Knowledge and Needs of Nursing in Relation to the Treatment Complex Wounds

April 24, 2024 updated by: Francisco Zamora Carmona, Corporacion Parc Tauli

Knowledge and Needs of Nursing Professionals in Relation to the Treatment of People With Complex Wounds at Parc Taulí University Hospital

Study with cross-sectional and descriptive mixed methodology. With questionnaires with likert-type questions (0-10) being the 10 with the highest score, and open questions in relation to knowledge in wound care; include all Corporaciló Sanitària Parc Taulí (CCSPT) nurses who voluntarily want to participate in a pseudo-anonymized surv

Study Overview

Status

Active, not recruiting

Detailed Description

INTRODUCTION A complex wound is a skin injury with little or no tendency to heal as long as the cause that produces it is present. Complex wounds that are difficult to heal or develop torpid or refractory to the usual treatments, do not evolve adequately in the expected time (> 6 weeks).

The clinical practice we find is completely heterogeneous among professionals who care for people with injuries.

OBJECTS Describe the knowledge and training needs perceived by nurses in the approach to people with complex wounds of the CCSPT.

To explore the difficulties and facilitating elements that professionals perceive when dealing with people with complex wounds, from the reference area of the Parc Taulí University Hospital, over a period of 12 months.

Explain tools with scientific evidence for correct continuity of care.

METHODOLOGY:

Study with cross-sectional and descriptive mixed methodology. With questionnaires with likert-type questions and open questions in relation to knowledge in wound care; include all CCSPT nurses who voluntarily want to participate in a pseudo-anonymized survey.

EXPECTED RESULTS:

Current situation of the knowledge, needs, limiting and facilitating elements that nursing professionals have to address people with injuries.

Study Type

Observational

Enrollment (Estimated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Barcelona
      • Sabadell, Barcelona, Spain, 08208
        • Corporacio Sanitaria Parc Tauli

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Acute and social healthcare hospital nurses

Description

Inclusion Criteria:

  • Nurses who take care of people with both adult and pediatric injuries.
  • Nurses who give their informed consent to participate in the study voluntarily.

Exclusion Criteria:

  • Nurses who do not want to participate in the study voluntarily.
  • Nurses who do not have healthcare activities (due to workplace, due to long-term illness, absence from work)

Study Plan

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

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
"What not to do in chronic wounds?"
Time Frame: 1 month
made up of socio-demographic variables of the participants: gender, age, level of education, years working as a nurse, training on wounds. And 37 items with three answer options "true", "fake" in relation to the 37 recommendations of the document "What not to do in chronic wounds?", the more correct, the more knowledge about wounds.
1 month
ReAc-PUKT (Renobato-Acosta Pressure Ulcer Knowledge Test)
Time Frame: 1 month
To determine knowledge of nurses about the prevention and treatment of pressure injuries (LPP). The instrument is made up of two sections: The first collects general data on professionals and academic-work information, including socio-demographic data (age, gender), service to which they belong, work shift, years of experience, academic training and training in LPP. The second measures the level of scientific knowledge about pressure injuries) generalities, prevention and treatment, the more correct, the more knowledge about LPP. The higher the value, the better the knowledge about LPP.
1 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ad hoc open questions
Time Frame: 1 month

Researchers want to know the training needs perceived by nursing staff and the limiting and facilitating elements they experience in dealing with people with complex injuries.

The qualitative methodology of descriptive phenomenological approach, through 10 open questions that will give us relevant information for the study:

  • Learn about their experiences in care.
  • Learn about their experiences with people with injuries.
  • Explore the difficulties and facilitating elements when making referrals and interconsultations with specialists.
  • Explain the tools we have with scientific evidence for correct continuity of care
  • Know the facilitating elements in the continuity of care.
1 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Francisco Zamora Carmona, Grupo emergente enfermeria I3PT

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2023

Primary Completion (Actual)

June 1, 2023

Study Completion (Estimated)

June 1, 2024

Study Registration Dates

First Submitted

April 18, 2024

First Submitted That Met QC Criteria

April 24, 2024

First Posted (Actual)

April 29, 2024

Study Record Updates

Last Update Posted (Actual)

April 29, 2024

Last Update Submitted That Met QC Criteria

April 24, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UFCIN1_2022

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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