Nursing Activity Score (Nursing Activities Score-NAS) Verification of Turkish Version

January 4, 2024 updated by: Ozgur Komurcu, Samsun University

Various tools for measuring nursing workload have been described in the national and international literature. For this purpose, Cullen et al. The Therapeutic Intervention Scoring System (TISS)-28, created by Miranda et al. Nursing Activities Score (NAS) was created by revising by. NAS covers 80.8% of all nursing activities, surpassing the 43.3% coverage of TISS-28.

Critical Nursing Situation Index (CNSI) has been validated and adapted in our country and has been found to be a valid and reliable scale for the Turkish society. The aim of this study is to adapt the Nursing Activities Score (NAS) to Turkish and determine its correlation with CNSI scores.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Various tools for measuring nursing workload have been described in the national and international literature. The Therapeutic Intervention Scoring System (TISS)-28, which is designed to classify the nursing workload of patients in intensive care units according to the severity of their illness to be evaluated by a panel of experts, evaluates 43.3% of nursing activities. Miranda et al. In order to reduce possible erroneous evaluations, some changes were made to TISS-28 and the Nursing Activities Score (NAS) was created. NAS covers 80.8% of all nursing activities, surpassing the 43.3% coverage of TISS-28.

The Critical Nursing Situation Index (CNSI), which was finalized with 84 items developed by Binnekade et al., was validated and adapted in our country and was found to be a valid and reliable scale for the Turkish society.

In this study, which was carried out to adapt and validate the Nursing Activities Score (NAS) into Turkish, the internal consistency Cronbach's alpha coefficient was found to be p = 0.718 after a pilot study with a sample of 30 adult intensive care patients and 30 nurses. After the significant internal consistency obtained in the pilot study, it was aimed to examine the correlation of NAS internal consistency and CNSI scores in 150 work shift.

Study Type

Observational

Enrollment (Actual)

150

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

      • Samsun, Turkey, 55270
        • Özgür Kömürcü

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

Yes

Sampling Method

Probability Sample

Study Population

Nurses providing 3rd level intensive care services at Samsun University

Description

Inclusion Criteria:

  • Nurses who serve patients over the age of 18 who stay in Level 3 intensive care for at least 24 hours

Exclusion Criteria:

  • Those nurses; Serving patients under the age of 18, Caring for patients who are scheduled to be discharged from intensive care within 24 hours, Those who change their workplace for any reason during the work shift Who did not agree to participate in the study

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
Nurse
Nurses working in tertiary intensive care
NAS Turkish language validation will be carried out. NAS and CNSI scores will be recorded during the shifts of nurses serving patients in Level 3 intensive care units by the nurse in charge and another independent evaluator, and the correlation between the two scores will be investigated.
Other Names:
  • CNSI

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of NAS Turkish validity and applicability
Time Frame: 6 month
NAS was developed to measure the workload of nurses in patient care. Scores refer to the average time spent caring for patients, not the severity of the disease. Total NAS can range from 0 to 177 points. A score above 100 points indicates that more than one nurse is needed to provide care.
6 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Investigating the correlation between NAS and CNSI
Time Frame: 6 month
CNSI, which has previously been validated in Turkish, will be applied together with NAS in the same nurse shift, so that the correlation between the two scores will be investigated.
6 month

Collaborators and Investigators

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

Investigators

  • Study Director: özgür kömürcü, 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)

May 5, 2023

Primary Completion (Actual)

November 11, 2023

Study Completion (Actual)

November 12, 2023

Study Registration Dates

First Submitted

December 20, 2023

First Submitted That Met QC Criteria

January 4, 2024

First Posted (Actual)

January 16, 2024

Study Record Updates

Last Update Posted (Actual)

January 16, 2024

Last Update Submitted That Met QC Criteria

January 4, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • SUKAEK 2023-12/2

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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