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.
調査の概要
詳細な説明
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.
研究の種類
介入
入学 (実際)
48
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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Massachusetts
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Boston、Massachusetts、アメリカ、02215
- Joslin Diabetes Center
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Boston、Massachusetts、アメリカ、02215
- Beth Isreal Deaconess Medical Center
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
69年歳以上 (高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
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
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：処理
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：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.
他の名前：
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介入なし：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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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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change in hemoglobin A1c
時間枠：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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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Change in clinical, functional and psycho social tests and questionnaires
時間枠：6 and 12 months
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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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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- 主任研究者：Medha N Munshi, MD、Joslin Diabetes Center
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
一般刊行物
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研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始
2006年11月1日
一次修了 (実際)
2012年12月1日
研究の完了 (実際)
2012年12月1日
試験登録日
最初に提出
2011年11月16日
QC基準を満たした最初の提出物
2011年11月23日
最初の投稿 (見積もり)
2011年11月29日
学習記録の更新
投稿された最後の更新 (見積もり)
2014年3月28日
QC基準を満たした最後の更新が送信されました
2014年3月26日
最終確認日
2014年3月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。