跳至主要内容
临床试验/NCT07184489
NCT07184489招募中不适用

Validation of the Effectiveness of the CFIR - ERIC Matching Tool in Implementation Research of Pediatric Venous Access Device Selection

Children's Hospital of Fudan University2 个研究点 分布在 1 个国家目标入组 394 人开始时间: 2025年6月20日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
394
试验地点
2
主要终点
error rate of appropriate venous access device selection

研究概览

简要总结

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.

详细描述

Currently,the evidence-based practice research often isolates barrier assessment from implementation strategy development. At tne same time, many implementation science models being overly complex for clinicians. In Chinese, certain studies still neglect barrier assessment, demonstrate inconsistent conceptualization of implementation strategies, and rarely classify developed strategies.

As a tool for matching and selecting implementation strategies, the CFIR - ERIC matching tool has the characteristics of strong pertinence, repeatability, structuring, systematization, and simple and convenient operation compared with other models. Researchers can identify barrier factors through CFIR and use the CFIR - ERIC matching tool to match strategies to promote the implementation of clinical intervention measures.

This implementation study adopted a pre-post design using the CFIR-ERIC Matching Tool to analyze barriers and develop strategies. Grounded in the "Pediatric Venous Access Device Selection Decision Tree" from the 2021 clinical practice guideline on infusion therapy in children, the intervention was rolled out across 21 wards at the Children's Hospital of Fudan University.

The implementation process of the evidence was evaluated from four aspects using the RE-AIM framework , including the evaluation indicators corresponding to each dimension of patient reach, intervention efficacy, medical adoption, and guideline implementation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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).

排除标准

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

结局指标

主要结局

error rate of appropriate venous access device selection

时间窗: 6 months

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

次要结局

  • 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)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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