Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06261398

Better Birth Outcomes Through Technology, Education, and Reporting

Led by Ohio State University · Updated on 2025-05-15

550

Participants Needed

3

Research Sites

209 weeks

Total Duration

On this page

Sponsors

O

Ohio State University

Lead Sponsor

A

American Heart Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a pragmatic randomized control trial to evaluate the BETTER intervention compared to standard obstetrical care (control) to determine whether it helps to reduce maternal anemia and other adverse pregnancy outcomes. The BETTER intervention includes one motivational interviewing session and bi-weekly text messages to encourage patients to connect with resources that address their social needs, including housing, food, and transportation. Quantitative data will be used to study participant outcomes, including surveys, and electronic health record data.

CONDITIONS

Official Title

Better Birth Outcomes Through Technology, Education, and Reporting

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Less than 20 weeks and 6 days pregnant upon enrollment
  • At least 18 years of age
  • Receiving obstetric care at OSU McCampbell Hall or OSU Outpatient Care East
  • Singleton pregnancy and fetus with a heartbeat
  • English speaking
  • Able to receive text messages
Not Eligible

You will not qualify if you...

  • Has a significant medical condition (eg sickle cell disease) that is a cause of anemia
  • Has a plan for transfusion during pregnancy

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 3 locations

1

The Ohio State University Outpatient Care East

Columbus, Ohio, United States, 43203

Actively Recruiting

2

McCampbell Hall

Columbus, Ohio, United States, 43210

Actively Recruiting

3

The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

A

Ann McAlearney, ScD, MS

CONTACT

N

Nicole Thomas, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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