The result of the PaliEnf application in relation to improving the records of nurses working in a pediatric oncology intensive care unit
- Conditions
- Information TechnologyNursing ProcessClassificationStandardized Nursing TerminologyQuality ImprovementE05.318.308.940.984
- Registration Number
- RBR-5qq77rs
- Lead Sponsor
- Programa Acadêmico em Ciências do Cuidado em Saúde - Faculdade de Medicina da Universidade Federal Fluminense
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Phase 1 predictive usability assessment – researchers; professionals; professors with expertise in the development of health information technologies belonging to the GESAEUFF and NUPESICA research groups registered in the Directory of Research Groups in Brazil of the National Council for Scientific and Technological Development (CNPq); both genders. Prospective usability assessment - professional nurses with experience in pediatric oncology or pediatric palliative care; both genders. Training nurses' clinical reasoning through fictitious case studies and training with the PaliEnf application: clinical nurses who are actively working in the Pediatric Oncology Intensive Care Unit (PICU) during the research period; both genders. Phase 2: Quasi-experiment - nurses' records in the medical records of children and adolescents who were admitted to the Pediatric Oncology Intensive Care Unit (PICU) during the research period
Phase 1 (stage 1) predictive assessment: participants with experience period less than five years. Phase 1 (stage 1) prospective assessment: none, all nurses considered specialists in pediatric oncology according to the criteria proposed by Jasper who participate will have their analyzes considered. Phase 1 (stage 3): none, everyone who enters and remains in the research will be trained and their progress will be evaluated. Phase 2: records of children and adolescents who remained hospitalized for less than four days and records selected post-intervention whose nurse's progress was not generated by the PaliEnf application report
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method