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临床试验/NCT00583310
NCT00583310终止2 期

Telephone-Based Lifestyle Intervention to Reduce Blood Pressure in Prehypertensive Patients

NYU Langone Health2 个研究点 分布在 1 个国家目标入组 125 人开始时间: 2007年1月最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
125
试验地点
2
主要终点
Ambulatory blood pressure change

研究概览

简要总结

Individuals with prehypertension are at risk for developing cardiovascular disease and sustained hypertension. Modifying lifestyle behaviors (diet, weight loss, sodium intake, physical activity, alcohol intake) has been shown to reduce blood pressure in hypertensives. Participants in this study will be enrolled in one of two groups. Participants in the first group will receive usual care, and participants in the second group will receive a 4 session telephone-based lifestyle intervention. The goal of the study is to determine whether this intervention is effective in promoting behavior change and reducing blood pressure among prehypertensives.

详细描述

Individuals with prehypertension are at increased cardiovascular risk compared with normotension, as well as increased risk of progression to sustained hypertension. The recommended treatment for prehypertension is lifestyle modification, including weight loss, adoption of the Dietary Approaches to Stop Hypertension (DASH) diet, reduction of dietary sodium, physical activity, and moderation of alcohol intake. The proposed pilot study will test the effect of a 4 session telephone-based lifestyle intervention on blood pressure change in 125 prehypertensive participants. The intervention includes education and behavioral counseling strategies that have been shown to be effective in promoting behavior change and reducing blood pressure among hypertensives.

Following baseline assessment, participants will be randomized to the intervention or usual care, and will complete follow-up assessments at 6 weeks and 3 months post-randomization. The primary aim of the study is to examine the effect of the intervention on blood pressure at 3 months. Secondary aims include examining intervention effects on lifestyle behavior changes at 6 weeks and 3 months. This study will provide pilot and feasibility data for a future application to study effects of the intervention on risk factor modification, blood pressure reduction, and cardiovascular morbidity and mortality. If successful, this brief, cost-effective intervention could easily be incorporated into routine care, and could have a significant impact on the management of prehypertension.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Screening BP in prehypertensive range (SBP of 120-139 mmHg or DBP of 80-89 mmHg). If SBP or DBP is below these ranges, the patient is eligible. However, if either SBP or DBP is above the upper cutoffs (i.e., patient meets criteria for HTN), the patient will not be eligible.
  • Able to read and communicate in English or Spanish.
  • Must have access to a telephone at home or at work.
  • Age 18 years or older

排除标准

  • Patients who are currently taking anti-hypertensive medication will be excluded.
  • Patients with diabetes or kidney disease will be excluded, because pharmacologic treatment may be initiated to achieve the JNC 7 recommended BP goal of 130/80 mmHg in patients with these compelling indications.
  • Patients who are currently participating in another HTN-related clinical trial will be excluded.

结局指标

主要结局

Ambulatory blood pressure change

时间窗: 3 months

次要结局

  • Change in physical activity level(6 weeks and 3 months)
  • Change in dietary habits(6 weeks and 3 months)
  • Weight change(3 months)

研究者

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

Tanya Spruill

Associate Clinical Professor, Department of Medicine Behavioral Cardiology

Columbia University

研究点 (2)

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