Identifying and Overcoming Barriers to Diabetes Management in the Elderly: An Intervention Study (DISCO)
2014年3月26日 更新者：Medha Munshi、Joslin Diabetes Center
The purpose of this research study is to identify barriers affecting self care in older patients with diabetes and to provide coping strategies for these barriers with help from a care manager (Geriatric Life Specialist) to improve clinical, economical, functional and psychosocial parameters.
研究概览
详细说明
This is a study to evaluate whether short term focused intervention by a geriatric diabetes team, with addition of a care manager, to help overcome barriers to diabetes care in older adults will result in improved clinical, functional, and quality of life measures compared to usual care.
In addition, we will assess whether the support network formed during intervention by the geriatric diabetes team will empower patients, resulting in long lasting improvement in parameters after intervention is completed.
We will also explore whether improved blood glucose control will improve blood circulation in the brain that is compromised in elderly with diabetes.
研究类型
介入性
注册 (实际的)
48
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
-
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Massachusetts
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Boston、Massachusetts、美国、02215
- Joslin Diabetes Center
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Boston、Massachusetts、美国、02215
- Beth Isreal Deaconess Medical Center
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
69年 及以上 (年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Age 70 years and older
- Diagnosis of type 1 or type 2 diabetes
- Seen at Joslin Clinic or Beth Israel Deaconess Medical Center for at least one year
- HbA1c 8% X 2 in past 6 months without fluctuation of more than 0.5% (i.e. stable poor control)
- No major change in medications in past 3 months, e.g. addition of insulin or another hypoglycemic agent
Exclusion Criteria:
- Patients with terminal diseases, e.g. malignancy with life expectancy of 12 months or less
- Patients who live more than 25 miles from Joslin Clinic/ Beth Israel Deaconess Medical Center
- Patients who live in an institutional setting, e.g. nursing home, group home, etc
- Patients who are not able to complete outcome assessments,(e.g. poor vision, diminished mental capacity/severe cognitive decline, unable to speak/read/write English, etc)
- Patients will be excluded from participation in Study Aim 3 if they have a history of orthostatic hypotension, TIA, or vertebral basilar insufficiency
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：Geriatric diabetes team intervention group
The subjects in this group underwent evaluation for barriers to self care by a diabetes educators well versed with age specific barriers.
After consideration of patients clinical, functional, and psychosocial background a geriatric diabetes team devised strategy to help patients cope respective barriers.
A care manager then implemented the coping strategies by educating patients and caregivers.
She also made home visits to assess any safety issues not know to clinic based geriatric team.
She helped the patients and caregivers with all aspects of care coordination.
Patients in this group received phone contact from care managers as many times as needed over the six month intervention period.
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The intervention included developing strategies to help patients cope with their barriers to self care.
The intervention were implemented by care manager over 6 month period in person and by phone calls.
During the six to twelve month period subjects did not have any contact with study staff or care manager.
其他名称：
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无干预：Attention Control Group
The subjects in the group received similar, in person, contact as the intervention group.
An educator, separate from the one involved in the intervention team, called patents in this group for a total of eleven time within the first six months.
The phone calls were forces toward general discussion without any diabetes related advice.
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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change in hemoglobin A1c
大体时间：6 and 12 months
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The primary outcome of the study is to measure change in A1c before and after intervention at 6-months and at 12-months
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6 and 12 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in clinical, functional and psycho social tests and questionnaires
大体时间：6 and 12 months
|
Tests, surveys and questionnaires used during study visits are as follows: Demographic and medical history, hypoglycemia history and calendar, medication adherence survey, modified clock making test, trail making test A and B, verbal fluency test, activities of daily living, instrumental activities of daily living, 6 minute walk test, Tinetti test, geriatric depression scale, problem areas in diabetes assessment, self care inventory, determine nutrition test, social support assessment.
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6 and 12 months
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：Medha N Munshi, MD、Joslin Diabetes Center
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
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研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2006年11月1日
初级完成 (实际的)
2012年12月1日
研究完成 (实际的)
2012年12月1日
研究注册日期
首次提交
2011年11月16日
首先提交符合 QC 标准的
2011年11月23日
首次发布 (估计)
2011年11月29日
研究记录更新
最后更新发布 (估计)
2014年3月28日
上次提交的符合 QC 标准的更新
2014年3月26日
最后验证
2014年3月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.