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临床试验/NCT02126605
NCT02126605Unknown不适用

Accuracy of Blood Glucose Detection by Diabetes Alert Dogs

University of Virginia1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2014年7月最近更新:
适应症

试验速览

阶段
不适用
入组人数
16
试验地点
1
主要终点
Percent agreement between DAD alerts and glucose readings

研究概览

简要总结

Even though there is growing interest in and use of trained Diabetes Alert Dogs (DADs) as a way to monitor blood glucose in type 1 diabetes (T1D), no scientific studies have confirmed the ability of DADs to accurately detect extreme high and low blood sugar. The current project is the first preliminary investigation into the accuracy of DADs, using scientifically rigorous research methods similar to those required to demonstrate accuracy in blood glucose meters. The primary aim of the project is to test the hypotheses that DADs are accurate at detecting extreme blood sugar levels in adults and children with T1D. The proposed project has several other secondary aims, which include determining: 1) the glycemic thresholds and time course for hypo- and hyperglycemic DAD alerts, 2) the degree to which alert accuracy is consistent across different DADs, and 3) whether or not DAD owners appear to experience better psychosocial status and quality of life compared to other individuals with T1D.

详细描述

In the proposed project, DAD alerts will be compared to blood glucose (BG) readings from a continuous glucose monitoring (CGM) device, as well as a BG meter. CGM, BG meter, and DAD alert data will be collected over a 4-wk period. CGM devices will be "blinded" so that BG readings will not be shown. This will allow for a direct comparison between objective glucose readings generated by approved BG monitoring devices and DAD alerts. This study will also utilize two methods for measuring DAD alerts: (1) use of the event recorder mechanism of the CGM device, and (2) collection of more detailed and qualitative data on DAD alerts using diaries (Daily DAD Diaries) to collect information concerning the occurrence, timing, and type of DAD alerts.

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
6 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The participant must have had type 1 diabetes for at least 1 year and been taking insulin since diagnosis
  • The participant must have a DAD placed in their home for a minimum of 6 months.
  • Participants must not currently be using a continuous glucose monitor (CGM) in their diabetes management.
  • Participants must be capable of performing all tasks involved in the study protocol, including filling out questionnaires and diaries in English.
  • Participants must have an internet-connected computer compatible with study software.
  • Willingness to avoid consumption of acetaminophen-containing products for the duration of the study.

排除标准

  • Pregnant women-self reported
  • Current use of a CGM
  • History of a systemic deep tissue infection with methicillin-resistant staph aureus or Candida albicans

结局指标

主要结局

Percent agreement between DAD alerts and glucose readings

时间窗: 5 weeks

次要结局

  • Psychosocial variables (quality of life, fear of hypo-/hyperglycemia, diabetes distress, self-efficacy, and DAD experiences)(Baseline, 5 weeks)

研究者

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

Linda Gonder-Frederick

Associate Professor

University of Virginia

研究点 (1)

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