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The Effects Of Discharge Education Program On Recovery And Quality Of Life After Cardiac Surgery

The Effects Of Discharge Education Program On Recovery And Quality Of Life After Cardiac Surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05631340
Enrollment
70
Registered
2022-11-30
Start date
2022-04-01
Completion date
2023-11-30
Last updated
2026-04-06

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

Conditions

Cardiac Disease, Cardiac Surgical Procedures

Keywords

Cardiac Surgical Procedures, Education of Patients, QoL

Brief summary

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.

Detailed description

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.

Interventions

Researcher's newly prepared discharge education supported by a booklet and mobile app

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Masking description

participants do not know the group they belong, case or control

Intervention model description

same follow up time

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* To agree to participate in the research, * Open heart surgery patients * Being 18 years or older, * Being able to read, write, understand and communicate in Turkish, * No vision, hearing and perception problems, * Being conscious, oriented, cooperative and open to communication.

Exclusion criteria

• Having surgery other than open heart surgery

Design outcomes

Primary

MeasureTime frameDescription
Recovery status after cardiac surgery12 weeksRecovery-40 Questionnaire
Quality of Life after cardiac surgery12 weeksMultidimensional Index of Life Quality

Countries

Turkey (Türkiye)

Contacts

STUDY_CHAIRAyfer Özbaş

Istanbul University-Cerrahpasa Florence Nightingale Faculty of Nursing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 18, 2026