Preliminary Examination of a Mobile Behavior Change Program for Weight Loss in Breast Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Noom Inc.
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Program satisfaction
研究概览
简要总结
The purpose of this study is to evaluate the preliminary efficacy of a Noom Breast Cancer Weight Loss Program on weight loss outcomes, quality of life, and physical activity. Also, to qualitatively determine acceptability of this novel program among breast cancer survivors with overweight or obesity.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Able to understand and provide informed consent
- •18 years and older
- •Overweight or obesity (BMI ≥ 27.5)
- •Not 6 months postpartum
- •Not planning to become pregnant in the next 7 months
- •Have a smartphone that is compatible with Noom's mobile app
- •Breast cancer survivor with stage I, II, or III
- •Completed active treatment (e.g, surgery, chemo, radiation, etc.) > 6 months ago
排除标准
- •Inability or unwillingness of a participant to give written informed consent
- •Currently pregnant or < 6 months postpartum
- •Plans to become pregnant within the next 7 months
- •Stage IV, metastatic cancer or DCIS
- •Currently taking insulin
- •Uncontrolled hypertension
结局指标
主要结局
Program satisfaction
时间窗: week 1 - 26 week
Satisfaction assessed via an in-house survey
Program engagement
时间窗: weeks 1-26
Engagement with the Noom program; measured as 1. Number of App opens 2. Messages to coach 3. Number of Steps 4. Logged food 5. Logged exercise 6. Group messages and likes 7. Articles read
Weight
时间窗: baseline to 6 months
Self-reported weight
Program retention
时间窗: weeks 1-26
i.e. % = (total participants - number of drop out) / Total number of participants) \* 100%
次要结局
未报告次要终点