GlObal Secondary Prevention strategiEs to Limit Event Recurrence After Myocardial Infarction. GOSPEL Study

February 2, 2021 updated by: Heart Care Foundation
Cardiac rehabilitation programmes are a proven treatment for individuals with recent myocardial infarction, resulting in reduced morbidity and mortality compared to usual care. Unfortunately, following completion of a cardiac rehabilitation programme, risk factors and lifestyle behaviours may deteriorate. The GOSPEL study investigates the benefits of a programme of continued educational and behavioural intervention to achieve optimal long-term secondary prevention goals.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Detailed Description

Study partially sponsored by Società Prodotti Antibiotici

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
3200

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Italy
      • Aosta, Italy
        • Ospedale Beauregard
      • Aurisina, Italy
        • Casa di Cura Pineta del Carso
      • Bergamo, Italy
        • Ospedali Riuniti
      • Como, Italy
        • Casa di Cura Villa Aprica
      • Mezzolombardo, Italy
        • Presidio Ospedalier S Giovanni
      • Milano, Italy
        • Fondazione Don Gnocchi
      • Milano, Italy
        • Istituti Clinici Perfezionamento
      • Milano, Italy
        • Ospedale S Luca-Centro Auxologico
      • Milano, Italy
        • Pio Albergo Trivulzio
      • Napoli, Italy
        • Policlinico Universitario Federico II
      • Napoli, Italy
        • Azienda Ospedaliera Vincenzo Monaldi
      • Pavia, Italy
        • Fondazione Salvatore Maugeri
      • Roma, Italy
        • Ospedale Santo Spirito
      • Roma, Italy
        • Ospedale Forlanini
      • Roma, Italy
        • Villa Betania
      • Torino, Italy
        • Ospedale Evangelico Valdese
      • Torino, Italy
        • Ospedale Mauriziano
      • Vicenza, Italy
        • ospedale Civile S Bortolo
    • AR
      • Arezzo, AR, Italy
        • Ospedale San Donato
    • AV
      • Avellino, AV, Italy
        • Az Osp Giuseppe Moscati
    • BA
      • Cassano delle Murge, BA, Italy
        • Fondazione Salvatore Maugeri
    • BG
      • Romano Lombardo, BG, Italy
        • Ospedale Romano di Lombardia
    • BN
      • Telese Terme, BN, Italy
        • Fondazione Salvatore Maugeri
    • BO
      • Bologna, BO, Italy
        • Ospedale Bellaria
    • BS
      • Gazzaniga, BS, Italy
        • Presidio Gazzaniga
      • Gussago, BS, Italy
        • Fondazione Salvatore Maugeri
    • CE
      • Caserta, CE, Italy
        • Azienda Ospedaliera S Anna e S Sebastiano
    • CH
      • Chieti, CH, Italy
        • Casa di Cura Villa Pini d'Abruzzo
    • CR
      • Rivolta d'Adda, CR, Italy
        • Ospedale Santa Marta
    • CS
      • Mormanno, CS, Italy
        • Ospedale Civile Minervini
      • Trebisacce, CS, Italy
        • Ospedale Civile C Chidichino
    • CT
      • Catania, CT, Italy
        • Ospedale Ascoli Tomaselli
      • Catania, CT, Italy
        • Ospedale Cannizzarro
    • CZ
      • Catanzaro, CZ, Italy
        • Azienda Ospedaliera Mater Domini
    • Como
      • Bellano, Como, Italy
        • Ospedale Umberto I
    • FI
      • Firenze, FI, Italy
        • Az Ospedaliera-Universitaria Careggi
    • GE
      • Arenzano, GE, Italy
        • Ospedale La Colletta
      • Rapallo, GE, Italy
        • Polo Ospedaliero Rapallo S Margherita
    • GO
      • Gorizia, GO, Italy
        • Ospedale Generale provinciale
    • LE
      • Casarano, LE, Italy
        • Presidio Ospedaliero F Ferrari
    • LI
      • Cecina, LI, Italy
        • Ospedale Civile Bassa Val di Cecina
    • LU
      • Lucca, LU, Italy
        • Ospedale Civile Campo di Marte
    • Lecco
      • Merate, Lecco, Italy
        • Ospedale San Leopoldo
    • MI
      • Bozzolo, MI, Italy
        • Presidio di Riabilitazione Multifunzionale
      • Cesano Boscone, MI, Italy
        • Casa di Cura Ambrosiana
      • Monza, MI, Italy
        • Ospedale San Gerardo
      • Passirana - Rho, MI, Italy
        • Presidio Ospedaliero di Passirana
      • Tradate, MI, Italy
        • Fondazione Salvatore Maugeri
    • Novara
      • Veruno, Novara, Italy
        • Fondazione Salvatore Maugeri
    • PA
      • Palermo, PA, Italy
        • Ospedale Buccheri La Ferla Fatebenefratelli
    • PC
      • Ponte dell'Olio, PC, Italy
        • Casa di Cura San Giacomo
    • PD
      • Camposanpiero, PD, Italy
        • Ospedale di Camposanpiero
    • PG
      • Città di Castello, PG, Italy
        • Predisio Ospedaliero Città di Castello
      • Foligno, PG, Italy
        • Nuovo Ospedale S Giovanni Battista
      • Gualdo Tadino, PG, Italy
        • Ospedale Calai
      • Perugia, PG, Italy
        • Azienda Ospedaliera di Perugia
      • Perugia, PG, Italy
        • Ex Ospedale Grocco
    • PV
      • Montescano, PV, Italy
        • Fondazione Salvatore Maugeri
    • PZ
      • Potenza, PZ, Italy
        • Azienda Ospedaliera San Carlo
    • Point
      • Pescia, Point, Italy
        • ospedale della Val di Nievole
    • Pordenone
      • Sacile, Pordenone, Italy
        • Ospedale Civile
    • RA
      • Cotignola, RA, Italy
        • Casa di Cura Villa Maria Cecilia
      • Rimini, RA, Italy
        • Ospedale Infermi
    • RC
      • Reggio Calabria, RC, Italy
        • Policlinico Madonna della Consolazione
    • RE
      • Castelnuovo Ne' Monti, RE, Italy
        • Ospedale Sant'Anna
      • Correggio, RE, Italy
        • Ospedale Civile San Sebastiano
    • SO
      • Sondalo, SO, Italy
        • Ospedale E Morelli
    • TA
      • Taranto, TA, Italy
        • Ospedale SS Annunziata
    • TN
      • Ala, TN, Italy
        • Ospedale di ALA
      • Arco, TN, Italy
        • Ospedale Provinciale S Pancrazio
    • TV
      • Montebelluna, TV, Italy
        • Presidio Ospedaliero
    • VE
      • Mirano, VE, Italy
        • Ospedale Civile
      • San Donà di Piave, VE, Italy
        • Ospedale Civile
  • Switzerland
      • Lugano, Switzerland
        • Cardiocentro Ticino

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Recent myocardial infarction (within 3 months after the index event)
  • Standard rehabilitation program of 3-6 weeks performed
  • Informed consent (obtained before any study specific procedure)

Exclusion Criteria:

  • Age > 75 years
  • Any condition that in the opinion of the investigator would jeopardize the evaluation of efficacy or be associated with poor adherence to the protocol;
  • Presence of any non-cardiac disease (e.g. cancer) that is likely to significantly shorten life expectancy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
cardiovascular mortality
non fatal re-MI
angina requiring hospitalization
urgent revascularization procedures
hospitalization for heart failure
non fatal stroke

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Heart Care Foundation

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Chair: Pantaleo Giannuzzi, MD, Fondazione Maugeri - Veruno (NO)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
December 1, 2000

Study Completion

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
December 1, 2005

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
January 12, 2007

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
January 12, 2007

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
January 15, 2007

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
February 3, 2021

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
February 2, 2021

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
January 1, 2007

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • 60

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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