- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01336374
Vacant Lot Greening and Violence-Related Outcomes
December 2, 2011 updated by: University of Pennsylvania
A Pilot Randomized Controlled Trial of Vacant Lot Greening and Violence-related Outcomes
The purpose of this study is to determine the impact of vacant lot greening on perceptions of safety and violence for residents living around the lots.
We hypothesize that people living around lots that are greened will have improved perception of safety.
Study Overview
Status
Completed
Conditions
Detailed Description
Violence is a serious health problem in the US, and especially in Philadelphia, as the city ranks first in violent crime amongst the ten largest US cities.
The determinants of violent crime range from individual to community level factors.
In this study, we focus on physical incivilities in the built environment, specifically vacant lots, as they have been associated with violent crime.
Physical incivilities are also associated with individual perceptions of crime and safety, and subsequently, negative health outcomes.
However, prior research has been observational and retrospective.
We aim to expand this body of work through a randomized community intervention trial of vacant lot greening to explore causal mechanisms between vacant lots and violent crime outcomes.
This pilot study, in partnership with the Pennsylvania Horticultural Society, will investigate the feasibility of a vacant lot greening intervention, and explore how vacant lot greening changes resident perception about violence, fear, stress, and neighborhood disorder, as well as violent crime in the surrounding area.
We will interview residents living around the greened and non-greened lots during a joint walk around a pre-determined route, which will ensure exposure to our intervention.
We will also use violent crime data (homicide, aggravated assault, robbery, and rape) from the Philadelphia Police Department.
Results of this pilot trial will be used to develop a full scale vacant lot greening grant to be submitted to the National Institutes of Health or the National Institute of Justice.
Study Type
Observational
Enrollment (Actual)
29
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Residents living around two seperate sites (one site where vacant lots are greened and a control site where vacant lots are not greened).
Description
Inclusion Criteria:
- Age 18-65
- Lives in home
- Ability to walk unassisted and without difficulty for 10 blocks
Exclusion Criteria:
- One resident per house
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Greened Vacant Lot
A cluster of vacant lots is greened.
People living around this area make up this cohort.
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Control Site
The control site is a cluster of vacant lots that will not be greened.
The people living around these lots make up the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceptions of safety and violence
Time Frame: measured twice - once during first month of study and once during 4th or 5th month.
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We will be performing qualitative interviews to assess perceptions of safety and violence.
We will compare these perceptions over time between two groups.
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measured twice - once during first month of study and once during 4th or 5th month.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart Rate
Time Frame: measured twice - once during first month of study and once during 4th or 5th month of study
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Participants wear a heart rate monitor during a walk around their neighborhood.
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measured twice - once during first month of study and once during 4th or 5th month of study
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Violent crime statistics
Time Frame: Measured 6 months before intervention and 6 months after intervention
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We will obtain crime statistics, including homicide, robbery, rape, and assault in the area around each cluster of vacant lots.
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Measured 6 months before intervention and 6 months after intervention
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Safe/Unsafe items in the environment
Time Frame: measured twice - once during the first month of the study and once during the 4th or 5th month.
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During a walk around the neighborhood, participants will point out items in the environment which they feel are safe or unsafe.
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measured twice - once during the first month of the study and once during the 4th or 5th month.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Eugenia C Garvin, MD, University of Pennsylvania
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2011
Primary Completion (ACTUAL)
August 1, 2011
Study Completion (ACTUAL)
September 1, 2011
Study Registration Dates
First Submitted
April 13, 2011
First Submitted That Met QC Criteria
April 13, 2011
First Posted (ESTIMATE)
April 15, 2011
Study Record Updates
Last Update Posted (ESTIMATE)
December 5, 2011
Last Update Submitted That Met QC Criteria
December 2, 2011
Last Verified
December 1, 2011
More Information
Terms related to this study
Other Study ID Numbers
- 813112
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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