跳至主要内容
临床试验/NCT05648721
NCT05648721Unknown不适用

The Effects of a Digital Application for Gestational Diabetes Management in Improving Patients' Compliance and Satisfaction, Glycemic Control and Pregnancy Outcomes: A Multicenter Randomized Controlled Trial

The Baruch Padeh Medical Center, Poriya5 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2023年5月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
110
试验地点
5
主要终点
Patient compliance

研究概览

简要总结

Gestational diabetes mellitus (GDM) is the most prevalent complication in pregnancy. Patients' follow-up and treatment is performed in specialized GDM clinics that teach and support women in implementing lifestyle changes, blood glucose self-monitoring, and nutritional and pharmacologic therapy.

Recently, mobile health (mHealth) applications have been introduced as a resource to improve self-management and follow-up among pregnant women. The proposed study will examine the efficacy of the GDM management mHealth application in improving patients' compliance and satisfaction, glycemic control, and pregnancy outcomes.

A multicenter randomized controlled trial of women with GDM treated in the GDM clinics. Women will be randomly allocated to a research group that will use the GDM application and a control group that will receive regular follow-up without the GDM application. The primary outcome is patient compliance, defined as the actual blood glucose measurements/instructed measurements ×100. Secondary outcomes include glycemic control parameters, and maternal and neonatal complications.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • •Pregnant women diagnosed with GDM from 13.0 gestational week
  • •Recruitment until 34.0 gestational week
  • •18 years old and older
  • •Singleton pregnancy

排除标准

  • •Women with pre-gestational diabetes mellitus
  • •Multiple pregnancy
  • •Women without a Smartphone that can support the GDM application
  • •Refusal to participate

研究组 & 干预措施

Mobile health application

Experimental

Use of GDM application for GDM management

干预措施: Datos mobile health application (Other)

Control

Other

Regular follow-up without the GDM application

干预措施: Regular follow-up (Other)

结局指标

主要结局

Patient compliance

时间窗: During the follow up in the clinic (around 4 months)

Defined as the actual blood glucose measurements/instructed measurements ×100

次要结局

  • Induction of labor(At birth)
  • Neonatal intensive care unit admission(A week after delivery)
  • Neonatal hypocalcemia(During hospitalization after delivery (around the first week))
  • Neonatal hypomagnesemia(During hospitalization after delivery (around the first week))
  • Percentage of off-target glucose measurements(During the follow up in the clinic (around 4 months))
  • Instrumental or cesarean delivery(At birth)
  • shoulder dystocia(At birth)
  • Neonatal birth weight(At birth)
  • Number of neonates who needed phototherapy(During hospitalization after delivery (around the first week))
  • Neonatal death(During hospitalization after delivery (around the first week))
  • Apgar score(One and Five minutes after birth)
  • Patients' satisfaction from the monitoring protocol(Will be evaluated up to 2 months after birth)
  • Mean blood glucose of the daily glucose charts(During the follow up in the clinic (around 4 months))
  • Preeclampsia/gestational hypertension(During the follow up in the clinic (around 4 months))
  • Respiratory morbidity of the newborn(During hospitalization after delivery (around one week))
  • polyhydramnios(During the follow up in the clinic (around 4 months))
  • Hypoglycemia of the newborn(During hospitalization after delivery (around one week))
  • Need for pharmacotherapy for glycemic control(During the follow up in the clinic (around 4 months))
  • Third- or fourth-degree perineal tears(At birth)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (5)

Loading locations...

相似试验