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CompletedNCT05660707Updated Feb 2, 2024

Patients Who Underwent Surgical Procedures State of Readiness for Discharge

An observational study in Surgery, Patients and Discharge Readiness, sponsored by Akdeniz University. Completed at 1 site in Turkey. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-02-02.

Sponsored by Akdeniz University · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
870
Ages
18 Years and older
Sex
All
01

Study summary

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

Read the 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.

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Conditions studied

  • Surgery
  • Patients
  • Discharge Readiness
03

In context

Lead sponsor

Akdeniz University is the lead sponsor of 289 studies on the registry; 60 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
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.

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

Exclusion Criteria:

  • Be under the age of 18,
  • Being discharged without surgical procedure,
  • Transfer to another department
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Study design

Observational model
Other
Time perspective
Other
Enrollment
870 participants (actual)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Readiness status of patients whose discharge is planned

    Readiness for Hospital Discharge Scale/Short Form

    Time frame: within 24 hours before discharge

Secondary outcomes

  1. Reasons why patients are not ready for discharge

    semi-structured interview form

    Time frame: within 24 hours before discharge

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Study locations

1 site
  • Akdeniz University
    Antalya, Turkey
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 2, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05660707
Lead sponsor
Akdeniz University
Responsible party
Fatma CEBECİ (Principal Investigator, Akdeniz University) — Principal investigator
First posted
Dec 21, 2022
Start date
Feb 1, 2022
Primary completion
Dec 29, 2023
Completion
Dec 29, 2023
Last update
Feb 2, 2024

Study contacts

Fatma CEBECİ, Prof.
principal investigator · Akdeniz University
Songül BİŞKİN ÇETİN, PhD.
study chair · Akdeniz University
Arzu TAT ÇATAL, RN
study chair · Akdeniz University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2022. You cannot join it, but the record below documents what was studied.

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