This study is accepting new patients by invitation only

Study to Understand Risk Information to Support and Empower

a study on Diabetes Gestational Diabetes Diabetes Type 2

Summary

Eligibility
for females ages 18 years and up (full criteria)
Location
at UC Davis
Dates
study started
study ends around

Description

Summary

The aim of this trial is to test components of a digital health outreach intervention to promote uptake of postpartum screening and lifestyle programs for diabetes prevention among patients with gestational diabetes (GDM). The outreach intervention, designed to be interactive and delivered online, includes standard health information plus up to four theory-based components, targeting motivational and logistical barriers to engaging in diabetes preventive care during the postpartum period. The trial leverages the Multiphase Optimization Strategy (MOST) using a randomized factorial study design.

Official Title

Optimizing a Scalable Intervention to Maximize Guideline-recommended Diabetes Testing After GDM

Keywords

Diabetes, Gestational, Diabetes Mellitus, Type 2, Gestational Diabetes, Diabetes Mellitus, Type 2 Prevention, Preventive Health Services, Health Communication, Type 2 Diabetes Mellitus, Diabetes Mellitus, Values Affirmation (VA), Tailored Risk Information (TRI), Motivational Interviewing-based (MI), Action planning (AP)

Eligibility

You can join if…

Open to females ages 18 years and up

  • Current pregnancy complicated by gestational diabetes mellitus (GDM)
  • Age: 18 years and older
  • Contact with the Kaiser Permanente Northern California (KPNC) Regional Perinatal Service Center
  • Able to communicate in English

You CAN'T join if...

  • Diagnosis of diabetes before pregnancy
  • Maternal or infant current hospitalization
  • Pregnancy loss
  • History of eating disorder
  • Previously requested not to receive research invitations

Location

  • Kaiser Permanente Northern California
    Pleasanton 5383777 California 5332921 94588 United States

Details

Status
accepting new patients by invitation only
Start Date
Completion Date
(estimated)
Sponsor
University of California, Davis
ID
NCT05752292
Study Type
Interventional
Participants
Expecting 2000 study participants
Last Updated