- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06388980
Knowledge and Needs of Nursing in Relation to the Treatment Complex Wounds
Knowledge and Needs of Nursing Professionals in Relation to the Treatment of People With Complex Wounds at Parc Taulí University Hospital
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Barcelona
-
Sabadell, Barcelona, Spain, 08208
- Corporacio Sanitaria Parc Tauli
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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:
|
1 month
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Francisco Zamora Carmona, Grupo emergente enfermeria I3PT
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UFCIN1_2022
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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