A Mobile Health (mHealth)-Enabled Lifestyle Intervention Among Women With History of Gestational Diabetes (GDM): a Pilot Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 61
- 试验地点
- 2
- 主要终点
- Mobile health application feasibility
研究概览
简要总结
This study aims to explore: (1) the relationship between lifestyle factors (eating, movement behaviour, sleep and stress) and glycaemic profile, and (2) the feasibility of delivering lifestyle intervention through the proposed mHealth strategy.
详细描述
A 2-week observational period, followed by a 8-week parallel 2-arm, single-centre, randomized controlled trial (RCT) study involving 60-80 multi-ethnic healthy women (Chinese, Malay, Indian, others) subjects aged between 21 and 45 years who had a previous diagnosis of Gestational diabetes mellitus (GDM).
Type 2 diabetes is the most common type of diabetes and if left untreated or is ill-managed, can lead to detrimental long-term health problems such as heart disease, kidney disease and stroke. Type 2 diabetes is often related to lifestyle and develops over time; with proper interventions, it could be avoided in some cases. GDM stands for Gestational Diabetes Mellitus and can occur in some pregnant women, usually from week 24 of pregnancy. Women with a history of GDM have also been connected to a lifetime risk of developing type 2 diabetes and cardiovascular disease. In Singapore, it is estimated that 4 in 10 women with GDM could develop pre-diabetes or diabetes within five years of their pregnancy. Therefore, postpartum follow-up is essential in early detection of, preventing or delaying the development of Type 2 diabetes in this group.
The study hypothesize that there is an association between glycaemic profile and daily lifestyle (i.e. eating behavior, physical activity sleep and stress) among women with a history of GDM. The study also hypothesize that it is feasible to adopt a holistic approach and introduce a personalized mHealth intervention to promote metabolic and mental health among women with a history of GDM. The study is a parallel 2-arm, single-centre randomized controlled trial based on 1:1 allocation ratio.
The study arms are; Group 1 (Intervention group) and Group 2 (Control group). The study will begin with baseline data collection (anthropometric measures, body composition, biochemistry tests, questionnaires) and 14-day observation of interstitial glucose and lifestyle (diet, physical activity, sleep and stress). Every subject, irrespective of their group allocation, will use Oura ring and Oura App throughout the study duration. Every subject randomized to Group 1( Intervention group) will additionally receive HealthifySG App which provides personalized lifestyle interventions that last for 4 weeks. Lifestyle recommendations (targeting diet, physical activity, sleep and stress) will be delivered by study team member through the HealthifySG App on a weekly basis. On the contrary, subjects randomized to Group 2 (Control group) will not receive the HealthifySGApp and lifestyle interventions during this period. Subsequently, both groups will be followed-up for 4 weeks.
The overall aim of the REVERSE DIABETES programme is three pronged: (1) to be more proactive in screening to identify women with a history of GDM in polyclinics and the community, (2) to explore the potential of mobile health (mHealth) strategies to engage these women and deliver holistic and personalized interventions for promoting metabolic health and mental wellbeing, and (3) to engage primary care physicians to use mHealth if proven acceptable and useful in the long term follow up of these GDM women in the polyclinics and communities. We hope to optimize the preventive measures within the community in the long term.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
盲法说明
60-80 female subjects will be randomized to either Group 1 (Intervention group) or Group 2 (Control group) based on 1:1 allocation. HealthifySG App will only be installed on the phones of subjects for Group 1(Intervention group).
入排标准
- 年龄范围
- 21 Years 至 45 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Healthy female volunteers (age 21-45 years)
- •A history of GDM in the past 5 years
- •Not planning to conceive during the study period
- •Not performing full breastfeeding during the study period
- •Own a smart phone(mobile phone) compatible with study App (Android v10 and above)
- •Proficient in English language
- •Plan to stay in Singapore for the next 1 year
- •Willing to comply to study protocol
- •Able to provide a written informed consent
排除标准
- •Current and/or previous diagnosis of diabetes except GDM
- •Currently pregnant
- •Given birth within last 12 weeks
- •Following special diet or dietary restriction
- •Experiencing severely limited mobility (e.g. wheelchair bound, need walking aid etc.)
- •Diagnosed with malnutrition, eating disorder, severe insomnia
- •Diagnosed with cancers, unstable heart related diseases, severe kidney disease
- •Diagnosed with severe unstable mental conditions, dementia or cognitive impairment
- •Alcohol or drug abuse
- •Medications known to influence glucose metabolism e.g. peroral corticosteroids
结局指标
主要结局
Mobile health application feasibility
时间窗: 10 weeks
Number of participants that show a change in lifestyle behaviour through the mobile health application usage.
次要结局
- Postprandial glucose(14 days)
- Oral glucose tolerance test (OGTT) measurements(Week -1 and 10)
- Change in depression (if any)(Week -1 and 10)
- Change in sleep quality as assessed by the Oura Ring Sleep Score.(10 weeks)
- Change in daily physical activity levels as assessed by the Oura Ring Activity Score.(10 weeks)
- Change in quality of life(Week -1 and 10)
- Change in anxiety (if any)(Week -1 and 10)
- Change in intake of meals(14 days)
研究者
Johan Eriksson
Executive Director & Programme Director (Human Development)
Institute for Human Development and Potential (IHDP), Singapore
