Michigan Healthy Mom (MI-MOM) Pregnancy Improvement Web Application Trial
This study is looking at whether using the MI MOM App can improve health during and after pregnancy. You would be in one of two groups: one uses the MI MOM App, and the other receives standard care. Both groups will answer questions about their pregnancy health, and researchers will also look at health records. If you're in the MI MOM App group, you'll get app content and text messages with health information. You can also choose to involve up to three friends or family members to receive text messages, and you'll have the option to contact a community health worker. The study aims to see if the app can improve overall pregnancy and postpartum health, especially for women who are 20 weeks pregnant or less, 18 or older, have a smartphone with internet, speak English, and are enrolled in Medicaid. The study is currently unclear on its recruitment status and plans to enroll 500 participants.
- Study design
- This is an interventional study with two groups: one using the MI MOM App and one receiving usual care. It plans to enroll 500 participants.
- What's involved
- You will be asked to answer questions about your pregnancy health. If in the MI MOM App group, you will receive app content and text messages.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed through one year postpartum for pregnancy-associated morbidity and mortality. A composite index of risk factors will be measured at specific time points up to one year postpartum.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Michigan Healthy Mom (MI-MOM) Pregnancy Improvement Web Application Trial
At a glance
Conditions
Where it's being run
8 sites across 1 statesWho to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Total pregnancy-associated morbidity through one year postpartumStart of pregnancy through 1 year postpartum
Total pregnancy-associated non-severe and severe maternal morbidity through 1 year postpartum. Non-severe maternal morbidity will be indexed using ICD codes taken from Medicaid records, with conditions taken from World Health Organization-identified Maternal Morbidity conditions (e.g., anemia, hypertension, depression). Severe maternal morbidity will use ICD codes identified for the 21 severe maternal morbidity indicators developed by the CDC.
- Pregnancy-Associated Mortality through one year postpartumStart of Pregnancy through 1 year postpartum
Total pregnancy-associated mortality through 1 year postpartum as measured using a preexisting linked dataset of Medicaid claims, deaths, birth records, and Evidence-Based Practice Center (EPC) program data.
- Composite Index, total number of maternal morbidity and mortality risk factorsMeasured at 6 weeks post-baseline, 35 weeks of pregnancy, 6 weeks postpartum, 6 months postpartum, and 1 year postpartum.
A composite index evaluating multiple maternal morbidity and mortality behavioral risk factors including the Tobacco, Alcohol, Prescription medication, and other Substance use Tool for substance use (TAPS); the Humiliation, Afraid, Rape, Kick questionnaire for intimate partner violence (HARK); the Patient Health Questionnaire (PHQ-9) and Generalized Anxiety Disorder Screener (GAD-7) for symptoms of depression and anxiety; patient understanding of early warning signs of pregnancy complications and appropriate responses; confidence in ability to communicate effectively with healthcare providers; help-seeking behaviors/service utilization, and prenatal care adherence. Total score on this composite index will be the number of risks on which the participant is positive at that assessment point. All risks will refer to the time since becoming pregnant (baseline) or since the last assessment point (follow-up observations) except for depression and anxiety, which refer to the past two weeks.