Rhode Island - Statewide Postpartum Hypertension Remote Surveillance
Recruiting
N/A
Interventional Study
Hypertension in Pregnancy
Postpartum Preeclampsia
Postpartum Complication
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 60
- Sex
- Female
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 1,536 (estimated)
- Sponsor
- Women and Infants Hospital of Rhode Island · Other
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About This Trial
This is a hybrid type 1 non-inferiority implementation effectiveness trial among postpartum patients with hypertension (N=1536) that will test the hypothesis that RI-SPHERES (a technologically enabled collaborative care model) is non-inferior to a standard self-measured blood pressure program in terms of persistent hypertension at six weeks postpartum and preventive care receipt within one year of…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Postpartum patient aged 18 years or more at any birthing hospital in Rhode Island
* Diagnosed during pregnancy or after delivery with hypertensive disorder of pregnant
* English-, Spanish-, Portuguese-, or Haitian-Creole-speaking
* Smartphone ownership
Exclusion Criteria:
* …
Contacts