Diet Therapy Versus Prescriptive Educational Group Intervention in Overweight / Obese Patients at First Episode of AMI: a Randomized Controlled Trial

Not Applicable

• Conditions: Obesity /Overweight; Acute Myocardial Infarction (STEMI/ NSTEMI)

• Registration Number: NCT02323802
• Lead Sponsor: Fondazione IRCCS Policlinico San Matteo di Pavia

Brief Summary

Results after interventions on lifestyle in the secondary prevention of ischemic heart disease are not always consistent, and the Guidelines multidisciplinary measures aren't easily achievable.

Therefore, the purpose of this research project is the identification of an interventional approach to effective secondary prevention and realistic feasibility, in a field of multifactorial risk. The study is open to patients who totaled a double chronic disease, obesity/overweight and coronary heart disease, and who experienced a first event of ischemic cardiac infarction (AMI). The aim is to evaluate the effectiveness of a group educational intervention in a sample of overweight and obese patients (BMI \> 24.9) incurred in a first episode of acute myocardial infarction (non-STEMI and STEMI), comparing with the classic approach of prescriptive diet therapy.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-07
• Status Verified: 2014-12
• Study First Submitted: 2014-12-18
• Study First Submitted QC: 2014-12-18
• Last Update Submitted: 2014-12-18
• Study First Posted: 2014-12-23
• Last Update Posted: 2014-12-23
• Primary Completion: 2015-07
• Study Completion: 2015-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Subjects of both sexes and age ≥ of 18 years consecutively admitted to the Coronary Unit of IRCCS Foundation Policlinico S. Matteo, at first episode of STEMI or non-STEMI AMI, with BMI greater than 24.9.

Exclusion Criteria

Patients who can not provide informed consent (because illiterate or with significant language barrier or severe deficit/cognitive decays). Subjects with diseases and/or disabling organ damage. Subjects affected by active neoplasm. Individuals who have submitted arhythmic complications in acute and/or heart failure, or people referring to post-AMI residential rehabilitation. Subjects that are carriers of severe psychiatric disorders diagnosed by DSM-V -TR.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
reduction of body weight	6 months	The proportion of subjects with a 10% reduction in body weight at 6 months

Secondary Outcome Measures

Name	Time	Method
quality of life	6 months	quality of life (assessed by SF-36 questionnaire at baseline and 6 months after infarction).
Reduction of reinfarction and revascularization	1 year
general and specific mortality	1 year	relative risk of death from all causes and from ischemic heart disease (no. of overall deaths and cardiovascular causes).

Trial Locations

Locations (2)

Internal Medicine Department, Clinica Medica II, IRCCS San Matteo Foundation; 🇮🇹 Pavia, PV, Italy

Cardiology department; 🇮🇹 Pavia, Italy