UNMET CARE PERCEPTIONS OF INTENSIVE CARE NURSES

August 13, 2024 updated by: Dilek KIYMAZ, Ondokuz Mayıs University

UNMET NURSING CARE PERCEPTIONS OF INTENSIVE CARE NURSES: A QUALITATIVE STUDY

This study was conducted to determine the perceptions of intensive care nurses regarding unmet care. A qualitative descriptive approach. The study was completed between April and September 2023 by conducting semi-structured individual interviews with 20 intensive care nurses in a Training and Research Hospital in Turkey and analyzed using the inductive content analysis method.

Study Overview

Status

Completed

Conditions

Detailed Description

Unmet nursing care may occur due to systemic, institutional or nursing-related reasons. Reasons such as insufficient staff and equipment, excessive workload (Pereira et al., 2020), confusion between disciplines, and failure to prioritize care play an important role in missed care (Chaboyer et al., 2021; Dutra & Guirardello, 2021; Kılıç et al., 2023). In summary, while improvements should be made in nursing care practices to ensure patient safety and quality of care, systemic improvements should also be made. In order to make these improvements, it should be determined what the missed nursing care experienced and perceived in the clinical field is and what causes them. This research was conducted to determine the perceptions of intensive care nurses about unmet nursing care. This study is a qualitative design research conducted with intensive care nurses. In the study, a purposeful sample selection was made in accordance with the qualitative research approach. The number of participants was determined according to data saturation and is based on the volunteering of a total of 20 intensive care nurses. During the interview, the participants were asked a personal information form and expert opinion on the subject, as well as in-depth interview questions in a semi-structured information form consisting of eight questions.

Study Type

Observational

Enrollment (Actual)

1

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

    • Atakum
      • Samsun, Atakum, Turkey, 55100
        • Ondokuz Mayıs 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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

This study comprised research with qualitative design completed with intensive care nurses.

Description

Inclusion Criteria:

  • working in intensive care
  • volunteering to participate in the study

Exclusion Criteria:

  • not volunteering 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
What is the perception of care among intensive care nurses?
Time Frame: April-September 2023
This study is a qualitative design study conducted with intensive care nurses. In the study, a purposeful sampling method was used in accordance with the qualitative research approach. The number of participants was determined according to data saturation and was based on the voluntary participation of a total of 20 intensive care nurses. During the interview, participants were asked to fill out a personal information form and expert opinions on the subject, as well as in-depth interview questions in a semi-structured information form consisting of eight questions. Data were collected through face-to-face individual interviews with nurses working in the intensive care unit of a Training and Research Hospital between April and September 2023. In-depth interview questions were prepared in line with literature knowledge and expert opinions were obtained.
April-September 2023
What are the thoughts of intensive care nurses regarding the perception of unmet care?
Time Frame: April-September 2023
After the interviews were completed, the raw data were manually transcribed by the researchers. The content analysis method was used in the evaluation of the data. The data were read several times by the researchers and codes were created from each word, sentence and paragraph. The analysis of the data was carried out manually using the level coding system and themes were created. Level coding was applied as open coding (first level), selective coding (second level), themes (third level) (Yıldırım & Şimşek 2016). After this stage, the relevant codes were classified and themes and sub-themes were created (Elo & Kyngäs, 2008; Vaismoradi et al., 2013).
April-September 2023

Collaborators and Investigators

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

April 1, 2023

Primary Completion (Actual)

September 30, 2023

Study Completion (Actual)

September 30, 2023

Study Registration Dates

First Submitted

August 7, 2024

First Submitted That Met QC Criteria

August 13, 2024

First Posted (Actual)

August 16, 2024

Study Record Updates

Last Update Posted (Actual)

August 16, 2024

Last Update Submitted That Met QC Criteria

August 13, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • UNMET NURSING CARE PERCEPTIONS

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

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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