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

Sponsor
Istanbul University - Cerrahpasa (IUC) (Other)
Overall Status
Recruiting
CT.gov ID
NCT05631340
Collaborator
(none)
64
Enrollment
1
Location
2
Arms
14.9
Anticipated Duration (Months)
4.3
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Discharge education
 N/A

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 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
same follow up timesame follow up time
Masking:
Single (Participant)
Masking Description:
participants do not know the group they belong, case or control
Primary Purpose:
Health Services Research
Official Title:
The Effects Of Discharge Education Program On Recovery And Quality Of Life After Cardiac Surgery
Actual Study Start Date :
Apr 1, 2022
Actual Primary Completion Date :
Nov 18, 2022
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: case group

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

Other: Discharge education
Researcher's newly prepared discharge education supported by a booklet and mobile app
Active Comparator: control group

Recieving standart hoapital discharge education

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

Outcome Measures

Primary Outcome Measures

  1. Recovery status after cardiac surgery [12 weeks]

    Recovery -40 Questionnaire mesure recovery status before discharge and 12 weeks after discharge

  2. Quality of Life after cardiac surgery [12 weeks]

    Multidimensional Index of Life Quality questionnaire to mesure QoL before discharge and 12 weeks after discharge

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istanbul Univesity-Cerrahpasa Florence Nightingale Faculty of Nursing Istanbul Şişli Turkey 34000

Sponsors and Collaborators

  • Istanbul University - Cerrahpasa (IUC)

Investigators

  • Study Chair: Ayfer Özbaş, Istanbul University-Cerrahpasa Florence Nightingale Faculty of Nursing

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Eva Kajti, Lecturer, Istanbul University - Cerrahpasa (IUC)
ClinicalTrials.gov Identifier:
NCT05631340
Other Study ID Numbers:
  • Eva Kajti
First Posted:
Nov 30, 2022
Last Update Posted:
Nov 30, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Eva Kajti, Lecturer, Istanbul University - Cerrahpasa (IUC)
Cardiac Surgery, Heart Surgery, Discharge Education, Nursing, Telenursing, m-Health, Quality of Life, Recovery

Study Results

No Results Posted as of Nov 30, 2022