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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02388958
Other study ID # 140295
Secondary ID P30DK092986
Status Completed
Phase N/A
First received March 9, 2015
Last updated January 18, 2017
Start date June 2014
Est. completion date December 2016

Study information

Verified date January 2017
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Gestational diabetes mellitus (GDM) is associated with short-term and long-term complications for infants and mothers. The management of GDM during pregnancy focuses on reducing risks to the infant associated with hyperglycemia. The postpartum management of GDM focuses on reducing maternal risk of developing type 2 diabetes (T2DM). A diagnosis of GDM identifies up to 31% of parous women who will eventually develop T2DM and approximately 50% of women diagnosed with GDM will develop T2DM in the first 5 years postpartum. The perceived risk of developing short-term and/or long-term complications of GDM may influence women's likelihood of engaging in diet modification, the mainstay of treatment of GDM, both during and after pregnancy. If sustained after delivery, diet modifications introduced as treatment for GDM could affect maternal weight changes during and after pregnancy, which could in turn affect T2DM risk. It is unknown if and how women with GDM differ in their perceived risk of developing T2DM, dietary choices, or weight gain (and retention) during versus after pregnancy. Therefore, the project proposed in this application seeks to (1) characterize the perceived risk of developing T2DM among women with GDM during and after pregnancy, (2) characterize dietary choices of women with GDM during and after pregnancy, and (3) characterize weight changes of women with GDM during and after pregnancy as compared to women without GDM.


Recruitment information / eligibility

Status Completed
Enrollment 89
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria for women with GDM:

- Patient is currently pregnant with a singleton pregnancy.

- Laboratory confirmed diagnosis of GDM between weeks 24-28 gestation.

- Patient is receiving routine prenatal care at Vanderbilt University Medical Center.

Inclusion Criteria for women without GDM:

- Patient is currently pregnant with a singleton pregnancy.

- Patient does not have GDM based on non-fasting and/or fasting GTT results.

- Patient is receiving routine prenatal care at Vanderbilt University Medical Center.

Exclusion Criteria for both cohorts:

- Diagnosis of type 1 or type 2 diabetes prior to pregnancy.

- Diagnosis of GDM prior to 20 weeks gestation.

- Patient does not speak English.

Study Design


Locations

Country Name City State
United States Vanderbilt University Medical Center Nashville Tennessee

Sponsors (2)

Lead Sponsor Collaborator
Vanderbilt University National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postpartum weight change measured in kilograms 6 months (change in weight from the time of delivery to 6 months postpartum)
Secondary Rate of pregnancy weight gain prior to GDM diagnosis measured in kilograms per week 24-28 weeks
Secondary Rate of pregnancy weight gain after GDM diagnosis measured in kilograms per week 10-16 weeks
Secondary Change in perceived risk of developing diabetes during versus after pregnancy measured with the Risk Perception Survey for Developing Diabetes (RPS-DD) 10 months
Secondary Change in dietary choices during versus after pregnancy measured with the Personal Diabetes Questionnaire 10 months
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