CClinicalTrials.gg
Not yet recruitingNCT06832241ECCOLicoFUpdated Feb 18, 2025

Cognitive Load Assessment of Helicopter Pilots in Training

An observational study in Cognitive Impairment, Situational Anxiety and Skills, Coping, sponsored by Direction Centrale du Service de Santé des Armées. Not yet recruiting. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-02-18.

Sponsored by Direction Centrale du Service de Santé des Armées · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
32
Ages
18 Years to 50 Years
Sex
All
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Study summary

The aim of this study is to identify the effect of the increase of the situation demands, with or without a thread, on military helicopter pilot's cognitive load, depending on their skills acquisition (at the beginning, midway and end of training course). This study is carried out on a simulator, in virtual reality and allows to identify the moments of cognitive load enhancement and the associated indicators such as subjective, physiological and behavioural indicators. Recommendations will be done to go towards an individualization of the lessons during the pilots education, by anticipating an overload which has a deleterious effect on learning.

02

Conditions studied

  • Cognitive Impairment
  • Situational Anxiety
  • Skills, Coping

Keywords

  • Cognitive load
  • Military helicopter pilots
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In context

Cognitive Dysfunction

3,843 studies on the registry are indexed under Cognitive Dysfunction; 1,100 are open to participants now.

This study's planned enrollment of 32 is below the median of 150 across 950 observational studies indexed under Cognitive Dysfunction.

Browse Cognitive Dysfunction studies →

Lead sponsor

Direction Centrale du Service de Santé des Armées is the lead sponsor of 93 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Military helicopter pilots trainees

Inclusion criteria

  • Being a trainee at the Instructional center of helicopter crews
  • Being more than 18 years old
  • Being insured under the French social security system
  • Having the bases to pilot helicopters
  • Having signed the non-opposition form

Exclusion criteria

Exclusion Criteria:

  • Being minor or an incapacitated adult
  • Being in a motor handicap situation
  • Having a cardiac pathology
  • Having a visual pathology that is uncorrected by glasses or lens
  • Having a bad audition
  • Having a psychiatric disorder, a neurologic or organic disorder requiring a medical treatment
  • Taking psychotropics
  • Drinking more than 28 units of alcohol per week
  • Being epileptic
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
32 participants (estimated)
Target follow-up
3 Years
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Subjective level of cognitive load

    The NASA-TLX questionnaire is used to assess the subjective level of cognitive load

    Time frame: It is completed during 5 minutes after each of the six scenarios

Secondary outcomes

  1. Objective level of cognitive load

    It is measures by physiological indicators ( cardiac activity and electroencephalogram) and behavioural indicators (tasks performance, ocular saccades and blinks)

    Time frame: It is measured during each of the six scenarios lasting around 5 minutes

  2. Subjective level of anxiety

    It is measured by a visual analogue scale

    Time frame: It is measured during 1 minute after each of the six scenarios

  3. Objective level of anxiety

    It is measured by the electrodermal activity

    Time frame: It is measured during each of the six scenarios lasting around 5 minutes

  4. Subjective level of fatigue

    It is measured by the Karolinska Sleepiness Scale

    Time frame: It is measured during 1 minute before each of the six scenarios

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06832241
Lead sponsor
Direction Centrale du Service de Santé des Armées
Responsible party
Sponsor
First posted
Feb 18, 2025
Start date
Mar 2025 (estimated)
Primary completion
Jan 2027 (estimated)
Completion
Jan 2028 (estimated)
Last update
Feb 18, 2025

Study contacts

Julie ALBENTOSA
Contact
julie.albentosa@intradef.gouv.fr
+33 1 78 65 12 17
Julie ALBENTOSA
study chair · IRBA, 1 place Valérie André, 91 223 Brétigny-sur-Orge cedex

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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