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

NCT07184489 | Recruiting

• 1 other identifier: CHFudanU0814
• Study Type: interventional
• Target: 394
• Locations: 1 country
• Sites: 1

Brief 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. 1.Does the implementation strategies developed by CFIR-ERIC matching tool improve nurses knowledge in venous access devices selection.
2. 2.Does the implementation strategies developed by CFIR-ERIC matching tool lower the error rate of appropriate venous access device selection.
3. 3.Receive the implementation strategies made by CFIR-ERIC matching tool.
4. 4.Using the pediatric venous access device selection decision trees in daily catheterization.
5. 5.Record their venous access device selection informantion, consumables usage and pediatric patients' outcome.

Conditions

Infusions, Intravenous; Implementation Science

Keywords

implementation strategy; CFIR-ERIC

Outcome Measures

Primary Outcomes (1)

• error rate of appropriate venous access device selection

  According to the recommendations in the guidelines, selecting the infusion device is considered correct, while failing to select according to the recommendations is considered incorrect. Error rate = Number of incorrect selections / Total number of catheter insertions by nurses

  6 months

Secondary Outcomes (5)

• Score of nurses' knowledge questionaire of venous access device selection

  The third and sixth months of the research.

• Nurses' compliance with evidence-based practice behaviors

  6 months

• Complication rate

  6 months

• The cost of venous access device consumables

  6 months

• Implementing process evaluated based on "Reach*Efficacy(RE)-Adoption, Implementation, and Maintenance(AIM)" framework

  6 months

Study Arms (1)

CFIR-ERIC group

EXPERIMENTAL

Develop implementation strategies for applying evidence to clinical practice using CFIR - ERIC matching tool.

Other: implementation strategies

Interventions

implementation strategies OTHER

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.

Also known as: pediatric venous access device selection decision tree

CFIR-ERIC group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Having worked at the research site for ≥ 1 year;
• Being able to independently perform nursing operations (having completed the content related to intravenous infusion in the standardized training of this hospital and passed the assessment).

You may not qualify if:

• Not having obtained the nurse practice license;
• Refusing to participate in this study.

Sponsors & Collaborators

• Children's Hospital of Fudan University: lead

Study Sites (1)

Children's Hospital of Fudan University

Shanghai, 201102, China

RECRUITING

Central Study Contacts

Yaliuhui WANG

CONTACT

+86 18085293862; ylhwang@126.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: OTHER
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 25, 2025
• First Posted: September 19, 2025
• Study Start: June 20, 2025
• Primary Completion: December 31, 2025
• Study Completion: December 31, 2025
• Last Updated: September 19, 2025

Record last verified: 2025-09

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)