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临床试验/NCT02064647
NCT02064647已完成不适用

Evaluation of a Novel CGM Trend Arrow Adjustment Tool in Children & Adolescents With Type 1 Diabetes Using Insulin Pump Therapy and Continuous Glucose Monitoring (TAAT Study)

Children's Hospital of Eastern Ontario2 个研究点 分布在 1 个国家目标入组 20 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
状态
已完成
入组人数
20
试验地点
2
主要终点
Time spent with postprandial glucose level in target range

研究概览

简要总结

Continuous glucose monitoring (CGM) provides up to 288 blood glucose levels per day, updated every 5 minutes and displayed in real-time on the insulin pump, which can be used to enhance delivery of insulin through pump therapy. In addition this real-time CGM data includes "trend arrows" which indicate when the blood glucose is rapidly falling or rising thus enabling the pump user to make immediate adjustments in insulin delivery to prevent subsequent low or high blood sugars. The trend arrows are displayed when the blood glucose is rapidly falling or rising. For example, if the glucose is increasing by 1-2 mmol/L over 20 minutes, a single upward arrow alerts the pump wearer, who can then decide to give a bolus of insulin or increase the meal bolus. Should the glucose level be increasing at a rate greater than 2mmol/L over 20 minutes, 2 upward arrows are displayed and the user could decide to give a larger bolus. The purpose of the bolus adjustment is to add insulin for the predicted rise in glucose to prevent or reduce subsequent hyperglycemia. Similarly, a decrease in the insulin bolus is advised if glucose levels are falling as evidenced by one or two downward arrows.

However, effective strategies for adjusting insulin boluses based on CGM trend arrows are lacking. The JDRF CGM Study Group recommended that boluses be adjusted based on trend arrows using a standard 10-20% increase/decrease of the total original recommended bolus dose (10% for one arrow up or down, and 20% for two arrows up or down), with the original bolus dose calculated by the pump calculator (i.e. Bolus Wizard). However, the original recommended bolus dose is dependent on the amount of food to be consumed (grams of carbohydrate) and the current blood glucose (if above or below target range), as well as the amount of active insulin, and therefore increasing or decreasing the total recommended bolus by 10-20% may overcompensate for the trend arrows and result in postprandial hypoglycemia. Attempts to use the10/20% formula within CHEO's large pediatric pump/CGM population resulted in low acceptance and adherence by CGM users.

The CGM TIME Trial Study Group develop an innovative tool for adjusting boluses for CGM trend arrows based on the patient's own insulin sensitivity factor (ISF). The Trend Arrow Adjustment Tool formula is: if CGM shows a single arrow up or down: adjust bolus by +/- (1.5/ISF) and for 2 arrows up or down +/- (3/ISF). Use of the Trend Arrow Adjustment Tool within the CGM TIME Trial appears to lead to more appropriate adjustment in bolus dosing, and more effective prevention of subsequent hyper- and hypoglycemia. Furthermore, this tool appears to have excellent uptake amongst the TIME Trial participants, with observations that there is continued usage of the tool throughout the 12 month study, and greater satisfaction with this component of CGM. However, the tool has not been systematically evaluated.

The proposed study will evaluate the Trend Arrow Adjustment Tool, to determine its effectiveness in reducing postprandial hyper- and hypoglycemia, as well as parent, child/youth satisfaction, and ease of use of the tool based on self-report measures. Comparison will be made with the 10/20% bolus adjustment & also to no adjustments to meal boluses (i.e. ignoring CGM trend arrows). Should use of the Trend Arrow Adjustment Tool lead to more time spent within the target glucose range, this will have immediate clinical benefit for patients, including improved quality of life, and potentially a reduction in HbA1c and prevention of long-term complications.

详细描述

Detailed protocol:

Phase 1(inpatient evaluation):

This part of the study will take place in a standardized outpatient setting (CHEO Medical Day Unit/Clinic). The CGM trend arrows will be stimulated using two typical clinical scenarios: oral fast acting carbohydrate (to stimulate upward trend arrows) and exercise (to stimulate downward trend arrows).

40 participants will be enrolled in this phase of the study (20 of whom will have oral fast acting carbohydrate and 20 of whom will engage in exercise). Once trend arrows have been triggered, the subjects will receive a standardized meal, and an adjusted insulin bolus. Comparison will be made between the Trend Arrow Adjustment Tool (based on the patient's own insulin sensitivity factor) and the standard bolus adjustment recommendations (i.e. +/- 10/20%, based on the STAR 1 Trial and JDRF CGM Study Group). Phase 1 of the study will lead directly to Phase 2's outpatient evaluation.

Upward CGM trend arrows (Group 1):

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Investigator)

入排标准

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

入选标准

  • Participants will be children and youth aged 5-18 years, attending CHEO diabetes clinic
  • Established Type 1 diabetes for more than 1 year,
  • Who have used an insulin pump and CGM for at least 3 months.
  • Willing to wear iPro2 blinded CGM and to use the Trend Arrow Adjustment Tool and the 10/20% bolus adjustment method.
  • Internet access at home (to upload CGM data).

排除标准

  • Conditions which may interfere with the subject's ability to participate in the study.
  • Has received oral and/or intravenous steroid therapy (for any indication, at any dose and/or for any duration) on more than 2 separate occasions in the past 12 months. Use of inhaled and/or topical steroid therapy in the last 12 months does not exclude the subject

结局指标

主要结局

Time spent with postprandial glucose level in target range

时间窗: during 3 week trial

Glucose target level is 4-10mmol/L post meals

次要结局

  • Frequency & duration of postprandial hyperglycemia(during 3 week study period)
  • Frequency & duration of postprandial hypoglycemia(during 3 week study period)

研究者

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

Margaret Lawson

Senior Scientist, Evidence to Practice Research Program, CHEO Research Institute, Pediatric Endocrinologist, CHEO, Associate Professor, Faculty of Medicine, University of Ottawa, Director, JDRF Canadian Clinical Trial Network

Children's Hospital of Eastern Ontario

研究点 (2)

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