Cognitive Vitality Pilot Study

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Aging, Healthy Aging, Cognition, Memory, Brain

In brief

This study's purpose is to evaluate the effects of a dietary supplement on cognitive function and psychological well-being in community-dwelling older adults aged 55+. The study involves taking a commercially available dietary supplement daily for 45 days. A 45-minute assessment will be conducted at the beginning and again at the end of the study.

Key facts

Study ID

NCT07208279

Run by

Arizona State University

People needed

16

Starts

2025-09-01

Expected to finish

2026-08-11

Last updated by the study team

2025-10-28

Who can join

Age: 55 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Adults aged 55 years and older
• Live independently,
• Self-report as healthy
• Adequate vision
• Fluent in English
• No history of mild cognitive impairment
• Currently not taking dietary supplements with the same active ingredients in Axolt or naturally flavored water
• A Montreal Cognitive Assessment [12] (MOCA) score ≥ 24
• Able to provide written informed consent, and medical clearance to participate.

You may not qualify if…

• Previous participation in a cognitive dietary supplement study in the last 12 months
• A score of < 24 on the Montreal Cognitive Assessment (MoCA) as a potential risk for obtaining informed consent
• History of seizures
• Epilepsy
• Parkinson's disease
• History of severe head trauma
• Uncontrolled hypertension
• On psychoactive medications
• Substance abuse
• Unwilling or unable to discontinue current dietary supplements with similar ingredients
• Planned surgery during the study period
• Medications known to interact with active ingredients with Axolt
• Minors and prisoners will be excluded.

Where it is running

• Community — West Palm Beach, Florida, United States (enrolling)

Full record on ClinicalTrials.gov

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