Improving birth outcomes through technology and education
Official title: Better Birth Outcomes and Experiences Through Technology, Education, and Reporting (BETTER)
Run by Ohio State University · NCT06261398 · Data updated 2026-11-12
This study is testing a new program that uses text messages and support to help pregnant women in Ohio have healthier pregnancies and reduce issues like anemia.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 550 (estimated) |
| Sponsor | Ohio State University Academic / other |
| Locations | 3 sites (Columbus, Ohio and 2 other locations) |
| Status | Recruiting |
| Started | February 26, 2024 |
| Main results expected | September 2027 |
| Study ends | March 2028 |
| Registry record updated | June 9, 2026 |
| Trial ID | NCT06261398 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are pregnant individuals under 20 weeks, at least 18 years old, receiving care at designated Ohio State University clinics, and able to communicate in English.
✕Probably not a fit
Patients with significant medical conditions causing anemia or those planning for transfusion during pregnancy may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This pragmatic randomized control trial evaluates the BETTER intervention, which includes motivational interviewing and bi-weekly text messages, against standard obstetrical care to reduce maternal anemia and other adverse pregnancy outcomes. The study focuses on addressing social determinants of health by connecting patients with resources for housing, food, and transportation. A total of 550 obstetric patients will be enrolled from specific clinics at Ohio State University, and their health outcomes will be assessed using surveys and electronic health records.
Why it matters
Potential benefit: If successful, this intervention could significantly improve maternal and child health outcomes by addressing social needs that contribute to adverse pregnancy outcomes.
How similar studies have gone: Other studies have shown promise in addressing social determinants of health in maternal care, suggesting potential for success with this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria * 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 Exclusion Criteria * Has a significant medical condition (eg sickle cell disease) that is a cause of anemia * Has a plan for transfusion during pregnancy
Where it's running
-
The Ohio State University Outpatient Care East
Columbus, Ohio, United States Recruiting -
McCampbell Hall
Columbus, Ohio, United States Recruiting -
The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine
Columbus, Ohio, United States Recruiting
Study contacts
- Principal investigator: William Grobman, MD, MBA — Ohio State University
- Study coordinator: Ann McAlearney, ScD, MS
- Email: Ann.McAlearney@osumc.edu
- Phone: 614-293-3716
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.