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临床试验/NCT06214221
NCT06214221进行中(未招募)不适用

A Randomized Controlled Trial Evaluating the Safety and Effectiveness of the Intelligently-Driven Signos System for Personalized Weight Management in Overweight and Obese Adults

Signos Inc10 个研究点 分布在 1 个国家目标入组 380 人开始时间: 2024年1月2日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Signos Inc
入组人数
380
试验地点
10
主要终点
Average Total Body Weight Loss (TBWL%)

研究概览

简要总结

Metabolic syndrome and resulting downstream health effects remains a growing health concern. In published trials, the use of continuous glucose monitoring (CGM) assists behavioral changes efforts, leading to improved adherence and results from diet and exercise changes in individuals with obesity. Mobile health (mHealth) platforms provide satisfactory, easy-to-use tools that help participants in the pursuit of weight change goals. The investigators hypothesize that the use of CGM data and targeted coaching and nutrition education will assist with weight optimization goals in the general (non-diabetic) population using the Signos mHealth platform, with associated health benefits.

详细描述

The scope of this study is to enroll participants into a study that utilizes a continuous glucose monitor (CGM) and mobile health application [Signos] to optimize general wellness and body weight and composition. The Signos users will be compared against a control arm.

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
None

入排标准

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

入选标准

  • To join our study, participant need to:
  • Be at least 22 years old.
  • Be overweight or obese, which we define as having a Body Mass Index (BMI) between 25 and
  • HbA1c test result should be below 6.5% at the start of the study.
  • Have and know how to use a smartphone that's compatible with the Signos app.
  • Be able to understand, speak, and read English well enough to participate fully in the study.

排除标准

  • Participant can't join our study if participant has:
  • Have Type 1 or Type 2 diabetes.
  • Are already using a device to monitor glucose level.
  • Have severe allergies to the sticky part of glucose monitors.
  • Suffer from an eating disorder like anorexia or bulimia.
  • Are currently taking certain medications for diabetes or weight loss.
  • Have had or are planning to have weight loss surgery.
  • Have major health issues like severe kidney disease, untreated thyroid problems, or skin conditions where the glucose monitor would be placed.
  • Have been part of another clinical trial recently.

结局指标

主要结局

Average Total Body Weight Loss (TBWL%)

时间窗: 6 Months

Investigators will measure how much weight, on average, participants have lost after 6 months in the study. This will be calculated as a percentage of their initial weight. This measure helps us understand the effectiveness of the Signos System in helping participants reduce their body weight over a 6-month period.

Responder Rate

时间窗: 6 Months

Investigators will measure how many participants successfully reached their weight management goals by the end of 6 months. This 'Responder Rate' tells us the percentage of people in our study who effectively managed their weight using the methods we provided, whether it's through the Signos System or standard lifestyle education.

次要结局

未报告次要终点

研究者

发起方
Signos Inc
申办方类型
Industry
责任方
Principal Investigator
主要研究者

Stephanie Kim, M.D., MPH

Clinical Trial Investigator, Signos Inc

Signos Inc

研究点 (10)

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