NCT05752292
Study to Understand Risk Information to Support and Empower
Enrolling by Invitation
NAAges 18+InterventionalHealth servicesUniversity of California, DavisInvestigator-initiated
~2,000 participants
Updated 2026-05-12 on ClinicalTrials.gov
What's tested:Standard Health InformationValues Affirmation (VA)Tailored Risk Information (TRI)Motivational Interviewing-based (MI)Action planning (AP)
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Completion of recommended postpartum diabetes screening.
Measured over 4-12 weeks postpartum
Conditions
Where it's being run
1 sites across 1 statesCalifornia1
Study leadership
- Susan D Brown, PhD · PRINCIPAL_INVESTIGATOR · University of California, Davis
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
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
Exclusion
Diagnosis of diabetes before pregnancy
Maternal or infant current hospitalization
Pregnancy loss
History of eating disorder
Previously requested not to receive research invitations
What this trial measures
- Completion of recommended postpartum diabetes screening.4-12 weeks postpartum
Completion of a 75-gram, 2-hour oral glucose tolerance test (OGTT)