NCT07184489 Validation of the Effectiveness of the CFIR - ERIC Matching Tool in Implementation Research
| NCT ID | NCT07184489 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Children's Hospital of Fudan University |
| Condition | Infusions, Intravenous |
| Study Type | INTERVENTIONAL |
| Enrollment | 394 participants |
| Start Date | 2025-06-20 |
| Primary Completion | 2025-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 394 participants in total. It began in 2025-06-20 with a primary completion date of 2025-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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. 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.
Eligibility Criteria
Inclusion Criteria: * 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). Exclusion Criteria: * Not having obtained the nurse practice license; * Refusing to participate in this study.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07184489 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Infusions, Intravenous. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07184489 currently recruiting?
Yes, NCT07184489 is actively recruiting participants. Contact the research team at ylhwang@126.com for enrollment information.
Where is the NCT07184489 trial being conducted?
This trial is being conducted at Shanghai, China.
Who is sponsoring the NCT07184489 clinical trial?
NCT07184489 is sponsored by Children's Hospital of Fudan University. The trial plans to enroll 394 participants.