Clinical trial Recruiting at 1 site Interventional Ages 18 to 39

Acute Mental Fatigue and Lower-Body Muscle Strength in Young Adults

Official title: Influence of Acute Mental Fatigue on Muscle Strength and Limb Symmetry in Healthy Adults

Run by Florida Institute for Human and Machine Cognition · NCT07846618 · Data updated 2026-11-12

This study tests whether a computer-based mental fatigue task changes knee and leg muscle strength and limb symmetry in healthy young adults.

More Mental Fatigue trials

Quick facts

Study typeInterventional
Ages18 Years to 39 Years
SexAll
Enrollment50 (estimated)
SponsorFlorida Institute for Human and Machine Cognition
Academic / other
Locations1 site (Pensacola, Florida)
StatusRecruiting
StartedSeptember 23, 2026
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedSeptember 29, 2026
Trial IDNCT07846618 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are healthy adults aged 18–39 who can perform maximal leg movements on the Biodex and have no recent lower-extremity injuries or neurological conditions.

Probably not a fit

Individuals with recent lower-extremity injuries, neurological or cognitive impairments, or other conditions affecting maximal force production may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Healthy young adults undergo baseline lower-extremity strength tests using a Biodex dynamometer, then complete a standardized mental fatigue protocol, and repeat strength testing to see if fatigue affects strength and limb symmetry. The study uses isokinetic measurements and surface EMG to assess muscle activity, with subjective fatigue and exertion ratings collected as well. It follows a within-subject, repeated-measures design conducted over a single session at IHMC Healthspan, Resilience, and Performance Research Complex. Heart rate monitoring will accompany testing, and brain activity may be evaluated during cognitive tasks. Primary outcome is peak torque and limb symmetry index before and after the mental fatigue task.

Why it matters

Potential benefit: If successful, results could help understand how mental fatigue might influence leg strength and symmetry, informing performance strategies and safety.

How similar studies have gone: prior work using mental fatigue protocols has explored cognitive and physical performance links, but applying isokinetic leg testing with neuromuscular measures is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age 18-39 years
2. Able to produce maximal force against Biodex protocol
3. Able to perform required lower extremity movements through range of motion necessary for Biodex protocol
4. No known cognitive impairment
5. Sufficient musculoskeletal health to complete the tasks

Exclusion Criteria:

1. History of a neurological disorder, disease, or cognitive impairment that may affect cognition, motor control, reaction time, or force production
2. History of musculoskeletal injury affecting the lower extremities within the past 6 months
3. History of lower extremity surgery affecting force production of the hip, knee, or ankle
4. Color-vision impairment
5. Significant visual or hearing impairment
6. History of migraine headaches
7. Current significant sleep disturbances or sleep deprivation
8. Head injury that may affect cognitive function
9. Medical condition affecting ability to produce maximal force safely
10. Allergy to adhesive tape, parabens, or propylene glycol
11. Scalp lacerations, open wounds, or sutures on the scalp
12. Cranial surgery or skull defects
13. History of unexplained dizziness or fainting in the past 6 months
14. Individuals who are pregnant, prisoners, or not yet adults
15. Inability to communicate with investigators
16. Inability to provide written informed consent

Where it's running

  • Florida Institute for Human and Machine Cognition
    Pensacola, Florida, United States
    Recruiting

Study contacts

  • Principal investigator: Nicole K Rendos, PhD — Florida Institute for Human and Machine Cognition
  • Study coordinator: Nicole K Rendos, PhD
  • Email: nrendos@ihmc.org
  • Phone: 850-202-4442

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.