Actively Recruiting
Biological and Behavioral Outcomes of Community Nature Walks
Led by Charlotte Tate · Updated on 2023-09-28
200
Participants Needed
1
Research Sites
186 weeks
Total Duration
On this page
Sponsors
C
Charlotte Tate
Lead Sponsor
U
University of California, San Francisco
Collaborating Sponsor
AI-Summary
What this Trial Is About
The investigators will test the efficacy of our proposed intervention to reduce embodied stress in four racial/ethnic groups (Black, Latinx, Pilipinx, and Pacific Islander) as a preventative intervention for health disparities found in these communities. The intervention is comprised of two phases. The first consists of community nature walks in a pristine redwood forest for six months. This is followed by chosen nature activities with family and/or friends for three months. The investigators will test the ability of these activities in nature to reduce chronic stress that underpins many health disparities using validated biological, behavioral, and sociocultural measures. The use of these measures is in alignment with the National Institute of Minority Health and Health Disparities (NIMHD) Research Framework, and will increase understanding of individual, interpersonal, community, and social level factors that lead to, and that can eliminate health disparities.
CONDITIONS
Official Title
Biological and Behavioral Outcomes of Community Nature Walks
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years or older
- Able to commit to a 9-month Nature Intervention (6-month walks; 3-month chosen nature activity)
- Spoken languages: English, Spanish, or Tagalog
- Able-bodied and must be able to walk
You will not qualify if you...
- Pregnant women and other gender identities who are pregnant
- Prisoners
- Cognitively impaired individuals
AI-Screening
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Trial Site Locations
Total: 1 location
1
San Francisco State University
San Francisco, California, United States, 94132
Actively Recruiting
Research Team
C
Charlotte Tate, Ph.D.
CONTACT
L
Leticia Marquez-Magana, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
PREVENTION
Number of Arms
1
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