- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04901403
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
Status
Completed
Intervention / Treatment
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
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Belleville, Michigan, United States, 48197
- SOS Community Services
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Croswell, Michigan, United States, 48422
- Sanilac Intermediate School District
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Houghton, Michigan, United States, 49931
- Keweenaw Family Resource Center
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Kalamazoo, Michigan, United States, 49048
- Catholic Charities Diocese of Kalamazoo
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Marysville, Michigan, United States, 48040
- St Clair RESA
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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.
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, 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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