Actively Recruiting

Age: 18Years +
All Genders
ID07278427

Reducing Parental Substance Use, Improving Child Health Outcomes, and Enhancing Family Resilience Among Rural Families Through Ohio START

Led by Ohio State University · Updated on 2026-05-14

400

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

Sponsors

O

Ohio State University

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to understand how parental activity spaces and social networks influence reducing substance use and improving child and family health outcomes within the Ohio START program, which supports families in rural areas facing substance use and child welfare challenges. It investigates whether having substance use treatment services nearby and support from family peer mentors helps parents recover and strengthens family resilience, especially comparing rural and urban differences. The study focuses on families involved in child welfare due to substance use and maltreatment, emphasizing the importance of accessible treatment and social support for lasting family health. Participants in this observational study are parents enrolled in Ohio START, an intervention linking child welfare and behavioral health services to provide timely substance use treatment and family peer mentoring. Parents engage with peer mentors through weekly face-to-face visits for 90 days, who support recovery and resource coordination. The study collects data over three waves—at enrollment, 6 months, and 12 months—tracking changes in treatment access, social connections, and family outcomes. During the study, participants will complete surveys about their substance use, parenting, child health, and family well-being at three time points. They will share information about their regular activity locations and social support networks. Researchers will measure parental substance use severity, child psychosocial and behavioral health, child maltreatment, substance use treatment utilization, and family resilience. The study aims to provide insights to improve interventions for families in rural communities, with the overall participation lasting up to 12 months.

CONDITIONS

Brief Title

Reducing Parental Substance Use and Enhancing Family Resilience Among Rural Families Through Ohio START

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 or older
  • Currently enrolled in Ohio START
  • Unemployed or family income at or below the federal poverty level
  • Designated as the primary parent in the Ohio START case plan
Not Eligible

You will not qualify if you...

  • None explicitly stated in the eligibility criteria

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Approximately 3 months

Participants engage in Ohio START services, which include weekly face-to-face visits with family peer mentors for 90 days to support recovery and coordination of resources.

Weekly visits for 12 weeks

Long-term Monitoring

Duration - 12 months

Participants are observed over time to assess parental substance use severity, child psychosocial and behavioral health, child maltreatment, substance use disorder treatment service use, and family resilience.

3 visits at baseline, 6 months, and 12 months

Trial Site Locations

Total: 1 location

1

The Ohio State University

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

S

Susan Yoon, PhD

E

Elinam Dellor, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Development and preliminary psychometric properties of the multidimensional neglectful behavior scale-child report.

Glenda Kaufman Kantor, Melissa K Holt, Carolyn J Mebert...

https://pubmed.ncbi.nlm.nih.gov/15538039