Caffeine and vitamin c may fight mental fatigue to improve strength — a trial puts the combo to the test
NCT ID NCT07726745
First seen Jul 24, 2026 · Last updated Jul 28, 2026 · Updated 2 times
Summary
This trial investigates whether caffeine, vitamin C, or their combination can improve maximum strength and strength endurance in female adolescents experiencing mild mental fatigue. Forty healthy college students will complete strength tests after a mental fatigue task, with each participant trying all supplement conditions in a random order. The study aims to see if these common substances can counteract the physical effects of mental tiredness.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- caffeine and vitamin C
- What this could lead to
- If effective, a simple combination of caffeine and vitamin C could help counteract mental fatigue and improve physical performance in young athletes.
- What could go wrong
- This is a small, early-stage trial in healthy female college students, so results may not apply to other groups. Caffeine can cause side effects like jitters or sleep disruption.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 19 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Aged between 18and 19years (adolescent) 2. Able to complete standardized 1RM maximal strength test and muscular endurance protocol for back squat and bench press 3. Meet criteria for mild mental fatigue verified by validated scale (PVT + VAS Mental Fatigue ≥4/10 or Brief Fatigue Inventory) prior to experimental session 4. Habitual daily caffeine intake ≤ 150 mg/day (low-to-moderate habitual consumption) 5. Non-smoker; no regular alcohol consumption 6. Consistent strength training status: No physical training for the past 3 months, or maintenance of a consistent daily activity routine throughout the study 7. Able to attend all scheduled testing visits, comply with pre-test restrictions (diet, sleep, exercise, supplements) 8. Participant provides written assent; parent/legal guardian provides written informed consent 9. Able to understand and follow verbal and written study instructions Exclusion Criteria: 1. History of cardiovascular disease, arrhythmia, hypertension, asthma requiring regular medication 2. Known hypersensitivity or adverse reaction to caffeine, vitamin C 3. Chronic neurological disorders: epilepsy, migraine disorder, ADHD with stimulant medication 4. Current psychiatric diagnosis (anxiety, depression) receiving psychotropic medication 5. Musculoskeletal injury in the past 3 months limiting lower/upper body maximal strength testing 6. Regular intake of ergogenic supplements (creatine, beta-alanine, energy drinks) within 4 weeks before screening 7. Use of any stimulants, anti-fatigue drugs, corticosteroids within 30 days prior to enrollment 8. Chronic gastrointestinal disease, kidney stone history (vitamin C related risk) 9. Irregular sleep-wake cycle, diagnosed sleep disorder 10. Females: current pregnancy; regular oral contraceptive use 11. Participated in other human intervention trials within past 8 weeks 12. Investigator judges any condition that compromises participant safety or interferes with outcome measurements
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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