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Exploring the Feasibility of Kōmmour Prenatal to Reduce Maternal and Infant Health Disparities

Exploring the Feasibility of a Group Prenatal Program, Kōmmour Prenatal, to Reduce Maternal and Infant Health Disparities Among Marshallese Pacific Islander Women

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04558619
Enrollment
38
Registered
2020-09-22
Start date
2022-04-05
Completion date
2026-03-01
Last updated
2026-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kōmmour Prenatal Among Marshallese Pregnant Women

Keywords

Kōmmour, Prenatal, Marshallese

Brief summary

The purpose of the study is to culturally adapt and examine the feasibility of a group prenatal program (Kōmmour Prenatal) to reduce maternal and infant health disparities among Marshallese Pacific Islander women in the US. The study will also gather information from providers of Kōmmour Prenatal and stakeholders in the Marshallese community familiar with the program to learn of their experience with the program.

Interventions

BEHAVIORALKōmmour Prenatal

Centering Pregnancy, a group prenatal care model, is a promising intervention that challenges the standard model of one-on-one counseling of prenatal care. The model, is currently implemented at the UAMS, but as of yet to be adapted for Pacific Islanders. Centering Pregnancy replaces the individual prenatal care visit with a group model for obstetrically low-risk women. This model provides substantially more health promotion content than the traditional one-on-one prenatal care model. The intervention occurs from week 14 of pregnancy through birth, following the same same schedule as individual care. Group visits are 90-120 minutes each and follow a unique structured curriculum that incorporates standards of care. In the group setting, credentialed prenatal providers conduct a one-on-one assessment with each patient (30 min) and then facilitate group discussions on the topics of pregnancy, using adult learning principles (60-90 min).

Sponsors

University of Arkansas
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women who self-identify as Marshallese * 18 years of age or older * And 8-20 weeks pregnant

Exclusion criteria

* Women who do not self-identify as Marshallese * Not 18 years of age or older * And not 8-20 weeks pregnant

Design outcomes

Primary

MeasureTime frameDescription
Gestational Weight Gain9 monthsGestational weight gain will be measured by weight of first and last group prenatal visit along with information from the birth record data. We will use independent samples tests for proportions to compare treatment groups. We will also use generalized linear models to examine treatment group differences including important covariates such as income, education, age and marital status. Further, data from the proposed study will be use the data from the Kommour treatment group to estimate intraclass correlations as an indicator of clustering due to the nesting of participants within groups.

Secondary

MeasureTime frameDescription
Breastfeeding initiation, birth weight of infant, preeclampsia, primary cesarean birth, and gestational diabetes mellitus9 monthsThe research team will abstract medical record information about the mother and child.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORBritni Ayers, PhD

University of Arkansas for Medical Sciences Northwest

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 8, 2026