CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 2,350 enrolled
Drug / intervention
CenteringPregnancybehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02640638
NCT02640638N/ACompleted
CompareCT.gov

Reducing Disparities in Birth Outcomes: a Randomized Controlled Trial of CenteringPregnancy

Clemson University·interventional·Posted Dec 29, 2015·Updated Aug 26, 2022

In Brief

A clinical study evaluating CenteringPregnancy for Pregnancy and Preterm Birth. Completed, enrolled 2,350 participants across 4 sites.

Detailed Summary

The purpose of this study is to evaluate whether CenteringPregnancy group prenatal care can improve preterm birth rate and other birth outcomes, maternal psychosocial and behavioral outcomes, and decrease the racial difference in selected birth outcomes among African American and White women, compared to individual prenatal care.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPregnancy, Preterm Birth
CountriesUnited States
CollaboratorsPrisma Health-Upstate, University of California, Los Angeles, Georgia State University

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedDec 29, 2015
Enrollment StartFeb 24, 2016
Primary CompletionOct 14, 2020
Study CompletionJan 21, 2021
TodayJul 2, 2026
Enrollment to primary: 4.6 yearsPosted 10.5 years ago

Interventions

CenteringPregnancybehavioral

8-12 pregnant women whose due dates are in the same month will receive ten 2-hour group prenatal care sessions according to the standard curriculum provided by the Centering Healthcare Institute.