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Physical Exercise Prescription With PEdometeR in General Practice for Patients With Cardiovascular Risk Factors - PEPPER

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02317003
Acronym
PEPPER
Enrollment
126
Registered
2014-12-15
Start date
2015-03-16
Completion date
2018-08-01
Last updated
2022-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Diabetes Mellitus, Type 2, Hypercholesterolemia, Hypertension, Sedentary Lifestyle

Keywords

physical exercise, sedentarity, general practice, family medicine, pedometer

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALIntervention PPIL
BEHAVIORALControl OR

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to 74 Years
Healthy volunteers
No

Inclusion criteria

* 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?

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Change in total energy expenditure by accelerometry at 3 months compared to baselinebaseline and 12 weeksThe 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.

Secondary

MeasureTime frameDescription
Change in total energy expenditure by questionnaire at 3 months compared to baselinebaseline and 12 weeksThe total energy expenditure is calculated with the self-administered International Physical Activity Questionaire (IPAQ) short version covering the past 7 days. It is expressed in Metabolic Equivalent Task-Minutes per Week.
Change in total energy expenditure by questionnaire at 12 months compared to baselinebaseline and 52 weeksThe total energy expenditure is calculated with the self-administered International Physical Activity Questionaire (IPAQ) short version covering the past 7 days. It is expressed in Metabolic Equivalent Task-Minutes per Week.
Change in quality of life at 3 months compared to baselinebaseline and 12 weeksChange in quality of life as measured by the self-administered Short Form 36 questionnaire
Change in quality of life at 12 months compared to baselinebaseline and 52 weeksChange in quality of life as measured by the self-administered Short Form 36 questionnaire
Change in waist circumference at 3 months compared to baselinebaseline and 12 weeks
Change in waist circumference at 12 months compared to baselinebaseline and 52 weeks
Change in total energy expenditure by accelerometry at 12 months compared to baselinebaseline and 52 weeksThe 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.
Change in weight at 12 months compared to baselinebaseline and 52 weeks
Change in arterial blood pressure at 3 months compared to baselinebaseline and 12 weeks
Change in arterial blood pressure at 12 months compared to baselinebaseline and 52 weeks
Perceived obstacles to physical exercise52 weeksPerceived obstacles to physical exercise as measured by the Determinant of Physical Activity Questionnaire (DPAQ)
Adherence of doctors and patients to the suggested strategy12 weeks
Change in weight at 3 months compared to baselinebaseline and 12 weeks

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026