- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05660707
Patients Who Underwent Surgical Procedures State of Readiness for Discharge
Patients Who Underwent Surgical Procedures State of Readiness for Discharge: Mixed Methods Research
Study Overview
Status
Conditions
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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Antalya, Turkey
- Akdeniz University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
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
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
Sponsor
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
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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