Monitoring the Effect of Mental Fatigue on Physical Performance Using Wearable Sensors and Physiological Parameters
NCT ID: NCT07323810
Last Updated: 2026-01-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
30 participants
INTERVENTIONAL
2026-01-31
2026-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
SINGLE
Study Groups
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Mental Fatigue Condition
The mental fatigue task will involve a modified Stroop test, adapted from previous research. Words will appear on the screen in 34-point font for 1000 milliseconds, with the inter-stimulus interval personalized based on each participant's Stroop max test performance. Stroop task duration will be 60 minutes for every participant. Participants will be instructed to respond as quickly and accurately as possible.
Mental Fatigue
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.
Control condition
The control task will consist of watching a pre-approved, emotionally neutral 60-minute documentary.
No interventions assigned to this group
Interventions
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Mental Fatigue
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.
Eligibility Criteria
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Inclusion Criteria
* Male or female
* No prior knowledge of the concept of MF
* No medication
* Non-smoker
* 18-35 years of age
* Experienced runners: (≥15km/week and/or ≥2u/week during the last 6 months)
Exclusion Criteria
* 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
* Use of medication
* Use of caffeine and heavy efforts 24 hours prior each trial
* Suffering from colour vision deficiencies
* Not eating a standardized meal, the morning of each trial and the evening before each trial
18 Years
35 Years
ALL
Yes
Sponsors
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Vrije Universiteit Brussel
OTHER
Responsible Party
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Bart Roelands
Professor Doctor
Locations
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Brussels Labo voor Inspanning en Topsport
Brussels, , Belgium
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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EC-2025-113
Identifier Type: -
Identifier Source: org_study_id
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