Cardiovascular patients undergoing angioplasty. Presence of coronary angioplasty implant and graft
Conditions
Interventions
Intervention 1: Intervention group: In the intervention group, at first, a how to use website guidance pamphlet and a card containing username and password to login the website will be given. in the n
Lifestyle
Intervention group: In the intervention group, at first, a how to use website guidance pamphlet and a card containing username and password to login the website will be given. in the next step, patien
Control group: the control group patients receive routine training of the ward. Evaluating will be done through questionnaire before the intervention, two weeks and 3 months after the end of the inter
Sponsors
Deputy of research of Bushehr University of Medical Sciences
Eligibility
Sex/Gender
All
Age
78 Years to 27 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: over 18 years and less than 70 years old? having coronary artery disease and being in the first-degree angioplasty treatment (angina, acute coronary syndrome, myocardial infarction)? not having cognitive problems based on medical records? not participating in another self-care program? a specific diet for the patient is not recommended ? left ventricular drainage fraction 40% =? no need for surgery and access to the internet. Exclusion criteria: developing new physical problems? unwillingness to continue participation in the study at any time? not seeing web-based educational content.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Self-care behaviors. Timepoint: Before the intervention, two week after the intervention and 3 months after intervention. Method of measurement: Self-care behaviors questionnaire (researcher provided). | — |
Secondary
| Measure | Time frame |
|---|---|
| Awareness. Timepoint: Before the intervention, two week after the intervention and 3 months after intervention. Method of measurement: Questionnaire awareness (researcher provided).;Perceived benefits. Timepoint: Before the intervention, two week after the intervention and 3 months after intervention. Method of measurement: Perceived benefits questionnaire (researcher provided).;Perceived barriers. Timepoint: Before the intervention, two week after the intervention and 3 months after intervention. Method of measurement: Perceived barriers questionnaire (researcher provided).;Perceived Self-efficacy. Timepoint: Before the intervention, two week after the intervention and 3 months after intervention. Method of measurement: Perceived Self-efficacy questionnaire (researcher provided).;Perceived social support. Timepoint: Before the intervention, two week after the intervention and 3 months after intervention. Method of measurement: Perceived social support questionnaire (researcher provided). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHomamodin Javadzadeh
Bushehr University of Medical Sciences
Outcome results
None listed