Team Management of High Blood Pressure
Collaborative Management of Hypertension
調査の概要
詳細な説明
BACKGROUND:
The Healthy People 2010 target calls for controlled BP in 50% of the 50 million Americans with hypertension. BP is currently controlled in only 27% of the population. These population figures are in contrast to data from clinical trials (efficacy) in which BP has been controlled in 70 to 80% of study participants. Poor BP control exists in spite of six sets of guidelines generated over the last 30 years in the United States. While there are many causes for poor control, several studies have found that physicians are frequently satisfied with uncontrolled BPs. Numerous strategies exist to assist physicians with achieving better BP control, but a consistent, effective approach to solving the problem has not been found.
DESIGN NARRATIVE:
The objective of this study is to test whether BP control can be improved by physician education and feedback provided through the development of physician/pharmacist collaborative teams. The rationale for this proposal is generated from studies demonstrating that physician knowledge, quality of prescribing, and attainment of treatment goals can be improved when physicians collaborate with clinical pharmacists. Previous studies have suffered from insufficient sample size and controls and did not include a structured intervention. This study will address these gaps in knowledge by conducting a randomized, prospective study in 5 clinics (2 intervention and 3 control) with 27 physicians who care for 180 patients with uncontrolled BP. The structured intervention will involve clinical pharmacists who evaluate BP therapy and treatment strategies and make specific recommendations to the physician. Patients will be seen at baseline and at 2, 4, 6, 8, and 9 months, at which time random zero BP measurements will be performed. The specific aims of this study are (1) to determine if better BP control can be achieved by the use of physician/pharmacist teams that utilize physician education and feedback when compared to usual care, (2) to determine if improvements in BP control are related to an increase in physician knowledge of and adherence to BP guidelines when they are involved in physician/pharmacist teams, and (3) to determine if changes in BP control are associated with the level and scope of the physician/pharmacist relationships. This model utilizes an innovative system approach to improve BP control. This intervention has the potential to achieve marked improvements in BP control. This model could become one additional strategy to help achieve the BP goals for Healthy People 2010.
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
-
-
Iowa
-
Iowa City、Iowa、アメリカ、52242
- University of Iowa
-
-
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:
- Males or females, age 21-85
- Taking 0-3 antihypertensive medications with no changes in regimen or dose within the past 4 weeks
- Non-diabetic with clinic BP 145-179 / 95-109 or diabetic with BP greater than 135/85
Exclusion Criteria:
- Previous 24 hour BP monitoring consult service within the past 6 months
- Stage 3 hypertension greater than 180/110
- Recent MI or stroke within the past 6 months
- Class III or IV congestive heart failure
- Unstable angina
- Uncontrolled atrial fibrillation
- Serious renal disease (serum creatinine greater than 3.5)
- Serious hepatic disease (total bilirubin greater than 3.0)
- Pregnancy
- Poor prognosis with less than a 3 year life expectancy
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
- 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: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 |
|---|---|
|
実験的:Intervention
Intervention patients receive care from a clinical pharmacist to improve blood pressure.
|
The patient's physician collaborates with a clinical pharmacist to improve management of hypertension
|
|
介入なし:Control
Control patients receive usual care and do not have a clinical pharmacist included in their care.
|
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 |
|---|---|
|
Blood pressure control
時間枠:Measured by zero blood pressure measurements at baseline and 2, 4, 6, 8, and 9 months
|
Measured by zero blood pressure measurements at baseline and 2, 4, 6, 8, and 9 months
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Mean number of antihypertensives
時間枠:Measured when each patient completed the study.
|
Measured when each patient completed the study.
|
|
Side effect score
時間枠:Measured when each patient completed the study.
|
Measured when each patient completed the study.
|
|
Physician knowledge
時間枠:Measured at the beginning and at the end of the study.
|
Measured at the beginning and at the end of the study.
|
協力者と研究者
スポンサー
捜査官
- スタディチェア:Barry L. Carter、University of Iowa
出版物と役立つリンク
一般刊行物
- Carter BL, Rogers M, Daly J, Zheng S, James PA. The potency of team-based care interventions for hypertension: a meta-analysis. Arch Intern Med. 2009 Oct 26;169(19):1748-55. doi: 10.1001/archinternmed.2009.316.
- Carter BL, Hartz A, Bergus G, Dawson JD, Doucette WR, Stewart JJ, Xu Y. Relationship between physician knowledge of hypertension and blood pressure control. J Clin Hypertens (Greenwich). 2006 Jul;8(7):481-6. doi: 10.1111/j.1524-6175.2006.05601.x.
- Carter BL. Antihypertensive prescribing: do we have reason to celebrate? Hypertension. 2006 Nov;48(5):816-7. doi: 10.1161/01.HYP.0000240978.77934.3a. Epub 2006 Sep 18. No abstract available.
- Carter BL, Sica DA. Strategies to improve the cardiovascular risk profile of thiazide-type diuretics as used in the management of hypertension. Expert Opin Drug Saf. 2007 Sep;6(5):583-94. doi: 10.1517/14740338.6.5.583.
- Carter BL, Bergus GR, Dawson JD, Farris KB, Doucette WR, Chrischilles EA, Hartz AJ. A cluster randomized trial to evaluate physician/pharmacist collaboration to improve blood pressure control. J Clin Hypertens (Greenwich). 2008 Apr;10(4):260-71. doi: 10.1111/j.1751-7176.2008.07434.x.
- Weber CA, Ernst ME, Sezate GS, Zheng S, Carter BL. Pharmacist-physician comanagement of hypertension and reduction in 24-hour ambulatory blood pressures. Arch Intern Med. 2010 Oct 11;170(18):1634-9. doi: 10.1001/archinternmed.2010.349.
研究記録日
主要日程の研究
研究開始
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
本研究に関する用語
その他の研究ID番号
- 271
- R01HL069801 (米国 NIH グラント/契約)
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。