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Behavioural Intervention
Simulation Airway Coaching for Anesthesia Trainee Skills
N/A
Waitlist Available
Led By Stephen Flynn, MD
Research Sponsored by Boston Children's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, anticipated 12-15 months
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to see if a special training method can help new pediatric anesthesia trainees perform better at helping infants breathe. The trainees will practice with guidance to improve their skills. The goal is to make sure they can successfully help infants breathe on the first try, reducing potential complications.
Who is the study for?
This trial is for novice pediatric anesthesia trainees, specifically fellows and residents in that field. It's not open to medical students or off-service rotators who are temporarily working in different specialties.
What is being tested?
The study is testing a training method called Just-In-Time Rapid Cycle Deliberate Practice Simulation. This method aims to improve the skills of new pediatric anesthesia trainees in performing laryngoscopy, which is a procedure used to view someone's vocal cords.
What are the potential side effects?
Since this trial involves educational simulation training rather than medication or invasive procedures, there aren't any direct medical side effects associated with it.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, anticipated 12-15 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, anticipated 12-15 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
1st attempt success rate
Secondary study objectives
Cognitive Load in intubating patient
Complication rate
Evaluation of utility of JIT/RCDP
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
The experimental group will review a pre-induction airway management plan for their upcoming case and undergo a scripted 10-minute RCDP session with an airway coach within 1 hour of patient intubation. The intubation approach (DL vs. video assisted DL) will be chosen by the primary case attending and communicated to the airway coach to simulate the planned laryngoscopy attempt. The experimental group will then proceed with their scheduled case with a member of the research team observing the laryngoscopy attempt(s) to capture data.
Group II: ControlActive Control1 Intervention
The trainees in the control group will have no interventions by the research team, only observation of the intubation and documentation of the same details.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Anesthesia treatments commonly involve agents such as propofol, sevoflurane, and fentanyl, which work through various mechanisms to induce unconsciousness, analgesia, and muscle relaxation. Propofol enhances the inhibitory neurotransmitter GABA, leading to sedation and hypnosis.
Sevoflurane, an inhalational agent, modulates ion channels to produce a reversible loss of consciousness. Fentanyl, an opioid, binds to mu-opioid receptors to provide potent analgesia.
These mechanisms are crucial for anesthesia patients as they ensure a pain-free and immobile state during surgery, allowing for precise and safe surgical interventions. The emphasis on skill acquisition and competency through methods like J-I-T RCDP Simulation Training is vital as it ensures that anesthesia providers can effectively and safely administer these agents, manage potential complications, and improve patient outcomes.
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Who is running the clinical trial?
Boston Children's HospitalLead Sponsor
786 Previous Clinical Trials
5,582,159 Total Patients Enrolled
Stephen Flynn, MDPrincipal Investigator - Boston Children's Hospital
Boston Children's Hospital, Chmc Anesthesia Foundation Inc
Brown University Program In Medicine (Medical School)
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- This clinical trial does not include anesthesia residents.Medical students are not eligible to participate.
Research Study Groups:
This trial has the following groups:- Group 1: Experimental
- Group 2: Control
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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