- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07463131
Negative Income Tax Trial (NITT)
September 4, 2026 updated by: University of Pennsylvania
In partnership with a local community college in in Omaha, Nebraska, the Center for Guaranteed Income Research (CGIR) at the University of Pennsylvania will conduct a randomized controlled trial to determine the impacts of a negative income tax for MCC students, with particular attention to educational and career advancement outcomes.
The sample will include students in a degree-seeking program, as well as those in non-degree programs, such as those working towards professional certificates.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
750
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
- Name: Stacia West, PhD
- Phone Number: 215-898-5512
- Email: swest11@utk.edu
Study Locations
-
-
Nebraska
-
Omaha, Nebraska, United States, 68111
- Recruiting
- Metropolitan Community College (MCC)
-
-
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:
- 19 years of age or older, and
- Currently in 2nd semester of MCC Associate's program OR completed at least one Level-1 credential OR within one month of completing a Level 2 credential, and
- Have a total adjusted gross income (AGI) $6,000 below the SPM for the reported family size, and
- Compliant with community college's enrollment, participation, and documentation requirements
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 |
|---|---|
|
Experimental: Associate's Degree Seekers with NIT
Students currently enrolled in an Associate's Degree program at the community college will receive a negative income tax for a duration of two years followed by a linear titration of payments for one year
|
Negative income tax calculated by the supplemental poverty measures less the household's prior tax year adjusted gross income, then divided by 12 to arrive at a monthly cash transfer
|
|
Experimental: Credential Seekers with NIT
Students currently enrolled in a credential program at the community college will receive a negative income tax for a duration of one year followed by a linear titration of payments for six months
|
Negative income tax calculated by the supplemental poverty measures less the household's prior tax year adjusted gross income, then divided by 12 to arrive at a monthly cash transfer
|
|
Active Comparator: Control
These students will not receive the negative income tax
|
No negative income tax payment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Educational Program Completion
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
Number of participants who complete academic program, whether Associate's Degree or credential
|
Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
|
Workforce participation
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
Number of participants who become employed in industry associated with earned degree or credential
|
Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Food security (Household Food Insecurity Access Scale)
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 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, 18 months, 24 months, 30 months, 36 months, 42 months
|
|
Financial wellbeing (Consumer Financial Protection Bureau Financial Wellbeing Scale)
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 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, 18 months, 24 months, 30 months, 36 months, 42 months
|
|
Psychological distress (Kessler 6)
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 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, 18 months, 24 months, 30 months, 36 months, 42 months
|
|
Health Behavior Inventory-20
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
Assessment of health promotion and risk behaviors, Likert scaled inventory with 5 subscales
|
Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
|
Housing status
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
Number of participants who report a change in housing status (e.g., renter, homeowner, rent-to-own, etc.) or report stable housing status in the prior month.
|
Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
|
General health
Time Frame: Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
Self-reported general health as measured by one question from the RAND Short Form Health Survey (known as SF-36): "In general, would you say your health is:", with a 5-point scale from Poor to Excellent.
|
Baseline, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
June 1, 2026
Primary Completion (Estimated)
June 1, 2030
Study Completion (Estimated)
June 1, 2030
Study Registration Dates
First Submitted
March 4, 2026
First Submitted That Met QC Criteria
March 4, 2026
First Posted (Actual)
March 11, 2026
Study Record Updates
Last Update Posted (Actual)
September 8, 2026
Last Update Submitted That Met QC Criteria
September 4, 2026
Last Verified
September 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 26-6149
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.