- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06001008
Validity of the Turkish Version of "Perception of Quality in Anesthesia": A Prospective Observational Cohort Study
April 17, 2024 updated by: dilan akyurt, Samsun University
The aim of this study is to test the validity of the Perception of Quality in Anesthesia (PQA) and language compatibility.
Study Overview
Detailed Description
The Perception of Quality in Anesthesia (PQA) scale was developed by Hocking et al. in 2013 to measure the quality of anesthesia service received by patients who underwent surgery under anesthesia.
The survey consists of 16 questions.
Researchers ask patients undergoing surgery to complete the PQA questionnaire 24 hours after surgery.
The researcher visits patients in hospital rooms or makes phone calls the day after surgery.
Study Type
Observational
Enrollment (Estimated)
140
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Dilan Akyurt
- Phone Number: +905062344791
- Email: dilanakyurt@gmail.com
Study Contact Backup
- Name: Şenay C Adıgüzel
- Phone Number: +90533 543 54 22
- Email: senaycanikli@gmail.com
Study Locations
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-
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Samsun, Turkey, 55270
- Recruiting
- Dilan Akyurt
-
Contact:
- Dilan Akyurt
- Phone Number: +905062344791
- Email: dilanakyurt@gmail.com
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-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
Adult patients undergoing electiveinguinal or umbilical hernia surgery under general or regional anesthesia in Samsun University Hospital
Description
Inclusion Criteria:
- Patients scheduled for elective inguinal or umbilical hernia surgery under general or regional anesthesia
- Age between 18 and 80 years
- Ability to understand the content of surveys
- Native speaker of Turkish
Exclusion Criteria:
- Emergency operation
- The need for postoperative intensive care
- Existence of mental disability
- Pregnancy
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
General or regional anesthesia
Patients who have undergone inguinal or umbilical hernia surgery
|
PQA is a questionnaire consisting of 16 questions developed to measure the quality of anesthesia service received by patients based on their experiences.
Patients will be asked to answer questions by the researcher 24 hours after surgery.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Construct Validity of PQA (Perception of Quality in Anesthesia)
Time Frame: 24 hours after the surgery
|
PQA is a 16-item questionnaire that measures the satisfaction of the patient with the anesthesia approach applied in the perioperative period.
Survey questions assess 5 topics: Factor A: attention/courtesy; Factor B: pain management; Factor C: knowledge/trust; Factor D: POB; and Factor E: concerns addressed.
For each question, the patient is asked to answer using a five-point Likert scale.
The extremes of the scale are labeled 'very poor' to 'very good' or 'definitely no' to 'definitely yes' depending on the question.
Patient responses to each PQA Likert scale and visual analog questions are scored from 1 to 5. 'Absolutely no' or 'very poor' is scored as 1 and 'definitely yes' or 'very good' is scored 5.
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24 hours after the surgery
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Response success rate of the PQA
Time Frame: 24 hours after the surgery
|
Defined as success if the patient has answered all items
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24 hours after the surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Mustafa SÜREN, Samsun University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
August 1, 2022
Primary Completion (Actual)
December 30, 2023
Study Completion (Estimated)
May 31, 2024
Study Registration Dates
First Submitted
July 29, 2023
First Submitted That Met QC Criteria
August 13, 2023
First Posted (Actual)
August 21, 2023
Study Record Updates
Last Update Posted (Actual)
April 18, 2024
Last Update Submitted That Met QC Criteria
April 17, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SÜKAEK-2022/5/12
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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