NCT07754604

Brief Summary

"This study investigates whether the length of time spent on a mentally demanding task affects brain activity and jumping performance in physically active young men. Twelve healthy male university students, all regularly engaged in sport, completed four separate testing sessions on different days, each at least 72 hours apart. In one session (the control condition), participants watched a calm nature documentary. In the other three sessions, mental fatigue was induced by having participants perform a demanding attention task (the Stroop color-word test) continuously for 10, 15, or 30 minutes. Before and after each session, brain activity was recorded using electroencephalography (EEG), a painless method that measures electrical activity through sensors placed on the scalp. Immediately afterward, participants performed a countermovement jump test, a standard measure of explosive leg power used in sports science. The study examines whether longer periods of mental fatigue produce progressively larger changes in brain activity and jump performance, and whether changes in brain activity are related to changes in jumping ability. The findings may help athletes, coaches, and students better understand how mentally tiring activities, such as studying or exams, could affect physical performance shortly afterward."

Trial Health

87
On Track

Trial Health Score

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

Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

August 4, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 10, 2026

Completed
Last Updated

August 10, 2026

Status Verified

August 1, 2026

Enrollment Period

2 months

First QC Date

August 4, 2026

Last Update Submit

August 4, 2026

Conditions

Keywords

Mental FatigueCountermovement JumpElectroencephalographyCognitive-Motor InteractionDose-ResponseStroop Task

Outcome Measures

Primary Outcomes (1)

  • Countermovement Jump (CMJ) Height

    Countermovement jump (CMJ) height was assessed using the My Jump Lab application (version 5.2; C. Balsalobre-Fernández, Madrid, Spain) via video recorded at 240 frames/s on an iPad Air 11-inch (M3), positioned on a tripod approximately 2 m from the participant. Take-off and landing frames were identified manually by the same investigator using the application's frame-by-frame function, and jump height was calculated from flight time using the equation h = (g·t²)/8. Two jump attempts were performed in each experimental session, with 60 seconds of rest between trials, and the better performance was retained for analysis.

    Immediately after completion of each experimental protocol (control, and 10-, 15-, and 30-minute Stroop-task mental fatigue conditions); sessions were separated by a minimum 72-hour washout period.

Secondary Outcomes (8)

  • Countermovement Jump-Derived Mechanical and Kinematic Parameters

    Immediately after completion of each experimental protocol.

  • EEG Absolute Band Power (Delta, Theta, Alpha, Beta)

    Recorded immediately before and immediately after each experimental protocol (control, and 10-, 15-, and 30-minute Stroop-task mental fatigue conditions); each recording lasted 3 minutes with eyes closed.

  • EEG Theta/Beta Ratio

    Immediately before and immediately after each experimental protocol.

  • EEG Spectral Entropy

    Immediately before and immediately after each experimental protocol.

  • EEG Sample Entropy

    Immediately before and immediately after each experimental protocol.

  • +3 more secondary outcomes

Study Arms (4)

Control

SHAM COMPARATOR

Participants viewed a neutral, cognitively undemanding nature documentary for a duration matched to the mental-fatigue protocols, without performing the Stroop task.

Behavioral: Nature Documentary (Control)

MF10 (10-min Mental Fatigue)

EXPERIMENTAL

Participants performed the Stroop color-word task continuously for 10 minutes to induce mental fatigue.

Behavioral: 10-Minute Stroop Task

MF15 (15-min Mental Fatigue)

EXPERIMENTAL

Participants performed the Stroop color-word task continuously for 15 minutes to induce mental fatigue.

Behavioral: 15-Minute Stroop Task

MF30 (30-min Mental Fatigue)

EXPERIMENTAL

Participants performed the Stroop color-word task continuously for 30 minutes to induce mental fatigue.

Behavioral: 30-Minute Stroop Task

Interventions

Viewing of a neutral, cognitively undemanding nature documentary matched in duration to the mental-fatigue protocols, serving as a non-fatiguing control condition.

Control

Continuous performance of the Stroop color-word interference task for 10 minutes to induce mental fatigue.

MF10 (10-min Mental Fatigue)

Continuous performance of the Stroop color-word interference task for 15 minutes to induce mental fatigue.

MF15 (15-min Mental Fatigue)

Continuous performance of the Stroop color-word interference task for 30 minutes to induce mental fatigue.

MF30 (30-min Mental Fatigue)

Eligibility Criteria

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

You may qualify if:

  • Healthy male volunteers aged 18-30 years
  • Enrolled in the Faculty of Sport Sciences at İnönü University
  • Engaged in structured exercise at least three days per week
  • Free of any neurological, psychiatric, cardiovascular, or musculoskeletal disorder
  • Normal or corrected-to-normal vision
  • Physically capable of completing the experimental protocol safely

You may not qualify if:

  • Diagnosed neurological, psychiatric, cardiovascular, or musculoskeletal disorder
  • Lower-limb injury within the preceding 6 months
  • Use of medication known to affect central nervous system function
  • Prior diagnosis of a sleep disorder
  • Uncorrectable visual impairment or any disturbance of color perception
  • Cognitive or sensory limitation likely to interfere with performance of the Stroop task
  • Failure to complete a session in full, non-compliance with investigator instructions during testing, inability to produce an EEG recording of analyzable quality for technical reasons, or discontinuation of the experimental procedure for any reason
  • Non-compliance with pre-session restrictions (vigorous physical exercise or alcohol consumption within 24 hours before each session; caffeine, energy drinks, or other stimulant substances within 12 hours before each session)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

İnönü University, Faculty of Sport Sciences

Malatya, 44280, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Mental Fatigue

Interventions

Stroop Test

Condition Hierarchy (Ancestors)

FatigueSigns and SymptomsPathological Conditions, Signs and SymptomsBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Neuropsychological TestsPsychological TestsBehavioral Disciplines and Activities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Statistical analyses were performed by biomedical-engineering collaborators who were not involved in data collection, providing a degree of blinding at the analysis stage.
Purpose
TREATMENT
Intervention Model
CROSSOVER
Model Details: Single-group, repeated-measures crossover design; all participants completed all four conditions (control, MF10, MF15, MF30) in a randomized, counterbalanced order across session positions, with a minimum 72-hour washout between sessions.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 4, 2026

First Posted

August 10, 2026

Study Start

May 1, 2026

Primary Completion

July 1, 2026

Study Completion

August 1, 2026

Last Updated

August 10, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared because the study includes a small sample size, and no data-sharing plan was included in the approved study protocol or informed consent. Aggregate study results will be reported in scientific publications.

Locations