Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04159389
Other study ID # CESAR002
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 6, 2020
Est. completion date March 5, 2022

Study information

Verified date November 2023
Source University Grenoble Alps
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the benefit of adding mental visualization to a training program in medical education. Undergraduate medical students will be randomized before participating in a training program on airway management during rapid sequence induction. In the control group, participants will receive traditional teaching including theoretical courses and procedural simulation. In the intervention group, in addition to traditional teaching, participants will be trained and encouraged to practice mental visualization. The main outcome will be clinical performance during a standardized high-fidelity simulation of rapid sequence induction assessed using a specific pre-established checklist.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date March 5, 2022
Est. primary completion date December 5, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Undergraduate medical students from the Grenoble Alps university hospital - From the 2nd to the 6th year - Volontary Exclusion Criteria: - /

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mental visualization
Instruction in mental visualization by theoretical lessons and support of practice by audio guide and session of experience sharing.

Locations

Country Name City State
France University Grenoble Alps La Tronche

Sponsors (1)

Lead Sponsor Collaborator
University Grenoble Alps

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical performance for airway management in a standardized high-fidelity simulation of rapid sequence induction. All simulations will be videotaped and the clinical performance of each participant will be assessed by an independent evaluator using a specific pre-established checklist 2 weeks
Secondary "Material preparation" score, subpart 1 of the clinical performance grid All simulations will be videotaped and the score of the subpart "Material preparation" of the clinical performance of each participant will be assessed by an independent evaluator using a specific pre-established checklist 2 weeks
Secondary "Intubation procedure" score, subpart 2 of the clinical performance grid All simulations will be videotaped and the score of the subpart "Intubation procedure" of the clinical performance of each participant will be assessed by an independent evaluator using a specific pre-established checklist 2 weeks
Secondary Physiological stress response : SDNN Heart rate variability evaluated by SDNN (Standard Deviation Normal to Normal), in miliseconds. Physiological stress response is higher when SDNN is lower. 2 weeks
Secondary Psychological stress response : Stress-VAS Stress Visual Analogical Scale, from 0 to 100, psychological stress response is higher when score is higher. 2 weeks
Secondary Psychological stress response : STAI STAI (State-Trait Anxiety Inventory), from 20 to 80, psychological stress response is higher when score is higher. 2 weeks
Secondary Adesion to Mental visualization Frequency questionnaire for the use of mental visualization, from "0" to ">1 per day". We ask the participant to use it once a day 2 weeks
Secondary Quality to Mental visualization : MIQ Mental Imagery Questionnaire, from 8 to 56, mental visualisation is better when score is higher. 2 weeks
Secondary Memorization of key messages at three months Specific pre-established checklist : 5-point grid. Assessed by an independent evaluator using a phone call. 3 months
See also
  Status Clinical Trial Phase
Active, not recruiting NCT04580030 - Tricuapid Annular Plane Sistolic Excursion Before General Anesthesia Can Predict Hypotension After Induction
Active, not recruiting NCT04279054 - Decreased Neuraxial Morphine After Cesarean Delivery Early Phase 1
Completed NCT03640442 - Modified Ramped Position for Intubation of Obese Females. N/A
Recruiting NCT04099693 - A Prospective Randomized Study of General Anesthesia Versus Anesthetist Administered Sedation for ERCP
Terminated NCT02481999 - Pre- and Postoperative EEG-Monitoring for Children Aged From 0,5 to 8 Years
Completed NCT04235894 - An Observer Rating Scale of Facial Expression Can Predict Dreaming in Propofol Anesthesia
Recruiting NCT05525104 - The Effect of DSA on Recovery of Anaesthesia in Children (Het Effect Van DSA op Het Herstel na Anesthesie Bij Kinderen). N/A
Recruiting NCT05024084 - Desflurane and Sevoflurane Minimal Flow Anesthesia on Recovery and Anesthetic Depth Phase 4
Completed NCT04204785 - Noise in the OR at Induction: Patient and Anesthesiologists Perceptions N/A
Completed NCT03277872 - NoL, HR and MABP Responses to Tracheal Intubation Performed With MAC Blade Versus Glidescope N/A
Terminated NCT03940651 - Cardiac and Renal Biomarkers in Arthroplasty Surgery Phase 4
Terminated NCT02529696 - Measuring Sedation in the Intensive Care Unit Using Wireless Accelerometers
Completed NCT05346588 - THRIVE Feasibility Trial Phase 3
Terminated NCT03704285 - Development of pk/pd Model of Propofol in Patients With Severe Burns
Recruiting NCT05259787 - EP Intravenous Anesthesia in Hysteroscopy Phase 4
Completed NCT02894996 - Does the Response to a Mini-fluid Challenge of 3ml/kg in 2 Minutes Predict Fluid Responsiveness for Pediatric Patient? N/A
Completed NCT05386082 - Anesthesia Core Quality Metrics Consensus Delphi Study
Terminated NCT03567928 - Laryngeal Mask in Upper Gastrointestinal Procedures N/A
Recruiting NCT06074471 - Motor Sparing Supraclavicular Block N/A
Completed NCT04163848 - CARbon Impact of aNesthesic Gas