Diabetes Prevention Programming for Women With a History of Gestational Diabetes

Indiana University

Status: Completed

Conditions: Diabetes Mellitus, Type 2

Treatments: Behavioral: Positive Outcomes for Women

Study type: Interventional

Funder types: Other

Identifiers

NCT03971838

1812789354

Details and patient eligibility

About

The purpose of this study is to offer women with a history of gestational diabetes access to diabetes prevention programming; their children 10 and older can participate.

Full description

The purpose of this study is to offer women with a history of gestational diabetes access to diabetes prevention programming; their children 10 and older can participate. There are two potential types of participants:

1. Women and their children 10+ can consent to participate in the diabetes prevention programming offered through Dr. Hannon's center (called Encourage). Researchers 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.

Enrollment: 117 patients

Sex: Female

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• History of gestational diabetes in a previous pregnancy
• Age 18+

Exclusion criteria

·Currently pregnant

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

117 participants in 1 patient group

Intervention Arm

Experimental group

Description:

Women with a history of gestational diabetes will be offered 4-6 months of a diabetes prevention program.

Treatment:

Behavioral: Positive Outcomes for Women