Actively Recruiting

Phase Not Applicable
Age: 50Years - 85Years
All Genders
ID07334366

A 12-week Randomized, Double-blind, Placebo-controlled Trial of Broccoli Sprout Extract to Improve Cognitive Function in Adults With Mild Cognitive Impairment

Led by Pusan National University Yangsan Hospital · Updated on 2026-01-13

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate whether broccoli sprout extract can improve cognitive function in adults aged 55 to 85 with mild cognitive impairment. The study also assesses the safety and possible side effects of taking this extract. Participants will be adults with mild cognitive issues but without dementia, capable of reading Korean, and meeting specific memory impairment criteria. Participants will be randomly assigned to receive either 1,000 mg of broccoli sprout extract or a placebo daily for 12 weeks. The study is double-blind, meaning neither the participants nor the researchers know who is receiving the extract or placebo. Clinic visits will occur at screening, week 0, week 6, and week 12 for health checks and cognitive testing. During the trial, researchers will evaluate changes in cognitive function using computerized neurocognitive tests, verbal learning, digit span, and auditory continuous performance tests, as well as the Korean Mini-Mental State Examination. Blood tests will measure brain-related proteins and oxidative stress markers. Participant safety will be monitored throughout, with the primary outcome measured at 12 weeks from the start.

CONDITIONS

Brief Title

Broccoli Sprout Extract for Cognitive Function

Who Can Participate

Age: 50Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 55 to 85 years, male or female
  • Global Deterioration Scale score of 2 or 3 indicating subjective or mild objective memory impairment
  • No diagnosis of dementia based on established criteria
  • Ability to read Korean
Not Eligible

You will not qualify if you...

  • Severe medical conditions within past 6 months such as major stroke, cardiac disease, or cancer (stable cases may be included at investigator discretion)
  • Diseases linked to cognitive impairment like dementia, Parkinson's disease, cerebral infarction
  • Uncontrolled high blood pressure (160/100 mmHg or higher)
  • Poor blood sugar control in diabetes (fasting glucose 160 mg/dL or higher)
  • Uncontrolled thyroid problems under treatment
  • Significant kidney or liver impairment
  • Severe gastrointestinal symptoms
  • Use of medications or supplements affecting cognition within past month
  • Participation in other drug trials within past month or planned during this study
  • Severe alcohol use disorder
  • Allergies to study product ingredients
  • Any other condition deemed unsuitable by the investigator

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants take dietary broccoli sprout extract or a placebo daily to evaluate effects on cognitive function.

Clinic visits at 0, 6, and 12 weeks for checkups and tests

Trial Site Locations

Total: 1 location

1

Pusan National University Yangsan Hospital

Yangsan, South Korea, 50612

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Research Team

S

Sang Yeoup Lee, Professor, MD, PhD

Y

Ye Li Lee

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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