跳至主要内容
临床试验/NCT02518217
NCT02518217已完成不适用

ShapeUp Empower Study

The Miriam Hospital2 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2015年12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
130
试验地点
2
主要终点
Body Weight (kg)

研究概览

简要总结

This randomized controlled trial will evaluate patterns of use and health outcomes of the ShapeUp Empower online program with and without financial incentives for program engagement.

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
Single (Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-70 years
  • Body mass index (BMI) between 25 and 45 kg/m2
  • English speaking
  • Have access to the Internet via a computer and smartphone compatible with Empower and Commercial Apps, and basic knowledge of how to use this technology.
  • Agree to sharing of data entered in the Empower and Commercial Apps intervention systems.
  • Agree to ShapeUp's privacy policy and user agreement.

排除标准

  • Report health problems that make weight loss or unsupervised exercise unsafe or unreasonable
  • Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire
  • Are currently pregnant or breastfeeding, or intend to become pregnant in the next 12 months
  • Are planning to move outside of the greater Providence area within the next 12 months
  • Report any cognitive or physical limitations that preclude use of a personal computer
  • Have participated in a study conducted by the WCDRC in the past 2 years
  • Have followed a commercial weight-loss program within the previous 6 months or who are currently following a commercial weight loss program
  • Weight loss of ≥ 5% of initial body weight in the last 6 months
  • History of clinically diagnosed eating disorder excluding Binge Eating Disorder.
  • Previous surgical procedure for weight loss
  • Currently taking weight loss medication\
  • Treatment of cancer within the last 6 months
  • Have any medical or psychological condition, or life situation, that would make participation in a weight loss program inadvisable in the opinion of the principal investigator.

结局指标

主要结局

Body Weight (kg)

时间窗: 6 months after randomization

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

Rena R. Wing

Professor, Director of the Weight Control and Diabetes Research Center

The Miriam Hospital

研究点 (2)

Loading locations...

相似试验