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临床试验/NCT02368600
NCT02368600已完成不适用

A Randomized Controlled Trial Examining the Effectiveness of a Lifestyle Intervention in Reducing Gestational Diabetes Mellitus in High Risk Chinese Pregnant Women in Hong Kong

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 220 人开始时间: 2015年4月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
220
试验地点
1
主要终点
Proportion of subjects developed GDM

研究概览

简要总结

The number of women with gestational diabetes mellitus (GDM) had been increasing. Maternal GDM has a great impact on both the health of the mothers and the offspring. Antenatal lifestyle interventions, in particular dietary intervention appear to be feasible to improve maternal GDM and weight gain. To the best of our knowledge, there has been no such trial examining the feasibility of a lifestyle intervention in pregnant women in Hong Kong. Therefore, we plan to conduct a randomized controlled trial comparing a lifestyle modification program (LMP) in early pregnancy and the usual antenatal care in high risk Chinese pregnant women in Hong Kong. Intervention group subjects (n=110) will participate in a dietitian-led LMP including dietary and exercise component from the first antenatal (AN) booking to 24 weeks gestation. 110 women in the control group will receive routine hospital antenatal care. The primary endpoint will be the prevalence of GDM measured using a 75 g oral glucose tolerance test at 24-28 weeks gestation. The secondary endpoints will be the proportion of infant born with large for gestational age (>=95th percentile of the customized birth weight) and macrosomia (>=4 kg at birth). The intervention group involves dietary and exercise advice and monitoring. No drug or invasive procedure is involved. The control group will receive routine antenatal care and will be provided with an educational pamphlet on diet and exercise during pregnancy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Chinese origin
  • Reside normally in Hong Kong
  • Singleton pregnancy
  • Gestational age <= 12 weeks at the time of recruitment
  • Could speak and understand Chinese
  • Fulfill at least one of the following criteria for high risk of GDM at the time of recruitment based on the update hospital protocol implemented since 1st May 2014
  • Maternal age >= 35 years old at expected date of confinement.
  • Prior history of GDM or birth of child >= 4 kg
  • Pre-pregnant BMI or BMI at 1st trimester >= 25 kg/m2
  • Family history of diabetes at 1st degree relatives
  • Willing to give informed written consent and follow the study procedures

排除标准

  • Concurrent participation in any clinical trial or study
  • With renal, liver or thyroid dysfunction, cognitive impairment, or any other indication of a major medical or psychological illness, as judged by the investigators as ineligible to participate the study
  • Multiple pregnancies
  • Pre-existing DM
  • With physical restriction that prevents from exercising
  • Substance abuse

结局指标

主要结局

Proportion of subjects developed GDM

时间窗: 24-28 weeks gestation

次要结局

  • Proportion of neonates born with macrosomia(within 48 hours after delivery)
  • Proportion of neonates born with large for gestational age (LGA)(within 48 hours after delivery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ruth Chan

Research assistant professor

Chinese University of Hong Kong

研究点 (1)

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