Skip to content

The effect of patients early mobilization program on the Physical and mental conditions of patients with MI

A survey effect of patients early mobilization program on the Physical and mental conditions of patients with MI hospitalized in CCU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201201138717N1
Enrollment
40
Registered
2012-01-26
Start date
2012-02-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Acute myocardial infarction. Acute myocardial infarction

Interventions

Intervention 1: A) Intervention group: the first day, the first stage: In this stage, patients 12-18 hours after admission in hospital, setting from prone position to sitting position and after checki
Rehabilitation
A) Intervention group: the first day, the first stage: In this stage, patients 12-18 hours after admission in hospital, setting from prone position to sitting position and after checking blood pressur
B) control group According to the ward routine, 48 hours after admission, patients are ambulated with the help and supervision of researcher.

Sponsors

Semnan University of Medical Sciences, Semnan, Iran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criterias: (1) age of participants less than 70 years, (2) lack of hemodynamic dysfunction (systolic blood pressure Under 100 mmHg and more than 180 mmHg), absence of arrhythmias, and absence of shortness of breath or chest pain before the start of each stage, (3) lack of atrial ventricular block grade two and three, (4) lack of cardiac complications which is confirmed by a cardiologist after echocardiography, (5) lack of acute psychiatric disorders, (6) lack of motor disorders. Exclusion criterias: (1) Patients addicted to narcotic substances, (2) Patients who have a history of cardiopulmonary resuscitation, (3) Patients with myocardial infarction complicated by [hemodynamic disorder, congestive heart failure, signs of carcinogenic shock, continuity of atrial and ventricular arrhythmias, existence of atrial ventricular block grade two and three, pericarditis, pulmonary embolism, stroke or transient ischemic attack, stroke], (4) Patients during stages of the walk have intolerance procedure for three times consecutive, (5) Unwillingness of patients to perform the early mobilization program, (6) Patients who undergoing percutaneous coronary intervention [PCI] and (7) Patients who are treated with thrombolytictherapy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hear Rate. Timepoint: Every 6 hours. Method of measurement: To view the monitor screen.;Blood pressure. Timepoint: Every 6 hours. Method of measurement: According to mmHg by the Pointer manometer.;Ejection fraction. Timepoint: 18-12 and 72 hours after MI. Method of measurement: Echocardiography machine.;Anxiety. Timepoint: In the first 12-18 and 72 hours after of admission. Method of measurement: By Hospital Anxiety and Depression Scale (HADS).;Depression. Timepoint: In the first 12-18 and 72 hours after of admission. Method of measurement: By Hospital Anxiety and Depression Scale (HADS).;Duration of stay in hospital. Timepoint: Time of discharge. Method of measurement: According to hours.;Frequency of pain. Timepoint: After 72 hours. Method of measurement: Looking at records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Asgari

Mohammad Reza Asgari

asgari@sem-ums.ac.irasgari5000@gmail.com+98 23 1445 3365

Outcome results

None listed

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