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临床试验/NCT01751230
NCT01751230已完成不适用

E-Moms: A Personalized Telehealth Intervention for Health and Weight Loss in Postpartum Women

Pennington Biomedical Research Center2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2013年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Body Weight Change

研究概览

简要总结

The purpose of this study is to help women lose the weight they gained during their pregnancy using a SmartPhone app the investigators have developed called E-Moms. The investigators hypothesize that the moms given the app to use during the study will lose more weight than the moms who do not use the app.

详细描述

The E-Moms Study will last about 4 months. The weight management program is 4 months long and will end about 6 months after the participant's baby is born. All participants will receive Women, Infants and Children (WIC) services.

For the weight management program, participants will be put into one of these groups:

  1. WIC Moms: receive advice and services for nutrition and weight management after pregnancy from their WIC clinic.
  2. WIC E-Moms: receive a personalized diet and exercise plan to help them lose the weight they gained during their pregnancy. All information will be given to them using a SmartPhone, such as an iPhone. They will also get advice and services from your WIC clinic.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Investigator)

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

  • Are a female who has delivered a baby within the last 2 months
  • Are 18 years of age or older
  • Have a body mass index ≥25 kg/m2 or <40 kg/m2
  • Are accepted for post-pregnancy WIC services
  • Are English-speaking

排除标准

  • Are participating in the Nurse Family Partnership program
  • Had multiples in your most recent pregnancy
  • Are unwilling to be assigned at random to either of the 2 study groups
  • Are planning to move out of the study area within the next 6 months
  • Have a history of psychiatric conditions or chronic disease than can impact body weight, appetite, or energy intake such as HIV/AIDS, cancer, bipolar disorder or schizophrenia
  • Currently use antipsychotic medications or have used such medications in the previous 12 months
  • Have been diagnosis with type I diabetes
  • Report having a heart attack, stroke, or being hospitalized or treated for chest pain
  • Currently taking medications or supplements to aid in weight loss
  • Have had weight loss surgery in the past year or plan to have it prior to study completion.
  • Currently participating in another interventional study that influences weight control
  • Currently abusing drugs or alcohol (up to 14 drinks per week allowed)

结局指标

主要结局

Body Weight Change

时间窗: Baseline and 16 weeks

The primary outcome measure is weight change after the 16 week intervention.

次要结局

未报告次要终点

研究者

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

Leanne Redman

Principal Investigator

Pennington Biomedical Research Center

研究点 (2)

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