Comparison of the impacts of early physical rehabilitation & early comprehensive rehabilitation on patients' outcomes in patients undergoing coronary artery bypass graft surgery

Comparison of the impacts of progressive early physical rehabilitation & early comprehensive rehabilitation on illness outcome including fatigue, functional independence, anxiety, depression, medication adherence & quality of life in patients undergoing coronary artery bypass graft surgery (CABG): A randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160110025937N8

Enrollment

105

Registered

2024-04-19

Start date

2024-04-04

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Chronic ischemic heart disease. Chronic total occlusion of coronary artery

Interventions

Intervention 1: Control group: common rehabilitation in cardiac wards. Intervention 2: Intervention group 1: A comprehensive rehabilitation intervention will be used, conducted by the comprehensive re

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: ?Four Score scale equal to 16 patients who are candidates for non-emergency coronary artery bypass surgery over 18 years old patients with the ability to speak Farsi or Turkish stable hemodynamic status without taking cardiac inotropic drugs

Exclusion criteria

Exclusion criteria: Cardiac and respiratory arrest during surgery and after admission to the ward Syncope caused by activity and exercise Duration under mechanical ventilation for more than 24 hours Heart rate above 100 or having ventricular dysrhythmias Open sternum SpO2 below 90 Inability to establish correlation New ischemic changes in ECG Tachypnea Neuromusculoskeletal problems Unstable fractures limb amputation Hearing, vision and cognitive problems History of cerebrovascular accidents or traumatic brain injury Radiotherapy or chemotherapy in the last 6 months

Design outcomes

Primary

Measure	Time frame
Functional independence. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: modified barthel scale.;Quality of life. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: SF-12 scale.;Fatigue. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: MFI scale.;Anxiety and depression. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: HADS scale.;Medical adherence. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: MARS scale.	—

Measure

Time frame

Functional independence. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: modified barthel scale.;Quality of life. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: SF-12 scale.;Fatigue. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: MFI scale.;Anxiety and depression. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: HADS scale.;Medical adherence. Timepoint: Before intervention , at discharge, a month after discharge. Method of measurement: MARS scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAefeh Allahbakhshian

Tabriz University of Medical Sciences

allahbakhshiana@tbzmed.ac.ir+98 41 3479 6770

Outcome results

None listed

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