RECRUITING

Rhode Island - Statewide Postpartum Hypertension Remote Surveillance

Description

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.

Study Overview

Study Details

Study overview

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.

Effect of a Technology-based Collaborative Model on Persistent Hypertension and Preventive Care Attendance Among Postpartum People With Hypertensive Disorders of Pregnancy

Rhode Island - Statewide Postpartum Hypertension Remote Surveillance

Condition
Hypertension in Pregnancy
Intervention / Treatment

-

Contacts and Locations

Newport

Newport Hospital, Newport, Rhode Island, United States, 02840

Providence

Women & Infants Hospital of Rhode Island, Providence, Rhode Island, United States, 02903

Wakefield

South County Hospital, Wakefield, Rhode Island, United States, 02879

Warwick

Kent Hospital, Warwick, Rhode Island, United States, 02886

Woonsocket

Landmark Hospital, Woonsocket, Rhode Island, United States, 02895

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * 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

Ages Eligible for Study

18 Years to 60 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Women and Infants Hospital of Rhode Island,

Study Record Dates

2029-03-01