- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07265375
Cash Transfers for Reentry
Study Overview
Status
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Stacia West Principle Investigator, PhD
- Phone Number: 215-898-5512
- Email: west.stacia@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Amy Castro, PhD, The University of Pennsylvania
- Principal Investigator: Stacia West, PhD, The University of Pennsylvania
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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