Better Birth Outcomes Through Technology, Education, and Reporting
Recruiting
N/A
Interventional Study
Pregnancy
Maternal Anemia
Pre-Term Birth
Hypertensive Disorders
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 550 (estimated)
- Sponsor
- Ohio State University · Other
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About This Trial
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 need…
Trial Locations
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Eligibility 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 Criteri…
Contacts