Skip to content

Forest Bathing Intervention for Persons Living with Dementia and Family Carers

Forest Bathing Intervention for Persons Living with Dementia and Family Carers: a Feasibility Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06813196
Enrollment
107
Registered
2025-02-06
Start date
2024-04-22
Completion date
2024-08-17
Last updated
2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregiver Mental Health, Dementia

Keywords

Forest bathing

Brief summary

This study assessed the feasibility and acceptability of a forest bathing intervention for people living with dementia and their family carers, and examined its effectivness on care burden and quality of life by comparing to an art activty programme as control group.

Interventions

BEHAVIORALForest Bathing

Forest bathing intervention is a group structured psychosocial intervention. Its core therapeutic element is its nature-based activities that took place in an outdoor green space. During the session, participants would be guided by a trained forest therapy guide to engage in nature-based activities, such as walking in the woods, listening to the nature, and interacting with objects in the nature through different sensations.

BEHAVIORALArt activity

Art activity intervention is a group semi-structured psychosocial intervention. Its main therapeutic element is its engagement in art-based activites. During the session, participants would be guided in individual or collaborative art activities of different forms, such as painting, paper arts, and dried flower art, by an experienced interventionist in an activity room.

Sponsors

Hong Kong Young Women's Christian Association
CollaboratorOTHER
The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* For family careivers: * taking care of a family member living with dementia in the community, * For people living with dementia: * Clinical diagnosis of mild to moderate dementia

Exclusion criteria

* For both: * Unable to communicate in Chinese or Cantonese * Unable to participate meaningfully in group activities due to intellectual disability, visual impairment, hearing impairment, or other health conditions, were excluded.

Design outcomes

Primary

MeasureTime frameDescription
Change in Caregiver's Care Burden measured by 12-item version of Zarit Burden Interview (ZBI-12)Baseline and 6 weeksPossible range: 0-48, with higher scores indicate a worse outcome
Change in Caregiver's Depressive Symptoms measured by the Depression subscale of Hospital Anxiety and Depression Scale (HADS-D)Baseline and 6 weeksPossible range: 0-21, with higher scores indicate a worse outcome
Change in Caregiver's Anxiety Symptoms measured by the Anxiety subscale of Hospital Anxiety and Depression Scale (HADS-A)Baseline and 6 weeksPossible range: 0-21, with higher scores indicate a worse outcome

Secondary

MeasureTime frameDescription
Change in Neuropsychiatric Symptoms of Person Living with Dementia measured by the Neuropsychiatric Inventory - Questionnaire (NPI-Q)Baseline and 6 weeksPossible range: 0-12, with higher scores indicate a worse outcome
Change in Caregiver's Positive Aspect of Caregiving measured by the Positive Aspect of Caregiving Scale (PACS)Baseline and 6 weeksPossible range: 11-55, with higher scores indicate a better outcome
Change in Health-related Quality of Life of Person Living with Dementia measured by the Visual Analogue Scale of EuroQol 5-dimension 5-level (EQ5D5L VAS)Baseline and 6 weeksPossible range: 0-100, with higher scores indicate a better outcome
Change in Caregiver's Caregiving Self-Efficacy measured by the Revised Scale for Caregiving Self-Efficacy (CSE-R)Baseline and 6 weeksPossible range: 0-100, with higher scores indicate a better outcome
Change in Caregiver's Health-related Quality of Life measured by the Visual Analogue Scale of EuroQol 5-dimension 5-level (EQ5D5L VAS)Baseline and 6 weeksPossible range: 0-100, with higher scores indicate a better outcome

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026