Type 2 Diabetes Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have just given birth and are still admitted to the delivery hospital
- People who are 18 years of age or older and are able to give their own consent to participate
- People who were diagnosed with gestational diabetes (diabetes that develops during pregnancy, not before) during their pregnancy, confirmed either by a one-hour glucose screening test result plus a doctor's record of the diagnosis, or by two abnormal results on a three-hour glucose tolerance test plus a doctor's record of the diagnosis
- People who speak English or Spanish
- People who are receiving their pregnancy and postpartum care at OSU (Ohio State University)
Who may not be able to join:
- People who are unable to complete a two-hour oral glucose tolerance test — for example, those who have had gastric bypass surgery
- People who do not speak English or Spanish
- For the follow-up part of the study (called PP CARE): Spanish-speaking participants are not eligible, as the study team does not currently have Spanish-speaking staff members available for that phase (confirm with trial site)
- For the follow-up part of the study (called PP CARE): participation is only open to English-speaking participants who are between 12 and 24 months after giving birth
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Christine Field, MD, MPH, Ohio State University
Phone: 614-293-2222
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Rate of postpartum diabetes mellitus screening; Patient reported outcome of postpartum Cardiovascular health (CVH) counseling received within the first 12 months after delivery; Patient perspectives, preferences and barriers to engagement with respective to postpartum interventions to improve CVH.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.