Nature and Well-Being Project
1 other identifier
interventional
74
1 country
1
Brief Summary
The investigators pilot test two intervention strategies to increase green space use- place-based and person-based, as well as evaluate the dose-response relationship between green space use and 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 Apr 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 13, 2020
CompletedFirst Posted
Study publicly available on registry
November 24, 2020
CompletedStudy Start
First participant enrolled
April 12, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 23, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
August 23, 2022
CompletedSeptember 1, 2022
August 1, 2022
1.4 years
November 13, 2020
August 31, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Green Space Use
This will measured using GPS data to see the amount of time spent in green space.
12 months
Secondary Outcomes (3)
Mental health and well-being: CES-D
12 months
Mental health and well-being: PSS-10
12 months
Mental health and well-being: WHO-5
12 months
Study Arms (4)
Nature Nook
EXPERIMENTALNature Nook builds on our prior work with a standard vacant lot greening intervention involving: removing trash, grading the land, planting new grass and trees, installing a low wooden perimeter fence, and regular maintenance. This greening intervention was designed as a blight removal strategy. People in this arm receive no intervention.
Nature Coach
EXPERIMENTALThe Nature Coach intervention, developed in a prior study (NCT04146025), will be delivered to people in their homes. Participants will live in the blocks immediately surrounding the study vacant lots randomized to this arm. The lots in this arm receive no intervention.
Nature Nook + Nature Coach
EXPERIMENTALThis is a combined arm: a place-based intervention (Nature Nook) and a person-based intervention (Nature Coach).
Control
NO INTERVENTIONThe study lots randomly selected for this arm, as well as the participants living near them, receive no intervention.
Interventions
The Nature Nook intervention will take place on lots that already have the standard greening intervention. In addition, design elements will be added such as a simple path and benches to explicitly invite people into the space. An additional difference is the exclusive use of larger, corner lots, rather than smaller mid-block spaces, to maximize visibility.
The Nature Coach Intervention consists of 3 components - home visit, text message follow up, and goal feedback. Home visit. During the 1-hour home visit, the coach will (a) provide education about the health benefits of nature, (b) identify nearby nature targets for the participant to visit, (c) complete a pre-commitment contract based on individualized weekly nature goals, and (d) brainstorm barriers and solutions to reaching the goals. Personalized weekly text messages. Texts will serve as reminders of goals set with the Nature Coach, as well as encouragement to meet the goals. The context of text messages with change slightly based on individual participants, the goals they set, and the barriers they identify. Goal feedback- At the end of each week, participants will receive a progression badge via text message that shows the amount of days and time they spent in nature, and how this matched up to the goal set with the Nature Coach.
The combined intervention will involve the installation of Nature Nooks to blighted vacant lots followed by the delivery of the Nature Coach intervention to people living in the immediate surrounding blocks. The intervention will be tailored to explicitly direct participants to use the Nature Nook.
Eligibility Criteria
You may qualify if:
- years or older
- Live in one of the 8 target neighborhoods identified
- Have a smartphone
- Able to understand and respond to an oral interview in English.
You may not qualify if:
- Unwilling to go outside
- Not ambulatory
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Pennsylvanialead
- American Heart Associationcollaborator
- Pennsylvania Horticultural Societycollaborator
- United States Forest Servicecollaborator
- OLIN Studiocollaborator
Study Sites (1)
University of Pennsylvania, Department of Emergency Medicine
Philadelphia, Pennsylvania, 19104, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Eugenia South, MD MS
University of Pennsylvania
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 13, 2020
First Posted
November 24, 2020
Study Start
April 12, 2021
Primary Completion
August 23, 2022
Study Completion
August 23, 2022
Last Updated
September 1, 2022
Record last verified: 2022-08