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Completed

NCT Number: NCT05238870

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

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

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Key information

Age range

Up to 65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

UZ Gent, Ghent, Oost-Vlaanderen, Belgium

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About this study

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

  • the results of our recently published gap-analysis study,
  • the needs assessment results from the interviews, keeping the optimal conditions (facilitators) in mind for successful implementation, and
  • the critical review and evaluation by eleven key opinion leaders from the established international expert panel

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Interviews for the needs analysis. No intervention.

Other

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

Primary outcomes

  1. Opinion and information regarding the training needs critical care clinicians have regarding prone positioned patients, with a specific focus on skin damage prevention.

    Time frame: Interviews will be conducted within 1-2 months.

    • Information regarding the training needs critical care clinicians have regarding prone positioning,
    • Opinions regarding the optimal conditions for effective implementation of the educational interventions in an intensive care setting,

Secondary outcomes

  1. 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 position

    Time frame: 2-4 months

    Development of online educational materials based on evidence, training needs assessments and expert opinions.

Sponsors and collaborators

Lead sponsor

University Ghent

Other

Collaborators

  • Örebro University, Sweden

Registry information

Official study title

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.

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Feb 14, 2022
Registry last updated
Oct 13, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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