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Walking Green: The Effects of Walking in Forested and Urban Areas (NUWG)

Primary Purpose

Mood, Stress, Anxiety

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Walking
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mood focused on measuring nature, walk, stress, Green Walking, Physical Activity, Environment, anxiety, mood

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • over the age of 18
  • under the age of 35
  • no current infections / recent infections (<2weeks)
  • PAR-Q+ scores indicative of readiness to engage in physical activity

Exclusion Criteria:

  • Women who are pregnant or breast-feeding
  • Inability to consent
  • Incarcerated Persons
  • non-adults

Sites / Locations

  • Northwestern University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Forest

Urban

Arm Description

Each subject is exposed to a 50 minute walk in a "green location" at some point during the crossover experiment. The psychological and physiological measurements taken during these walk location weeks are compared to the measurements from the other location. In addition a 'control' day is assigned for each location (ADL).

Each subject is exposed to a 50 minute walk in a "gray location" at some point during the crossover experiment. The psychological and physiological measurements taken during these walk location weeks are compared to the measurements from the other location. In addition a 'control' day is assigned for each location (ADL).

Outcomes

Primary Outcome Measures

Psychological Effects - Mood
Change in Positive and Negative Affect scale 0 = never, 4 = very often. Higher Positive Affect scores reflect better reported mood scores. Lower Negative Affect Scores reflect better mood scores. Average values based on age
Psychological Effects - Anxiety
change in STAI (STAI-TRAIT anxiety) score based on a Likert scale self reported score. Higher scores indicate a higher level of self-reported anxiety.
Psychological Effects - Attention
change in vBDS (backward digit span) score lower scores indicate a increased inability to properly recall the numbers in the test.
Psychological Effects - Depression
change in CESD score. Possible range of scores is 0 to 60, with the higher scores indicating the presence of more symptomatology. Citation: Radloff LS: The CES-D Scale: a self-report depression scale for research in the general population.

Secondary Outcome Measures

Physiological Effects - Blood Glucose
Glucose levels as markers of health and wellness. (mg/dL)
Physiological Effects - Salivary Cortisol
Diurnal cortisol dynamics measured by salivary cortisol (ug/dl), as the normal drop in cortisol during the day is attenuated by exposure to chronic stress.
Physiological Effects - Blood
Pro- and anti-inflammatory cytokine concentrations in blood (pg/mL), as stress typically induces an inflammatory response
Physiological Effects - Heart Rate Variation
changes in HRV is indicative of parasympathetic input (milliseconds), higher HRV correlating to reduced stress.

Full Information

First Posted
May 13, 2019
Last Updated
May 1, 2023
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT03950661
Brief Title
Walking Green: The Effects of Walking in Forested and Urban Areas
Acronym
NUWG
Official Title
Walking Green: The Effects of Walking in Forested and Urban Areas on Health and Well-being
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
June 1, 2016 (Actual)
Primary Completion Date
August 14, 2017 (Actual)
Study Completion Date
December 8, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This research hypothesizes that moderate physical activity in a "green environment" (e.g. a forest preserve path) has increased benefits on psychological measures (stress, anxiety, mood, depression, attention) and on physiological measures (Heart Rate Variability, Blood Glucose, Salivary Cortisol) when directly compared to activity in a "gray environment" (urban or suburban sidewalks). The study design is a randomized crossover design in which each subject is assigned randomly to a group which determines the order in which participants will walk in each location. Subjects will take three 50-minute walks per location in one week, with half of the subjects taking the urban walks first as per group assignment. Control data are collected on days when participants do not walk. Physiological data are taken during walks and control periods (heart rate, heart rate variation). Biomarker samples (saliva, dried blood spots) are taken on selected days. Psychological data are take before and after walks and control periods.
Detailed Description
This study records the psychological and physiological effects of green vs gray walks during a longitudinal crossover study on 41 participants. In accordance with the Attention Restoration and Stress Recovery theories we hypothesize that exposure to a green environment will have beneficial health outcomes for participants both psychologically (mood, stress, anxiety, depression, attention) and physiologically (blood glucose, heart rate variability, cortisol). Participants will be randomly assigned to a study group which determines the order in which they will walk in either the gray or green location. The study takes place for 29 days of which only 9 are active study dates. The cross-over design controls for training effects that may result from the regular physical activity. Participants provided informed consent on Day 1. Walks will be monitored on Days 8, 12, 22, 26, while walks on days 10 and 24 have no monitoring to reduce testing burden. Days 15 and 29 are control days in which the participants are monitored during the day (Activities of Daily Living) as a control against the location they had previously walked in. No walks will be taken between days 12 and 21 to provide a washout period from the previous location. Psychological tests are administered by computer using the Qualtrics software platform to assess: Positive and Negative Affect Scale (PANAS) Center for Epidemiological Studies Depression Scale (CESD) State and Trait Anxiety Inventory (STAI) Cohen's Perceived Stress Scale (UCLA) Perceived Isolation Scale Nature Relatedness Scale (NR-6) Anthropometric measures are taken on days 1, 8, 15, 22, and 29. Physiological effects are studied through heart rate monitoring during all monitored walks via a Zephyr Omnisense which records heart information as well as activity, temperature and breathing rate. Salivary cortisol is collected on days 7, 14, 21, and 28 by the participant. Blood glucose is measured on days 8, 12, 15, 22, 26, and 29; dried blood spots are collected for future analysis of inflammatory biomarkers. Hypotheses will be tested using fixed and random effects linear regression models using the appropriate statistical procedures in SAS 9.4 to test for main effects, covariates, and other confounding variables that were measured throughout the study including individuals' reported stress and tiredness, and the weather conditions of the day.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mood, Stress, Anxiety, Depression, Obesity, Health Behavior, Physical Activity
Keywords
nature, walk, stress, Green Walking, Physical Activity, Environment, anxiety, mood

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Randomized cross over design. Repeated measures.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
82 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Forest
Arm Type
Experimental
Arm Description
Each subject is exposed to a 50 minute walk in a "green location" at some point during the crossover experiment. The psychological and physiological measurements taken during these walk location weeks are compared to the measurements from the other location. In addition a 'control' day is assigned for each location (ADL).
Arm Title
Urban
Arm Type
Experimental
Arm Description
Each subject is exposed to a 50 minute walk in a "gray location" at some point during the crossover experiment. The psychological and physiological measurements taken during these walk location weeks are compared to the measurements from the other location. In addition a 'control' day is assigned for each location (ADL).
Intervention Type
Other
Intervention Name(s)
Walking
Primary Outcome Measure Information:
Title
Psychological Effects - Mood
Description
Change in Positive and Negative Affect scale 0 = never, 4 = very often. Higher Positive Affect scores reflect better reported mood scores. Lower Negative Affect Scores reflect better mood scores. Average values based on age
Time Frame
29 days
Title
Psychological Effects - Anxiety
Description
change in STAI (STAI-TRAIT anxiety) score based on a Likert scale self reported score. Higher scores indicate a higher level of self-reported anxiety.
Time Frame
29 days
Title
Psychological Effects - Attention
Description
change in vBDS (backward digit span) score lower scores indicate a increased inability to properly recall the numbers in the test.
Time Frame
29 days
Title
Psychological Effects - Depression
Description
change in CESD score. Possible range of scores is 0 to 60, with the higher scores indicating the presence of more symptomatology. Citation: Radloff LS: The CES-D Scale: a self-report depression scale for research in the general population.
Time Frame
29 days
Secondary Outcome Measure Information:
Title
Physiological Effects - Blood Glucose
Description
Glucose levels as markers of health and wellness. (mg/dL)
Time Frame
29 days
Title
Physiological Effects - Salivary Cortisol
Description
Diurnal cortisol dynamics measured by salivary cortisol (ug/dl), as the normal drop in cortisol during the day is attenuated by exposure to chronic stress.
Time Frame
29 days
Title
Physiological Effects - Blood
Description
Pro- and anti-inflammatory cytokine concentrations in blood (pg/mL), as stress typically induces an inflammatory response
Time Frame
29 days
Title
Physiological Effects - Heart Rate Variation
Description
changes in HRV is indicative of parasympathetic input (milliseconds), higher HRV correlating to reduced stress.
Time Frame
29 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: over the age of 18 under the age of 35 no current infections / recent infections (<2weeks) PAR-Q+ scores indicative of readiness to engage in physical activity Exclusion Criteria: Women who are pregnant or breast-feeding Inability to consent Incarcerated Persons non-adults
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Teresa Horton
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Evanston
State/Province
Illinois
ZIP/Postal Code
60208
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Walking Green: The Effects of Walking in Forested and Urban Areas

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