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临床试验/NCT07734259
NCT07734259尚未招募不适用

Voice-activated and Touchscreen-controlled Smart Speaker Intervention for Older Adults With Poorly Controlled Type 2 Diabetes

Medical College of Wisconsin0 个研究点目标入组 30 人开始时间: 2026年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
30
主要终点
HemoglobinA1C

研究概览

简要总结

This is a pre-post pilot study that will test the feasibility and acceptability of a health educator delivered diabetes education and skills training intervention using a voice-activated, touch screen controlled, smart speaker. We will enroll 30 adults aged 50 and older with poorly controlled type 2 diabetes as defined by a hemoglobin A1C of 8% in the study.

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
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 1) Aged 50 and older; 2) clinical diagnosis of poorly controlled type 2 diabetes, defined as HbA1C greater than or equal to 8% at the screening visit; 3) willing to install and use the VATC-SS for the 3 months of the study.

排除标准

  • 1) Mental confusion at screening assessment suggesting significant dementia; 2) alcohol or drug abuse/dependency at screening assessment; 3) active psychosis or acute mental disorder at screening assessment.

结局指标

主要结局

HemoglobinA1C

时间窗: Baseline and 3-months post enrollment

About 10cc of blood will be drawn by phlebotomist and sent to the lab for testing

Blood Pressure

时间窗: Baseline and 3-months post-enrollment

Blood pressure readings will be obtained using automated blood pressure monitors (OMRON IntelliSenseTM HEM-907 XL). The device will be programmed to take 3 readings at 2-minute intervals and give an average of the 3 blood pressure readings.

Low-Density Lipoprotein Cholesterol

时间窗: Baseline and 3-months post-enrollment

About 10cc of blood will be drawn by phlebotomist and sent to the lab for testing

次要结局

  • Depression(Baseline and 3-months post-enrollment)
  • Social Isolation(Baseline and 3-months post-enrollment)
  • Loneliness(Baseline and 3-months post-enrollment)

研究者

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

Aprill Z. Dawson, PhD, MPH

Associate Professor

Medical College of Wisconsin

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