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Simulation clinical trials

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NCT ID: NCT03428269 Completed - Simulation Clinical Trials

Serious Game Versus Traditional Teaching to Improve Clinical Reasoning Skills

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Detection of patient deterioration is a major healthcare problem. Indeed, acute clinical deterioration of the patient is often preceded by changes of several physiological parameters within 6 to 24h before the event occurs. The combination of i) early detection ii) rapid response and iii) efficient clinical management influences the patient's prognosis. Education of nurses, who are frontline healthcare providers, is therefore essential. Serious games might represent an interesting immersive educational tool to train a large number of healthcare professionals with high flexibility but assessment of their learning efficacy should be demonstrated. A serious game named LabforGames Warning has been developed for nursing students with the aims of improving their ability to detect clinical deterioration and to promote adequate interprofessional communication. The objective of this study will be to compare the respective value of digital simulation (using the above mentioned serious game) and a traditional teaching method to improve the clinical reasoning skills necessary to detect patient deterioration.

NCT ID: NCT03356717 Completed - Simulation Clinical Trials

Effect of an Observer Tool on Learning Outcomes During High Fidelity Simulation

Start date: June 23, 2017
Phase: N/A
Study type: Interventional

The increasing use of high-fidelity simulation is limited by the imbalance between the growing number of students and the human resources available in such a way that all residents cannot play a role during scenarios. The learning outcomes of observers need to be studied in more depth. Previous studies have provided controversial results but overall no significant differences in learning outcomes can be demonstrated between observers and participants engaged as players in scenarios. Moreover, preliminary data suggest that learning outcomes of observers might be improved by using an observer tool during the scenario. However, no high-quality study has yet shown if this assumption is verified. In the present study, 3rd-4th year residents in anesthesia will be randomized before high fidelity scenarios to act as observers only or active participants in some scenarios and observers in others. The main outcome parameter will be the learning outcomes by comparing data obtained before and after the sessions by using questionnaires specifically dedicated to the knowledge of technical skills in the management of crisis scenarios.

NCT ID: NCT03176251 Completed - Endoscopy Clinical Trials

Applying Gamification to Postgraduate Endoscopic Training

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

Simulation-based training curricula for gastrointestinal endoscopy have been developed and have been shown to be effective. It is possible that these curricula may be further improved. Gamification, the application of game-design principles to non-game contexts, has been shown to improve learning and skill performance in medical education. In gastrointestinal endoscopy, however, no dedicated curricula have been developed using gamification principles. We aim to evaluate the impact of applying gamification to a curriculum using SBT in endoscopy on clinical performance, compared to an identical curriculum without gamification. 36 novice endoscopists from the general surgery and gastroenterology programs at the University of Toronto will be recruited. Participants will be randomized into two groups: the Conventional Training Curriculum (CTC) Group, in which participants will receive 6 hours of training on a simulator augmented with expert feedback and interlaced with 4 hours of didactic training on the theory of colonoscopy; and the Gamified Integrated Curriculum (GIC) Group, in which participants will receive the same curriculum, using the following applications of gamified learning: a leaderboard of participant performances; badges for achievement of training landmarks; and rewards for top performance. Participants will be trained to perform colonoscopies progressively moving from a low to high complexity simulators, starting with the bench-top model (1 hour) and then moving to the EndoVR® virtual reality (VR) gastroenterology simulator (5 hours). Performance will be assessed at three points: prior to training (pre-test), immediately after training (acquisition post-test) and 4-6 weeks after training (retention test). Assessment will take place on the simulator at all three time points and during two live colonoscopies at the retention test. The primary outcome measure will be the difference in clinical colonoscopy performance between the two training groups, as assessed by the Joint Advisory Group for GI Endoscopy Direct Observation of Procedural Skills (JAG/DOPS). We aim to have data collection finished by 2018. Our results have the potential to improve existing curricula for training in colonoscopy. Moreover, the development of a gamified curriculum in procedural skills may have applicability to other specialities, such as general surgery and anesthesiology.

NCT ID: NCT02995785 Not yet recruiting - Simulation Clinical Trials

The First Aid Skill Simulation Training of Nurses of General Wards.

Start date: December 2016
Phase: N/A
Study type: Interventional

[Background and Objective]First-aid skill training plays an important role in the education of nurses. How to implement stable and efficient skill is very important. (Kardong-Edgren, Oermann, Odom-Maryon, & Ha, 2010). Simulation-based workshops,or training, as the most common enhancing skills.(Topping et al., 2015) .This study was designed to assist nurses enhancing the clinical ability and safety the patients in the first aid-related skills and knowledge. The purpose of this study is to compare the two groups of(1) first aid knowledge online test. (2) first aid skills test.【Methods】This study is a general ward nurses first aid technical examination, pre-test and post-test, the random control trial. Review by the hospital ethics committee and execution date on105/12/12-107/03/08, a total of 92 cases, obtained consent of all cases, then the case will be test in our hospital clinical skills center. Subject condition: general ward nurse (minimum age> 20 years),exclusion conditions: intensive care unit nurses, emergency department nurses. Study Procedure: Subjects who obtained the informed consent were randomly assigned to the first aid skill simulation training group (FAST) or the traditional group (T) by using a computer generated number. Randomization envelopes were opened and randomization performed by the study nurse after informed consent was obtained. Each group consisted of 46 subjects. All the subjects were pre-test first aid knowledge online test, followed were pre-test first aid skills test at the Clinical Skills Center.After pre-test,the experimental group are give the first aid skill simulation training with debriefing(75-min) and online lecture(15-min).While the traditional group only give online lecture(15-min). Two weeks later, the post-test include online test and skills test for two groups. After all the data were collected by the researchers who unknown the groups, the names of the cases were removed and the scores of the two groups were compared before and after.The test Based on 2015 AHA Guidelines for CPR & ECC (2015 Adult Basic Life Support and Cardiopulmonary Resuscitation Quality & 2015American Heart Association and 2015).The data will be archived in SPSS20.0 statistical package software. Statistical methods such as T-test and Anova variance analysis are used to analyze the data【Expected Result】: The knowledge and skills in the experimental group were better than the traditional group, and the first-aid simulation skill training was helpful for the clinical emergency situations.

NCT ID: NCT02988154 Recruiting - Hydrocephalus Clinical Trials

Simulation Efficacy in Neurosurgical Education

SENSE
Start date: June 2016
Phase: N/A
Study type: Observational

This study aims to investigate the efficacy of simulation in neurosurgical training.

NCT ID: NCT02886754 Completed - Performance Clinical Trials

Proficiency-Based Progression Training for Clinical Communication

Start date: September 14, 2016
Phase: N/A
Study type: Interventional

Importance: Clinical communication is an important source of medical error and preventable adverse events. Objective: To determine the effectiveness of proficiency-based progression (PBP) simulation training for ISBAR (Identify, Situation, Background, Assessment, Recommendation) communication in the deteriorating patient. Setting: The study will be conducted in University College Cork, Ireland. Participants: Third year undergraduate nursing and fifth year medical students, who are scheduled to undertake ISBAR training as part of the National Early Warning Score (NEWS) programme. Intervention: Participants will be prospectively randomized to one of three groups before undertaking a performance assessment of an ISBAR communication relevant to a deteriorating patient in a high fidelity simulation laboratory: HSE group (the national e-learning programme only); S group (national e- learning plus simulation training) and PBP group (national e-learning plus proficiency-based progression simulation). Main outcome and measures: A proficiency benchmark on the performance of ISBAR communication in the context of an acutely deteriorating patient.

NCT ID: NCT02676024 Recruiting - Cardiac Arrest Clinical Trials

Consolidating Tools for Outcomes in Resuscitation

CONTOUR
Start date: July 5, 2017
Phase: N/A
Study type: Interventional

In-hospital pediatric cardiac arrest is an important public health problem affecting almost 6000 children a year in the United States. As many as 3% of patients admitted to a children's hospital require cardiopulmonary resuscitation (CPR). Only a minority of children survive, of which around 35% go on to have a poor neurological outcome. International consensus guidelines on science and treatment recommendations for the management of pediatric resuscitation have existed for decades and are revised periodically by the International Liaison Committee on Resuscitation (ILCOR) based on available evidence. This consensus is then used by national councils such as the American Heart Association (AHA) and the Heart and Stroke Foundation of Canada (HSFC) to make guidelines for care. These guidelines focus on a structured approach to resuscitation, which emphasizes the rapid implementation of key interventions such as starting chest compressions, administering epinephrine and defibrillation. The goal of this study is to improve outcomes after cardiac arrest in children by improving adherence to consensus guidelines. The investigators aim to achieve this by conducting a multi-center, prospective, factorial randomized study with participating sites from the International Network for Simulation-based Pediatric Innovation, Research and Education (INSPIRE). The specific aims of this study are to: 1. To evaluate the effectiveness of knowledge-based cognitive aids, namely the Pediatric Advanced Life Support (PALS) algorithm cards, in healthcare teams. 2. To evaluate the effectiveness of teamwork-based cognitive aids, namely the Cognitive Aids with Roles Defined (CARD) system, in healthcare teams. 3. To determine if there is a synergistic effect when adding the CARD system to the use of knowledge-based cognitive aids or indeed whether using both these tools together has unintended consequences and reduces the added value of each technique. 4. To identify whether additional simulation-based team training in the use of cognitive aids results in a significant improvement in performance over an e-learning module. The investigators hypothesize that (i) knowledge-based cognitive aids will significantly improve the performance of healthcare teams in providing PALS in a simulated setting, (ii) that teamwork-based cognitive aids (CARD) will significantly improve the performance of healthcare teams in providing PALS in a simulated setting, and that (iii) adding the CARD system to knowledge-based aids will have an added and synergistic effect, (iv) that the team performance in all study arms will improve after simulation based training, but that the groups with cognitive aids will continue to out-perform the groups without cognitive aids.

NCT ID: NCT02168192 Completed - Medical Education Clinical Trials

Breaking Bad News in Obstetrics: A Trial of Simulation-Debrief Based Education

Start date: November 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the utility of training in Breaking Bad News (BBN) skills. We hypothesize that given little or no formal training in breaking bad news, obstetric providers will benefit from a curriculum of teaching breaking bad news techniques, but will benefit more from a simulation teaching technique than from a lecture in breaking bad news techniques. The investigators also hypothesize that providers who have undergone breaking bad news simulation will receive improved scores after the simulation debriefing compared to their pre-simulation scores, and their improvement with be greater than the control group.

NCT ID: NCT01792674 Completed - Education Clinical Trials

'In Situ Simulation' Versus 'Off Site Simulation' in Obstetric Emergencies

Start date: April 2013
Phase: N/A
Study type: Interventional

Care for pregnant is a field where unexpected emergencies occur, however emergencies are rare and hence competences difficult to learn. Therefore, it can be relevant to use simulation-based medical education. Many questions on how simulation can optimise learning remain unanswered. A major question is how simulation settings as 'in situ simulation' (i.e. in the actual patient care unit) versus 'off site simulation' (i.e. in training rooms or simulation center) impact learning. Objectives: To study the effect of 'in situ simulation' versus 'off site simulation' on learning outcome, safety-attitudes, team performance and clinical performance in the simulated setting plus stress and motivational inducing effect of simulation settings. Design: Randomised trial. Primary outcome: Written knowledge-test. Exploratory outcomes: Safety Attitudes Questionnaire, team- and clinical performance score, validated stress inventory, salivary cortisol, Intrinsic Motivation Inventory and questionnaire on perceptions of the simulation and organisational changes needed. Perspective: To provide new knowledge on contextual effects of different simulation settings.

NCT ID: NCT01688271 Completed - Pain Management Clinical Trials

Simulation-Based Training for Ultrasound-Guided Perineural Catheter Insertion

Start date: August 2012
Phase: N/A
Study type: Observational

This study will determine the efficacy of a teaching program incorporating hybrid simulation in training practicing anesthesiologists on ultrasound (US)-guided continuous peripheral nerve block (CPNB). This study will also examine the extent of practice change following participation in a regional anesthesia teaching program incorporating hybrid simulation. In addition, this study will assess remaining obstacles to incorporating the use of US-guided perineural catheters through identifying potential future interventions and "tool-kits" for setting up perineural catheter programs.