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A Clinical Trial to Investigate the Efficacy of the Brain Blossom Supplement to Improve Cognitive Function and Memory

A Clinical Trial to Investigate the Efficacy of the Brain Blossom Supplement to Improve Cognitive Function and Memory

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07564804
Enrollment
60
Registered
2026-05-04
Start date
2025-03-28
Completion date
2025-06-27
Last updated
2026-05-04

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

Conditions

Cognitive Decline, Cognitive Function, Memory

Keywords

Brain health, Dietary supplement

Brief summary

This study evaluates the efficacy of BioNatureHealth's Brain Blossom supplement in improving cognitive function and memory in adults aged 50-70 years. Participants will be randomized to receive either the test product or placebo over 8 weeks, with cognitive battery testing and questionnaires administered at multiple timepoints.

Interventions

DIETARY_SUPPLEMENTDietary Supplement: Brain Blossom

Six capsules taken once daily in the morning with water.

DIETARY_SUPPLEMENTPlacebo

Rice flour capsules

Sponsors

Bio Nature Health
Lead SponsorINDUSTRY
Citruslabs
CollaboratorINDUSTRY

Study design

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

Eligibility

Sex/Gender
ALL
Age
50 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Male or female * Aged 50-70 years * Seeking to support cognitive function and memory * Experiences at least three symptoms related to cognitive decline * Willing to avoid new cognitive-related medications/supplements * Generally healthy

Exclusion criteria

* Medical conditions affecting cognition * Psychiatric or neurological disorders * Diabetes or heart conditions * Use of anticoagulants, benzodiazepines, or pain medications * Substance abuse or heavy alcohol use * Allergies to product ingredients * Inability to comply with protocol

Design outcomes

Primary

MeasureTime frameDescription
Change in Cognitive Battery Composite ScoreBaseline, Week 2, Week 4, Week 6, Week 8Cognitive function and memory will be assessed using a cognitive battery consisting of Polygons, Double Trouble, Feature Match, Paired Associates, Digit Span, and Spatial Planning tasks.

Secondary

MeasureTime frameDescription
Change in Self-Reported Memory and RecallBaseline, Week 2, Week 4, Week 6, Week 8Assessed via study-specific questionnaires evaluating participants' perceived ability to retain and recall information.
Change in Self-Reported Focus and AttentivenessBaseline, Week 2, Week 4, Week 6, Week 8Measured using questionnaire items assessing the ability to concentrate and maintain attention.
Change in Self-Reported ComprehensionBaseline, Week 2, Week 4, Week 6, Week 8Assessed via questionnaire responses evaluating participants' perceived ability to understand and process information.
Change in Self-Reported Mental ClarityBaseline, Week 2, Week 4, Week 6, Week 8Measured through questionnaire items assessing clarity of thought and mental sharpness.
Change in Self-Reported Learning AcuityBaseline, Week 2, Week 4, Week 6, Week 8Assessed via questionnaire responses evaluating participants' perceived ability to learn and retain new information.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 5, 2026