Mindfulness and Wearable Biosensors to Prevent Hypertensive Disorders of Pregnancy
Recruiting now · Not applicable
Conditions studied: Preeclampsia
In brief
The MINDBP study will enroll 90 pregnant women at risk for HDP across two sites (MCW and Brown) and randomize them to: (1) mindfulness training (MT) plus wearable biosensors, (2) MT alone, or (3) routine prenatal care. MT participants will receive 8 weekly phone-based MT sessions plus two booster sessions at 1 and 2 months post-intervention. The primary outcome is study feasibility.
Key facts
- Study ID
- NCT07218237
- Run by
- Medical College of Wisconsin
- People needed
- 90
- Starts
- 2026-04-28
- Expected to finish
- 2028-10-01
- Last updated by the study team
- 2026-07-20
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Pregnant patients at gestational age <= 16 weeks
- Live, non-anomalous gestation
- Normotensive at enrollment
- Meet criteria consistent with 'moderate' to 'high' risk for preeclampsia based on ACOG/USPSTF guidelines for low-dose aspirin administration to prevent hypertensive disorders of pregnancy
You may not qualify if…
- Multiple gestation
- Chronic (pregestational hypertension)
- Inability of unwillingness to provide informed consent
- Active suicidality or psychosis
- Ongoing mind-body practice (e.g., yoga, meditation, mindfulness >= once per week)
Where it is running
- Brown University — Providence, Rhode Island, United States (enrolling)
- Medical College of Wisconsin — Milwaukee, Wisconsin, United States (enrolling)
Full record on ClinicalTrials.gov
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