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Not yet recruitingNCT07782372Updated Aug 24, 2026

Perceptions of Leadership in Quality Culture for Infection Prevention Among Intensive Care Nurses and Unit-Based Assessment of Antimicrobial Resistance Indicators in Intensive Care Units

An observational study in Healthcare-associated Infections, Quality Culture and Leadership in Intensive Care and Infection Prevention and Control, sponsored by Yeliz Sapulu Alakan. Not yet recruiting. Open to participants aged Up to 125 Years. Per ClinicalTrials.gov, last updated 2026-08-24.

Sponsored by Yeliz Sapulu Alakan · Observational

Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
127
Ages
Up to 125 Years
Sex
All
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Study summary

This study aims to examine intensive care nurses' perceptions of leadership in quality culture for infection prevention and to investigate antimicrobial resistance indicators at the intensive care unit level. Healthcare-associated infections (HAIs) remain a major global patient safety problem and are associated with prolonged hospital stays, increased healthcare costs, and higher mortality. The increasing prevalence of antimicrobial resistance (AMR) further complicates infection prevention and patient care.

Intensive care units are particularly vulnerable to healthcare-associated infections and antimicrobial resistance because of the high frequency of invasive procedures, the vulnerability of critically ill patients, and the extensive use of broad-spectrum antibiotics. Nurses play a central role in infection prevention and antimicrobial stewardship because they are continuously involved in patient care. However, previous studies have reported a gap between nurses' knowledge of infection prevention and adherence to recommended practices in clinical settings. Organizational culture and leadership may contribute to this gap.

Most previous studies have focused on healthcare professionals' self-reported perceptions of infection prevention. However, limited evidence is available regarding the relationship between nurses' perceptions of leadership and quality culture and objective antimicrobial resistance indicators at the intensive care unit level. Therefore, this study will assess nurses' perceptions using the Leadership in Quality Culture for Infection Prevention (LCQ-IP) instrument and examine their relationship with retrospective microbiological data from the participating intensive care units, including antimicrobial resistance rates and resistance profiles. The findings may provide evidence on the role of organizational leadership and quality culture in infection prevention and antimicrobial resistance management in intensive care settings.

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Conditions studied

  • Healthcare-associated Infections
  • Quality Culture and Leadership in Intensive Care
  • Infection Prevention and Control

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Keywords

  • Intensive care nurses
  • Infection prevention and control
  • Quality culture
  • Leadership
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In context

Cross Infection

285 studies on the registry are indexed under Cross Infection; 48 are open to participants now.

This study's planned enrollment of 127 is below the median of 351 across 115 observational studies indexed under Cross Infection.

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Lead sponsor

This is the only study on the registry with Yeliz Sapulu Alakan as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 125 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population will consist of nurses actively working in intensive care units in participating hospitals in Bursa and Iğdır, Türkiye. Eligible participants will be nurses who have been actively working in an intensive care unit for at least 1 year and who voluntarily agree to participate in the study. Student nurses, nursing interns, nurses working temporarily or on a rotational basis in intensive care units, and nurses with less than 1 year of intensive care experience will be excluded.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Nurses who have been actively working in an intensive care unit for at least 1 year.
  • Nurses who voluntarily agree to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Student nurses or nursing interns.
  • Nurses working temporarily or on a rotational basis in the intensive care unit.
  • Nurses who have been actively working in an intensive care unit for at least 1 year.
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Study design

Observational model
Cohort
Time perspective
Other
Enrollment
127 participants (estimated)
Patient registry
No

Groups and cohorts

  • Bursa

    Intensive Care Nurses and Intensive Care Units in Bursa

  • Iğdır

    Intensive Care Nurses and Intensive Care Units in Iğdır

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What researchers measure

Primary outcomes

  1. Leadership in Quality Culture for Infection Prevention (LCQ-IP) score among intensive care nurses

    Leadership for a culture of quality in infection prevention will be assessed using the Turkish version of the Leading a Culture of Quality for Infection Prevention Scale. The scale consists of 16 items rated on a 5-point Likert scale. Total scores range from 16 to 80, with higher scores indicating a more positive perception of leadership for a culture of quality in infection prevention.

    Time frame: Baseline

Secondary outcomes

  1. Antimicrobial Susceptibility Profiles of Bacterial Isolates from Intensive Care Units

    Time frame: The 1-year period preceding study enrollment

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No — Individual participant-level data will not be shared with other researchers. The study will use data collected from intensive care nurses and retrospective, unit-level microbiological and antimicrobial resistance data. Data will not be shared because of ethical, privacy, and confidentiality considerations. Only aggregated and de-identified results will be reported.

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Nov 2026, 2 months later.

Of 56 non-industry observational studies under Cross Infection, half reached primary completion within 28 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 65. This study's planned 2 months is below that.

Counting every sponsor, half of 56 studies reached it within 28 months; a quarter within 17 and three quarters within 65.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 17, 2026
First posted
Aug 24, 2026
StartEst.
Sep 1, 2026
Primary completionEst.
Nov 30, 2026
CompletionEst.
Dec 30, 2026
Last update
Aug 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07782372
Lead sponsor
Yeliz Sapulu Alakan
Responsible party
Yeliz Sapulu Alakan (Lecturer, Uludag University) — Sponsor-investigator
First posted
Aug 24, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Nov 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Aug 24, 2026

Study contacts

Yeliz Alakan, PhD lecturer
Contact
yelizsapulu@uludag.edu.tr
90 505 850 0222

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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