Turkish Validity and Reliability Study of Pediatric Anesthesia Satisfaction Scale (TVRPAS)

November 1, 2023 updated by: Yesim Senayli, Bozok University

Evaluation of Satisfaction Levels of Pediatric Patients and Parents After Anesthesia: A Turkish Validity and Reliability Study

Strategies to increase patient satisfaction have a positive effect on clinical care. Therefore, evaluation of emotional and psychological satisfaction and satisfaction can increase the quality of anesthetic care. The number of satisfaction evaluation studies, especially for pediatric patients who have undergone surgery, is very few, and the validity and reliability of the existing satisfaction scoring systems in the Turkish population has not yet been established. As a result of this study, it will be possible to use a Turkish validity and reliability scale that can evaluate the satisfaction levels of pediatric patients and parents after anesthesia, which is planned to be developed, to be used in the studies of improving health services, increasing the quality of the hospital, and using it in scientific studies by researchers and academicians in Türkiye.The aim of this study is to conduct a Turkish validity and reliability study by examining the reliability, validity, acceptability and reproducibility of a pediatric patient and parent satisfaction questionnaire previously validated in English.

The research data will be realized by the face-to-face filling of the Turkish version of the pediatric anesthesia satisfaction scale, which has been published in the literature, by the child and their parents.

The Turkish version of the scale in question will be asked to fill out the questionnaire within the first hour of being transferred from the operating room to the pediatric surgery service after the surgery/surgical procedure for all parents who have been operated by Yozgat Bozok University Research and Practice Hospital Pediatric Surgery. The delivery of the questionnaire and its face-to-face filling process will be carried out by an anesthesiologist (specialist or specialist student) different from the relevant anesthesiologist, who is responsible for the outpatient evaluation of the patient and the anesthesia management in the peroperative period, so that the respondent is not affected by any embarrassment, intentional reasons, etc.

Study Overview

Status

Enrolling by invitation

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Yozgat, Turkey
        • Bozok University

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

  • Child
  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

0-18 years old age pediatric patients who 0-18 year who will undergo surgical procedure

Description

Inclusion Criteria:

  1. Speaking Turkish of the child patient and the parent
  2. Absence of any known psychiatric disease
  3. Agreeing to participate in the study (patients and parents with cognitive development who can give consent)

Exclusion Criteria:

  1. Having any known psychiatric disease of the child patient or parent
  2. Having a history of drug use that will affect the cognitive functions of the child patient or parent
  3. Parent's refusal to participate in the study (patients and parents with cognitive development who can give consent)
  4. Child patient or parent does not know Turkish

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
Survey grup
No intervention is to be administered. Just a survey study
Non interventional. Pediatric anesthesia satisfaction scale validity and reliability is going to investigate by survey analyses

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Valid and reliable Turkish pediatric anesthesia satisfaction scale
Time Frame: One year
The reliability, test-retest reliability, and internal consistency will be examined. McNemar coefficient and a Cronbach's alpha coefficient will be applied to get validity conformation
One year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Yesim Senayli, ass profess, Bozok University Anesthesiology and Reanimation Department

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 (Estimated)

November 15, 2023

Primary Completion (Estimated)

April 30, 2024

Study Completion (Estimated)

July 1, 2024

Study Registration Dates

First Submitted

August 25, 2023

First Submitted That Met QC Criteria

November 1, 2023

First Posted (Actual)

November 7, 2023

Study Record Updates

Last Update Posted (Actual)

November 7, 2023

Last Update Submitted That Met QC Criteria

November 1, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Bozok University

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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