NCT06692413撤回不适用
Withings Devices Follow-up Study - Hypertension
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 发起方
- Withings
- 入组人数
- 1,000
- 试验地点
- 1
- 主要终点
- Prediction of uncontrolled hypertension
研究概览
简要总结
The primary objective is to evaluate the accuracy to predict uncontrolled hypertension with Withings device data.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
入排标准
- 年龄范围
- 21 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Male or female who are 21 years of age or older,
- •Participant living in the United States,
- •Participant with data recorded in WITHINGS database,
- •Active WITHINGS device users having at least 2 years of data,
- •Subject able to read, understand, and provide written informed consent,
- •Subject willing and able to participate in the study procedures as described in the consent form,
- •Subject able to communicate effectively with and willing to follow instructions from the study staff.
排除标准
- •Minors under 21 years old,
- •Subject who refused to participate in the study,
- •Subject who did not reply to the questionnaire,
- •Subject who objected to the processing of his or her data after the start of the study.
研究组 & 干预措施
Withings device users
Active Withings device users having at least 2 years of device data
干预措施: Questionnaire (Other)
结局指标
主要结局
Prediction of uncontrolled hypertension
时间窗: 2 years
Correlation between uncontrolled hypertension, Withings data, and survey answers
次要结局
- Correlation between Framingham risk score and EQ-5D-5L answers and Withings data(2 years)
- Number of Questionnaires answers per participant(2 years)
研究者
研究点 (1)
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