Competencies of Operating Room Nurses and Influencing Factors

August 4, 2022 updated by: Öğr. Gör. Ayşe UÇAK, Burdur Mehmet Akif Ersoy University

Perceptıons Of The Surgıcal Team Regardıng The Competencıes Of The Operatıng Room Nurse And Factors Affectıng The Competence

Aim: The aim of this study was to determine the perceived competence of operating room nurses and the opinions of the surgical team, regarding the competence of nurses and the influencing factors with a deep understanding.

Method: This convergent parallel mixed-methods study was carried out with members of the surgical team working in 17 hospitals including three public, two university, one city, one education and research, and ten private ones located in city center of Burdur, Isparta and Antalya provinces. The data were collected between May 1th, 2020 and August 20th, 2020 using Quantitative and Qualitative Personal Information Forms, Perceived Perioperative Competence Scale (PPCS-R) and semi-structured interview form. The quantitative data were assessed using the SPSS 24.0 package program, and the qualitative data were assessed using content analysis and thematic analysis. The quantitative and qualitative data were analyzed independently, and interpreted based on analytical generalization in the discussion section.

Study Overview

Detailed Description

Aim: The aim of this study was to determine the perceived competence of operating room nurses and the opinions of the surgical team, regarding the competence of nurses and the influencing factors with a deep understanding.

Method: This convergent parallel mixed-methods study was carried out with members of the surgical team working in 17 hospitals including three public, two university, one city, one education and research, and ten private ones located in city center of Burdur, Isparta and Antalya provinces. The sample of the quantitative dimension of the study consisted of 224 operating room nurses working in authorized institutions, and the qualitative dimension consisted of 54 team members including 21 operating room nurses, 21 surgeons, 3 anesthesiologists, and 9 technicians/operators. The data were collected between May 1th, 2020 and August 20th, 2020 using Quantitative and Qualitative Personal Information Forms, Perceived Perioperative Competence Scale (PPCS-R) and semi-structured interview form. The quantitative data were assessed using the SPSS 24.0 package program, and the qualitative data were assessed using content analysis and thematic analysis. Quantitative data were analyzed using descriptive analysis, ANOVA, Mann Whitney U and Kruskal-Wallis H tests. Qualitative data were assessed through descriptive content analysis. The quantitative and qualitative data were analyzed independently, and interpreted based on analytical generalization in the discussion section.

Study Type

Observational

Enrollment (Actual)

224

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

      • Muratpaşa, Turkey, 07160
        • Fatma Cebeci

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
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The universe of the research consists of the hospitals located in the city centers of Burdur, Isparta and Antalya in the Western Mediterranean Region. The sample consists of surgical team members working in the operating rooms of 17 hospitals, two of which are university, one is research practice, four are state and ten are private.

Description

Inclusion Criteria:

  • Quantitative At least six months of operating room experience nurses Qualitative At least six months of operating room experience surgical team members

Exclusion Criteria:

Willingness to withdraw from the study at any time

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

  • Observational Models: Case-Only
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
surgical team members
The aim of this study is to determine with a deep understanding the perceptions of the operating room nurses' competence and the surgical team's views on the competence of nurses and the factors affecting them. In the research, parallel data type in convergent parallel mixed design (convergent parallel) was used to obtain rigorous, valid and reliable data with survey questions and individual interviews. In the quantitative dimension of the study, it was aimed to determine the perceptions of the operating room nurses about their competencies, and in the qualitative aspect, the thoughts/opinions of the entire surgical team about the competency of the operating room nurses and the factors affecting them.

The quantitative part of the study is a descriptive study with the Perceived Perioperative Competence Scale-Revised to determine the perceptions of operating room nurses about their competencies.

It is a case study in order to reveal the opinions of the surgical team members about the competencies of the operating room nurses and the affecting factors through individual in-depth interviews and to better explain the current situation at the qualitative stage, which is carried out simultaneously.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
competence Factors affecting the competence of operating room nurses
Time Frame: 6 week

In the quantitative dimension of the study, the competency areas of operating room nurses were evaluated in 6 dimensions with the revised perioperative competency scale. The factors of the scale included "foundational knowledge and skills" (9 items), "leadership" (8 items), "collaboration" (6 items), "proficiency" (6 items), "empathy" (5 items), and "professional development" (6 items). In the qualitative aspect of the research, individual in-depth interviews with the surgical team members were made by descriptive and content analysis, and competency areas were determined.

security non-technical arae

6 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
factors
Time Frame: 6 week

In the quantitative aspect of the study, the Perceived Perioperative Competence Scale-Revised and the sociodemographic characteristics of nurses were compared.

In the qualitative aspect of the study, descriptive and content analysis were made in the interviews with the members of the surgical team and the influencing factors were determined.

6 week

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Ayşe Uçak-lecturer, Akdeniz University

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)

March 1, 2020

Primary Completion (Actual)

August 20, 2020

Study Completion (Actual)

June 20, 2022

Study Registration Dates

First Submitted

July 7, 2022

First Submitted That Met QC Criteria

August 4, 2022

First Posted (Actual)

August 8, 2022

Study Record Updates

Last Update Posted (Actual)

August 8, 2022

Last Update Submitted That Met QC Criteria

August 4, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • AUCAK

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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