A Clinical Trial to Evaluate the Effects of a Supplement on Cognitive Function and Energy Levels (NCT07755475) | Clinical Trial Compass
CompletedNot Applicable
A Clinical Trial to Evaluate the Effects of a Supplement on Cognitive Function and Energy Levels
United States50 participantsStarted 2025-06-13
Plain-language summary
This study evaluates the effects of Artah's Cellular Hydration electrolyte supplement on cognitive function and energy levels in healthy adults aged 25-60 who experience mild to moderate fatigue, brain fog, or related symptoms. The trial is a single-arm, unblinded, virtual study in which all 50 participants will use the test product daily for 4 weeks.
Participants will complete self-reported questionnaires at Baseline, Week 1, Week 2, Week 3, and Week 4, and will undergo cognitive battery testing at Baseline and Week 4. The primary endpoint is change in cognitive performance scores as measured by a standardized cognitive battery. Secondary endpoints include participants' self-reported perceptions of mental clarity, alertness, mood, physical performance, overall energy levels, and frequency of food cravings.
Who can participate
Age range
25 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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 …
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in Cognitive Battery Test Score (Polygons)
Timeframe: Baseline and Week 4
2
Change in Cognitive Battery Test Score (Double Trouble)
Timeframe: Baseline and Week 4
3
Change in Cognitive Battery Test Score (Feature Match)
Timeframe: Baseline and Week 4
4
Change in Cognitive Battery Test Score (Paired Associates)
Timeframe: Baseline and Week 4
5
Change in Cognitive Battery Test Score (Digit Span)
Timeframe: Baseline and Week 4
6
Change in Cognitive Battery Test Score (Spatial Planning)