Coronary Artery Disease. presence of aortocoronary bypass graft
Conditions
Interventions
Control group took routine educations.
Intervention 1: Education based on stages of change model of Prochaska for intervention group took 8 weeks.These educations started immediately after discharge and continued in 2,4,6,8 weeks. Interven
Behavior
Education based on stages of change model of Prochaska for intervention group took 8 weeks.These educations started immediately after discharge and continued in 2,4,6,8 weeks.
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
40 Years to 75 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria:Has only CABG surgery; Residence in shiraz city or province; Access to telephone follow-up program by the researcher; Ability to read and write; Ability to understand the content based on the researcher,s judgment; Willing to participate in the study; Exclusion criteria: History of CABG surgery; Family members have expertise in medical sciences field; Have severe and life-threatening diseases alongside with coronary artery disease such as CVA and cancer; Have hearing problems; Have psychiatric or cognitive disorders.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: Before and 2 months after intervention. Method of measurement: Mac New questionnaire.;Anxiety and Depression. Timepoint: pre test and post test (2 months after intervention). Method of measurement: Hospital Anxiety and Depression Scale.;Triglyceride. Timepoint: Before and 2 months after intervention. Method of measurement: mg\dl.;Stages of change of patients. Timepoint: Before and 2 months after intervention. Method of measurement: Stages of change allgoritm.;Cholesterol. Timepoint: Before and 2 months after intervention. Method of measurement: mg\dl.;Cholesterol / High Density Lipoprotein (HDL). Timepoint: Before and 2 months after intervention. Method of measurement: ---.;Low Density Lipoprotein (LDL) / High Density Lipoprotein (HDL). Timepoint: Before and 2 months after intervention. Method of measurement: ---.;Body Mass Index (BMI). Timepoint: Before and 2 months after intervention. Method of measurement: Weight / ( Height)2.;Smoking. Timepoint: Before and 2 months after intervention. Method of measurement: Demografic Form. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Marzieh Moattari
Shiraz University of Medical Sciences
Outcome results
None listed