Patients Who Underwent Surgical Procedures State of Readiness for Discharge

February 1, 2024 updated by: Fatma CEBECİ, Akdeniz University

Patients Who Underwent Surgical Procedures State of Readiness for Discharge: Mixed Methods Research

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

Study Overview

Status

Completed

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 Type

Observational

Enrollment (Actual)

870

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Antalya, Turkey
        • Akdeniz University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

In the Turkish validity and reliability study, the minimum sample size for the 95% confidence interval was calculated as 1251 (t=1.96; d=0.1) by using the standard deviation value (σ=1.85) found for the Discharge Readiness Scale.

Considering that there would be missing or missing data, it was planned to take 10% more than the number of samples.

As a result, the number of samples was determined as 1376.

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Other

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Readiness status of patients whose discharge is planned
Time Frame: within 24 hours before discharge
Readiness for Hospital Discharge Scale/Short Form
within 24 hours before discharge

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reasons why patients are not ready for discharge
Time Frame: within 24 hours before discharge
semi-structured interview form
within 24 hours before discharge

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2022

Primary Completion (Actual)

December 29, 2023

Study Completion (Actual)

December 29, 2023

Study Registration Dates

First Submitted

December 9, 2022

First Submitted That Met QC Criteria

December 19, 2022

First Posted (Actual)

December 21, 2022

Study Record Updates

Last Update Posted (Estimated)

February 2, 2024

Last Update Submitted That Met QC Criteria

February 1, 2024

Last Verified

December 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • KAEK-959-2021

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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