Cash Transfers for Reentry

April 16, 2026 updated by: University of Pennsylvania
Investigators will execute a mixed methods randomized controlled trial to determine the impacts of cash transfers of $1,000 per month for one month followed by $750 for eleven months. Investigators will measure the impacts of the cash transfers on physical and mental health, housing stability, healthcare utilization, financial stability, and interactions with the criminal legal system.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

The transition from incarceration to community reintegration represents a finite time period of unique challenges, often exacerbated by fines and other structural constraints associated with limited access to housing, the workforce, and public benefits. As such, individuals exiting prisons are most vulnerable for recidivism and other poor wellbeing outcomes during the initial period after their release.

The project will enroll approximately 200 individuals in the Omaha, NE area to receive cash transfers over a one year period. Another 250 will be assigned to the control group and will not receive the cash transfers but will be eligible to participate in research activities. Adults exiting Nebraska state prisons will be eligible to participate if they are exiting prison during the specified time frame and do not have a conviction of a sex crime or homicide.

Longitudinal repeated measures will be utilized through surveys conducted at baseline, 6 months, 12 months, and 18 month intervals. Future involvement with the criminal legal system will be measured using linked administrative data from the Department of Corrections. A select group of 30 participants across study groups will also be invited to participate in in-depth interviews with a CGIR research scientist and team at multiple time points.

Study Type

Interventional

Enrollment (Estimated)

450

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion criteria:

  • Aged 18 or older
  • Exiting Nebraska state prisons during the study enrollment period

Exclusion criteria:

- Conviction of a sex crime or homicide

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
No intervention
Experimental: Treatment
Recipients of stipend
Provision on monthly cash transfer

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Post-release compliance with payment of fees
Time Frame: 1 year post release date or for the duration of required supervision, whichever is sooner
Compliance/non-compliance with post-release payment of fees. A count of fee payments (continuous) and on-time payment as a binary outcome variable (y/n) for each instance.
1 year post release date or for the duration of required supervision, whichever is sooner
Recidivism
Time Frame: 1 year following release date
As applied to adults, recidivism shall mean a final conviction of a Class I or II misdemeanor, a Class IV felony or above, or a Class W misdemeanor based on a violation of state law within 1 year of being successfully released.
1 year following release date
Post-release compliance with conditions
Time Frame: 1 year post release date or for the duration of required supervision, whichever is sooner
Compliance/non-compliance with post-release conditions. A count of instances for each condition bounded by dates of conditions imposed.
1 year post release date or for the duration of required supervision, whichever is sooner

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Housing status
Time Frame: Baseline, 6 months, 12 months
Housing status (e.g., renter, homeowner, rent-to-own, etc.) reported in the prior month.
Baseline, 6 months, 12 months
Food security (Household Food Insecurity Access Scale)
Time Frame: Baseline, 6 months, 12 months
9 items to assess past four week food insecurity: 1) worry about not having enough food, 2) inability to eat preferred foods, 3) eating a limited variety of foods, 4) having to eat foods that they did not want to eat, 5) eating a smaller meal than needed, 6) eating fewer meals in a day, 7) having no food to eat, 8) going to sleep at night hungry, and 9) going a whole day and night without eating. Items scored as "yes" (1) or "no" (0).
Baseline, 6 months, 12 months
Employment
Time Frame: Baseline, 6 months, 12 months
Employment status as measured by one item with attributes per the U.S. Department of Labor.
Baseline, 6 months, 12 months
Financial wellbeing (Consumer Financial Protection Bureau Financial Wellbeing Scale)
Time Frame: Baseline, 6 months, 12 months
Each item is scored 0 to 4 and summed to a total. The sum total is then converted to a total response value on the CFPB Financial Well-Being Scale score from 0-100, where higher scores indicate a greater sense of financial well-being.
Baseline, 6 months, 12 months
Psychological distress (Kessler 6)
Time Frame: Baseline, 6 months, 12 months
Each item is scored from zero "none of the time" to four "all of the time." Scores of the 6 items are then summed, yielding a minimum score of 0 and a maximum score of 24. Low scores indicate low levels of psychological distress and high scores indicate high levels of psychological distress.
Baseline, 6 months, 12 months
General health
Time Frame: Baseline, 6 months, 12 months
Self-reported general health as measured by one question from the SF-36: "In general, would you say your health is:", with a 5-point scale from Poor to Excellent.
Baseline, 6 months, 12 months
Substance use (UNCOPE)
Time Frame: Baseline, 6 months, 12 months
Six items, each scored 0 (no) or 1 (yes). A score of two or more indicates possible substance misuse.
Baseline, 6 months, 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Amy Castro, PhD, The University of Pennsylvania
  • Principal Investigator: Stacia West, PhD, The 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 (Estimated)

June 1, 2026

Primary Completion (Estimated)

December 15, 2028

Study Completion (Estimated)

December 15, 2029

Study Registration Dates

First Submitted

November 17, 2025

First Submitted That Met QC Criteria

December 2, 2025

First Posted (Actual)

December 4, 2025

Study Record Updates

Last Update Posted (Actual)

April 22, 2026

Last Update Submitted That Met QC Criteria

April 16, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 11235 (DAIDS ES Registry Number)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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