Effect of online rehabilitation versus control group on physical and psychosocial function in patients undergoing coronary artery bypass graft surgery

Effect of online rehabilitation versus control group on physical and psychosocial function in patients undergoing coronary artery bypass graft surgery: a randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N561

Enrollment

Registered

2025-06-25

Start date

2025-07-11

Completion date

Unknown

Last updated

2025-07-21

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. Atherosclerosis of autologous artery coronary artery bypass graft(s) with unspecified angina pectoris

Interventions

Intervention 1: Intervention group: Routine treatment and rehabilitation measures plus the American College of Sports Medicine (ASCM) protocol at home using a formula (frequency, intensity, time, and

Eligibility

Sex/Gender

All

Age

30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 30 to 65 years Patients undergoing coronary artery bypass graft surgery Candidate for physiotherapy and rehabilitation measures Proper access to cyberspace

Exclusion criteria

Exclusion criteria: Suffering from delirium, delusions or dementia

Design outcomes

Primary

Measure	Time frame
Musculoskeletal disorders. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the Cornell Musculoskeletal Discomfort Questionnaire.;Quality of life. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the WHO Quality of Life-BREF (WHOQOL-BREF) Questionnaire.;Anxiety and depression. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the General Health Questionnaire 28 (GHQ-28).	—

Measure

Time frame

Musculoskeletal disorders. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the Cornell Musculoskeletal Discomfort Questionnaire.;Quality of life. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the WHO Quality of Life-BREF (WHOQOL-BREF) Questionnaire.;Anxiety and depression. Timepoint: Before intervention and 6 and 12 weeks later. Method of measurement: Using the General Health Questionnaire 28 (GHQ-28).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactPaniz Ghasemi Nesari

Hamedan University of Medical Sciences

panizghasemi028@gmail.com+98 81 3838 0572

Outcome results

None listed

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