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临床试验/NCT05204706
NCT05204706招募中不适用

A Feasibility Randomised Controlled Trial of a Mobile Phone Application for the Primary Prevention of Type 2 Diabetes in Malaysian Women With Gestational Diabetes Mellitus.

Universiti Putra Malaysia6 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年1月24日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
6
主要终点
Number of women withdrawn or loss to follow up

研究概览

简要总结

Gestational diabetes mellitus (GDM) is an increasingly common condition of pregnancy and is associated with adverse foetal, infant, and maternal outcomes. Over 50% of women with history of GDM will develop type 2 diabetes (T2D) in later life. Asian women experience disproportionate risk of both GDM and T2D compared to women from other ethnic groups. Lifestyle interventions have been proven to be effective in preventing progression to T2DM in high-risk populations. This is a two-arm, parallel feasibility RCT. Sixty Malaysian women with GDM will be randomized to receive the intervention or standard care in the antenatal period to 12 months postpartum. The intervention is a diabetes prevention intervention delivered via a smartphone application developed based on the Information-Motivation-Behavioral Skills (IMB) model of behavior change and group support utilizing motivational interviewing, which will provide women with tailored information and support to encourage weight loss through adapted dietary intake and physical activity. Women in the control arm will receive standard care.

详细描述

Gestational diabetes mellitus (GDM) is a global health challenge, with rates increasing around the world. The adverse short and long-term health outcomes of GDM for both mother and their offspring have been well established. In the long-terms women are up to ten times more likely to develop T2D after GDM and approximately 50% of mothers with GDM will develop diabetes within 10 years. Considerable evidence from several landmark studies has shown that healthy lifestyle interventions and behaviour change can delay or even prevent the onset of T2D in high-risk populations. Given women with prior GDM are at high risk of developing T2D earlier in their lifespan than women with normoglycemic pregnancies, intervening early with an effective diabetes prevention intervention offers a unique window of opportunity along the life-course for the prevention of T2D for the mother. Mobile health (mHealth) is a rapidly growing field of public health, defined as the use of mobile phones and other wireless technology to support the achievement of health objectives. Due to the increasing ownership rate of smartphones, significant numbers of mHealth applications 'apps' have been developed. Pregnant and postpartum women are increasingly utilising such technologies as sources of health information and services for pregnancy self-care and infant care.

The overall aim of the RCT is to test the feasibility of undertaking a definitive trial of a diabetes prevention intervention delivered via a smartphone app over 15-months in women with GDM from randomisation in the antenatal period to 12 months postpartum.

Sixty participants will be recruited from three public health clinics within the southern Selangor state of Malaysia. Women will be eligible for recruitment if they meet the following criteria: i) aged above 18 years, ii) diagnosed with GDM defined using fasting blood glucose > 5.1mmol/1 or 2-hour postprandial >7.8mmol/1 which are the standard guidelines for diagnosis of GDM in Malaysia, iii) permanent resident in the state of Selangor, iv) registered in one of the study health clinics v) owning a smartphone (iOS 11 or Android 7), vi) able to speak, read, and understand English and/or Malay. Women will be excluded if they meet any of the following criteria: i) are having a twin pregnancy, ii) have type 1 or 2 diabetes, iii) have severe physical disability that would prevent any increased uptake of physical exercise, iv) have severe mental illness (psychosis, bipolar, substance dependence or active suicidal ideation), v) are currently participating in a weight loss program or diabetes prevention intervention.

Women who meet study inclusion criteria and consent to study participation will be randomised to either the intervention or control arm. The intervention consists of a smartphone app for women with GDM called MyManis (the English meaning of MyManis is 'my sweet (baby)' and a virtual peer support group. The development of the app was guided by the Information-Motivation-Behavioural Skills (IMB) model of behaviour change. The MyManis app aims to provide women with information and support and motivation to act on this information to make lifestyle behaviour changes in diet and physical activity from pregnancy to post-partum. The app is available for women in both Malay and English. Women allocated to the control arm will receive standard care and no digital intervention.

The overall aim of the RCT is to test the feasibility of undertaking a definitive trial of a diabetes prevention intervention including a smartphone app and group support over 15-months in women with GDM from randomization in the antenatal period to 12 months postpartum.

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

入选标准

  • aged above 18 years,
  • diagnosed with GDM defined using fasting blood glucose > 5.1mmol/1 or 2-hour postprandial >7.8mmol/1 which are the standard guidelines for diagnosis of GDM in Malaysia,
  • permanent resident in the state of Selangor,
  • registered in one of the study health clinics
  • owning a smartphone (iOS 11 or Android 7) with internet connection,
  • able to speak, read, and understand English and/or Malay.

排除标准

  • are having a twin pregnancy,
  • have type 1 or 2 diabetes,
  • have severe physical disability that would prevent any increased uptake of physical exercise,
  • have severe mental illness (psychosis, bipolar, substance dependence or active suicidal ideation),
  • are currently participating in a weight loss program or diabetes prevention intervention.

结局指标

主要结局

Number of women withdrawn or loss to follow up

时间窗: Collected antenatally at 12 months after delivery

The proportion of women who are withdrawn or lost to follow-up (numerator) out of those randomised (denominator)

Number of women who were randomised to the treatment groups.

时间窗: Collected antenatally at 30 weeks pregnancy

The proportion of women who were randomised (numerator) out of those identified from the clinical registers (study population as denominator)

Number of women that take up the intervention

时间窗: Collected antenatally at 12 months after delivery.

The proportion of women who take up the intervention (numerator) out of those in the intervention arm (denominator)

次要结局

  • Number of women completed the secondary outcomes(Collected antenatally at 12 months after delivery)
  • Number of women consented(Collected antenatally at 24-28 weeks pregnancy)
  • Number of women randomised(Collected antenatally at 30 weeks pregnancy)

研究者

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

Boon-How Chew

Principal Investigator

Universiti Putra Malaysia

研究点 (6)

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