Istanbul Atlas University
Istanbul, 34000, Turkey (Türkiye)
NCT Number: NCT05631340
This study aims to build a new discharge education, booklet and mobile application based, and assess it's effects on recovery and quality of life in cardiac surgery patients. This is a randomised control trial. 12 weeks follow up will be done by phone calls.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Istanbul, 34000, Turkey (Türkiye)
Patients following cardiac surgery will be part of the study. Patients will be randomized in control and case groups. Control group receive standart discharge education from the nurses of the hospital, they will be interviewed by the researcher to gather general information and also information about recovery and quality of life. Case group will be given a discharge education by the researcher before discharge. After education patients will be given a booklet and a mobile application with the neccesary discharge information. Both groups will be followed for 12 weeks by monthly phone calls. In the last call recovery and quality of life will be reassessed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Researcher's newly prepared discharge education supported by a booklet and mobile app
Time frame: 12 weeks
Recovery-40 Questionnaire
Time frame: 12 weeks
Multidimensional Index of Life Quality
Istanbul University - Cerrahpasa
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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