Mixed Methods Evaluation of the Pomona Household Universal Grant (HUG) Program

May 6, 2026 updated by: Judith L. Perrigo, University of California, Los Angeles

City of Pomona's Guaranteed Income Program for Parents With Children Under the Age of Give

The City of Pomona is launching the Pomona Household Universal Grant (HUG) program in the Summer of 2024. Pomona HUG is a pilot project that will provide 250 parents/caregivers with children under 5 years old $500 a month for 18 months. Pomona's guaranteed income (GI) initiative provides relief for the most economically vulnerable households. The study will investigate the impacts of GI on financial security, material hardship, health and well-being, food security, social support, parenting, and childhood development. The intervention group will be compared to a control group of 350 parents/caregivers receiving only a nominal ($20) amount per month during the 18 month period.

Study Overview

Detailed Description

GI programs are commonly depicted as catalysts for reshaping social welfare paradigms. Such programs not only address immediate material hardship through consistent and unconditional financial support but also have the potential to confer broader societal benefits. For instance, GI programs can reduce income inequality, enhance socio-economic conditions, and improve health outcomes and overall well being.

The early years of a child's life hold profound significance, as approximately 90% of brain development occurs before age five. This period lays the crucial foundation for lasting effects, presenting a valuable opportunity to implement an innovative, two-generation GI initiative in Pomona, California. By adopting a comprehensive two-generation approach, Pomona can pave the way for transformative change in equipping parents/caregivers with the means to secure basic necessities such as food, clothing, and shelter for themselves and their children. By alleviating the stress of financial instability, parents/caregivers are empowered to focus on their education, skill development, career prospects, and responsive parenting. Consequently, the ripple effects hold promise to disrupt the cycle of poverty, offering a brighter future for both children and their families.

The investigators guiding research questions are to examine how GI impacts child, parent/caregiver, and family outcomes. The evaluation utilizes a mixed methods approach, employing a randomized controlled trial (RCT) design which includes parent surveys, home-based observations, and semi-structured qualitative interviews.The study includes a total of N=600 dyads (parent/caregiver and child), with n=250 receiving $500 GI monthly for 18 months and a control group of n=350 receiving $20 per month for the same duration. Baseline, and follow-up surveys at year 1 and year 2 will be administered to all participants. Home observations will be conducted with all 600 participants to better understand the impact of GI on parent-child relationships. Lastly, qualitative interviews will be conducted with a subset of parents receiving GI (n=30) and those who do not (n=30) to gain a deeper understanding of the intervention's impact.

Study Type

Interventional

Enrollment (Estimated)

600

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 Locations

    • California
      • Los Angeles, California, United States, 90095
        • University of California, Los Angeles

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:

Must live in the City of Pomona;

Must be 18 years old upon application submission;

Must be the parent or legal guardian of a child aged prenatal to under 4 years old at the time of application;

Must meet at least one of the following qualifiers (#1-4):

Experienced negative impact due to the Covid-19 pandemic including:

  • The participant or anyone in the participant's household experienced unemployment during the pandemic.
  • The participant or anyone in the participant's household experienced increased food or housing insecurity during or as a result of the pandemic.

Home address is located within a qualified census tract (QCT).

Participant currently receiving any of the below benefits:

  • Federal Pell Grants
  • Free-and Reduced-Priced Lunch (NSLP) and/or School Breakfast (SBP) programs
  • Head Start and/or Early Head Start
  • Low Income Housing Energy Assistance Program (LIHEAP)
  • Section 8 Vouchers : Public Housing & Housing Choice Vouchers
  • Supplemental Security Income (SSI) - Social Security
  • CalFresh or SNAP (Supplemental Nutrition Assistance Program)
  • Temporary Assistance for Needy Families (TANF)
  • Supplemental Nutrition Program for Women, Infants, and Children (WIC)
  • Medicaid or MediCal
  • Children's Health Insurance Program (CHIP)
  • Childcare Subsidies through Child Care Development Fund (CCDF) Program
  • Household income is at or below 65% AMI (Area Median Income)

In order to be approved for the program, the participant agrees to Informed Research Consent.

Exclusion Criteria:

Individuals that do not meet one or more of the inclusion criteria listed above.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Treated Group ($500 GI for 18 months)
Treated Group will receive $500 per month for 18 months (anticipated n=250)
Participants receive $500 monthly for up to 18 months.
Active Comparator: Comparison Group ($20 GI for 18 months)
Comparison Group will receive $20 per month for 18 months (anticipated n=350)
Participants receive $20 monthly for up to 18 months.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Financial Security
Time Frame: Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)
Investigators use the Financial Well-being Scale developed and tested by the Consumer Financial Protection Bureau. Raw totals are derived from the participant responses which is then converted to a financial well-being score. Scores for the self-administered abbreviated version of the scale range from 19-90. Higher scores represent a higher level of reported financial well-being.
Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)
Early Childhood Well-being
Time Frame: Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period) (Update Feb2026: this measure was mistakenly left off 1-year survey, so it is available just at baseline and 6mos post-interverention)
Investigators use the developmental milestones subdomain from the Survey of Well-being of Young Children (SWYC) to measure early childhood well-being. The SWYC milestones subdomain assesses the cognitive, language, and motor development of children. Respondents are asked a set of 10 questions based on their child's age. Responses are scored and total scores range from 0 - 20. A cut off is provided for each age group and when the score is above this cutoff, it indicates that a child appears to be meeting age expectations for development.
Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period) (Update Feb2026: this measure was mistakenly left off 1-year survey, so it is available just at baseline and 6mos post-interverention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Parent-child interactions
Time Frame: Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)
Investigators measure this using the Healthy Families Parenting Inventory (HPFI) - Subdomain: Parent/Child Interaction, comprised of 10 questions. Reverse scoring is implemented for a set of questions. Total scores range from 10-50.
Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)
Food security
Time Frame: Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)
Investigators use the six-item short form of the United States Department of Agriculture Food Security Survey Module. Total scores range from 0-6 with higher scores indicating increased levels of food insecurity.
Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)
Parent/caregiver stress
Time Frame: Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)
Investigators use the Parental Stress Scale to measure parent/caregiver stress. Scores from the Parents Stress Scale range from 18-90. Before summing participant scores, reverse scoring is implemented for several items. Higher scores represent higher levels of parental stress.
Measured at baseline, 1-year after the start of the intervention, and at follow-up (6 months post-intervention period)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Judith L Perrigo, PhD, University of California, Los Angeles
  • Principal Investigator: Daniel Eisenberg, PhD, University of California, Los Angeles

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 17, 2024

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

July 11, 2024

First Submitted That Met QC Criteria

July 11, 2024

First Posted (Actual)

July 17, 2024

Study Record Updates

Last Update Posted (Actual)

May 11, 2026

Last Update Submitted That Met QC Criteria

May 6, 2026

Last Verified

August 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Deidentified participant survey data and home observation data will be available upon request and completion of a data access agreement. The deidentified data will be available to investigators with a proposal approved by an Institutional Review Board (or other independent review committee).

IPD Sharing Time Frame

Proposals may be submitted for PI review 6 months following publication of the study's primary results (which is estimated to be 1-2 years following project completion). The PI will review such requests for up to 5 years after such publication.

IPD Sharing Access Criteria

Proposals should be directed to Dr. Judith Perrigo at jperrigo@luskin.ucla.edu.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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.

Clinical Trials on Parental Stress

Clinical Trials on Guaranteed Income ($500/monthly)

  • University of Pennsylvania
    The City of Los Angeles
    Completed
    Stress | Psychological Distress | Family Dynamics | Health | Food Security | Educational Attainment | Housing | Employment | Income | Physical Functioning | Well-being/Quality of Life | Financial Wellbeing
    United States
  • University of California, San Francisco
    National Institutes of Health (NIH); Oregon Health and Science University; My...
    Completed
    Mental Health Wellness 1 | Health Care Utilization | Financial Hardship | Education, Professional
    United States
  • Harvard Medical School (HMS and HSDM)
    University of Michigan; Brigham and Women's Hospital; Harvard University
    Active, not recruiting
    Health Care Utilization | Health Care Costs
    United States
  • University of California, San Francisco
    Destination: Home SV; Sí Se Puede Collective; Sacred Heart Community Service; County...
    Enrolling by invitation
    Families Experiencing Homelessness and/or Housing Instability | Housing Stability
    United States
  • University of Pennsylvania
    Children's Hospital of Philadelphia; Rutgers University; Redlich Horwitz Foundation
    Completed
  • Stanford University
    Silicon Valley Community Foundation; Valhalla Foundation; Health Plan of San... and other collaborators
    Recruiting
    Child Development | Child Health | Healthcare Disparities | Mothers | Community Health Workers | Infant, Newborn | Poverty | Child Care | Income | Health Services Utilization | Hispanic or Latino | United States | Medicaid | Social Services Utilization
    United States
Subscribe