Comparison of the effect of educational program on cardiac rehabilitation by multimodality and face to face on self-efficacy and spirometric indices

Not Applicable

• Conditions: I00-I99; I70-I79; Coronary Artery Bypass Graft surgery.

• Registration Number: IRCT2017070734630N1
• Lead Sponsor: Vice Chancellor for Research, Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

voluntary of non-emergency coronary artery bypass graft surgery; no history of heart surgery.
Exclusion criteria: patient's death

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Maximum expiratory flow rate. Timepoint: Before intervention, 5 days after intervention, 9 weeks after intervention. Method of measurement: Spirometry device.;Self efficacy. Timepoint: Before intervention, 5 days after intervention, 9 weeks after intervention. Method of measurement: Heart Self Efficacy Questionnaire.;Forced Vital Capasity. Timepoint: Before intervention, 5 days after intervention, 9 weeks after intervention. Method of measurement: Spirometry device.;Forced Expiratory Volume 1. Timepoint: Before intervention, 5 days after intervention, 9 weeks after intervention. Method of measurement: Spirometry device.