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The Effect of Care Bundle in Preventing Pressure Ulcers Caused by Medical Devices in the Pediatric Intensive Care Unit

The Effect of Care Bundle in Preventing Pressure Ulcers Caused by Medical Devices in the Pediatric Intensive Care Unit

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05406986
Enrollment
80
Registered
2022-06-07
Start date
2022-07-15
Completion date
2022-10-15
Last updated
2022-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Device Induced Injury, Nursing Caries, Pressure Ulcer

Keywords

medical devices, pressure ulcers, Care Bundles

Brief summary

With the development of technology in medicine, more medical instruments are used in the treatment of diseases. Although the use of these instruments provides great benefits for the patients, it can also cause some complications.One of the most important of these complications is pressure ulcer.Some care and evaluation are needed to prevent these complications.This study aims to prevent pressure ulcers with a care package for patients with high risk scores.

Detailed description

A care package will be created with the Delphi method to prevent pressure ulcers caused by medical devices.Experimental and control groups will be formed by randomized control method.The care package created for 14 days will be applied to the experimental group. standard care will be applied to the control group.As a result, the rates of medical device-induced pressure ulcers in both groups will be compared.Children between the ages of 1 and 10 years and treated in the pediatric intensive care unit will be included in the study.Patients with any skin-related disease will not be included in the study.

Interventions

OTHERcare bundle application

The patients in the experimental group will be given care according to the current care bundle for 14 days

Sponsors

Kilis 7 Aralik University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Intervention model description

Experimental and control groups will be selected using the randomized control method.

Eligibility

Sex/Gender
ALL
Age
1 Years to 10 Years
Healthy volunteers
Yes

Inclusion criteria

* being in the pediatric intensive care unit. * nasogastric tube, intubation tube and saturation probe attached. * Voluntary consent of family to participate in the study

Exclusion criteria

* Patients with skin disease * Patients staying less than 14 days

Design outcomes

Primary

MeasureTime frameDescription
Pressure ulcer14 dayMedical devices related pressure ulcer

Secondary

MeasureTime frameDescription
medical device induced pressure ulcer14 dayThe rate of pressure ulcers caused by medical devices in the care package group will be compared with the rates of pressure ulcers caused by medical devices in patients receiving normal care.

Contacts

Primary ContactErhan Elmaoğlu
erhan.elmaoglu@kilis.edu.tr+903488142666

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026