Actively Recruiting

Phase 1
Age: 18Years +
All Genders
Healthy Volunteers
NCT06056375

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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