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Starting soon Not applicable

Mental Fatigue Effects on Posture and Spinal Reflexes

NCT07650903 · tracked via the Priya Life Science Belgium tracker
Phase
Not applicable
Started
2026-07-01
Last updated
2026-06-16

Condition(s) studied

Mental Fatigue

Investigational drug(s) / intervention(s)

Mental Fatigue InductionControl Condition

Mental Fatigue Induction: Participants complete a 60-minute computerized Stroop color-word task designed to induce mental fatigue. The task consists of repeated incongruent stimuli requiring rapid and accurate responses, with difficulty individualized based on a prior maximal Stroop performance test. Performance (reaction time and accuracy) is continuously recorded. Subjective mental fatigue is assessed intermittently during the task using a visual analogue scale.

Control Condition: Participants watch a 60-minute neutral documentary of their choice. This condition is designed to match the mental fatigue intervention in duration and general sensory engagement without inducing cognitive fatigue. No cognitive task performance is required. Subjective mental fatigue is assessed at equivalent time points using a visual analogue scale.

Study summary

This randomized crossover study investigates the effects of mental fatigue on postural control and spinal reflex excitability in healthy physically active adults aged 18-35 years. Participants will complete two experimental conditions: a mentally fatiguing Stroop task and a control condition involving passive documentary watching, separated by at least 48 hours. Postural control will be assessed using force plate measures of center of pressure displacement during bipedal and unipedal stance, with and without concurrent cognitive dual-tasking. In parallel, spinal reflex excitability will be evaluated using H-reflex recordings from the triceps surae muscles across sitting and standing postures.

The primary aim is to determine whether mental fatigue increases postural sway, particularly in more challenging balance conditions such as single-leg stance. The secondary aim is to examine whether mental fatigue alters the normal modulation of spinal reflex excitability across progressively demanding postural tasks. Additional biomechanical and neuromuscular measures, including EMG activity and hip kinematics, will be recorded to provide insight into underlying control mechanisms.

The study will include approximately 26 participants, with each serving as their own control. Data will contribute to understanding how cognitive fatigue influences balance control and spinal-level neuromuscular regulation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy participants aged between 18 and 35 years * Recreational active Exclusion Criteria: * Previous major lower limb injury (last 6 months) * Present neurological or musculoskeletal disorders * Involvement in another concurrent physical or cognitive intervention study

Primary outcome measure(s)

  • Center of Pressure (CoP) Displacement (Postural Sway) — Pre-intervention and immediately post-intervention (each experimental session)
    Postural sway will be assessed using center of pressure (CoP) displacement area and oscillation parameters measured during bipedal and unipedal stance on a force plate. Higher values indicate greater postural instability. Comparisons will be made between mental fatigue and control conditions, pre- and post-intervention.
  • Subjective Mental Fatigue — During intervention (every 15 minutes) and immediately post-intervention
    Subjective mental fatigue will be assessed using a visual analog scale (VAS) ranging from 0 (no fatigue) to 100 (extreme fatigue).

Trial sites (1)

FacilityCityRegionStatus
Vrije Universiteit Brussel Brussels Pleinlaan 2

More Izmir Bakircay University trials in Belgium

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07650903 on ClinicalTrials.gov ↗ ← All trials in Belgium