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临床试验/NCT07140848
NCT07140848招募中不适用

A Novel Continuous Glucose Monitoring Enhanced DPP Intervention to Prevent Type 2 Diabetes in Adults With Prediabetes

State University of New York at Buffalo1 个研究点 分布在 1 个国家目标入组 214 人开始时间: 2026年4月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
214
试验地点
1
主要终点
Glycemic Control (HbA1c)

研究概览

简要总结

Prediabetes affects over one-third of adults in the United States, placing them at a higher risk for developing type 2 diabetes and heart disease, which can lead to serious health complications and increased medical costs. Although a program called the Diabetes Prevention Program (DPP) has been shown to lower the risk of diabetes through healthy lifestyle changes, many people find it difficult to stick with these changes over the long term. This study seeks to find out if combining DPP coaching with continuous glucose monitoring (CGM) technology can help people stay on track with their health goals.

详细描述

CGM devices give individuals real-time information about their blood sugar levels, which can help them understand how their diet, exercise, and daily habits impact their health. By pairing CGM technology with support from trained DPP coaches, this approach aims to make it easier for participants to maintain healthy behaviors. The study will involve 214 adults with prediabetes who will follow a 12-month program with regular check-ins to measure improvements in blood sugar control, weight loss, physical activity, and overall quality of life.

The goal is to show whether using CGM in combination with coaching can lead to better health outcomes and whether it is a cost-effective way to prevent diabetes. If successful, this approach could be used in healthcare settings across the country, helping more people prevent diabetes and lead healthier lives.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • adults aged 18 years or older,
  • diagnosis of prediabetes, as defined by current clinical guidelines (HbA1c 5.7% to 6.4%, fasting plasma glucose 100-125 mg/dL, or 2-hour plasma glucose 140-199 mg/dL following a 75g oral glucose tolerance test),
  • body mass index (BMI) of at least 24 kg/m² (or 22 kg/m² for Asian Americans),
  • willingness to comply with all aspects of the study protocol, including attending coaching sessions and using CGM devices.

排除标准

  • Individuals will be excluded from the study if they
  • have a diagnosis of type 1 or type 2 diabetes,
  • are currently using CGMs or have medical contraindications to CGM use, such as severe skin allergies or implantable defibrillators, or
  • are currently enrolled in another clinical trial for prediabetes. Additionally, using validated assessments, we will exclude participants with significant dementia, alcohol or drug abuse/dependency, active psychosis, or life expectancy less than 12 months as these conditions are likely to interfere with adherence to the intervention.

研究组 & 干预措施

Control

Active Comparator

Diabetes Prevention Program

干预措施: Control (Behavioral)

Intervention

Experimental

Diabetes Prevention Program + Continuous Glucose Monitors/Coaching

干预措施: CGM-DPP (Behavioral)

结局指标

主要结局

Glycemic Control (HbA1c)

时间窗: Change from baseline HbA1c at 12 months post intervention follow-ups

Blood specimens (10 cc of blood) will be obtain by trained phlebotomists or nurse for HbA1c.

次要结局

  • Quality of Life as measured by SF-12(Change from baseline quality of life measure at 12 months post intervention follow-ups)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Raphael Fraser, PhD

Associate Professor of Medicine

State University of New York at Buffalo

研究点 (1)

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