A Shared Decision Making Intervention for Diabetes Prevention in Women With a History of Gestational Diabetes Mellitus
Gestational Diabetes Mellitus, Pre-diabetes, Diabetes Mellitus, Type 2
About this trial
This is an interventional prevention trial for Gestational Diabetes Mellitus focused on measuring Diabetes Prevention, Shared Decision Making
Eligibility Criteria
Inclusion Criteria:
- BMI 25 kg/m2 or above (23 or above if Asian American woman)
- History of gestational diabetes mellitus
- History of prediabetes in prior 36 months defined by either 1) most recent HbA1c 5.7-6.4% or 2) most recent FPG 100-125 mg/dL or 3) prior diabetes diagnostic codes + abnormal labs
- Patient at UCLA or Intermountain Healthcare Systems with provider visit or labs in prior 12 months
Exclusion Criteria:
- Delivery within prior 12 months
- History of diabetes (i.e., prior HbA1c 6.5% or above, or 2 or more fasting plasma glucose 125 or above, or prior diagnostic code)
- Use of an anti-glycemic medication in prior 12 months
- Last available glomerular filtration rate (eGFR) <45 ml/min
- BMI >60 kg/m2
- Bariatric surgery with prior 12 months
- Active eating disorder
- Currently pregnant or planning to get pregnant in the next 12-24 months
- Currently breastfeeding
- Completed a prediabetes SDM consult in past
- Currently enrolled in a CDC recognized Diabetes Prevention Program (DPP)
- Inability or concerns about doing >150 minutes of physical activity per week
- History of metformin intolerance
- Non-English primary language
Sites / Locations
- University of California, Los AngelesRecruiting
- Intermountain Healthcare SystemRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Shared decision-making with pharmacists
Usual Care
Participants randomized to the intervention arm will have an in-person visit to complete the baseline survey, record the participant's weight and receive a pharmacist-coordinated shared decision making intervention. Intervention participants will have follow-up research assessments visits at 6, 12 and 24 months.
Participants randomized to the usual care control arm will have an in-person visit with the research study team to complete the baseline survey and record the participant's weight. These participants will then return to usual care with research assessments at 6, 12 and 24 months follow-up.