Clinical trial for Hypertensive Disorders of Pregnancy
Official title MH-Rx Study (Baby on Board: Check-in on You, Your Medication, & Your Blood Pressure)
ClinicalTrials.gov ID: NCT07842341
What this study is testing
- What it's testing
- This controlled trial will evaluate whether adding Community Health Worker (CHW)/Social Worker (SW)-led support for non-medical health related needs (NMHRN) and clinician-led Medication Therapy Management (MTM) to remote blood pressure monitoring improves outcomes for pregnant women with chronic hypertension or gestational hypertension (i.e high blood pressure that was present before pregnancy or developed during pregnancy).
Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 45, women only
You may be able to join if
- Female, pregnant ≤34 weeks
- Pregnancy Status: Pregnant, up to 34 weeks of gestation. Able to provide medical confirmation of pregnancy
- Age 18-45
- Diagnosis of chronic hypertension or Gestational Hypertension ( i.e: high blood pressure that was present before pregnancy or developed during...
- Currently taking ≥1 medication
You likely can't join if
- Inability to Provide Legal Consent: Individuals who cannot legally consent to participate in the research study will be excluded.
- Availability Constraints: Individuals who are unavailable or unable to commit to the required study sessions and self-led surveys throughout the...
- Language Barrier: Individuals who do not speak and read English.
- Inability or Unwillingness to Provide Required Information: Individuals who are unable or unwilling to provide reliable contact information (phone...
See the full eligibility criteria
- Female, pregnant ≤34 weeks
- Pregnancy Status: Pregnant, up to 34 weeks of gestation. Able to provide medical confirmation of pregnancy
- Age 18-45
- Diagnosis of chronic hypertension or Gestational Hypertension ( i.e: high blood pressure that was present before pregnancy or developed during pregnancy).
- Currently taking ≥1 medication
- Smartphone user
- Able to speak and read English
- Ability to participate in self-led surveys and perform remote blood pressure monitoring
- Inability to Provide Legal Consent: Individuals who cannot legally consent to participate in the research study will be excluded.
- Availability Constraints: Individuals who are unavailable or unable to commit to the required study sessions and self-led surveys throughout the duration of their pregnancy and the 14-week postpartum follow-up period.
- Language Barrier: Individuals who do not speak and read English.
- Inability or Unwillingness to Provide Required Information: Individuals who are unable or unwilling to provide reliable contact information (phone, email, or address for app/text-based study communications), basic...
The study team makes the final eligibility decision.
Where it is enrolling
- Houston, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
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, but 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, 18 years to 45 years. The study team makes the final eligibility decision.
Where is this trial taking place?
This study is enrolling now at Houston, Texas, United States. Enter your location above to see the nearest enrolling site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.