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Benefits of Outdoor Walks in Reducing Depressive Symptoms

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University of Washington

Status

Enrolling

Conditions

Depressive Symptoms

Treatments

Behavioral: Active Nature Walk
Behavioral: Nature Walk
Behavioral: Urban Walk

Study type

Interventional

Funder types

Other

Identifiers

NCT06989801
STUDY00022242

Details and patient eligibility

About

The goal of this clinical trial is to determine whether outdoor walking in different environments-urban or natural-can reduce depressive symptoms among college students. The study also tests whether providing prompts for active engagement during nature walks enhances the benefits compared to unstructured nature walks.

Participants will be randomly assigned to one of three groups: (1) urban walk, (2) nature walk, or (3) active nature walk with guided interaction. Each participant will walk for 30 minutes, twice a week, for 3 weeks, complete questionnaires, and participate in interviews.

Our primary outcome (PHQ-9) will be used to test the following two primary hypotheses:

  • Hypothesis 1: Participants in both nature walk conditions (combined) will show greater reductions in depressive symptoms (PHQ-9) than those in the urban walk group.
  • Hypothesis 2: Participants in the active nature walk will show greater reductions than those in the regular nature walk.

Full description

The investigators aim to compare how walking in different outdoor environments influences depressive symptoms among college students. Specifically, the investigators will assess:

  1. walking in an urban environment (like a busy city street),
  2. walking in a natural environment regularly (e.g., walking without specific guidance), and
  3. walking in a natural environment with guided interaction prompts (e.g., noticing birds, listening to sounds, touching flowers).

Standardized questionnaires will measure changes in depressive symptoms, anxiety, affect, cognitive flexibility, nature connection, and Presence across all three groups.

The investigators will also explore potential mechanisms behind any observed effects, including interaction patterns, presence, cognitive changes, and emotional responses to the different environments.

Enrollment

180 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • College students in Seattle
  • Aged over 18.
  • Having depressive symptoms with self-rated Patient Health Questionnaire-9 (PHQ-9) scored higher than 5.
  • Normal or corrected-to-normal visual acuity.
  • No identified hearing impairment.
  • No history of neurological or mental disorders.

Exclusion criteria

  • Receiving clinical psychiatric treatment or psychological counseling.
  • Failing in providing consent form.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

180 participants in 3 patient groups

Urban Walk
Active Comparator group
Description:
Regular walks in an urban area, 30 minutes twice a week for 3 weeks.
Treatment:
Behavioral: Urban Walk
Nature Walk
Experimental group
Description:
Regular walks in a natural area, 30 minutes twice a week for 3 weeks.
Treatment:
Behavioral: Nature Walk
Active Nature Walk
Experimental group
Description:
Regular walks in a natural area, 30 minutes twice a week for 3 weeks. Prior to the walk, participants will be instructed to actively interact with the natural environment.
Treatment:
Behavioral: Active Nature Walk

Trial contacts and locations

2

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Central trial contact

Xuanyi Wang; Peter H Kahn, Ph.D.

Data sourced from clinicaltrials.gov

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