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临床试验/NCT02212158
NCT02212158Unknown不适用

Diabetes Intervention Program for Adolescents With Persistent High HA1c

University of Manitoba2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2014年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
20
试验地点
2
主要终点
Change from Baseline HA1c at 6 months post baseline

研究概览

简要总结

The purpose of this project is to assess the feasibility and efficacy of a new group therapy program for adolescents with Type 1 diabetes and compromised metabolic control (high A1c). This intervention is aimed at addressing issues frequently found to be associated with poor control: knowledge deficits, parental supervision, parent-teen communication and psychosocial barriers. In order to test this new group therapy program, adolescents' HA1c and psychosocial functioning will be monitored pre- and post-intervention. It is hypothesized that individuals who participate in the group therapy program will show an improvement in their HA1c levels and quality of life, self-efficacy, supportive behaviors from family members, readiness to make improvements in their diabetes care and decrease symptoms of depression.

详细描述

Basic Design:

This study will pilot a group therapy intervention for adolescents seen in the diabetes clinic who have had elevated HA1c's for at least 3 months. This group will be offered in fall of 2014. Group therapy sessions will include 8 teen sessions that cover the following topics: acceptance of diabetes, family issues, division of diabetes management, communication and facilitating motivation and skill development to improve diabetes care. Motivational interviewing and cognitive behavioral techniques will be the therapeutic modalities used in sessions. Parents will be involved in 3 therapy sessions that cover topics regarding family functioning, division of responsibility and parenting strategies. Participants will complete questionnaires measuring self-efficacy, family support, quality of life, readiness to change and symptoms of depression. Questionnaires will be administered at an initial assessment prior to participation in the group, at completion of the 8 week program, at a follow-up visit 2 months following the completion of the group and 1 year post-intervention. Questionnaires will take approximately 45 minutes to complete. HA1c levels will be evaluated for participants every 3 months as per regular clinic care. This intervention program will be offered to teens upon an elevated HA1c result.

Primary Outcomes:

HA1c levels will be tested every three months as per regular clinic care. Basic demographic information will be obtained from participants during the initial assessment for the group (age, family size, and date of diagnosis of diabetes).

Secondary Outcomes:

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • The therapy group will be composed of teens that currently have a documented history of elevated HA1c's that have persisted for at least 3 months
  • Potential candidates for the group will be recruited from all the physician's caseloads in the clinic.

排除标准

  • Patients with Type II diabetes
  • Those who are medically unstable due to other medical conditions
  • Those who refuse to participate will not be included in the study

结局指标

主要结局

Change from Baseline HA1c at 6 months post baseline

时间窗: Baseline, 6-months post baseline

Change from baseline HA1c at 3 months post baseline

时间窗: Baseline, 3-months post baseline

Change from Baseline HA1c at 9 months post baseline

时间窗: Baseline, 9-months post baseline

Change in Baseline HA1c at 12 months post baseline

时间窗: Baseline, 12-months post baseline

次要结局

  • Change from baseline in Diabetes Family Behavior Scale at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Diabetes Family Behavior Scale at 60 weeks(baseline, 60 weeks)
  • Change from baseline in Self-efficacy for Diabetes scale (SED) at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Self-efficacy for Diabetes scale (SED) at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Self-efficacy for Diabetes scale (SED) at 60 weeks(baseline, 60 weeks)
  • Change from baseline in Diabetes Family Behavior Scale at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Beck Depression Inventory for Youth (BDI-Y) at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Beck Depression Inventory for Youth (BDI-Y) at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Beck Depression Inventory for Youth (BDI-Y) at 60 weeks(baseline, 60 weeks)
  • Change from baseline in Diabetes Quality of LIfe for Youth at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Diabetes Quality of LIfe for Youth at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Diabetes Quality of LIfe for Youth at 60 weeks(baseline, 60 weeks)
  • Change from baseline in Diabetes Management Questionnaire at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Diabetes Management Questionnaire at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Diabetes Management Questionnaire at 60 weeks(baseline, 60 weeks)
  • Change from baseline in Child Behavior Checklist (Parent form) at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Child Behavior Checklist (Parent form) at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Child Behavior Checklist (Parent form) at 60 weeks(baseline, 60 weeks)
  • Change from baseline in Low Blood Sugar Survey at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Low Blood Sugar Survey at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Low Blood Sugar Survey at 60 weeks(baseline, 60 weeks)
  • Change from baseline in Children's Hope Scale at 8 weeks(baseline, 8 weeks)
  • Change from baseline in Children's Hope Scale at 16 weeks(baseline, 16 weeks)
  • Change from baseline in Children's Hope Scale at 60 weeks(baseline, 60 weeks)

研究者

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

Dr. Heather MacKenzie

Ph.D., C. Psych. Candidate

University of Manitoba

研究点 (2)

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