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Study to Improve Quality of Care and Patient Health in the Field of Cardiovascular Risk Factors in General Practice

Effects of a Series of Intensified Prevention Consultations on the Changes in Goals and Risk Factors in Hypertensive Patients at High Cardiovascular Risk

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00348855
Acronym
ESCAPE
Enrollment
1836
Registered
2006-07-06
Start date
2006-11-30
Completion date
2010-03-31
Last updated
2011-11-15

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

Conditions

High Risk Hypertensive Patients

Keywords

High Blood Pressure, High cardiovascular risk, Type 2 diabetes, Reaching goals

Brief summary

Observational studies performed in France and abroad in hypertensive patients at high cardiovascular risk have shown a wide gap between the therapeutic targets reached in ambulatory patients and those set by guidelines. In primary prevention, in hypertensive patients at high cardiovascular risk (+ at least 2 risk factors), the gap is secondary to 1) the ignorance of the validated therapeutic targets and strategies, 2) the absence of global cardiovascular risk management, 3) the usual ambulatory medical practice, which is not adapted to a global cardiovascular prevention approach. Objectives Principal. To demonstrate that a series of 5 specific prevention consultations over 2 years allows a greater number of hypertensive patients at high cardiovascular risk to reach the goals set by guidelines with no deterioration of their quality of life compared with no particular intervention. Method Pragmatic, cluster-randomised controlled trial. At least 1904 high cardiovascular risk hypertensive patients will be included and followed up during two years by 268 teaching general practitioners from 23 regional teaching colleges. The regional teaching colleges will be randomised to avoid a contamination bias. The study will be coordinated by local coordinators at the college level. Intervention In the intervention group, the investigators will have training, information, and feed back regarding the management of high risk hypertensive patients. The training will concern the targets to be reached, therapeutic strategies recommended by the AFSSAPS/HAS, and scientific data. The investigators will have an easy guide that can be used during consultations, and will be informed about tobacco withdrawal programs and education for improving diet, exercise and compliance. In the control group, investigators will care for their patients as usual. End points Main: number of patients who reach all the therapeutic targets defined by the guidelines in the total study population, in the sub-group of patients with hypertension, but free of type-2 diabetes (T2D), and in the sub-group with hypertension and DT2. Secondary: number of targets reached by the patients, changes in level of blood pressure, LDL-cholesterol, HbA1c, tobacco consumption, and use of aspirin if needed in the total population and its two subgroups, estimated cardiovascular risk, quality of life.

Detailed description

Cluster randomised pragmatic controlled trial in general practice

Interventions

OTHERCardiovascular drugs strategies

Implementation of drug strategies according to guidelines to try to reach goals proposed in these guidelines.

BEHAVIORALCompliance

Discussion about compliance and questionnaire to assess compliance at inclusion, Year 1 and Year 2.

BEHAVIORALExercise

Discussion with the patient on necessity to have regular exercise. Assessment of exercise by questionnaire at inclusion, year 1 and year 2.

BEHAVIORALStop Smoking

Minimal intervention

BEHAVIORALDiet

Discussion with the patient on his (her) alimentation during each of the six consultations and assessment of daily diet at inclusion, year 1 and year 2.

OTHERFeed Back

Feed back on results in the intervention group at baseline, Year 1 ans Year 2.

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
CollaboratorOTHER
Laboratoires Takeda
CollaboratorINDUSTRY
Merck Serono International SA
CollaboratorINDUSTRY
Collège National des Généralistes Enseignants
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Treated High blood Pressure patients with at least two other cardiovascular risks

Exclusion criteria

* Secondary prevention

Design outcomes

Primary

MeasureTime frame
Number of patients who reach all the therapeutic goals defined by the guidelines in the total study population, in the sub-group of patients with hypertension, but free of type-2 diabetes (T2D), and in the sub-group with hypertension and T2D.At inclusion, year 1 and year 2

Secondary

MeasureTime frame
Quality of life measured with SF8At inclusion, year 1 and year 2
ComplianceAt inclusion, year 1 and year 2
Number of targets reached by the patientsAt inclusion, year 1 and year 2
DietAt inclusion, year 1 and year 2
Levels of blood pressure, LDL-Cholesterol, tobacco consumption in the whole population plus levels of HbA1c and aspirin use in the TD2 populationinclusion, year 1 and year 2
ExerciseAt inclusion, year 1 and year 2

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026