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A Clinical Trial to Investigate the Efficacy of a Supplement to Improve and Maintain Cognitive Function and Memory

A Clinical Trial to Investigate the Efficacy of a Supplement to Improve and Maintain Cognitive Function and Memory

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06523218
Enrollment
50
Registered
2024-07-26
Start date
2024-05-17
Completion date
2024-08-17
Last updated
2024-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Decline, Cognitive Function

Keywords

Cognitive Health, Healthy Aging

Brief summary

This study will evaluate the efficacy of 1MD Nutrition's MindMD supplement in improving and maintaining cognitive function and memory. The randomized controlled trial will include 50 healthy participants aged 50-75 years, lasting for 3 months. Participants will be randomized to receive either the test product or a placebo.

Interventions

DIETARY_SUPPLEMENTMindMD Supplement

Participants will take two capsules of the MindMD supplement once daily with their morning meal for a duration of 3 months. The supplement is designed to improve and maintain cognitive function and memory.

OTHERPlacebo

Participants will take two capsules of the placebo once daily with their morning meal for a duration of 3 months. The placebo is designed to be indistinguishable in appearance and administration from the MindMD supplement to ensure blinding.

Sponsors

Citruslabs
CollaboratorINDUSTRY
Scale Media Inc
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 50-75 years * Regular experience of symptoms related to cognitive decline (e.g., forgetfulness, lack of focus, brain fog) * Generally healthy without uncontrolled chronic diseases * Willingness to avoid certain medications and supplements during the study

Exclusion criteria

* Any medical condition or treatment impacting cognitive ability Mental health or neurological disorders * Severe allergies, particularly to soy or other product ingredients * Taking blood thinning medication * Recent or planned surgeries * Major illness in the past three months

Design outcomes

Primary

MeasureTime frameDescription
Cognitive Function and Memory ImprovementBaseline, Month 2, and Month 3Measurement of cognitive function and memory through Cognitive Battery Testing. The Cognitive Battery Testing includes assessments such as Polygons, Double Trouble, Feature Match, Paired Associates, Digit Span, and Spatial Planning. These assessments provide objective measurements of various cognitive functions, including processing speed, memory recall, selective attention, and executive function.

Secondary

MeasureTime frameDescription
Participants' Perceptions of Cognitive Function and Memory using the Cognitive Function QuestionnaireBaseline, Month 1, Month 2, and Month 3Evaluation of participants' self-reported perceptions of the effect of the MindMD supplement on cognitive function and memory. This includes aspects such as focus and attentiveness, comprehension and mental clarity, learning acuity, absentmindedness, and overall quality of life. These perceptions will be measured through the Cognitive Function Questionnaire (CFQ) at specified time points: Baseline (Day 0), Month 1, Month 2, and Month 3.
Participants' Quality of LifeBaseline, Month 1, Month 2, and Month 3Assessment of participants' quality of life using the WHO-5 Well-Being Index. These assessments will be conducted at Baseline (Day 0), Month 1, Month 2, and Month 3.
Participants' Focus and AttentivenessBaseline, Month 1, Month 2, and Month 3Evaluation of participants' focus and attentiveness using the Visual Analog Scale (VAS). These assessments will be conducted at Baseline (Day 0), Month 1, Month 2, and Month 3.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026