Training nurses in arteriovenous fistula puncture using simulations
Impact of Simulation-based Training in Addition to Theoretical Training Versus Theoretical Training Alone for Nurses on the Occurring of Adverse Events Related to Arteriovenous Fistula Puncture in Chronic Hemodialysis Patients.
This study tests if training nurses with hands-on simulations for arteriovenous fistula puncture helps reduce problems during treatments for patients on hemodialysis compared to just classroom learning.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 9600 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Caen Academic / other |
| Locations | 9 sites (Alençon and 8 other locations) |
| Trial ID | NCT05302505 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a simulation-based training program for nurses on the technique of arteriovenous fistula puncture in chronic hemodialysis patients. It aims to compare the incidence of adverse events related to punctures between two groups: one receiving both theoretical and simulation training, and another receiving only theoretical training. The study will be conducted across eight hemodialysis centers, utilizing a prospective, comparative, randomized, multicenter design. The goal is to optimize nursing practices and improve patient safety in hemodialysis care.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients undergoing arteriovenous fistula puncture in hemodialysis units.
Not a fit: Patients who may not benefit include those receiving punctures in emergency settings or those unable to provide informed consent.
Why it matters
Potential benefit: If successful, this training program could significantly reduce adverse events associated with arteriovenous fistula punctures, enhancing patient safety and care quality.
How similar studies have performed: While simulation-based training is a common educational approach, this specific application in arteriovenous fistula puncture is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients * Arteriovenous fistula puncture in the hemodialysis unit of the nephrology, dialysis, transplantation department * Nurses trained in hemodialysis Exclusion Criteria: * arteriovenous fistula puncture in the emergency area/foldout of the unit * Refuse of data collection * Not speak French * Minor * Under guardianship or unable to give informed consent * Not enrolled in a social security plan * Pregnant or breastfeeding women
Where this trial is running
Alençon and 8 other locations
- Center hospital of Alençon — Alençon, France (Not_yet_recruiting)
- University hospital center of Caen — Caen, France (Recruiting)
- Private Hospital St Martin — Caen, France (Not_yet_recruiting)
- Center Hospital of Dieppe — Dieppe, France (Not_yet_recruiting)
- Center Hospital of Flers — Flers, France (Not_yet_recruiting)
- Anider — Hérouville-Saint-Clair, France (Recruiting)
- Center Hospital of Lisieux — Lisieux, France (Not_yet_recruiting)
- Anider Alencon — Saint-Germain-du-Corbéis, France (Recruiting)
- Center Hospital of Memorial United States of St Lo — Saint-Lô, France (Recruiting)
Study contacts
- Principal investigator: Erwan Guillouët — University Hospital, Caen
- Study coordinator: Erwan Guillouët
- Email: guillouet-e@chu-caen.fr
- Phone: +33231063403
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.