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

Comparison of the effect of educational program on cardiac rehabilitation by multimodality and face to face on self-efficacy and spirometric indices of patients undergoing coronary artery bypass graft surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017070734630N1

Enrollment

Registered

2017-07-07

Start date

2017-07-11

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

Coronary Artery Bypass Graft surgery. I70-I79

Interventions

Group two: teaching cardiac rehabilitation by face to face

Intervention 1: Group one: teaching cardiac rehabilitation by multimedia. Intervention 2: Group two: teaching cardiac rehabilitation by face to face.

Group one: teaching cardiac rehabilitation by multimedia

Eligibility

Sex/Gender

All

Age

18 Years to 64 Years

Inclusion criteria

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

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Malekzadeh

Mashhad University of Medical Sciences

malekzadehj@mums.ac.ir+51 38591511

Outcome results

None listed

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