Actively Recruiting
Validation of the Effectiveness of the CFIR - ERIC Matching Tool in Implementation Research
Led by Children's Hospital of Fudan University · Updated on 2025-09-19
394
Participants Needed
1
Research Sites
27 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this implementation study is to learn if the CFIR-ERIC matching tool is effective indeveloping implementation strategies for pediatric nurse. The evidence practised in this study is the pediatric venous access device selection decision tree from clinical practice guideline on infusion therapy in children. The main questions it aims to answer are: 1. Does the implementation strategies developed by CFIR-ERIC matching tool improve nurses knowledge in venous access devices selection. 2. Does the implementation strategies developed by CFIR-ERIC matching tool lower the error rate of appropriate venous access device selection. Researchers will compare the CFIR-ERIC group to a blank group to see if CIFR-ERIC matching tool works to improve nurses knowleged and lower the error rate of venous access device selection. Participants will: 1. Receive the implementation strategies made by CFIR-ERIC matching tool. 2. Using the pediatric venous access device selection decision trees in daily catheterization. 3. Record their venous access device selection informantion, consumables usage and pediatric patients' outcome.
CONDITIONS
Official Title
Validation of the Effectiveness of the CFIR - ERIC Matching Tool in Implementation Research
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Having worked at the research site for 65 1 year
- Being able to independently perform nursing operations, including intravenous infusion, after standardized training and assessment
You will not qualify if you...
- Not having obtained a nurse practice license
- Refusing to participate in this study
AI-Screening
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Trial Site Locations
Total: 1 location
1
Children's Hospital of Fudan University
Shanghai, China, 201102
Actively Recruiting
Research Team
Y
Yaliuhui WANG
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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