Diabetes Prevention Programming for Women With a History of Gestational Diabetes

NACompletedINTERVENTIONAL
Enrollment

117

Participants

Timeline

Start Date

June 1, 2019

Primary Completion Date

June 30, 2022

Study Completion Date

June 30, 2022

Conditions
Diabetes Mellitus, Type 2
Interventions
BEHAVIORAL

Positive Outcomes for Women

"Women and their children 10+ can consent to participate in the diabetes prevention programming offered through the research center. We will collect data at three time points, baseline, 4-6 months, and 12 months.~2\. Instead of participating in Encourage, women may participate in other diabetes prevention programming/weight management programming offered by other entities. Researchers will consent these women into the study to complete 3 data collection points, baseline, 4-6 months, and 12 months. Additionally, researchers will consent women to obtain data from their chosen program. For instance, if a woman chooses to do a Diabetes Prevention Program through the YMCA, researchers will ask women to self report their weekly attendance and weight."

Trial Locations (1)

46202

Riley Hospital for Children, Indianapolis

All Listed Sponsors
lead

Indiana University

OTHER

NCT03971838 - Diabetes Prevention Programming for Women With a History of Gestational Diabetes | Biotech Hunter | Biotech Hunter