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Adaptation of Perioperative Satisfaction Scale in Regional Anesthesia and Investigation of Its Psychometric Properties

Sponsor
Ömer Faruk Boran (Other)
Overall Status
Unknown status
CT.gov ID
NCT04009018
Collaborator
(none)
380
Enrollment
1
Location
1
Arm
8.4
Anticipated Duration (Months)
45.4
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The aim of the study is to determine the psychometric properties of Perioperative Satisfaction Scale in Regional Anesthesia. In the Turkish version of the scale, a blind reverse translation method will use. And validity and reliability analyses will conduct.

Condition or Disease Intervention/Treatment Phase
  • Other: Perioperative Satisfaction Scale in Regional Anesthesia
 N/A

Detailed Description

The aim of the present research is to contribute to the international literature determining and describing the factor structure and psychometric qualities of the Perioperative Satisfaction Scale in Regional Anesthesia. An additional aim is to contribute to the national literature regarding the performance of the instrument in cross-cultural adaptation. The following steps will be taken: (a) translation of the scale from English into Turkish, (b) data collection, and (c) checking validity and reliability evidence for the adapted Perioperative Satisfaction Scale in Regional Anesthesia.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
380 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Adaptation of Perioperative Satisfaction Scale in Regional Anesthesia and Investigation of Its Psychometric Properties
Actual Study Start Date :
Jun 20, 2019
Actual Primary Completion Date :
Feb 20, 2020
Anticipated Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: Psycometric analyses

It will be a validation study of the Perioperative Satisfaction Scale in Regional Anesthesia. This study is not experimental research. This is a psychometric assessment study of a questionnaire and data will collect pencil-paper survey and face to face from the patients who will get regional anesthesia in the postoperative second day.

Other: Perioperative Satisfaction Scale in Regional Anesthesia
This study is methodological research. Perioperative Satisfaction Scale in Regional Anesthesia will be used to collect data.
Other Names:
  • Measurement tool (Questionnaire)

    		•

    Outcome Measures

    Primary Outcome Measures

    1. Patient satisfaction [postoperative 48 hours]

      Perioperative Satisfaction Scale in Regional Anesthesia will be applied, side effects such as nausea-vomiting, drowsiness will be noted. Patient satisfaction will be assessed with these methods as bad, medium, good, and very good.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Volunteer to participate in the research

    • Participants are over 18 years of age

    • Provided regional anesthesia

    • Postoperative second day

    • No cognitive problems in self-expression

    Exclusion Criteria:

    • Lack of Turkish literacy

    • Use of anesthesia technique other than regional anesthesia

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Kahramanmaras Sutcu Imam University Kahramanmaraş Turkey 46100

    Sponsors and Collaborators

    • Ömer Faruk Boran

    Investigators

    • Study Chair: Fatih Mehmet Yazar, MD, Kahramanmaras Sutcu Imam University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Ömer Faruk Boran, Clinical Professor, Kahramanmaras Sutcu Imam University
    ClinicalTrials.gov Identifier:
    NCT04009018
    Other Study ID Numbers:
    • Regional-1
    First Posted:
    Jul 5, 2019
    Last Update Posted:
    Feb 20, 2020
    Last Verified:
    Feb 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ömer Faruk Boran, Clinical Professor, Kahramanmaras Sutcu Imam University
    scale
    validity
    reliability
    Additional relevant MeSH terms:
    Intraoperative Awareness
    Anesthetics

    Study Results

    No Results Posted as of Feb 20, 2020