Validity of the Turkish Version of "Perception of Quality in Anesthesia": A Prospective Observational Cohort Study
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ClinicalTrials.gov Identifier: NCT06001008 |
Recruitment Status :
Recruiting
First Posted : August 21, 2023
Last Update Posted : April 18, 2024
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Condition or disease | Intervention/treatment |
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Patient Satisfaction | Other: PQA |
Study Type : | Observational |
Estimated Enrollment : | 140 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Official Title: | Validity of the Turkish Version of "Perception of Quality in Anesthesia": A Prospective Observational Cohort Study |
Actual Study Start Date : | August 1, 2022 |
Actual Primary Completion Date : | December 30, 2023 |
Estimated Study Completion Date : | May 31, 2024 |
Group/Cohort | Intervention/treatment |
---|---|
General or regional anesthesia
Patients who have undergone inguinal or umbilical hernia surgery
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Other: PQA
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. |
- 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.
- 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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Ages Eligible for Study: | 18 Years to 80 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Sampling Method: | Probability Sample |
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
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06001008
Contact: Dilan Akyurt | +905062344791 | dilanakyurt@gmail.com | |
Contact: Şenay C Adıgüzel | +90533 543 54 22 | senaycanikli@gmail.com |
Turkey | |
Dilan Akyurt | Recruiting |
Samsun, Turkey, 55270 | |
Contact: Dilan Akyurt +905062344791 dilanakyurt@gmail.com |
Study Director: | Mustafa SÜREN | Samsun University |
Responsible Party: | dilan akyurt, Specialist of Anaesthesiology and Reanimasion Principle investigator, Samsun University |
ClinicalTrials.gov Identifier: | NCT06001008 |
Other Study ID Numbers: |
SÜKAEK-2022/5/12 |
First Posted: | August 21, 2023 Key Record Dates |
Last Update Posted: | April 18, 2024 |
Last Verified: | April 2024 |
Anesthesia Perioperative complications PQA |