New York State Gun Violence Reduction Project

Last registered on January 23, 2024

Pre-Trial

Trial Information

General Information

Title
New York State Gun Violence Reduction Project
RCT ID
AEARCTR-0012863
Initial registration date
January 23, 2024

Initial registration date is when the trial was registered.

It corresponds to when the registration was submitted to the Registry to be reviewed for publication.

First published
January 23, 2024, 1:18 PM EST

First published corresponds to when the trial was first made public on the Registry after being reviewed.

Locations

Region

Primary Investigator

Affiliation
United States Air Force Academy

Other Primary Investigator(s)

PI Affiliation
Princeton

Additional Trial Information

Status
Completed
Start date
2012-09-01
End date
2022-01-01
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
Can gun violence be deterred at low cost? We report the results of a randomized experiment of a messaging intervention which was designed to reduce gun violence among individuals under parole supervision with a prior violent felony conviction or firearm arrest. The intervention consisted of a group meeting in which high-risk paroled individuals were notified of the sanction they would face upon reoffending while being offered community resources to support re-integration into the community. The program did not lead to a reduction in gun violence or create community spillover effects but did reduce parole violations by 15%.
External Link(s)

Registration Citation

Citation
LaForest-Tucker, Michael and Patrick Sharkey. 2024. "New York State Gun Violence Reduction Project ." AEA RCT Registry. January 23. https://doi.org/10.1257/rct.12863-1.0
Experimental Details

Interventions

Intervention(s)
Intervention Start Date
2013-02-01
Intervention End Date
2014-07-31

Primary Outcomes

Primary Outcomes (end points)
Arrests and parole violations
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
The New York State GVRP was implemented in five sites across the state of New York. Two sites were in Albany and Schenectady, mid-sized cities several hours north of New York City. The remaining three sites were in New York City, one each in the Bronx, Manhattan, and Brooklyn. Individuals living in these communities were eligible for the forums if they (1) were on parole, (2) had been convicted of a violent felony or had a prior firearm arrest, (3) did not have a mental health diagnosis or a prior sexual assault charge, (4) had lived within the targeted area for at least 30 consecutive days, and (5) had been released from prison within the prior two years. Forums took place between August 2012 and July 2014 in each of the five sites, with randomized assignment of attendees taking place between February 2013 and July 2014.

Treatment assignment involved two stages of randomization in each of the three NYC study sites. In a first stage of randomization, census tracts within each area were randomly assigned to a “neighborhood treatment group” and a “neighborhood control group.” Individuals who lived within the treated communities were eligible to be called in to the forums. Individuals in the control communities were not eligible to be called in. In the Albany and Schenectady sites, no neighborhood level randomization occurred due to the substantially smaller eligible populations in these cities. In these two sites, all eligible individuals were classified as belonging to the neighborhood treatment group.

In all five study sites, eligible individuals were then randomly assigned to an “individual treatment group” and an “individual control group.” Thus, in the NYC study sites, eligible individuals belonged to one of four study groups based on their combination of neighborhood treatment group and individual treatment group. Only individuals in both the neighborhood and individual treatment group (Group 1) were eligible to be called in to the forums. In the Albany and Schenectady sites, eligible individuals belonged to one of two study groups – an individual treatment group and an individual control group. In these sites, all individuals in the individual treatment group were eligible to be called in.
Experimental Design Details
Randomization Method
In office by a computer
Randomization Unit
Treatment assignment involved two stages of randomization in each of the three NYC study sites. In a first stage of randomization, census tracts within each area were randomly assigned to a “neighborhood treatment group” and a “neighborhood control group.” Individuals who lived within the treated communities were eligible to be called in to the forums. Individuals in the control communities were not eligible to be called in. In the Albany and Schenectady sites, no neighborhood level randomization occurred due to the substantially smaller eligible populations in these cities. In these two sites, all eligible individuals were classified as belonging to the neighborhood treatment group.
Was the treatment clustered?
Yes

Experiment Characteristics

Sample size: planned number of clusters
171
Sample size: planned number of observations
3557
Sample size (or number of clusters) by treatment arms
Neighborhood treatment + individual treatment: 1101
Neighborhood treatment + individual control: 1054
Neighborhood control + individual treatment: 710
Neighborhood control + individual control: 692
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
IRB

Institutional Review Boards (IRBs)

IRB Name
IRB Approval Date
IRB Approval Number

Post-Trial

Post Trial Information

Study Withdrawal

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Intervention

Is the intervention completed?
No
Data Collection Complete
Data Publication

Data Publication

Is public data available?
No

Program Files

Program Files
Reports, Papers & Other Materials

Relevant Paper(s)

Reports & Other Materials