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Nature-Focused Mindfulness and Spiritual Well-being Among Adults with Moderate Prolonged Grief Symptoms

U

University of Twente

Status

Not yet enrolling

Conditions

Grief
Spiritual Wellbeing

Treatments

Behavioral: Nature-focused mindfulness
Behavioral: Noticing-nature

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this randomized controlled trial is to evaluate whether a nature-focused mindfulness 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-focused mindfulness intervention improve spiritual well-being compared to an active control condition (noticing nature) and a waitlist control condition?

Does a nature-focused mindfulness 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-focused mindfulness 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-focused mindfulness 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

Enrollment

230 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

230 participants in 3 patient groups

Nature-focused mindfulness
Experimental group
Description:
10 minutes walking to a chosen natural location, 10 minutes guided mindfulness practice, 10 minutes walking back.
Treatment:
Behavioral: Nature-focused mindfulness
Noticing-nature
Active Comparator group
Description:
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.
Treatment:
Behavioral: Noticing-nature
Waitlist
No Intervention group

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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