NCT06954519

Brief Summary

The goal of this randomized trial is to learn if mental imagery works to improve non technical skills in residents. It will also learn about knowledge and technical skills. The main questions it aims to answer are: Does mental imagery of a cognitive aid improve non technical skills of residents ? Does mental imagery of a cognitive aid improve technical skills and knowledge of residents ? The invastigators will compare repeated mental imagery to repeated simple reading of a cognitive aid to see if mental imagery works to train non technical skills. Participants will:

  • participate in an initial training on neonatal resuscitation
  • be randomized in two groups: mental imagery or simple reading
  • Repeat training according to the group with predefined intervalls during 6 months
  • be evaluated 6 months after the initial training

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 27, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

March 27, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

May 1, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2025

Completed
Last Updated

May 1, 2025

Status Verified

April 1, 2025

Enrollment Period

6 months

First QC Date

March 27, 2025

Last Update Submit

April 24, 2025

Conditions

Keywords

mental imagerycognitive aidneonatal resuscitationsimulation

Outcome Measures

Primary Outcomes (1)

  • Behaviorally Anchored Rating Scale (BARS)

    Evaluation of Non-Technical Skills of anesthesia residents' (Originally published in Watkins et al., Simul in Healthc 2017). From 1 to 36 points. Better score means better skills

    6 months

Secondary Outcomes (1)

  • Neonatal Resuscitation Performance Evaluation (NRPE) scale

    6 months

Study Arms (2)

Mental Imagery

EXPERIMENTAL

Participant of the mental imagery group will have a specific training during the initial training and will repeat the mental imagery regularely during the 6 months (timing of repetition guided by messages sended by investigator)

Other: Mental imagery

Classical reading

ACTIVE COMPARATOR

Participant of the control group will have no specific training during the initial training, only presentation of the cognitive aid. They will also repeat the reading of the cognitive aid regularely during the 6 months (timing of repetition guided by messages sended by investigator)

Other: Cognitive aid reading

Interventions

The principle of guided mental imagery and helping students to mentally represent the key stages of a process, using an animated slideshow full of evocative elements, which we created specifically for this study. The mental imagery will be repeated by the students several times independently until the evaluation simulation at 6 months based on reminders via messages from investigators.

Mental Imagery

Participants of the control group will only read the cognitive aid on neonatal resuscitation at the same intervalls than the experimentation group

Classical reading

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Anesthesia residents in 1, 2, 3 o 4 year of training and volunteers

You may not qualify if:

  • Residents not volunteer

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

CHU de Reims

Reims, Grand Est, 51100, France

ENROLLING BY INVITATION

CHU de Reims

Reims, 51100, France

RECRUITING

Central Study Contacts

Daphné Michelet, Professor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Professor

Study Record Dates

First Submitted

March 27, 2025

First Posted

May 1, 2025

Study Start

March 27, 2025

Primary Completion

October 1, 2025

Study Completion

October 1, 2025

Last Updated

May 1, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations