Blood Pressure Self Management for Hypertension & Prehypertension Using an Internet Enabled, Automated Self Management Program
調査の概要
詳細な説明
We propose to conduct a randomized controlled trial of an Internet-enabled, automated self-management program. The study will be carried out through six local sites (offices) of a large employer. 3 sites will be intervention sites and 3 will be control sites.
Subjects enrolled from the intervention sites will receive a blood pressure meter and access to an Internet site where they can view their readings, read educational material regarding hypertension management and receive personalized tips and feedback.
Subjects enrolled from the control sites will have access to a blood pressure monitor located at their workplace but will only be provided with basic written information about hypertension at the start of the trial and will receive no feedback.
The trial will run for 6 months from the time of enrollment and the primary outcome measure will be a change in systolic blood pressure.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Massachusetts
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Boston、Massachusetts、アメリカ、02114
- Massachusetts General Hospital
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Full-time employees of EMC
- Aged 30 to 65 years at time of enrollment
- Any of the following
- A diagnosis of hypertension as defined by one of the following
- Taking an antihypertensive medication
- Being told at least twice by a physician or other health professional that the subject has high blood pressure†
- A BP > 140/90 detected at screening by the research team on 2 separate occasions.
- A diagnosis of prehypertension as defined by a systolic BP between 120-139 or a diastolic BP between 80-89 detected at screening by the research team on 2 separate occasions
- Access to the Internet at work and / or at home
Exclusion Criteria:
- Inability to self-monitor blood pressure due to musculoskeletal or cognitive impairment
- Known secondary cause of hypertension e.g. renal artery stenosis, Cushing's disease.
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：なし（オープンラベル）
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：Intervention
Internet-based hypertension self-management platform
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An internet platform to display blood pressure readings and provide subjects with automated messages and educational information about hypertension management.
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アクティブコンパレータ：Control
Installation of BP cuff for communal use at the worksite
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Provided BP cuff for communal use at the worksite
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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 |
時間枠 |
|---|---|
|
Change in systolic blood pressure.
時間枠：6 months
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6 months
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Assess whether the intervention increases the motivation and self-efficacy of patients managing blood pressure. Assess patient satisfaction with the intervention. Assess the impact of the intervention on healthcare utilization and expenditure
時間枠：6 months
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6 months
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協力者と研究者
捜査官
- 主任研究者：Joseph C. Kvedar, MD、Harvard Medical School (HMS and HSDM)
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
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。