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Nursing Care Bundle for Pressure Injury Prevention

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What is being tested

Intervention Group

+ Control Group

Other
Who is being recruted

Pressure Ulcer+1

+ Skin Diseases

+ Skin Ulcer

From 18 to 65 Years
+7 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: January 2025
See protocol details

Summary

Principal SponsorKoç University
Study ContactAyşe Sılanur Demir Demir
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 1, 2025

Actual date on which the first participant was enrolled.

Pressure injuries are a common problem for patients in hospitals, leading to significant discomfort and longer recovery times. These injuries can be difficult to treat and can cause both physical and emotional distress for patients. They also significantly increase the costs associated with healthcare due to prolonged hospital stays and the intensive care they require. This study focuses on developing a nursing care bundle, which is a set of evidence-based practices designed to prevent pressure injuries. By implementing this care bundle, the study aims to improve patient outcomes, reduce healthcare costs, and enhance the quality of care provided by nurses. Participants in this study will be involved in testing the new nursing care bundle. This care bundle will be based on existing research and best practices, and it will include a series of standardized care procedures. Nurses will apply these procedures to prevent pressure injuries in patients. The success of the care bundle will be measured by observing any reduction in the rates of pressure injuries among patients receiving care. Additionally, the study will evaluate whether the use of the care bundle helps in reducing the costs associated with treating pressure injuries. This approach is expected to promote teamwork and a consistent standard of care among healthcare professionals.

Official TitleDevelopment of Nursing Care Bundle for the Prevention of Pressure Injuries, the Impact on the Rate and Cost of Pressure Injuries
NCT06770686
Principal SponsorKoç University
Study ContactAyşe Sılanur Demir Demir
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

90 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Pressure UlcerSkin DiseasesSkin UlcerSkin and Connective Tissue Diseases

Criteria

4 inclusion criteria required to participate
Patients who fall into all risk categories assessed by the Braden scale

Not having developed a pressure injury anywhere on their body

Being 18 years of age or older

Expectation of a minimum of 24 hours or more in the intensive care unit

3 exclusion criteria prevent from participating
Being 18 years of age or younger

Having and developing a pressure injury anywhere on their body

Expectation of a less than 24-hour stay in the intensive care unit

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
A nursing care bundle will be applied to patients in the intervention group. The implementation status of the nursing interventions included in the care bundle for each patient will be observed by the researcher and recorded on the "Care Bundle Observer Form." Recording of the applications performed on the monitoring form will be encouraged.

Group II

Active Comparator
Patients in the control group will receive routine care related to pressure injury prevention administered by the institution. Routine care includes standard interventions such as checking pressure points at twice-daily shift changes, positioning every 2 hours, skin assessment, and wound assessment.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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