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Clinical Trials/NCT06390683
NCT06390683Active, not recruitingNot Applicable

Biodiversity Interventions for Well-Being - Research in Assisted Living Centers

Natural Resources Institute Finland2 sites in 1 country36 target enrollmentStarted: February 1, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
36
Locations
2
Primary Endpoint
Skin Gammaproteobacteria

Study Overview

Brief Summary

Biodiversity is essential for nature and human well-being. Land use has reduced biodiversity in cities, which weakens the functionality of the urban ecosystems and the well-being of citizens. This may also increase the risk of immune-mediated disorders among urban dwellers.

In Biodiversity interventions for assisted living centers (BIWE 2), microbial biodiversity interventions are performed to increase biodiversity in urban housing units for people with autism spectrum disorder, disabled people and elderly. Results from the intervention trials are combined with publicly available land cover and ecological data. These are analyzed from the viewpoint of shifts in ecosystems and human well-being and immune regulation, ecological quality, and urban planning.

The investigators set up an intervention study in which yards of the housing units are rewilded with diverse vegetation and decaying deadwood and plant residuals. The investigators aim to evaluate the effect of rewilding, and yard management practices on commensal microbiome, cortisol levels and well-being and salivary cytokine levels, and gene pathways.

Detailed Description

Our specific aims are:

To assess if rewilding diversifies health-associated skin microbiota and is associated with salivary cytokine levels, gene pathways, cortisol levels and commensal microbiota.

Assess whether there are patterns in the microbiome associated with the salivary cytokine levels and hair cortisol levels.

Assess whether rewilding affects health and psychological measures. The investigators will recruit approximately 36 study subjects living in assisted housing units in urban areas and aged between 18-82.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 82 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Person lives in assisted living center

Exclusion Criteria

  • Immunosuppressive medications
  • Immune deficiencies
  • a disease affecting immune response (colitis ulcerosa, rheumatoid arthritis, Crohn's disease, diabetes)
  • cancer diagnosis within the last year or on-going cancer treatment

Outcomes

Primary Outcomes

Skin Gammaproteobacteria

Time Frame: Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year

Change in skin gammaproteobacterial diversity

Secondary Outcomes

  • Saliva gene pathways(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Salivary cytokines(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Saliva microbiota(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Cortisol levels(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Warwick-Edinburgh Mental Wellbeing Scale(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Perceived Stress Scale(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Nature Relatedness Scale(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Skin bacteria(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Depression Scale(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Changes in nature contacts(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)
  • Infectious diseases(Baseline, 3 month, 1 year, 2 year, 3 year, 4 year, 5 year)

Investigators

Sponsor
Natural Resources Institute Finland
Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (2)

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