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Evaluation of the Effect of Early mobilization in Myocardial Infarction

Investigating the Effect of Early Mobilization Program on Physiological Indicators and Cardiac Anxiety of Patients with Acute Myocardial Infarction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220116053740N1
Enrollment
60
Registered
2022-05-01
Start date
2022-04-09
Completion date
Unknown
Last updated
2022-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute myocardial infarction. Other current complications following acute myocardial infarction

Interventions

Intervention 1: Intervention group: Patients with acute myocardial infarction who begin to move as planned after 6 hours of complete rest. Intervention 2: Control group: Patients with acute myocardial

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 75 Years

Inclusion criteria

Inclusion criteria: Personal Desire and Satisfaction of Patients to Participate in Research The Patient must be less than 75 Years old The Patient has Hemodynamic stability The Units to be studied are Uncomplicated Myocardial Infarction The Patient has no Previous history of Myocardial Infarction The Patient has no History of Overdosing on Beta-blockers No Sports Contraindications and Movement restrictions Absence of Acute psychiatric disorders Absence of Complete Heart Block, Atrioventricular Node two and three Block, Life-threatening Dysrhythmia, Inferior Myocardial Infarction, Life-Threatening Cardiac Complications and Thrombophlebitis Has not had any Open Heart Surgery Left Ventricular Ejection Fraction is more than 40%

Exclusion criteria

Exclusion criteria: The patient's unwillingness to continue participating in the study Inability to apply or follow the study protocol in terms of recurrence of previous physical and mental illness Physician diagnoses during the intervention that the subject units can not continue to participate in the study Occurrence of any threatening condition during the intervention in the patient that requires emergency nursing or medical intervention

Design outcomes

Primary

MeasureTime frame
Physiological indicators. Timepoint: Before intervention, 24 hours after intervention, 72 hours after intervention. Method of measurement: Hemodynamic monitoring system, Checklist.

Secondary

MeasureTime frame
Anxiety focused on the heart. Timepoint: Before and after the intervention. Method of measurement: The Cardiac Anxiety Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReihane Askari

Esfahan University of Medical Sciences

reyhaneaskari90@yahoo.com+98 31 3360 9397

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026