Actively Recruiting

Phase Not Applicable
Age: 1Year - 5Years
All Genders
Healthy Volunteers
NCT06390878

Nationwide Research on the Rewilding of Kindergarten Yards

Led by Natural Resources Institute Finland · Updated on 2024-06-24

320

Participants Needed

2

Research Sites

171 weeks

Total Duration

On this page

Sponsors

N

Natural Resources Institute Finland

Lead Sponsor

T

Tampere University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Biodiversity is essential for nature and human well-being. Land use has reduced biodiversity in cities that is associated with altered commensal microbiota and a rising burden of immunological disorders among urban children. The investigators will estimate how rewilding of kindergarten yards affects commensal microbiome, prevalence of allergies, asthma, atopic dermatitis and infections, cortisol levels, cognitive skills and plasma cytokine levels of children. Our specific aims are: To assess if rewilding diversifies health-associated skin, saliva and gut microbiota and reduces infectious diseases and atopic or allergic symptoms. Assess whether the rewilding has positive effects on cognitive skills. Assess whether the rewilding changes cortisol and plasma cytokine levels. The investigators will recruit altogether 320 (160 per treatment) study subjects aged between 1-5 to questionnaire study (Task 2), from which 120 study subjects will be analyzed more detailed using microbiological and blood samples (Task 1).

CONDITIONS

Official Title

Nationwide Research on the Rewilding of Kindergarten Yards

Who Can Participate

Age: 1Year - 5Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Attendance in kindergarten
Not Eligible

You will not qualify if you...

  • Use of antibiotics in the year before sampling

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Natural Resources Institute Finland

Helsinki, Uusimaa, Finland, 00970

Actively Recruiting

2

Tampere University

Tampere, Finland

Actively Recruiting

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Research Team

S

Sanna Hurtola

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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