NCT06965803招募中不适用
Continuous Glucose Monitor (CGM) Discharge Program
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 37
- 试验地点
- 1
- 主要终点
- Patient Satisfaction (using a 5-point likert scale)
研究概览
简要总结
The purpose of the study is to improve patient-reported outcomes by improving patient's satisfaction and quality of life (QOL) with glucose monitoring device through pre and post satisfaction survey of patient with diabetes.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •aged 18 or older
- •diagnosed with Type 1 or Type 2 Diabetes who are on insulin
- •able to speak and understand English language
- •scheduled to receive a standard inpatient diabetes education consultation
- •must not have used CGM in the six months prior to admission
- •owns a smartphone
- •demonstrates the ability to follow instructions and be capable of providing informed consent to participate in the program
排除标准
- •those who are known to be pregnant. This is due to complexity of pregnancy-related changes in glucose metabolism and increased skin sensitivity, or changes in skin condition to adhesives and materials used in CGM devices.
- •non-English speakers. As this is small study to evaluate which method is favorable using a survey only validated in English, enrolling non-English speakers would require additional resources/translations/personnel for evaluation and the education intervention that are not logistically possible right now.
结局指标
主要结局
Patient Satisfaction (using a 5-point likert scale)
时间窗: 15 days
Glucose Monitoring Satisfaction Survey
次要结局
未报告次要终点
研究者
Matthew Monterola
Associate Director, Clinical Support Programs
Cedars-Sinai Medical Center
研究点 (1)
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