BridgeMD
New treatment option for Postpartum Complication
Official title Healing, Equity, Advocacy and Respect for Mamas
ClinicalTrials.gov ID: NCT06273436
What this study is testing
- What it's testing
- The goal of the proposed research is to test the comparative effectiveness of AIM safety bundles for post-partum women delivered in-person vs. via text/phone to improve early detection of and timely care for complications during the first six weeks postpartum for women experiencing significant health disparities.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 16 to 49, women only
You may be able to join if
- for Postpartum Women
- Postpartum woman within approximately 2 weeks of delivering a baby of gestational age ≥ 26 weeks in South Carolina.
- Aged 16-49 years old.
- Insured by Medicaid.
You likely can't join if
- for Postpartum Women
- Plans to relocate outside of SC anytime during the postpartum year.
- Plans to discontinue Medicaid health insurance during the postpartum year.
- Speaks a language other than English or Spanish.
- Incarcerated/pending incarceration during peripartum period.
- Currently institutionalized.
See the full eligibility criteria
- for Postpartum Women
- Postpartum woman within approximately 2 weeks of delivering a baby of gestational age ≥ 26 weeks in South Carolina.
- Aged 16-49 years old.
- Insured by Medicaid.
- for Postpartum Women
- Plans to relocate outside of SC anytime during the postpartum year.
- Plans to discontinue Medicaid health insurance during the postpartum year.
- Speaks a language other than English or Spanish.
- Incarcerated/pending incarceration during peripartum period.
- Currently institutionalized.
- Enrolled in current MUSC study funded by PCORI (#Pro00123833)
- Does not have and/or does not wish to use their personal cell phone for the study. Inclusion Criteria for Obstetric Providers and Hospital Administrators \- OB provider working at a delivery hospital in SC and directly...
- Less than 1 month of HEAR 4 Mamas experience if involved in the hospital where participants are recruited from.
- Unable or unwilling to commit to completing surveys or an interview.
- Speaking a language other than English.
The study team makes the final eligibility decision.
Where it's taking place
- Charleston, South Carolina, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 16 years to 49 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Charleston, South Carolina, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.