Rhode Island - Statewide Postpartum Hypertension Remote Surveillance
Recruiting
N/AInterventional Study
Hypertension in PregnancyPostpartum PreeclampsiaPostpartum Complication
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
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
Who this trial is looking for
This trial is looking for postpartum patients in Rhode Island who have had high blood pressure during or after pregnancy. Participants will help test a new care model that uses technology to manage their blood pressure compared to a standard method.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older
I have had high blood pressure during pregnancy or after delivery
I can speak English, Spanish, Portuguese, or Haitian-Creole
I own a smartphone
You may not be able to join if
I have been in this trial before
I am currently in prison
I cannot provide informed consent
I cannot communicate with the study team, even with an interpreter
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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…
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 delivery.
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
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:
* …
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:
* Prior enrollment in this trial
* Prisoners or incarcerated people
* Inability or unwillingness to provide informed consent
* Inability to communicate with study team, despite an interpreter
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.