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Prevention of Skin Damage in the Patient in Prone Position: Development of Education Interventions Based on a Training Needs Assessment Study.

Prevention of Skin Damage in the Patient in Prone Position: Development of the ProneTection Education and Training Package and Study of Implementation Conditions in an Intensive Care Setting in Belgium and Sweden.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05238870
Enrollment
21
Registered
2022-02-14
Start date
2022-07-08
Completion date
2022-09-01
Last updated
2022-10-13

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

Conditions

Acute Respiratory Distress Syndrome, Pressure Ulcer, Skin Lesion

Keywords

prone position, pressure ulcer, moisture-associated skin damage, medical device-related skin injury, skin tear, prone ventilation

Brief summary

This is study 1 of 3 - of the overall project: The ProneTection Quality Improvement Project. The three aims of this study, study 1 are: 1. to establish the training needs critical care clinicians have regarding prone positioning, 2. to investigate the conditions for effective implementation as in an intensive care setting, 3. to develop an education and training package (The ProneTection package) for an interdisciplinary team of clinicians on skin damage prevention of patients in the prone position

Detailed description

Conduct a needs assessment by using semi-structured interviews with an interdisciplinary team of clinicians (Ghent University Hospital (UZ Gent), Brussels University Hospital (UZ Brussel) and several institutions in Sweden, mainly Örebro University Hospital). Concurrently, investigate the conditions for effective implementation in a critical care facility using the same interviews and participants (interviewees). Develop the education and training package (the ProneTection package). The ProneTection package will be based on 1. the results of our recently published gap-analysis study, 2. the needs assessment results from the interviews, keeping the optimal conditions (facilitators) in mind for successful implementation, and 3. the critical review and evaluation by eleven key opinion leaders from the established international expert panel

Interventions

OTHERInterviews for the needs analysis. No intervention.

To develop the education and training package, a needs-analysis is necessary. The clinicians' training needs will be established through interviews.

Sponsors

Örebro University, Sweden
CollaboratorOTHER
University Ghent
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* • Clinicians (nurses, allied health professionals and doctors) working in intensive care units (ICU) are eligible to participate. This can include critical care nurses, respiratory therapists, physiotherapists etc. and/or * Nurses studying towards their speciality as critical care nurses. and/or * Wound care specialists or those responsible for advising on skin damage prevention or managing skin damage/ wounds of the patient in the prone position. and/or • Educators / clinical training facilitators within the hospital or teaching at the university. and/or * Quality assurance managers or hospital managers. and * Signed informed consent and voluntary participation.

Exclusion criteria

* Other than the inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Opinion and information regarding the training needs critical care clinicians have regarding prone positioned patients, with a specific focus on skin damage prevention.Interviews will be conducted within 1-2 months.1. Information regarding the training needs critical care clinicians have regarding prone positioning, 2. Opinions regarding the optimal conditions for effective implementation of the educational interventions in an intensive care setting,

Secondary

MeasureTime frameDescription
The development of an education and training package (The ProneTection package) for an interdisciplinary team of clinicians on skin damage prevention of patients in the prone position2-4 monthsDevelopment of online educational materials based on evidence, training needs assessments and expert opinions.

Countries

Belgium

Outcome results

None listed

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