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Depressive SymptomsNCT06989801

Benefits of Outdoor Walks in Reducing Depressive Symptoms

A study testing Urban Walk, Nature Walk and Active Nature Walk in people with Depressive Symptoms, run by University of Washington at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Depressive Symptoms
What is being tested?
Urban Walk, Nature Walk and Active Nature Walk
Could I receive a placebo?
No, everyone receives an active treatment
How many people
138 participants
Where
2 sitesUnited States
Study dates
11 Apr 2025to 27 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

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

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Condon Hall

    Seattle, Washington, 98105

  • Merrill Hall

    Seattle, Washington, 98105

Other trials in United States

About this study

Official title: Benefits of a Nature Walk vs. an Urban Walk in Reducing Depressive Symptoms: A Randomized Controlled Study Among College Students

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.

Read more

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.
Read the detailed 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.

Being tested
Urban Walk, Nature Walk, Active Nature Walk
Medical subject headings
Depression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Urban WalkBehavioural

    For each session, participants will take a 30-minute walk in an urban environment along a designated looped route. They will walk at a comfortable pace and follow the assigned path. During the walk, participants will be instructed to experience their surroundings as naturally as possible. No specific activities beyond walking are required.

    To fully immerse in the experience, participants will be asked to avoid using their phones unless necessary (e.g., in case of an emergency). They should keep the GPS app recording throughout the walk without interacting with it-just allow it to run in the background.

    Once the loop is completed, participants will stop the GPS recording and return to the starting point, where a research team member will be waiting. They will then be guided indoors to complete a brief post-walk survey and participate in a short interview to share their experience.

  • Nature WalkBehavioural

    For each session, participants will take a 30-minute walk in a natural environment along a designated looped route. They will walk at a comfortable pace and follow the assigned path. During the walk, participants will be instructed to experience their surroundings as naturally as possible. No specific activities beyond walking are required.

    To fully immerse in the experience, participants will be asked to avoid using their phones unless necessary (e.g., in case of an emergency). They should keep the Gaia GPS app recording throughout the walk without interacting with it-just allow it to run in the background.

    Once the loop is completed, participants will stop the GPS recording and return to the starting point, where a research team member will be waiting. They will then be guided indoors to complete a brief post-walk survey and participate in a short interview to share their experience.

  • Active Nature WalkBehavioural

    For each session, participants will take a 30-minute walk in a natural area, following a designated looped route. Unlike a regular walk, participants will be encouraged to engage with nature (e.g., listening to natural sounds, looking for birds, and touching flowers).

    To make the most of the walk, participants will be asked to avoid using their phones unless necessary (e.g., in case of an emergency). They should keep the Gaia GPS app recording throughout the walk without interacting with it-just letting it run in the background.

    Once the loop is completed, participants will stop the GPS recording and return to the starting point, where a research team member will be waiting. They will then be guided indoors to complete a brief post-walk survey and participate in a short interview to share their experience.

Study groups in NCT06989801
Study groupRoleWhat they receive
Urban WalkActive comparatorRegular walks in an urban area, 30 minutes twice a week for 3 weeks.
Receives: Behavioral: Urban Walk
Nature WalkExperimentalRegular walks in a natural area, 30 minutes twice a week for 3 weeks.
Receives: Behavioral: Nature Walk
Active Nature WalkExperimentalRegular 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.
Receives: Behavioral: Active Nature Walk

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Patient Health Questionnaire

    Patient Health Questionnaire measures the severity of depressive symptoms. It includes nine items that evaluate symptoms such as persistent sad, loss of interest or pleasure in activities, fatigue, and lack of energy. Each item is rated on a 4-point Likert scale, ranging from 0 (not at all) to 3 (nearly every day). Higher scores indicate more severe symptoms of depression.

    Measured: Right before the first walking session, immediately after the sixth walking session, and one month after the sixth walking session.

Secondary outcomes (5)
  1. Generalized Anxiety Disorder 7-item scale

    Generalized Anxiety Disorder 7-item scale measures the severity of anxiety. It includes seven items, such as persistent nervousness, excessive worrying, difficulty relaxing, feeling restless, and becoming easily irritated. Each item is rated on a 4-point Likert scale, ranging from 0 (not at all) to 3 (nearly every day). Higher scores indicate more severe anxiety.

    Measured: Right before the first walking session, immediately after the sixth walking session, and one month after the sixth walking session.

  2. Positive and Negative Affect Scale

    Positive and Negative Affect Scale measures positive and negative affect. The scale consists of 20 items, with 10 assessing positive affect (e.g., "passionate," "excited") and 10 assessing negative affect (e.g., "distressed," "upset"). Participants rated how strongly they experienced each emotion on a 5-point Likert scale, from 1 (very slightly or not at all) to 5 (very strongly).

    Measured: Right before the first walking session, immediately after the sixth walking session, and one month after the sixth walking session.

  3. Cognitive Flexibility Inventory

    Cognitive Flexibility Inventory measures individuals' ability to adapt to changing situations and consider multiple perspectives. Participants rated each item on a 5-point Likert scale, ranging from 1 (never) to 5 (always). Higher scores indicate greater cognitive flexibility.

    Measured: Right before the first walking session, immediately after the sixth walking session, and one month after the sixth walking session.

  4. Extended Inclusion of Nature in Self scale

    Extended Inclusion of Nature in Self scale measures individuals' perceived connection with nature, which refers to the degree to which individuals incorporate nature into their self-concept. Each item consists of seven pictures, scored on a 7-point scale, with higher scores indicating a stronger connection to nature.

    Measured: Right before the first walking session, immediately after the sixth walking session, and one month after the sixth walking session.

  5. Presence Scale

    Presence Scale measures the state of being in which conditioned thinking ceases, and the mind is open, aware, non-reactive, and still; and often a witness of itself. Participants rated each item on a 7-point Likert scale, ranging from 1 (not at all) to 7 (completely). Higher scores indicate higher levels of Presence.

    Measured: Immediately after each walking session.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 May 2025
  2. Study start11 Apr 2025
  3. Primary completion17 Dec 2025
  4. Study completion27 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
138 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06989801
Sponsor's protocol ID
STUDY00022242
Status last verified
Apr 2026
First submitted
11 Apr 2025
Last updated
4 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Urban Walk, Nature Walk and Active Nature Walk in people with Depressive Symptoms, run by University of Washington at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Patient Health Questionnaire (time frame: Right before the first walking session, immediately after the sixth walking session, and one month after the sixth walking session.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 May 2026.

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Clinical Trial NCT06989801 | AzTrials