Actively Recruiting
Telehealth Multi-Component Optional Model (MOM) Study
Led by University of Arkansas · Updated on 2026-02-05
1500
Participants Needed
6
Research Sites
202 weeks
Total Duration
On this page
Sponsors
U
University of Arkansas
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aim of this study is to conduct a comparative effectiveness evaluation using a randomized control trail design among diverse women to compare two postpartum care models: 1) Telehealth Multicomponent Optimal Model (Telehealth MOM) and 2) enhanced standard of care (ESoC). This study will address critical gaps in knowledge about how best to deliver comprehensive postpartum care that ensures timely identification and treatment of complications and meets the needs and preferences of diverse patients, including disproportionately-impacted racial groups and rural residents.
CONDITIONS
Official Title
Telehealth Multi-Component Optional Model (MOM) Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women between 16-35 weeks gestation
- Age 18-44 years
- Ability to speak English, Spanish, or Marshallese
- Participants may have either a vaginal birth or cesarean section birth
You will not qualify if you...
- Type 1 diabetes on an insulin pump followed closely by endocrinology
- Uncontrolled Type 2 diabetes
- End stage renal disease followed closely by nephrology
- ICU admission at any point during pregnancy or delivery hospitalization
- Other maternal conditions requiring additional surgeries (e.g. cesarean hysterectomy or intrapartum or postpartum oophorectomy/appendectomy)
- Incarceration
- Mental disability limiting decision-making capacity
- Uncontrolled chronic hypertension
- HELLP syndrome during pregnancy
- Sickle cell disease
- Maternal heart condition or heart disease
- Opioid use disorder
- Lupus
- Thrombophilia or blood clots
- Need for blood transfusion during delivery hospitalization
- Other maternal conditions or complications requiring prolonged postpartum hospitalization
AI-Screening
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Trial Site Locations
Total: 6 locations
1
UAMS El Dorado FMC
El Dorado, Arkansas, United States, 71730
Not Yet Recruiting
2
UAMS Fayetteville FMC
Fayetteville, Arkansas, United States, 72703
Actively Recruiting
3
UAMS Fort Smith FMC
Fort Smith, Arkansas, United States, 72901
Actively Recruiting
4
UAMS Jonesboro FMC
Jonesboro, Arkansas, United States, 72401
Not Yet Recruiting
5
UAMS Health Women's Center
Little Rock, Arkansas, United States, 72205
Actively Recruiting
6
UAMS Springdale FMC
Springdale, Arkansas, United States, 72764
Actively Recruiting
Research Team
B
Brett Rowland, MA
CONTACT
K
Kacie Simpson, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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