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The Physical Activity Post Myocardial Infarction SWEDEHEART Prospective Cohort Study (ACTIVITY)

S

Sahlgrenska University Hospital

Status

Enrolling

Conditions

Myocardial Infarction

Treatments

Other: Accelerometer measurement

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The association between objectively measured physical activity intensities (light, moderate and vigorous), sedentary time and clinical outcomes has not been clarified in patients after a myocardial infarction.

The overall objective of the study is to explore associations between accelerometer measured physical activity and clinical outcomes after a myocardial infarction. Moreover, the association between changes in physical activity and outcomes will be assessed.

Full description

It is estimated to include 4000 patients with myocardial infarction during 2 years. Patients will wear the accelerometer for 7 days at follow-up visits (2 months and 1 year) after discharge. The investigators will examine the dose-response relations of several exposure variables from the accelerometer measurements with the outcomes.

Enrollment

4,000 estimated patients

Sex

All

Ages

18 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed informed consent
  • Diagnosis of a type 1 myocardial infarction registered in SWEDEHEART
  • Age 18-79 years at discharge from hospital
  • Attending the first visit in the cardiac rehabilitation (CR) registry SEPHIA (2 months after discharge)

Exclusion criteria

  • Inability to understand Swedish
  • Non-ambulatory
  • Any mental condition that may interfere with the possibility for the patient to comply with the study protocol

Trial design

4,000 participants in 1 patient group

Cohort group
Description:
Diagnosis of a type 1 myocardial infarction registered in SWEDEHEART Age 18-79 years at discharge from hospital
Treatment:
Other: Accelerometer measurement

Trial contacts and locations

35

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Central trial contact

Maria Bäck, PhD; Johanna Lilliecrona, MSc

Data sourced from clinicaltrials.gov

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