N/A N=30 Randomized Treatment

Barriers to Adherence to Recommended Follow-up in Women With a History of Gestational Diabetes

Gestational Diabetes Mellitus

Bottom Line

View on ClinicalTrials.gov: NCT01681147 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

May 2023

Primary outcome: Primary: Weight Loss — 0; 0; 2 Participants

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: 2 online nutrition and exercise education classes (Behavioral); Self monitoring of blood glucose levels (Behavioral)
Age: Adult · 21+ yrs
Sex: Female
Sponsor: Joslin Diabetes Center
Primary completion: Jan 2018

Outcome Measures

Outcome	Result	p-value
PRIMARY Weight Loss	0; 0; 2	—
PRIMARY Postpartum Diabetes Screening at One Year	0; 1; 1	—
PRIMARY Barriers Associated With Poorer Adherence to Diabetes Screening Guidelines and Weight Loss Goals	2.08; 2.20; 2.52; 1.60; 1.57; 1.97	—
SECONDARY Dietary Pattern Assessment of Women With Gestational Diabetes Postpartum	2.46; 2.77; 2.4; 1.57; 1.53; 1.69	—
SECONDARY Food Frequency Questionnaire	87.5; 20.0; 50.0; 57.1; 60.0; 42.9	—
SECONDARY Exercise Frequency in Women With Gestational Diabetes Post-Partum	3.4; 1.7; 2.2; 3.0; 2.2; 2.6	—

Summary

The purpose of this study is to find out whether women who have had gestational diabetes mellitus (GDM) will make healthier lifestyle choices, achieve weight goals, and complete postpartum care assessments after receiving two online classes on healthy nutrition and exercise classes at 6 weeks - 3 months and at 9 months postpartum.

Eligibility Criteria

Inclusion Criteria

Gestational Diabetes
Age between 21 and 45 years
Preconception BMI 19-40
Seen for at least 2 visits in the Diabetes in Pregnancy Program during their pregnancy
Singleton pregnancy

Exclusion Criteria

Preexisting diabetes or diabetes diagnosed at the 6 week 75 gram 2 hour OGTT
BMI >40
Multiple gestation (i.e., twins, triplets, etc.)

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01681147). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.