Comparative evaluation of discharge planning and cardiac rehabilitation on the health outcomes of patients undergoing coronary artery bypass graft surgery

Comparative evaluation of discharge planning based on continuous care model and routine cardiac rehabilitation on the health related outcomes of patients undergoing coronary artery bypass graft surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20130211012439N3

Enrollment

Registered

2019-01-16

Start date

2019-07-23

Completion date

Unknown

Last updated

2020-09-07

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

Conditions

Patients undergoing coronary artery bypass graft surgery. Atherosclerotic heart disease of native coronary artery

Interventions

Intervention 1: Intervention group: after introduction of the study and statement of the purposes, the patients will provide informed consents and complete the demographics form, quality of life quest

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients after coronary artery bypass graft surgery The family and patient's willingness to participate in educational programs based on a continuous care model Close relationship of family member with patient

Exclusion criteria

Exclusion criteria: Heart Failure class III and IV Severe musculoskeletal problems Positive exercise test did not have access to a smart phone on medication for psychiatric disorders

Design outcomes

Primary

Measure	Time frame
Quality of life score in the short form questionnaire 36 questions. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Short form questionnaire of quality of life.;Measure functional capacity. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Using a treadmill according to a modified Bruce protocol.	—

Measure

Time frame

Quality of life score in the short form questionnaire 36 questions. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Short form questionnaire of quality of life.;Measure functional capacity. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Using a treadmill according to a modified Bruce protocol.

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Secondary

Measure	Time frame
Re-hospitalization. Timepoint: Immediately after and 3 months after the end of the intervention. Method of measurement: through checking the computer system and directly querying patients (for potential hospitalizations elsewhere).;Depression score in depression, anxiety and stress questionnaire. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Depression Anxiety and Stress Scale.;Anxiety score in depression, anxiety and stress questionnaire. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Depression Anxiety and Stress Scale.;Stress score in depression, anxiety and stress questionnaire. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Depression Anxiety and Stress Scale.	—

Measure

Time frame

Re-hospitalization. Timepoint: Immediately after and 3 months after the end of the intervention. Method of measurement: through checking the computer system and directly querying patients (for potential hospitalizations elsewhere).;Depression score in depression, anxiety and stress questionnaire. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Depression Anxiety and Stress Scale.;Anxiety score in depression, anxiety and stress questionnaire. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Depression Anxiety and Stress Scale.;Stress score in depression, anxiety and stress questionnaire. Timepoint: Before, immediately after and 3 months after the end of the intervention. Method of measurement: Depression Anxiety and Stress Scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Pakrad

Faculty of Medical Sciences Tarbiat Modares University

f.pakrad@modares.ac.ir+98 21 8288 3590

Outcome results

None listed

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