The Impact of Intensive Care Nurses' Caring Behaviors on the Quality of Nursing Care

February 4, 2026 updated by: Saadet Can Çiçek, Abant Izzet Baysal University

Brief Summary The purpose of this observational study is to find out whether the caring behaviors of intensive care nurses affect the quality of nursing care for adult patients in the Intensive Care Unit (ICU) at Bolu Izzet Baysal State Hospital.

The study aims to answer the following questions:

Do nurses' caring behaviors influence the quality of care that patients receive?

Are nurses' personal and professional characteristics related to their caring behaviors and the quality of care?

In this study:

Nurses will complete questionnaires about their caring behaviors and personal information.

The researcher will observe patients and assess the quality of care they receive.

The study will be conducted between June 1, 2025, and June 1, 2026. The results are expected to support training programs and improvement efforts to enhance nursing care quality in ICUs.

Study Overview

Detailed Description

This observational study investigates whether the caring behaviors of intensive care nurses influence the quality of nursing care for adult patients in the intensive care unit (ICU) at Bolu Izzet Baysal State Hospital.

Nurses play a critical role in providing continuous, high-quality care to critically ill patients. Research suggests that nurses' behaviors and communication can significantly affect patient care experiences and outcomes.

Based on clinical observations, variations in the perceived quality of care have been noticed, especially during shift changes in the ICU. This study aims to assess both how nurses perceive their caring behaviors and how the quality of care is observed by the researcher.

Findings from the study are expected to help identify areas for improvement and inform potential training programs to enhance care quality, teamwork, and communication within ICU settings.

Study Type

Observational

Enrollment (Actual)

30

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

      • Bolu, Turkey (Türkiye), 14100
        • Bolu Abant Izzet Baysal Unıversıtesı
    • Bolu
      • Merkez, Bolu, Turkey (Türkiye)
        • Republic of Turkey, Ministry of Health, Bolu Izzet Baysal State Hospital

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

Non-Probability Sample

Study Population

Patients aged 18 and above, admitted to the intensive care unit and meeting the study's inclusion criteria and Intensive Care Unit (ICU) Nurses

Description

Inclusion Criteria for Nurses:

Registered nurses who have been working in intensive care units for at least 3 months,

Nurses who have provided both verbal and written informed consent to participate in the study,

Nurses who are rotationally responsible for patient populations whose nursing care quality is assessed during 24-hour shifts.

Inclusion Criteria for Patients:

Patients aged 18 years or older,

Patients whose legal guardians have provided verbal and written informed consent to participate in the study,

Patients with a Foley catheter in place for a minimum of 14 days, as this duration is required to evaluate urinary catheter management quality,

Patients who are intubated, mechanically ventilated, equipped with invasive catheters for nutrition and monitoring, and are fully dependent on nursing care.

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
Intensive Care Unit (ICU) Nurses

Nurses who have been working in intensive care units for at least 3 months with a registered nurse title,

Nurses who have provided verbal and written informed consent to participate in the study,

Nurses who are rotationally responsible for patient populations whose care quality is evaluated during 24-hour shifts.

This refers to the clinical observation performed by the nurse researcher
Patients admitted to the Intensive Care Unit (ICU)

Patients aged 18 years and older,

Patients whose legal representatives have provided verbal and written informed consent for participation,

Patients with a Foley catheter in place for a minimum of 14 days, as urine bag replacement is evaluated after this period,

Patients who are intubated, mechanically ventilated, possess invasive catheters for nutrition and monitoring, and are fully dependent on nursing care.

Observation by the Researcher

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total score of the Caring Behaviors Inventory-24 (CBI-24) completed by ICU nurses
Time Frame: Each nurse will complete the questionnaire once during the study period
The CBI-24 consists of 24 items rated on a 6-point Likert scale (1 = Never, 6 = Always). Higher total scores indicate higher levels of self-perceived caring behaviors by ICU nurses. Due to the rotational shift system, all ICU nurses contribute to the care of multiple patients over time. Therefore, each nurse will complete the questionnaire only once during the study period to capture their overall perception of caring behaviors.
Each nurse will complete the questionnaire once during the study period

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total score of the "Quality of Nursing Care in Intensive Care Units Scale" assessed by the researcher through bedside observation
Time Frame: Data collected during each patient's stay in the ICU
The scale includes 50 items rated on a 3-point Likert scale (0 = Not satisfactory, 2 = Highly satisfactory). Total scores range from 0 to 100. Higher scores indicate better nursing care quality as assessed by the researcher.
Data collected during each patient's stay in the ICU

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of ICU nurses' self-perceived caring behaviors (CBI-24 total score) and nursing care quality (Quality Scale total score)
Time Frame: Analyzed after completion of data collection
The relationship between ICU nurses' self-perceived caring behaviors (CBI-24 total scores) and nursing care quality scores observed by the researcher will be evaluated using linear regression analysis. The goal is to determine whether higher caring behaviors are associated with higher nursing care quality.
Analyzed after completion of data collection

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)

October 10, 2025

Primary Completion (Actual)

January 16, 2026

Study Completion (Actual)

January 30, 2026

Study Registration Dates

First Submitted

June 12, 2025

First Submitted That Met QC Criteria

July 7, 2025

First Posted (Actual)

July 9, 2025

Study Record Updates

Last Update Posted (Actual)

February 6, 2026

Last Update Submitted That Met QC Criteria

February 4, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The data will not be shared due to ethical considerations.

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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