

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.

Nature-based contemplation

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

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

Locations