Survey efficiency of cardiac rehabilitation program after coronary artery bypass graft on respiratory characteristics

Survey efficiency of the cardiac rehabilitation program after coronary artery bypass graft on respiratory characteristics.

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

IRCT

Registry ID

IRCT20101019004971N5

Enrollment

Registered

2018-07-22

Start date

2018-06-05

Completion date

Unknown

Last updated

2018-09-11

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

Conditions

efficiency of cardiac rehabilitation program after coronary artery bypass graft on respiratory characteristics. Chronic ischemic heart disease

Interventions

Intervention 1: Intervention group: In this group patients besides receiving routine incentive spirometery in their cardiac rehabilitation program use Continuous Positive Airway Pressure mask(CPAP) ti

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: No Emergency Operation No CABG history in the past clinical diagnosis of coronary artery disease, who underwent elective coronary Artery bypass graft (CABG) with cardiopulmonary bypass, a median sternotomy incision and use of a saphenous vein, internal thoracic artery, or radial artery grafts No use of intra-aortic balloon pump No use of permanent pacemaker Ability to perform exercise according to our protocol No valvular heart disease,chronic obstructive pulmonary disease No respiratory problems that cause to add length of intensive care unit stay No Atrial fibrilation arrhythmia and use of Amiodarone protocle

Exclusion criteria

Exclusion criteria: Unstable angina chronic disturbances in heart rhythm significant acute arrhythmias Do not tolerate Continuous Positive Airway Pressure (CPAP) with patient

Design outcomes

Primary

Measure	Time frame
Dyspnea in patients who reveived score above 5 in Modified Category Ratio-10 (CR-10). Timepoint: At the end of the first to third sessions after intervention. Method of measurement: Scoring in Modified Category Ratio-10 (CR-10).;Leg effort in patients who reveived score above 15 in Rate of Perceived Exertion (RPE- Scale). Timepoint: At the end of the first to third sessions after intervention. Method of measurement: Scoring in Rate of Perceived Exertion (RPE- Scale).	—

Measure

Time frame

Dyspnea in patients who reveived score above 5 in Modified Category Ratio-10 (CR-10). Timepoint: At the end of the first to third sessions after intervention. Method of measurement: Scoring in Modified Category Ratio-10 (CR-10).;Leg effort in patients who reveived score above 15 in Rate of Perceived Exertion (RPE- Scale). Timepoint: At the end of the first to third sessions after intervention. Method of measurement: Scoring in Rate of Perceived Exertion (RPE- Scale).

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Secondary

Measure	Time frame
Spirometery parameters changes. Timepoint: In the forth session. Method of measurement: Spirometery.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Taghi Moghadamnia

Rasht University of Medical Sciences

moghadamnia@gums.ac.ir+98 31 3326 0090

Outcome results

None listed

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