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临床试验/NCT03726983
NCT03726983已完成不适用

Randomized Controlled Trail of e-Health Management for Women With Prior Gestational Diabetes Mellitus

Chang Gung Memorial Hospital1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2017年1月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
112
试验地点
1
主要终点
Change of high-density lipoprotein cholesterol (HDL) level

研究概览

简要总结

The purpose of this study was to develop an e-heath management platform(eHMP) for women with high risk of gestational diabetes mellitus (GDM) and to evaluate the longitudinal effects between groups of eHMP intervention.

详细描述

Background: Women with previous gestational diabetes mellitus are at increased risk for developing type2 diabetes mellitus or metabolic syndrome in their later life. Infants of mothers with GDM are more susceptible to stillbirth and more serious health concerns. With limited time for visits and the predicament of education, applying web-based intervention has become a convenient tool for health management.

Objectives: The approved project aimed to develop an e-heath management platform(eHMP) for women with high risk of gestational diabetes mellitus (GDM) and to evaluate the longitudinal effects between groups of eHMP intervention. The eHMP integrate GDM health care knowledge, self-awareness of health, self-monitoring of health status (i.e., recording weight and measurement data of metabolic syndrome risk factors and monitoring changes in data trends); participation in discussions or browsing forums; healthy lifestyle guidance and counseling; reminder systems, a token system of earning points in exchange for prizes.

Methods: Pregnant women aged 18-45 years with high risk of metabolic syndrome who have a singleton pregnancy, are eligible to participate in this study. Women who agree to participate in the study will be given a participant information sheet and consent form. Participants will be recruited from the Pregnancy diabetes Clinic, at Chang Gung memorial hospital and introduced to the eHMP using the mobile phone in the clinic. Participants will also be given the URL to access to the program and they can learn the modules at home by using their home PCs, mobile phones, or tablets. They were followed up for three times: 28 weeks' gestation, 36-40 weeks' gestation and 6-12 weeks postpartum. SPSS version 20.0 software was used to compile and analyze the research data, including questionnaires and blood test for metabolic index.

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
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Pregnant women (pre-pregnancy body mass index ≧ 24) must meet at least one of the following conditions and agree to be interviewed:
  • •Age over 34 years old;
  • •Ever had giant infant delivery (weight ≧ 4.5 kg);
  • •Previous diagnosed with gestational diabetes ;
  • •Family history of diabetes.

排除标准

  • •Pre-existing diabetes (types 1 and 2);
  • •Unable to write and understand Chinese;
  • •Subject has cognitive impairment;
  • •Subject has intellectual disability or mental illness;
  • •Dependent on medical care (eg, anti-depressants, or any psychiatric medication)

研究组 & 干预措施

eHMP experimental group

Experimental

The experimental group received health management support and counseling,including:

  1. GDM health care knowledge
  2. self-awareness of health
  3. self-monitoring of health status (i.e., recording weight and measurement data of metabolic syndrome risk factors and monitoring changes in data trends)
  4. participation in discussions or browsing forums
  5. healthy lifestyle guidance and counseling
  6. reminder systems
  7. a token system of earning points in exchange for prizes.

干预措施: Experimental group (Other)

Control group

No Intervention

only received usual care

结局指标

主要结局

Change of high-density lipoprotein cholesterol (HDL) level

时间窗: Change from Baseline at 6-12 weeks after delivery

Blood sampling was performed in the fasting state. Normal HDL was ≥50 mg/dl; \<50mg/dl was abnormal

Change of Triglyceride Level

时间窗: Change from Baseline at 6-12 weeks after delivery

Blood sampling was performed in the fasting state. Normal triglyceride was \<150 mg/dl; ≥150mg/dl was abnormal

Change of Cholesterol level

时间窗: Change from Baseline at 6-12 weeks after delivery

Blood sampling was performed in the fasting state. Normal Cholesterol was \< 200 mg/dl; ≥200mg/dl was abnormal

Newborn baby weight

时间窗: at birth

Newborn baby weight in normal range (\>2500g - \<4500g) - dichotomous outcome Yes/No assessed using calibrated digital scales.

Change of Fasting Blood Glucose (FBG) Level

时间窗: Change from Baseline at 6-12 weeks after delivery

Blood sampling was performed in the fasting state. Normal FBG was \< 100 mg/dl; ≥100mg/dl was abnormal

Change of systolic blood pressure

时间窗: Change from Baseline at 6-12 weeks after delivery

Normal systolic blood pressure was \<130mmHg; ≥130mmHg was abnormal. Blood pressure was measured at the right arm twice after a 10-min rest in the supine position by using a calibrated sphygmomanometer and averaged.

Change of body weight

时间窗: Change from Baseline at 6-12 weeks after delivery

Women's weight following as assessed using calibrated digital scales

Change of diastolic blood pressure

时间窗: Change from Baseline at 6-12 weeks after delivery

Normal diastolic blood pressure was \<85mmHg; ≥85mmHg was abnormal. Blood pressure was measured at the right arm twice after a 10-min rest in the supine position by using a calibrated sphygmomanometer and averaged.

次要结局

  • Change of Pregnancy Physical Activity Assessment(Change from Baseline at 6-12 weeks after delivery)
  • Change of Dietary Behavioral Characteristics Scale(Change from Baseline at 6-12 weeks after delivery)
  • Change of Health Promotion Scale(Change from Baseline at 6-12 weeks after delivery)

研究者

发起方
Chang Gung Memorial Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mei-Chen Su

Director, Clinical Research

Chang Gung Memorial Hospital

研究点 (1)

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