Simulation-based Training of Rapid Evaluation and Management for Acute Stroke (STREAM) Trial
- Conditions
- Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety
- Interventions
- Other: Stroke team simulation training
- Registration Number
- NCT03228251
- Lead Sponsor
- Johann Wolfgang Goethe University Hospital
- Brief Summary
Acute stroke care is highly time critical for thrombolysis as well as thrombectomy. In both scenarios, each minute lost reduces the therapeutic efficacy. Therefore, an optimal implementation of these effective therapies into daily clinical practice is of utmost importance for the translation of the evidence from clinical trials into good clinical outcomes in routine care. In acute stroke therapy, the patient is cared for by an interdisciplinary team and often has to undergo several handovers between different caregivers with possible interface problems.
To facilitate a smooth workflow, the investigator developed an interdisciplinary stroke team algorithm and implemented regular simulation-based team trainings at the investigators institution. This multimodal intervention markedly improved the "door-to-needle" time for thrombolysis (time from the patient's arrival in the emergency department to the start of the tissue plasminogen activator (tPA) infusion) which is the most relevant benchmark parameter for acute stroke care. The investigators monthly stroke team training had a positive effect on the perceived degree of safety and staff satisfaction among the employees of the investigators departments.
The investigator plans to investigate the benefits of the multimodal intervention of a stroke team algorithm with regular stroke team simulation training in a controlled prospective pretest-posttest trial design at seven leading stroke centers in Germany. The investigator hypothesize that the implementation of a stroke team algorithm (defined team, defined tasks) and regular stroke team training with a focus on efficient team work and communication will improve process times, patient safety and staff satisfaction.
In the pretest period, the participating seven centers (tertiary care university hospitals with thrombectomy capacity 24/7/365) record the data of all consecutive patients receiving thrombolysis and/or thrombectomy during a three month period. Afterwards 3-4 leading employees of different professional backgrounds (e.g. senior neurologist of the stroke unit, neurointerventionalist, head nurse of emergency department) will be invited to a joint "train-the-trainer" seminar at the sponsors institution where the participating centers present their algorithm to the participants of all seven stroke centers for discussion to invite suggestions for streamlining and improvement and a train-the-trainer course of stroke simulation. After the seminar, the principal investigator and stroke team trainer will visit all centers for one in situ stroke team simulation training and provide teaching materials. Afterwards, each center will be invited to schedule two additional stroke team trainings a with stroke team trainer that will be led by e.g. the senior neurologist from the respective stroke unit with the aim of permanently starting up regular stroke team simulation. In the posttest period, the participating seven centers again record the data of all consecutive patients receiving thrombolysis and/or thrombectomy during a three month time period.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 379
- thrombolysis/thrombectomy in one of the seven participating stroke centers following EMS referral
- written informed consent from the patient and/or his/her legal representative.
- in-hospital stroke
- referred for thrombectomy by another Hospital.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Observation Group 2 Stroke team simulation training all stroke patients receiving thrombolysis and/or thrombectomy in a time period of three months after stroke team simulation training
- Primary Outcome Measures
Name Time Method Median "door-to-needle" time (median and 25-75 % interquartile range) in a pretest-posttest observation up to 1 hour
- Secondary Outcome Measures
Name Time Method Median thrombectomy process times of patients receiving thrombectomy in a before-after observation up to 2 hours
Trial Locations
- Locations (7)
Charite - Universitätsmedizin Berlin, Campus Benjamin Franklin
🇩🇪Berlin, Germany
Universitätsklinikum Hamburg-Eppendorf (UKE)
🇩🇪Hamburg, Germany
Klinikum Augsburg
🇩🇪Augsburg, Germany
Uniklinik Köln
🇩🇪Köln, Germany
Universitätsklinikum Heidelberg
🇩🇪Heidelberg, Germany
Klinikum der Universität München, Klinikum Großhadern
🇩🇪München, Germany
Universitätsklinikum Tübingen
🇩🇪Tübingen, Baden-Württemberg, Germany