Earned Income Tax Credit Access Study

January 5, 2024 updated by: Katie Maguire-Jack, University of Michigan
The EITC Access Study an intervention study provided to families in 7 counties in Michigan.The intervention involves appending a concentrated benefits advocacy intervention onto an existing home visiting program. There are 5 treatment counties and 2 control counties that will survey families in the home visiting program to compare the relative benefits of the added benefits advocacy intervention on the outcomes of parent mental health, intimate partner violence, economic hardship, earned income tax credit take-up, and child maltreatment.

Study Overview

Study Type

Interventional

Enrollment (Actual)

208

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

    • Michigan
      • Battle Creek, Michigan, United States, 49017
        • Calhoun Intermediate School District
      • Belleville, Michigan, United States, 48197
        • SOS Community Services
      • Croswell, Michigan, United States, 48422
        • Sanilac Intermediate School District
      • Houghton, Michigan, United States, 49931
        • Keweenaw Family Resource Center
      • Kalamazoo, Michigan, United States, 49048
        • Catholic Charities Diocese of Kalamazoo
      • Marysville, Michigan, United States, 48040
        • St Clair RESA
      • Portage, Michigan, United States, 49002
        • Kalamazoo KRESA

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 18 years of age, has a child in their home

Exclusion Criteria:

  • Does not speak or read English, Spanish, Burmese, or Arabic

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: Basic Science
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Education intervention
Parents in the treatment group will receive information about Earned Income Tax Credit, including how to sign up for free. They will also receive help with budgeting and finances from their home visitor.
Parents will be provided with information about Earned Income Tax Credits and budgeting
Parents as Teachers home visiting program
Other: Control group
Control group families will receive home visiting services as usual.
Parents as Teachers home visiting program

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Earned Income Tax Credit receipt
Time Frame: Within 2 years of receiving the intervention
Self-report
Within 2 years of receiving the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Child maltreatment behaviors
Time Frame: Within 2 years of receiving the intervention
Self-report on the Brief Child Abuse Potential Inventory. 34 Yes/No questions. E.g. "A child needs very strict rules."
Within 2 years of receiving the intervention
Intimate partner violence
Time Frame: Within 2 years of receiving the intervention
Self-report from Women's Experiences of Battering Scale. 10 items relating to how they would describe their life with their partner. Scale ranges from Strongly agree to strongly disagree. E.g. 1. He makes me feel unsafe even in my own home.
Within 2 years of receiving the intervention
Depression
Time Frame: Within 2 years of receiving the intervention
Self-report from the Center for Epidemiologic Studies Depression Scale (CES-D). 20 questions on a scale from "rarely" to "most or all of the time" relating to things experienced within the past week. E.g. "I was bothered by things that usually don't bother me."
Within 2 years of receiving the intervention
Anxiety
Time Frame: Within 2 years of receiving the intervention
Self-report from the General Anxiety Disorder (GAD-7). 7 questions relating to feelings experienced over the past 2 weeks, with response options ranging from "not at all" to "nearly every day." E.g. "Not being able to stop or control worrying."
Within 2 years of receiving the intervention
Economic hardship
Time Frame: Within 2 years of receiving the intervention
Self-report on 11 yes or no items indicating whether individual hardships were experienced in the past year. E.g. "Was there anyone in your household who needed to see a doctor or go to the hospital but could not go because of the cost?"
Within 2 years of receiving the intervention

Collaborators and Investigators

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

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, 2021

Primary Completion (Actual)

September 29, 2023

Study Completion (Actual)

September 29, 2023

Study Registration Dates

First Submitted

May 20, 2021

First Submitted That Met QC Criteria

May 20, 2021

First Posted (Actual)

May 25, 2021

Study Record Updates

Last Update Posted (Estimated)

January 8, 2024

Last Update Submitted That Met QC Criteria

January 5, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • HUM00190754

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Only aggregate information will be shared with other researchers.

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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