SurgeryNCT05660707
Patients Who Underwent Surgical Procedures State of Readiness for Discharge
An observational study of Surgery and Patients, run by Akdeniz University at 1 site in Turkey (Türkiye).
Trial 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 more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Surgery, Patients, Discharge Readiness
- How many people
- 870 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Feb 2022to 29 Dec 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
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.
Who may be able to join
- 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
Who cannot join
- Be under the age of 18,
- Being discharged without surgical procedure,
- Transfer to another department
Trial locations and contacts
1 site in 1 country.
About this study
Official title: 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.
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.
- Conditions
- Surgery, Patients, Discharge Readiness
What is being measured
The primary outcome is the main question the study is designed to answer.
Readiness status of patients whose discharge is planned
Readiness for Hospital Discharge Scale/Short Form
Measured: within 24 hours before discharge
Secondary outcomes (1)
Reasons why patients are not ready for discharge
semi-structured interview form
Measured: within 24 hours before discharge
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Dec 2022
- Study start1 Feb 2022
- Primary completion29 Dec 2023
- Study completion29 Dec 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SurgeryStudies of the same condition, open and under way.
- More trials run by Akdeniz UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Other
- Enrolment
- 870 participants (actual)
Sponsor and investigators
- Lead sponsor
- Akdeniz University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Fatma CEBECİ, Akdeniz University
- Investigators
- Fatma CEBECİ, Prof., Principal investigator, Akdeniz UniversitySongül BİŞKİN ÇETİN, PhD., Study chair, Akdeniz UniversityArzu TAT ÇATAL, RN, Study chair, Akdeniz University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05660707
- Sponsor's protocol ID
- KAEK-959-2021
- Status last verified
- Dec 2022
- First submitted
- 9 Dec 2022
- Last updated
- 2 Feb 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Patients Who Underwent Surgical Procedures State of Readiness for Discharge: Mixed Methods Research
- ClinicalTrials.gov ID
- NCT05660707
- Acronym / sponsor ID
- KAEK-959-2021
- Conditions
- Surgery, Patients, Discharge Readiness
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 870 participants (actual)
- Lead sponsor
- Akdeniz UniversityUniversity, hospital or other
- Study start
- 1 Feb 2022 (actual)
- Primary completion
- 29 Dec 2023 (actual)
- Study completion
- 29 Dec 2023 (actual)
- First posted
- 21 Dec 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In this study, it was aimed to evaluate the readiness status of patients who are planned to be discharged after the surgical procedure.
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
- Observational model
- Other
- Time perspective
- Other
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- 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.
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (3 listed)
- Be under the age of 18,
- Being discharged without surgical procedure,
- Transfer to another department
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Readiness status of patients whose discharge is planned
Time frame: within 24 hours before discharge
Readiness for Hospital Discharge Scale/Short Form
1 secondary outcome
Reasons why patients are not ready for discharge
Time frame: within 24 hours before discharge
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Feb 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Fatma CEBECİ, Prof. principal investigator
Akdeniz University
Songül BİŞKİN ÇETİN, PhD. study chair
Akdeniz University
Arzu TAT ÇATAL, RN study chair
Akdeniz University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Surgery and Patients, run by Akdeniz University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 2 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Readiness status of patients whose discharge is planned (time frame: within 24 hours before discharge). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Feb 2024.