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首页> 外文期刊>BMC Pregnancy and Childbirth >INTER-ACT: prevention of pregnancy complications through an e-health driven interpregnancy lifestyle intervention – study protocol of a multicentre randomised controlled trial
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INTER-ACT: prevention of pregnancy complications through an e-health driven interpregnancy lifestyle intervention – study protocol of a multicentre randomised controlled trial

机译:交互行为:通过电子医疗驱动的孕期生活方式干预预防妊娠并发症–一项多中心随机对照试验的研究方案

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Background Excessive maternal pre-pregnancy and gestational weight gain are related to pregnancy- and birth outcomes. The interpregnancy time window offers a unique opportunity to intervene in order to acquire a healthy lifestyle before the start of a new pregnancy. Methods INTER-ACT is an e-health driven multicentre randomised controlled intervention trial targeting women at high risk of pregnancy- and birth related complications. Eligible women are recruited for the study at day 2 or 3 postpartum. At week 6 postpartum, participants are randomised into the intervention or control arm of the study. The intervention focuses on weight, diet, physical activity and mental well-being, and comprises face-to-face coaching, in which behavioural change techniques are central, and use of a mobile application, which is Bluetooth-connected to a weighing scale and activity tracker. The intervention is rolled out postpartum (4 coaching sessions between week 6 and month 6) and in a new pregnancy (3 coaching sessions, one in each trimester of pregnancy); the mobile app is used throughout the two intervention phases. Data collection includes data from the medical record of the participants (pregnancy outcomes and medical history), anthropometric data (height, weight, waist- and hip circumferences, skinfold thickness and body composition by bio-electrical impedance analysis), data from the mobile app (physical activity and weight; intervention group only) and questionnaires (socio-demographics, breastfeeding, food intake, physical activity, lifestyle, psychosocial factors and process evaluation). Medical record data are collected at inclusion and at delivery of the subsequent pregnancy. All other data are collected at week 6 and month 6 postpartum and every subsequent 6?months until a new pregnancy, and in every trimester in the new pregnancy. Primary outcome is the composite endpoint score of pregnancy-induced hypertension, gestational diabetes mellitus, caesarean section, and large-for-gestational-age infant in the subsequent pregnancy. Discussion INTER-ACT is a unique randomised controlled lifestyle intervention trial in its implementation between pregnancies and during the subsequent pregnancy, with an e-health driven approach. Trial registration ClinicalTrials.gov Identifier: NCT02989142 . Registered August 2016.
机译:背景孕妇过度妊娠和妊娠体重增加与妊娠和分娩结果有关。怀孕时间间隔为您提供了一个独特的机会,可以进行干预,以便在开始新的怀孕之前获得健康的生活方式。方法INTER-ACT是一项以电子健康为基础的多中心随机对照干预试验,主要针对处于妊娠和分娩相关并发症高风险中的女性。在产后第2天或第3天招募符合条件的女性进行研究。产后第6周,将参与者随机分为研究的干预或对照组。干预措施着重于体重,饮食,身体活动和心理健康,并包括面对面的指导(其中行为改变技术为中心)以及使用移动应用程序,该应用程序通过蓝牙连接到体重计和活动跟踪器。干预措施将在产后(第6周至第6个月之间进行4次辅导)和新妊娠(3次辅导,每三个月进行一次)中推出。在两个干预阶段中都会使用移动应用程序。数据收集包括参与者的病历数据(妊娠结局和病史),人体测量数据(身高,体重,腰围和臀围,皮褶厚度和通过生物电阻抗分析的身体成分),来自移动应用程序的数据(体力活动和体重;仅干预组)和问卷(社会人口统计学,母乳喂养,食物摄入,体力活动,生活方式,社会心理因素和过程评估)。在入组和随后妊娠分娩时收集病历数据。所有其他数据在产后第6周和第6个月以及随后的每6个月直至新胎以及新胎的每个三个月收集。主要结局是妊娠后高血压,妊娠糖尿病,剖腹产和大胎龄婴儿的综合终点评分。讨论INTER-ACT是一项独特的随机对照生活方式干预试验,在妊娠之间和随后的怀孕期间均采用电子卫生驱动方法进行。试用注册ClinicalTrials.gov标识符:NCT02989142。 2016年8月注册。

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