Nature and Health: How Does Lifestyle and Environment Affect Health and Wellness
1 other identifier
interventional
134
1 country
1
Brief Summary
The purpose of this study is to examine if and how implementing nature prescriptions can increase time in nature and improve health to yield an actionable understanding of the nature-health connection. It aims to explore how public green spaces can be better used to improve individual and community health. Finally, this study aims to advance science by conducting a randomized controlled trial to improve understanding of the linkages between time in nature and human health.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 14, 2023
CompletedFirst Posted
Study publicly available on registry
August 21, 2023
CompletedStudy Start
First participant enrolled
December 18, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 23, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 23, 2025
CompletedMay 6, 2025
May 1, 2025
1.3 years
August 14, 2023
May 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Nature Exposure Scale II (NES-II)
Assess each participant's exposure to nature in everyday life. The Nature Exposure Scale II uses a 5-point likert scale for each item. Higher score means greater exposure to nature. The total score is an average of all the items included.
Baseline and 6-months
Secondary Outcomes (12)
CDC Health related quality of life - 14 (CDC-HRQOL-14)
Baseline and 6-months
Brief-Pittsburgh Sleep Quality Index (B-PSQI)
Baseline and 6-months
Perceived Stress Scale (PSS-10)
Baseline and 6-months
International Physical Activity Questionnaire Short form (IPAQ-S)
Baseline and 6-months
Patient Health Questionnaire (PHQ-8/PHQ-A)
Baseline and 6-months
- +7 more secondary outcomes
Study Arms (2)
Intervention
EXPERIMENTALThe treatment group will receive information regarding wellness factors by the doctor (health advice) and they will be asked to follow those recommendations for the duration of the study. In addition they will also receive a park prescription specifying a target amount of time to spend in nature, along with frequency of visits and recommended locations (e.g., specific parks), and information about parks and programming in the study area.
Control
OTHERThe control group will receive regular health advice and information regarding wellness factors by the doctor and they will be asked to follow those recommendations for the duration of the study.
Interventions
The park prescription given by the patients care-provider includes information about the health benefits of spending time in nature and detailed information about the parks in the neighboring area. As well as access to a web-based platform called ParkRx which includes information and details about events in the parks in the study area. Together with information about the frequency and duration of visits to the parks.
Regular health advice relating to lifestyle factors that can decrease the risk of chronic disease and/or reducing the burden of an existing chronic disease. Areas included are diet, physical activity, sleep, stress and medications.
Eligibility Criteria
You may qualify if:
- Participants must be a patient of the AHN Forbes Family Medicine clinic.
- Participants must have one or more chronic conditions, or significant lifestyle risks as identified by their healthcare provider.
- Participants must be between 13-65 years old.
- Participants must be willing and able to provide informed consent to participate
- Participants under 18 must be willing and able to assent for themselves and obtain parental consent.
- Participants must be willing to comply with all study procedures for the duration of the study.
- Participants must reside in the greater Pittsburgh area for the duration of 6-month study.
- Participants must have a smartphone that is capable of running the Urban Mind App and connecting to the Garmin wearable device (iPhone 6 and newer as well as most Android phones).
- Minors who participate must have their own smartphone.
- Participants must have their own email address to register with the Urban Mind App and the Garmin App.
- Only one participant from a household may enroll in the study.
- Participants must be able to comprehend written English (questionnaires will be provided to participants in English).
- Participants may not be an employee of Forbes Family Medicine clinic
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Forbes Family Medicine/AHN Research Institute
Monroeville, Pennsylvania, 15146, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gretchen Daily, PhD
Stanford University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 14, 2023
First Posted
August 21, 2023
Study Start
December 18, 2023
Primary Completion
April 23, 2025
Study Completion
April 23, 2025
Last Updated
May 6, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share