Design and evaluation of educational intervntion besed on PRECEDE model in improving sleep quality of patients after coronary artery bypass surgery
Phase 1
- Conditions
- Sleep disorders.Sleep disorder, unspecified
- Registration Number
- IRCT201305047132N5
- Lead Sponsor
- Vice chancellor for research of Iran University of Medical Sciences and Health Services
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
The patient’s agreement to participate, patients of two genders between 40-80 years of age, only CABG treatment (not combined with valve replacement surgery), current complaint of poor SQ (score>5 of SQ scale), no history of chronic insomnia for at least one year before surgery, body mass index (BMI) =35 kg/m2, no indication of receiving treatments for depression and anxiety and no history of a major and serious comorbidity except for the risk factors of arthrosclerosis such as diabetic.
exclusion criteria: patients who receive sleeping medications during the study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improving sleep quality. Timepoint: One month after intervention. Method of measurement: Quessionnaire.
- Secondary Outcome Measures
Name Time Method