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The Effect of Mental Fatigue on Upper Extremity Functional Performance

The Effect of Mental Fatigue on Upper Extremity Functional Performance

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07645404
Enrollment
16
Registered
2026-06-12
Start date
2026-07-01
Completion date
2026-12-01
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Fatigue

Keywords

Mental Fatigue, Upper Extremity, Physical Performance, Functional Testing, Sports Medicine, Cognitive Performance, Visuomotor Reaction Time, Upper Quarter Y Balance Test

Brief summary

Mental fatigue (MF) is known to impair cognitive performance and may negatively affect physical performance. While its effects on lower-extremity functional performance have been investigated, little is known about the influence of MF on upper-extremity physical performance tests commonly used in sports and rehabilitation settings. This randomized crossover study will investigate the effects of experimentally induced mental fatigue on upper-extremity physical performance in 16 healthy physically active adults. Participants will complete both a mental fatigue condition, involving a prolonged Stroop task, and a control condition consisting of watching an emotionally neutral documentary. Before and after each condition, participants will perform the Upper Quarter Y Balance Test, Reactive Upper Quarter Y Balance Test, Closed Kinetic Chain Upper Extremity Stability Test, and Seated Single-Arm Shot Put Test. Subjective mental fatigue, cognitive performance, motivation, and perceived exertion will also be assessed. The findings will improve understanding of whether mental fatigue influences upper-extremity physical performance test outcomes and may assist clinicians and researchers in interpreting these assessments in sports medicine and rehabilitation contexts.

Interventions

BEHAVIORALMental 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.

Sponsors

Izmir Bakircay University
Lead SponsorOTHER
Vrije Universiteit Brussel
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Age between 18 and 35 years * Healthy (no neurological, cardiovascular or musculoskeletal disorders of any kind) * Male or female * No prior knowledge of the concept of mental fatigue * Not currently taking medications that affect cognition or neuromuscular performance * According to the International Physical Activity Questionnaire, being physically active at a minimum level of 1500 MET-min/week

Exclusion criteria

* Previous major upper limb injury (last 6 months) * Involvement in another concurrent physical or cognitive intervention study * 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

Design outcomes

Primary

MeasureTime frameDescription
Reactive Upper Quarter Y Balance TestPre-intervention and immediately post-intervention (each experimental and control condition session)Measures visuomotor reaction time, reaching accuracy, and balance errors during a reactive upper quarter Y balance test performed under visual stimuli conditions.
Closed Kinetic Chain Upper Extremity Stability TestPre-intervention and immediately post-intervention (each session)Assesses upper-extremity muscular endurance and stability by counting the number of alternating hand touches performed in a 15-second push-up position task.
Upper Quarter Y Balance TestPre-intervention and immediately post-intervention (each session)Evaluates dynamic upper-extremity reach performance and composite score based on normalized reach distances in three directions.
Seated Single-Arm Shot Put TestPre-intervention and immediately post-intervention (each session)Measures upper-extremity explosive power based on throwing distance of a 6-lb medicine ball.

Secondary

MeasureTime frameDescription
Subjective Mental FatigueBaseline, every 5 minutes during intervention, and post-intervention (each session)Subjective Mental Fatigue measured using the Mental Visual Analog Scale (M-VAS). The scale ranges from 0 to 100, where 0 indicates no mental fatigue and 100 indicates the highest level of mental fatigue imaginable. Higher scores indicate worse mental fatigue.
Go/No-Go TaskImmediately post-intervention (each session)Assesses executive function using a computerized Go/No-Go task. Outcomes include reaction time (milliseconds) and response accuracy (percentage of correct responses, ranging from 0% to 100%). Higher accuracy indicates better executive function performance, while shorter reaction times indicate better performance.
Motivation StatePre- and post-intervention (each session)Assesses task-related motivation using the Assessment of Motivational States in Performance Environments questionnaire. The questionnaire includes two 7-item subscales: Interest Motivation and Success Motivation. Higher scores indicate greater task engagement, interest in the task, and motivation to perform successfully.
Perceived ExertionImmediately after physical performance testing (each session)Assesses perceived exertion using the Borg Rating of Perceived Exertion Scale. Scores range from 6 to 20, with higher scores indicating greater perceived exertion.
Stroop Task PerformanceDuring intervention (continuous, averaged per block)Assesses cognitive performance using a computerized Stroop task. Outcomes include reaction time (milliseconds) and response accuracy (percentage of correct responses, ranging from 0% to 100%). Higher accuracy and shorter reaction times indicate better cognitive performance.

Countries

Belgium

Contacts

CONTACTNieka Coryn, MSc
Nieka.Coryn@vub.be+32 (0)2 629 2222
CONTACTGürsu Sayar, MSc
6009015@bakircay.edu.tr+90 534 231 00 72
STUDY_DIRECTORBart Roelands, Professor

Vrije Universiteit Brussel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 16, 2026