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Clinical Trials/NCT06509399
NCT06509399
Completed
Not Applicable

Evaluation of the Effectiveness of a Pressure Ulcers Prevention Care Package in the Intensive Care Unit

Abant Izzet Baysal University2 sites in 1 country72 target enrollmentMay 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pressure Ulcer
Sponsor
Abant Izzet Baysal University
Enrollment
72
Locations
2
Primary Endpoint
Pressure Ulcer Formation
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of this study is to evaluate the effectiveness of the care package (CP) developed to prevent pressure injury (PI) in patients in intensive care and to evaluate the effect of the training given to nurses on their knowledge levels and attitudes.

Detailed Description

This experimental study was carried out in the anesthesia and reanimation intensive care unit of Düzce Atatürk State Hospital. The part with patients was completed with a total of 72 patients, 36 in the control group and 36 in the application group. The occurrence rate of PI was compared between the control group and the application group. In the section about nurses, no sample was selected and all 50 nurses working in intensive care were included in the study. Nurses' knowledge and attitudes about PI before and after the training were compared. Data were analyzed using a statistical program.

Registry
clinicaltrials.gov
Start Date
May 15, 2023
End Date
September 15, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ganime Esra Soysal

Assistant Professor of Surgical Nursing

Abant Izzet Baysal University

Eligibility Criteria

Inclusion Criteria

  • - 18 years of age or older,
  • No development of pressure ulcers in any part of the body,
  • Patients expected to stay in the clinic for at least 72 hours or more
  • patients with a braden score below 15 points
  • Obtaining written consent from the first-degree relatives of patients whose written consent is obtained, patients who are unconscious and unable to give consent

Exclusion Criteria

  • - 18 years of age or younger,
  • BY in any part of the body,
  • BBYRDS score more than 15
  • Failure to give written consent by himself/herself or his/her 1st degree relative
  • Exitus, discharge, change of department and the patient's wish to leave the study before completing the number of days determined during the data collection phase

Outcomes

Primary Outcomes

Pressure Ulcer Formation

Time Frame: through study completion, an average of 1 year

Ulcer formation was monitored. Patients were followed up for at least 10 days in this respect.

Secondary Outcomes

  • Knowledge levels of nurses(through study completion, an average of 1 year)

Study Sites (2)

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