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The Norwegian Trial of Physical Exercise After Myocardial Infarction

Study acronym: NorEx
StatusEnrolling by Invitation
PhaseNot applicable
Started
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Record History

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  1. Minor Re-verified, no change to tracked fieldsv6
  2. Notable Primary completion date: Dec 31, 2026 to Jul 31, 2028
    • Start date: Oct 29, 2020 to Sep 29, 2020
    • Collaborators revised (26)
    v5
  3. Minor Re-verified, no change to tracked fieldsv4
  4. Notable Primary completion date: Jun 2025 to Dec 31, 2026v3 Show 5 more changesShow less
    • Primary endpoint revised
    • Enrollment target: 13500 to 9700
    • Study completion date: Dec 2032 to Dec 31, 2036
    • Eligibility criteria revised
    • Secondary endpoints revised (12)
  5. Minor Re-verified, no change to tracked fieldsv2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Myocardial infarction (MI) remains the main cause of death in Europe with about 2 million deaths annually. According to WHO, 30 % of deaths caused by MI could be prevented if the populations adhere to official guidelines for physical activity. However, secondary prevention trials in MI patients have been of insufficient size or quality to provide conclusive evidence that physical activity reduces the risk of death or recurrent cardiovascular diseases. NorEx is the first study able to provide such evidence. NorEx is a registry-based prospective, three-arm, randomized multicenter secondary prevention clinical trial with blinded end-point evaluation (PROBE design). The aim of the study is to investigate whether, and to what extent, moderate to high intensity supervised physical activity will reduce the risk of recurrent cardiovascular disease and death among people who have suffered a myocardial infarction. The intervention group consists of Approximately 3185 participants who will be trained to exercise for 4 years under supervision of a personal trainer. The study design includes two control groups each consisting of approximately 3200 patients.The primary composite endpoint is time to all-cause death, nonfatal acute myocardial infarction or nonfatal stroke, whatever comes first during 4 years of follow-up. The study is powered to detect a 20 % difference in the incidence of the primary endpoint between the intervention group and the control groups. Novel health IT technology was specifically designed for NorEx, including a smart watch, a NorEx mobile application and a manager portal which allows the trainers to interact with the participants. Follow-up of the participants will be through national health registries for up to 10 years after study completion.
Trial Details
NCT Number NCT04617639
Lead Sponsor Norwegian University of Science and Technology
Collaborators: Universitetssykehuset i Nord-Norge Hospital Trust, Helse-Bergen HF, Helse Sorlandet Hospital Trust, Finnmark Hospital Trust, Helgelandssykehuset Hospital Trust, Nordlandssykehuset Hospital Trust, Helse Fonna Hospital Trust, Helse Forde Hospital Trust, Helse Møre og Romsdal Hospital Trust, Helse Nord-Trøndelag HF, Akershus University Hospital Trust, Diakonhjemmet Hospital AS, Sykehuset Innlandet Hospital Trust, Sykehuset Telemark Hospital Trust, Sykehuset i Vestfold Hospital Trust, Helse Stavanger Hospital Trust, Vestre Viken Hospital Trust, Helse Midt-Norge Hospital Trust, University of Oslo, University of Bergen, University of Tromso, Haraldsplass Hospital AS, Lovisenberg Hospital AS, Sykehuset Ostvold Hospital Trust, St. Olavs Hospital, Oslo University Hospital
Conditions
(from sponsor)
Myocardial Infarction
Related terms Myocardial Infarction
Enrollment 9,700 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov