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Could a daily electrolyte drink sharpen your mind?

NCT ID NCT07755475

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time

Summary

This trial tests whether a daily electrolyte supplement can improve cognitive function and energy levels in healthy adults aged 25-60 who experience mild fatigue, brain fog, or low mental clarity. All 50 participants take the supplement twice daily for 4 weeks and complete cognitive tests and questionnaires about their mental clarity, mood, and cravings. The study aims to see if this simple hydration approach can support everyday mental performance.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Cellular Hydration electrolyte supplement
What this could lead to
If effective, this supplement could offer a simple, non-drug way to support mental clarity and energy in healthy adults.
What could go wrong
This is a small, unblinded study without a placebo group, so results may be influenced by expectations and may not apply broadly.

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

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

50 people

The number who actually took part.

Started

Jun 2025

Finished

Aug 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

25 to 60 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Be male or female. * Be aged 25-60. * Anyone currently experiencing mild to moderate issues with at least three of the following: low energy or fatigue * difficulty concentrating or low mental sharpness * experiences of brain fog or lack of mental clarity * feeling of low productivity * muscle weakness * unwanted food cravings. * Undertakes moderate to high-intensity exercise such as jogging/running and/or heavy resistance training at least three times per week. * Willing to refrain from taking any products, medications, or supplements that target energy, cognition, or physical performance during the test period. * Anyone with a BMI 18.5 to 30. * Anyone who has access to a device (e.g., smartphone, laptop, computer) for reliable internet. * Anyone who is generally healthy - does not live with any uncontrolled chronic disease. * Anyone willing to maintain a consistent diet and physical activity throughout study duration. Exclusion Criteria: * Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders. * Anyone suffering from gastrointestinal disorders including but not limited to small intestinal bacterial overgrowth (SIBO), irritable bowel syndrome (IBS), and celiac disease. * Anyone suffering from hyperkalemia (high potassium), liver disease, or kidney disease. * Anyone taking ACE inhibitors or potassium-sparing diuretics, examples include: Spironolactone (Aldactone), Eplerenone (Inspra), Amiloride (Midamor), Triamterene (Maxzide), Lisinopril (Zestril, Prinivil), Enalapril (Vasotec), Ramipril (Altace), Benazepril (Lotensin), Quinapril (Accupril), Losartan (Cozaar), Valsartan (Diovan), Olmesartan (Benicar), Irbesartan (Avapro), Lithium carbonate (Lithobid, Eskalith). * Anyone taking antibiotics. * Anyone with any allergies or sensitivities to any of the study product ingredients. * Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period). * Anyone unwilling to follow the study protocol. * Anyone with a history of substance abuse. * Anyone who is a shift worker with an irregular sleep-wake cycle. * Anyone who drinks heavily (8 or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men). * Anyone who is currently a smoker or has been a smoker in the past 3 months. * Currently partaking in another research study, or planning to at any point during this study's duration.

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Conditions

The condition(s) this trial relates to.

Fatigue Mental Fatigue

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Citruslabs

    Las Vegas, Nevada, 89101, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.