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

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

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19104
        • University of Pennsylvania

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
Greened Vacant Lot
A cluster of vacant lots is greened. People living around this area make up this cohort.
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.

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.
We will be performing qualitative interviews to assess perceptions of safety and violence. We will compare these perceptions over time between two groups.
measured twice - once during first month of study and once during 4th or 5th month.

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
Participants wear a heart rate monitor during a walk around their neighborhood.
measured twice - once during first month of study and once during 4th or 5th month of study
Violent crime statistics
Time Frame: Measured 6 months before intervention and 6 months after intervention
We will obtain crime statistics, including homicide, robbery, rape, and assault in the area around each cluster of vacant lots.
Measured 6 months before intervention and 6 months after intervention
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.
During a walk around the neighborhood, participants will point out items in the environment which they feel are safe or unsafe.
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.

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.

Clinical Trials on Violence Prevention

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