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Completed

NCT Number: NCT01565564

Randomized Translational Study to Examine the Effects of Shared Care in Management of Gestational Diabetes

Research question (s)/hypothesis:

1. . The effectiveness of the shared care management of gestational diabetes mellitus; 2. . The cost-effectiveness of the shared care management; 3. . Its sustainability

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Key information

About this study

Method (s) Tianjin three-tier antenatal care network established a universal screening program for gestational diabetes mellitus (GDM) in 1998 and up to 2008, the screening program had screened 115348 pregnant women. GDM will be defined as either fasting plasma glucose (PG) ≥5.1 mmol/L or 1-hour PG≥ 10.0 mmol/L or 2-hour PG≥ 8.5 mmol/L after 75 g glucose tolerance test. A total of 920 pregnant women who have GDM and agree to participate will be randomly assign to have the shared care (diet, physical activity and insulin if indicated) or the local usual antenatal care. The sample size has ≥80% power at a 5% type I error to detect the difference in the primary endpoint, birth weight ≥4000 gram and the secondary endpoint, pregnancy-induced hypertension. Hyperglycemia and other clinical data in the two groups of women will be collected during the shared care or the usual care. Logistic regression and cost-effectiveness analysis will be used in the data analysis.

Public health significance: The introduction of the proven management of GDM in Tianjin antenatal care network will justify the universal screening for GDM and reduce the rate of macrosomic infants and reduce pregnancy-induced hypertension, and thus improve pregnancy outcomes of women with GDM.

Sustainability plan: Just as the universal GDM screening in 1998, the shared care model will be introduced into the Tianjin antenatal care network as part of the usual care routine after the proposed study. The success of the care model will also be publicized and expanded to suburban districts and rural counties of Tianjin, possibly other parts of world where universal screening for GDM is a routine practice.

ACKNOWLEDGEMENT This project is supported by a BRIDGES grant from the International Diabetes Federation. BRIDGES, an International Diabetes Federation project, is supported by an educational grant from Lilly Diabetes."

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All pregnant women who are diagnosed to have GDM.

Exclusion criteria

  • Diagnosis of overt diabetes during OGTT;
  • Younger than 18 years of age;
  • Non-singleton pregnancy;
  • Maternal-foetal ABO blood type incompatibility;
  • Maternal diseases such as chronic hypertension,thyrotoxicosis, prepregnancy diabetes and use of long-term medications that may affect glucose metabolism.

Treatment and study plan

Shared glycaemic control care within the local three-tier's antenatal care network

Behavioral
  • Individualized dietary and physical activity consultation plus group diabetes education
  • Self blood glucose monitoring
  • Insulin therapy if indicated
  • Self blood glucose monitoring
  • Insulin therapy institutions if indicated;

Other names: The shared lifestyle intervention arm

Primary outcomes

  1. The Rate of Macrosomia.

    Time frame: At the time of birth.

    Macrosomia is defined as birthweight ≥ 4000 gram.

Secondary outcomes

  1. The Rate of Pregnancy-induced Hypertension.

    Time frame: From enrolment at 24-28 gestational weeks till after delivery, an average of 12 weeks.

    Pregnancy-induced hypertension includes gestational hypertension and preeclampsia/eclampsia.

Sponsors and collaborators

Lead sponsor

Tianjin Women and Children's Health Center

Other

Collaborators

  • Pennington Biomedical Research Center
  • Tianjin Medical University

Registry information

Official study title

A Randomized Translational Study to Examine the Effects of Shared Care Versus Usual Care in Management of Gestational Diabetes in a Three-tier Prenatal Care Network in Tianjin, China

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Mar 28, 2012
Registry last updated
Jul 7, 2015

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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