Monitoring the Effect of Mental Fatigue on Physical Performance Using Wearable Sensors and Physiological Parameters

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-35
SponsorVrije Universiteit Brussel

About this trial

Mental fatigue (MF) negatively affects both cognitive and physical performance, increasing the risk of errors in high-stakes environments such as sports and surgery. Traditional methods to assess MF rely on subjective self-report scales, which are prone to bias, or on complex brain measurements (e.g. EEG) that are impractical outside laboratory settings. This study aims to develop a real-time, objective monitoring method for MF using wearable physiological sensors. The study will recruit healthy, trained runners (18-35 years old) who will complete both an MF-inducing cognitive task (Stroop test) and a control condition (watching a documentary) in a randomized, counterbalanced, crossover design. Heart rate variability, respiration rate, and pupil metrics will be continuously recorded using wearable devices. Machine learning models will be used to predict MF-level as well as the effect of MF on physical performance (5-km time trial on a treadmill) using the physiological data as input.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy (no neurological, cardiovascular or musculoskeletal disorders of any kind)

Male or female

No prior knowledge of the concept of MF

No medication

Disqualifiers

Injuries in the past 6 months, affecting running performance

Suffering from a chronic health condition (could be neurological, cardiovascular, internal or musculoskeletal)

Participating in any concomitant care or research trials

History of suffering from any mental/psychiatric disorders

Trial design

Design model

Crossover

Treatments tested in this trial

  • Mental Fatigue

    Behavioral

    Mental fatigue (MF) is a psychobiological state characterized by feelings of tiredness and/or a measurable decline in performance following prolonged or intense cognitive activity.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Mental Fatigue ConditionExperimental treatment 1 intervention
Group B: Control conditionNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Heart rate variability time-domain parameters

Root mean square of successive differences \[RMSSD\], standard deviation of normal-to-normal intervals \[SDNN\] in milliseconds.

Time frame
Continuously during the cognitive intervention and control condition on the study day (approximately 75 minutes).
2

Heart rate variability frequency-domain parameters

Low-frequency (LF), High-frequency (HF) in milliseconds squared (ms²) and Low/high-frequency ratio \[LF/HF\]

Time frame
Continuously during the cognitive intervention and control condition on the study day (approximately 75 minutes).
3

Respiration rate

Respiration rate (RR) will be measured as the number of breaths per minute (breaths/min)

Time frame
Continuously during the cognitive intervention and control condition on the study day (approximately 75 minutes).
4

Pupil diameter

Pupil diameter (PD) will be measured in millimeters (mm) as an index of autonomic nervous system activity.

Time frame
Continuously during the cognitive intervention and control condition on the study day (approximately 75 minutes).

Secondary outcomes

1

Subjective feeling of Mental Fatigue

The Mental Fatigue Visual Annalogue Scale (0-10cm) will assess how mentally fatigued the participant is feeling (100 point VAS scale), and ranges from 'not at all' to 'completely exhausted'.

Time frame
At baseline (pre-intervention), every 5 minutes during the 60-minute cognitive intervention, and immediately after completion of the intervention on the study day.
2

Mood

The Brunel Mood Scale (BRUMS) will be used to indicate mood, and serve as a control measure for both arousal as well as boredom. It features 24 mood descriptors (divided into 6 subscales (i.e. anger, confusion, depression, fatigue, tension and vigor)), where participants have to give a value for every mood on a 5-point Likert scale (i.e. 0=not at all to 4 = extremely) responding to the question: "how do you feel right now?"

Time frame
At baseline, prior to the start of each experimental and control trial on the study day.
3

Motivation

Moti-VAS: Motivation will be assessed using a VAS. Participants will be asked "How motivated do you feel for the upcoming task", and will be instructed to rate their answer on a 10cm line, with the statements "not at all" and "extremely motivated" at opposite ends of this line.

Time frame
At baseline (pre-intervention) and immediately after completion of the 60-minute cognitive intervention on the study day.
4

Sleepiness

The Karolinska Sleepiness Scale (KSS) will be conducted. This 10-point scale measures the subjective level of sleepiness and goes from 1 = 'extremely alert' to 10 = 'extremely sleepy, falls asleep all the time'.

Time frame
At baseline (pre-intervention) and immediately after completion of the 60-minute cognitive intervention on the study day.

Other outcomes

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