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Sponsored by: |
Resicard |
Information provided by: | Resicard |
ClinicalTrials.gov Identifier: | NCT00337480 |
The purpose of this study is to determine whether the follow up of patients with acute coronary syndrome and modifiable cardiovascular risk factors is efficient based on outpatients visits in a House of Education, underlining the importance of nicotinic weaning, weight loss and physical activity practice.
Condition | Intervention |
Acute Coronary Syndrome |
Behavioral: education |
MedlinePlus related topics: | Weight Control |
Study Type: | Interventional |
Study Design: | Prevention, Randomized, Open Label, Historical Control, Parallel Assignment, Efficacy Study |
Official Title: | A Network to Control Risk Factors After Acute Coronary Syndrome |
Estimated Enrollment: | 500 |
Study Start Date: | July 2006 |
Estimated Study Completion Date: | September 2009 |
Estimated Primary Completion Date: | July 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
conventional: No Intervention
This arm is the conventional way of taking care of patients after an acute coronary syndrome
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structured: Active Comparator
This arm is an active way to monitor and educate patients after their acute coronary syndrome, with the intervention of health members in a House of Education
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Behavioral: education
education of acute coronary syndrome patients, mostly about nicotinic weaning, weight loss and physical activity
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Objectives
Method
After randomization, patients are directed to one of the two following groups: the conventional network group or the structured network group. Six and twelve months after their hospitalization, a blood test will be performed and their weight, blood pressure, waist measurement and cardiac frequency will be recorded in order to monitor patients' cardiovascular risk factors.In any case, patients receive optimal care with the participation of different health members (such as nurses, doctors, dietician...).
a-The conventional network group
Patients are taken care of, according to good medical practice by their usual general practitioner and cardiologist. The frequency of consultations is set up according to symptoms. The follow up of patients is optimized as they are taken care of by a multidisciplinary health team.
b-The structured network group
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Ariel Cohen, Pr | 33-1-49-28-28-86 | ariel.cohen@sat.aphp.fr |
France | |||||
Hopital Saint Antoine | Recruiting | ||||
Paris, France, 75011 | |||||
Principal Investigator: Ariel Cohen, Pr | |||||
Hopital Bichat | Recruiting | ||||
Paris, France, 75018 | |||||
Hopital Tenon | Recruiting | ||||
Paris, France, 75020 | |||||
Clinique la Roseraie | Recruiting | ||||
Aubervilliers, France, 93300 | |||||
Hopital Pitie Salpetriere | Recruiting | ||||
Paris, France, 75013 | |||||
Hopital Lariboisiere | Recruiting | ||||
Paris, France, 75010 |
Resicard |
Principal Investigator: | Ariel Cohen, Pr | Hopital St Antoine |
Responsible Party: | Resicard ( Dr Assyag ) |
Study ID Numbers: | Resicard Prevention |
First Received: | June 14, 2006 |
Last Updated: | May 22, 2008 |
ClinicalTrials.gov Identifier: | NCT00337480 |
Health Authority: | France: Institutional Ethical Committee |
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