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Validation of the Effectiveness of the CFIR - ERIC Matching Tool in Implementation Research

NCT07184489 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 394

Last updated 2025-09-19

No results posted yet for this study

Summary

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

  • Infusions, Intravenous
  • Implementation Science

Interventions

OTHER

implementation strategies

1. Analysis of barrier factors: A focus group interview will be conducted. Purposive sampling was used to include senior nurses in the ward, members of the evidence-based group, and doctors for the analysis of barrier factors. Then the CFIR-ERIC matching tool will be used to develop implementation strategies based on the barrier factors. 2. The best - worst scaling method will be used to generate relatively reliable and valid preference evidence of stakeholders for implementation strategies from CFIR-ERIC matching tool. 3. The implementation strategies will be developed specifically by an expert group. This group includes nursing managers and experts in evidence-based practice. 4. Implement the strategies.

Sponsors & Collaborators

  • Children's Hospital of Fudan University

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-20
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07184489 on ClinicalTrials.gov