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临床试验/NCT03382132
NCT03382132已完成不适用

momHealth: Multiple Health Behavior Change Intervention in Teen Pregnancy & Parenting Using Mobile Technology

University of Kansas Medical Center1 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2017年9月20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
入组人数
78
试验地点
1
主要终点
Minutes of moderate to vigorous physical activity per week

研究概览

简要总结

The purpose of this study is to find out if information and support provided with a mobile-delivered (via iPad) momHealth Teen Pregnancy Program can promote healthy choices and behaviors during and after pregnancy.

详细描述

This is a RCT to pilot test an innovative multiple health behavior intervention to influence three areas of health for pregnant and parenting adolescents: breastfeeding, healthy eating/active living, and depression prevention. Intervention and control groups will be compared in the main outcomes of the study (see 4.2.c. and 4.3). Beginning in the last eight weeks of pregnancy and extending to one month after giving birth, we use mobile health technology (e.g., iPad minis) to deliver multi-media educational modules, text-messaging, virtual home visits with professionals using secure televideo, and real-time peer group support over televideo. At birth, five weeks, and three months after giving birth, effectiveness of the program outcomes will be assessed and compared to a usual care control group and include breastfeeding/infant-feeding practices; healthy eating and physical activity; and depressive symptoms. This is the first known study to address these multiple behaviors simultaneously with pregnant and parenting adolescent women.

研究设计

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

入排标准

年龄范围
15 Years 至 20 Years(Child, Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Pregnant females
  • •English-speaking
  • •Giving birth to first child
  • •Intending to keep the newborn
  • •Access to a telephone
  • •27-31 weeks gestation
  • •Low-risk pregnancy

排除标准

  • •Multiple gestation pregnancy
  • •High-risk pregnancy
  • •Women with active untreated mental health conditions such as affective disorder, substance use disorder, anxiety disorder (excluding simple phobia), or psychosis

研究组 & 干预措施

Control

Active Comparator

Participants will receive the normal support they would normally receive if they were not in a study.

干预措施: Standard of Care (Behavioral)

momHealth

Experimental

Participants will receive support and information via the momHealth program.

干预措施: momHealth (Behavioral)

结局指标

主要结局

Minutes of moderate to vigorous physical activity per week

时间窗: Change from Baseline to Month 3

Measure will be assessed using ActiGraph Physical Activity Monitors.

Rate of any and exclusive breastfeeding

时间窗: Month 3

Self-report data on breastfeeding continuation, either wholly or partially, out to 3 months postpartum.

Duration of breastfeeding

时间窗: Month 3

Number of days out to 3 months postpartum of any breastfeeding.

Consumption of "red" foods per day

时间窗: Change from Baseline to Month 3

Measure will be assessed using the Automated Self-Administered 24-hour Recall™ (ASA24™). Participants will provide information on food eaten through an online site and accessed with an individualized link.

Change in depressive symptoms

时间窗: Month 3

Assessed using the Edinburgh Postnatal Depression Scale (EPDS), a 10-item questionnaire. Each question response is coded from 0 to 3. Scores can range from a minimum of 0 to a maximum of 30. A score of 10 or greater detects a major depressive disorder with sensitivity.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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