跳至主要内容
临床试验/NCT01472159
NCT01472159已完成不适用

Optimizing CGM Use and Metabolic Outcomes in Youth With Type 1 Diabetes

Joslin Diabetes Center2 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2011年10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
130
试验地点
2
主要终点
Change in glycemic control, assessed by hemoglobin A1c

研究概览

简要总结

The purpose of this 2-year randomized controlled trial (RCT) is to implement and evaluate a family-focused behavioral teamwork intervention aimed at overcoming barriers to sustained continuous glucose monitoring (CGM) use in youth with type 1 diabetes (T1D). We hypothesize that CGM implemented with a family-focused, behavioral teamwork intervention will result in sustained CGM use and greater improvement in A1c compared to routine implementation of CGM.

详细描述

Consistent CGM use in youth with T1D has been difficult to sustain historically. Youth with T1D and their families have routinely felt burden related to the introduction of this technology into their care management. Additionally, there can be difficulties with calibration, skin irritation, frequent skips, excessive or nuisance alarms and inaccurate readings which often lead to diminished use or discontinuation entirely. The purpose of this protocol is to implement and evaluate a family-focused behavioral teamwork intervention aimed at overcoming barriers to sustained CGM use in youth with T1D. In this 2-year RCT, we will assess the long-term acceptability and durability of CGM use and its associated glycemic and psychological outcomes in youth with T1D and their families. We will randomize 120 families to one of two groups: (1) CGM implemented according to usual care (CGM-Usual Care, CGM-UC) or (2) CGM implemented with a family teamwork intervention (CGM-Teamwork, CGM-TW). This intervention will allow participants and families to overcome barriers to sustained CGM use and achieve glycemic benefits that have been afforded to adults using CGM as demonstrated in other research. In year 1, all CGM supplies will be provided and covered by study resources. In year 2, study participants will be asked to cover the costs associated with sensor use and any costs associated with replacement of CGM components in a manner consistent with routine clinical care as the investigators believe that it is important to assess durability of CGM use in clinical practice.

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
Single (Investigator)

入排标准

年龄范围
8 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age 8-17 years
  • Planning to be living at home for 2 years
  • Type 1 diabetes of at least 1 year duration
  • Daily insulin dose ≥0.5 units/kg
  • A1c ≥6.5% and ≤10.0%
  • Insulin therapy with continuous subcutaneous insulin infusion (CSII) or multiple daily injections (≥3 injections/day)
  • Blood glucose (BG) monitoring frequency ≥4 times/day
  • Agreement to wear a CGM device
  • Fluency in English for child and parent/guardian
  • Stable living situation for ≥6 months (e.g., no Department of Youth Services Involvement)
  • Joslin Clinic attendance: At least one Joslin Clinic visit in last year AND Anticipated care at Joslin Clinic for duration of study

排除标准

  • Consistent CGM use, defined as 6+ days/week during the previous 6 months
  • History of severe, life-threatening skin reactions to the adhesive used with the CGM device
  • Pregnancy in the youth participant or intention to become pregnant within the next 2 years
  • Significant developmental or cognitive disorder in the youth or parent/guardian that would prevent full participation in a family-based, behavioral intervention or implementation of CGM
  • Inpatient psychiatric admission within the previous 6 months
  • Participation in another intervention study during the previous 3 months
  • Intent to enroll in another intervention study during the study period

结局指标

主要结局

Change in glycemic control, assessed by hemoglobin A1c

时间窗: Baseline and 1 year

次要结局

  • Change in glycemic control, assessed by hemoglobin A1c(1 year and 2 years)
  • Change in psychosocial factors (e.g., self-efficacy, fear of hypoglycemia, quality of life, diabetes-specific family conflict, diabetes responsibility sharing, diabetes-specific burden, anxiety, depressive symptoms)(1 year and 2 years)

研究者

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

Lori Laffel

Chief, Pediatric, Adolescent, & Young Adult Section; Investigator, Genetics & Epidemiology Section

Joslin Diabetes Center

研究点 (2)

Loading locations...

相似试验

Can Glucose Monitoring Improve (CGMi Study) | 临床试验