Publication: Simulation Training to Improve Informed Consent and Pharmacokinetic/Pharmacodynamic Sampling in Pediatric Trials
| dc.contributor.author | Burckhardt, Bjoern B. (55383006300) | |
| dc.contributor.author | Ciplea, Agnes Maria (57203856912) | |
| dc.contributor.author | Laven, Anna (22634866000) | |
| dc.contributor.author | Ablonczy, László (36636785400) | |
| dc.contributor.author | Klingmann, Ingrid (6602830730) | |
| dc.contributor.author | Läer, Stephanie (7003476724) | |
| dc.contributor.author | Kleine, Karl (57209315896) | |
| dc.contributor.author | Dalinghaus, Michiel (6601975474) | |
| dc.contributor.author | Đukić, Milan (56835361300) | |
| dc.contributor.author | Breur, Johannes M. P. J. (6506168146) | |
| dc.contributor.author | van der Meulen, Marijke (57126909900) | |
| dc.contributor.author | Swoboda, Vanessa (56465046300) | |
| dc.contributor.author | Schwender, Holger (6506833490) | |
| dc.contributor.author | Lagler, Florian B. (14061979400) | |
| dc.date.accessioned | 2025-06-12T13:56:46Z | |
| dc.date.available | 2025-06-12T13:56:46Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | Background: Pediatric trials to add missing data for evidence-based pharmacotherapy are still scarce. A tailored training concept appears to be a promising tool to cope with critical and complex situations before enrolling the very first patient and subsequently to ensure high-quality study conduct. The aim was to facilitate study success by optimizing the preparedness of the study staff shift. Method: An interdisciplinary faculty developed a simulation training focusing on the communication within the informed consent procedure and the conduct of the complex pharmacokinetic/pharmacodynamic (PK/PD) sampling within a simulation facility. Scenarios were video-debriefed by an audio-video system and manikins with artificial blood simulating patients were used. The training was evaluated by participants' self-assessment before and during trial recruitment. Results: The simulation training identified different optimization potentials for improved informed consent process and study conduct. It facilitated the reduction of avoidable errors, especially in the early phase of a clinical study. The knowledge gained through the intervention was used to train the study teams, improve the team composition and optimize the on-ward setting for the FP-7 funded “LENA” project (grant agreement no. 602295). Self-perceived ability to communicate core elements of the trial as well as its correct performance of sample preparation increased significantly (mean, 95% CI, p ≤ 0.0001) from 3 (2.5–3.5) to four points (4.0–4.5), and from 2 (1.5–2.5) to five points (4.0–5.0). Conclusion: An innovative training concept to optimize the informed consent process and study conduct was successfully developed and enabled high-quality conduct of the pediatric trials as of the very first patient visit. © Copyright © 2020 Burckhardt, Ciplea, Laven, Ablonczy, Klingmann, Läer, Kleine, Dalinghaus, Đukić, Breur, van der Meulen, Swoboda, Schwender and Lagler. | |
| dc.identifier.uri | https://doi.org/10.3389/fphar.2020.603042 | |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85098274420&doi=10.3389%2ffphar.2020.603042&partnerID=40&md5=845a0c74e4ba06eaac8c28d6e07f5302 | |
| dc.identifier.uri | https://remedy.med.bg.ac.rs/handle/123456789/4617 | |
| dc.subject | clinical study | |
| dc.subject | communication | |
| dc.subject | patient recruitment | |
| dc.subject | pediatrics | |
| dc.subject | pharmacokinetic/pharmacodynamic | |
| dc.subject | simulation training | |
| dc.subject | study conduct | |
| dc.title | Simulation Training to Improve Informed Consent and Pharmacokinetic/Pharmacodynamic Sampling in Pediatric Trials | |
| dspace.entity.type | Publication |
