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临床试验/NCT02317003
NCT02317003已完成不适用

Physical Exercise Prescription With PEdometeR in General Practice for Patients With Cardiovascular Risk Factors - The PEPPER Pragmatic Randomised Controlled Trial

University Hospital, Angers1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2015年3月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
126
试验地点
1
主要终点
Change in total energy expenditure by accelerometry at 3 months compared to baseline

研究概览

简要总结

This study evaluates the efficacy, in terms of energy expenditure, physical activity level, quality of life, blood pressure, waist circumference and weight, of a general practice based intervention involving a personalised physical exercise medical prescription, the structured delivery of information on the benefits of physical activity, a pedometer, and a pedometer log book, in 35 to 74 year old patients with cardiovascular risks factors.

详细描述

Background: Health benefits of physical activity have been shown to be at least as important as drug therapies in the prevention of cardiovascular diseases in patients with hypertension, hyperlipidaemia or diabetes. However, few strategies have demonstrated efficacy and practicality in the promotion of physical exercise among these high risk patients in general practice.

The PEPPER clinical study is a pragmatic randomised trial over a period of 12 months to evaluate the efficacy, in terms of physical activity level, of an intervention based on structured information delivery according to cognitive and behavioural theories, a personalised written physical activity prescription in number of steps per day, a pedometer, and a pedometer logbook similar to diabetes logbooks, in 35 to 74 year old patients with cardiovascular risks factors. This strategy will be compared to the commonly used oral recommendation of physical activity. The primary outcome is the change in total energy expenditure measured by accelerometry over a 7-day period. Secondary outcomes include changes in physical activity levels (International Physical Activity Questionnaire), quality of life (SF-36), blood pressure, weight, waist circumference, perceived obstacles to physical activity, and patient and doctors compliance with the suggested strategy. 140 patients will be recruited and followed up in 15 GP practices. Measures will be assessed at baseline, at 3 months and at 12 months (end of intervention).

The results of the PEPPER study are expected at the end of 2016. If the intervention proves effective in increasing durably the level of physical activity, this relatively simple and cheap strategy could help decrease the occurrence of cardiovascular events in a large high-risk population seen in general practice.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
35 Years 至 74 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients consulting their general practitioner for a non-urgent matter
  • •with regular follow-up every 3 months for hypertension, hypercholesterolaemia or non insulin dependent type 2 diabetes.
  • •judged insufficiently active by their general practitioner based on negative answers to the questions : "Do you practice a physical activity or cycling more than an hour per week?" and "Does your occupation involve physical exertion?"

排除标准

  • •contraindication to moderate physical activity,
  • •non autonomous for walking,
  • •with cognitive or psychiatric impairment limiting the full understanding of the study,
  • •suffering from another limiting disease (coronary insufficiency, chronic cardiac failure, etc),
  • •who don't speak French,
  • •refusing to participate.

研究组 & 干预措施

Intervention PPIL

Experimental

Intervention delivered by the family doctor and based on structured information delivery according to cognitive and behavioural theories, a personalised written physical activity prescription in number of steps per day, a pedometer, and a pedometer logbook similar to diabetes logbooks.

干预措施: Intervention PPIL (Behavioral)

Control OR

Active Comparator

Oral recommendation of physical exercise delivered by the family doctor.

干预措施: Control OR (Behavioral)

结局指标

主要结局

Change in total energy expenditure by accelerometry at 3 months compared to baseline

时间窗: baseline and 12 weeks

The total energy expenditure is measured with a wGT3x-BT Actigraph accelerometer worn at the belt during 7 consecutive days from morning to evening. It is measured in Metabolic Equivalent Task-Minutes per Week.

次要结局

  • Change in total energy expenditure by questionnaire at 12 months compared to baseline(baseline and 52 weeks)
  • Change in total energy expenditure by questionnaire at 3 months compared to baseline(baseline and 12 weeks)
  • Change in total energy expenditure by accelerometry at 12 months compared to baseline(baseline and 52 weeks)
  • Change in quality of life at 3 months compared to baseline(baseline and 12 weeks)
  • Change in waist circumference at 12 months compared to baseline(baseline and 52 weeks)
  • Change in arterial blood pressure at 3 months compared to baseline(baseline and 12 weeks)
  • Change in waist circumference at 3 months compared to baseline(baseline and 12 weeks)
  • Change in weight at 3 months compared to baseline(baseline and 12 weeks)
  • Perceived obstacles to physical exercise(52 weeks)
  • Change in quality of life at 12 months compared to baseline(baseline and 52 weeks)
  • Change in weight at 12 months compared to baseline(baseline and 52 weeks)
  • Change in arterial blood pressure at 12 months compared to baseline(baseline and 52 weeks)
  • Adherence of doctors and patients to the suggested strategy(52 weeks)
  • Adherence of doctors and patients to the suggested strategy(12 weeks)

研究者

发起方
University Hospital, Angers
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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