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

NCT ID: NCT05631340

Last Updated: 2022-11-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

64 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-04-01

Study Completion Date

2023-06-30

Brief Summary

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This study aims to build a new discharge education, booklet and mobile application based, and assess it's efffects 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

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Patients following cardiac surgery will be part of the study. Patients will be randomized in control and case groups. Control group receive standart discharge eduation 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 neccasary 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 reassesed.

Conditions

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Cardiac Surgery, Heart Surgery, Discharge Education, Nursing, Telenursing, m-Health, Quality of Life, Recovery

Keywords

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Cardiac Surgery, Heart Surgery, Discharge Education, Nursing, Telenursing, m-Health, Quality of Life, Recovery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

same follow up time
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

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

Study Groups

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case group

Recieving additional discharge education by the researcher and supported by a booklet and mobile app

Group Type EXPERIMENTAL

Discharge education

Intervention Type OTHER

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

control group

Recieving standart hoapital discharge education

Group Type ACTIVE_COMPARATOR

Discharge education

Intervention Type OTHER

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

Interventions

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Discharge education

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

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role lead

Responsible Party

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Eva Kajti

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ayfer Özbaş

Role: STUDY_CHAIR

Istanbul University-Cerrahpasa Florence Nightingale Faculty of Nursing

Locations

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Istanbul Univesity-Cerrahpasa Florence Nightingale Faculty of Nursing

Istanbul, Şişli, Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Eva Kajti

Role: CONTACT

Phone: +905535213904

Email: [email protected]

Facility Contacts

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Eva Kajti

Role: primary

Other Identifiers

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Eva Kajti

Identifier Type: -

Identifier Source: org_study_id