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Patients Who Underwent Surgical Procedures State of Readiness for Discharge

Sponsor
Akdeniz University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05660707
Collaborator
(none)
1,376
Enrollment
1
Location
18.9
Anticipated Duration (Months)
72.7
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

In this study, it was aimed to evaluate the readiness status of patients who are planned to be discharged after the surgical procedure.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Objective: In this study, it was aimed to evaluate the readiness status of patients who are planned to be discharged after the surgical procedure.

    Method: Explanatory sequential mixed design will be used in accordance with the purpose of the study. The purpose of the exploratory sequential design is to clarify the relationships obtained with the quantitative data by applying the qualitative step.

    This pattern is applied in two stages. The first phase begins with the collection of quantitative data that will essentially answer the research question. In the second stage, qualitative data are collected and the collected data is interpreted to help explain the quantitative results.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    1376 participants
    Observational Model:
    Other
    Time Perspective:
    Other
    Official Title:
    Patients Who Underwent Surgical Procedures State of Readiness for Discharge: Mixed Methods Research
    Actual Study Start Date :
    Feb 1, 2022
    Anticipated Primary Completion Date :
    Aug 31, 2023
    Anticipated Study Completion Date :
    Aug 31, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Readiness status of patients whose discharge is planned [within 24 hours before discharge]

      Readiness for Hospital Discharge Scale/Short Form

    Secondary Outcome Measures

    1. Reasons why patients are not ready for discharge [within 24 hours before discharge]

      semi-structured interview form

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    • Being 18 years or older,

    • Willingness and willingness to participate in the study,

    • Having undergone a surgical procedure,

    • Healing / discharge as it is,

    • Not having difficulties in understanding

    • Patients who do not feel ready for discharge according to quantitative data and also agree to participate in the qualitative study

    Exclusion Criteria:

    • Be under the age of 18,

    • Being discharged without surgical procedure,

    • Transfer to another department

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Akdeniz University Antalya Turkey

    Sponsors and Collaborators

    • Akdeniz University

    Investigators

    • Principal Investigator: Fatma CEBECİ, Prof., Akdeniz University
    • Study Chair: Songül BİŞKİN ÇETİN, PhD., Akdeniz University
    • Study Chair: Arzu TAT ÇATAL, RN, Akdeniz University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fatma CEBECİ, Principal Investigator, Akdeniz University
    ClinicalTrials.gov Identifier:
    NCT05660707
    Other Study ID Numbers:
    • KAEK-959-2021
    First Posted:
    Dec 21, 2022
    Last Update Posted:
    Dec 21, 2022
    Last Verified:
    Dec 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Dec 21, 2022