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临床试验/NCT03168867
NCT03168867已完成不适用

Effectiveness Trial of an E-Health Intervention To Support Diabetes Care in Minority Youth (3Ms)

Wayne State University14 个研究点 分布在 1 个国家目标入组 149 人开始时间: 2017年9月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
149
试验地点
14
主要终点
Glycemic Control

研究概览

简要总结

The purpose of the study is to conduct a multicenter, randomized effectiveness trial of The 3Ms. The proposed study will use an effectiveness-implementation "Hybrid 1" design. In this design, the primary goal is to determine whether an intervention works in a real-world setting, but the design also answers secondary questions such as the relationship between treatment dose and treatment outcome and what factors affect the actual delivery of the intervention in the clinics (staff burden, workflow interference etc).

详细描述

The study will be conducted at 3 clinics in the Detroit area (Children's Hospital of Michigan (CHM); Ascension St. John Children's Hospital; William Beaumont Children's Hospital) and 4 clinics in the Chicago area. Wayne State University (WSU) will function as the coordinating center for the trial and will be responsible for overseeing the adequacy all aspects of trial management, including recruitment, retention, data collection, data management and statistical analyses. 212 African American (AA) adolescents with type 1 diabetes and their primary caregivers will be enrolled across all sites (half will be enrolled at WSU and half at the 4 Chicago sites). Families will be randomized to one of two arms: The 3Ms intervention (parental motivation for supervision of adolescent DSM) or standard educational control. In the 3Ms condition, parents will receive a brief (10-20 minute) computer delivered intervention at three consecutive routine diabetes clinic visits that is designed to increase parental motivation to supervise adolescent diabetes management. In the control condition, parents will receive computer-delivered education materials regarding type 1 diabetes. Data collection will be completed in the diabetes clinic at baseline and then at 6, 12 and 18 months after baseline in the families' home. Data collection is completed by the adolescent and caregiver on a tablet computer and includes questionnaires to assess adolescent diabetes management, parental supervision of diabetes management, family relationships and youth quality of life. Blood will also be collected to measure HbA1c (mean blood glucose level). Medical record data will also be collected. The data analyses will be intent-to-treat, meaning that all randomized participants are included regardless of the intervention dose received. Trial data will analyzed using the linear mixed effect model (LME) for repeated measures.

In addition to the clinical trial, 20 diabetes clinic staff members (5 at WSU from the CHM clinic; 15 from the Chicago clinics) will also be recruited to participate in qualitative interviews upon completion of the trial. The purpose of the interview is to identify barriers and facilitators of use of the 3Ms intervention at the level of the individual clinician, the diabetes clinic and the organization (hospital). Interviews will be audiotaped and subsequently transcribed for coding.

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
Triple (Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
10 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age: 10 years 0 months - 15 years, 11 months
  • Diagnosed with Type 1 diabetes
  • Diagnosed for at least 6 months
  • African American
  • Residence within 30 miles of a recruitment site (Children's Hospital of Michigan, Ann and Robert H. Lurie Children's Hospital of Chicago, Children's Hospital University of Illinois, or La Rabida Children's Hospital of Chicago)
  • Primary caregiver willing to participate

排除标准

  • Mental health conditions that might compromise data integrity (e.g., developmental delay, schizophrenia, psychosis, current suicidality, homicidality)
  • Co-morbid medical condition resulting in atypical diabetes management (e.g., cystic fibrosis)
  • Inability to speak or read English
  • Child is in out-of-home placement

结局指标

主要结局

Glycemic Control

时间窗: Baseline, 6, 13 and 18 month follow-up

Hemoglobin A1c (HbA1c)

次要结局

  • Diabetes Management (Self-reported)(Baseline, 6 months, 13 months, and 18 months)
  • Regimen Adherence (Objective)(Baseline, 6 months, 13 months, and 18 months)
  • Parental Monitoring of Diabetes Care (Self-reported)(Baseline, 6 months, 13 months, and 18 months)
  • Diabetes- Specific Family Functioning (Self-reported)(Baseline, 6 months, 13 months, and 18 months)
  • Executive Functioning (Self-reported)(Baseline, 6 months, 13 months, and 18 months)
  • Household Chaos (Self-reported)(Baseline, 6 months, 13 months, and 18 months)
  • Adolescent Depression (Self-reported)(Baseline, 6 months, 13 months, and 18 months)
  • Cost Analysis (Self-reported)(Baseline, 6 months, 13 months, and 18 months)
  • Diabetes Emotional Distress (Self-reported)(Baseline, 6 months, 13 months, and 18 months)

研究者

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

Deborah Ellis, Ph.D.

Professor of Family Medicine and Public Health Sciences Wayne State University School of Medicine

Wayne State University

研究点 (14)

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