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Blueberry Intervention Study for Brain Aging

Not Applicable
Completed
Conditions
Brain Aging
Interventions
Dietary Supplement: Control
Dietary Supplement: Intervention
Registration Number
NCT05024916
Lead Sponsor
University of Kansas Medical Center
Brief Summary

The purpose of this study is to determine if increased blueberry intake helps increase brain antioxidant (glutathione) and cerebral blood flow in older adults.

Detailed Description

Consuming blueberries may improve brain health of older adults by increasing the antioxidant levels in the brain to protect nerve cells in the aging brain. Researchers think that there may be a relationship between the brain's antioxidant defense system and blueberry intake due to the high antioxidant content in blueberries.

This study will investigate if blueberry intake may aid in enhancing glutathione levels and cerebral blood flow using special Magnetic Resonance Imaging (MRI) scans.

Participants will be asked to make a total of up to 4 visits to the research site. Participation will last about 3 months.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
63
Inclusion Criteria
  • Speak English as the primary language and be able to read and write.
  • Good general health with no concomitant diseases
  • Low berry consumption (≤1 serving/week)
  • Cognitively normal (Mini-Mental State Exam Score ≥24)
  • BMI range=18.5-35 kg/m2.
Exclusion Criteria
  • Presence of any central neurological diseases or prior major head trauma with loss of consciousness
  • Presence of an active unstable and life-threatening systemic illness
  • Presence of major psychiatric disorders within the past 3 years including depression, anxiety, and alcohol or drug abuse
  • Presence of diabetes mellitus; metabolic syndrome or uncontrolled hypertension
  • Use of psychoactive and investigational medications
  • MRI contraindications (pacemaker, aneurysm clips, artificial heart valves, metal fragments, foreign objects or claustrophobia)
  • Blueberry or salicylate allergy
  • Pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ControlControlParticipants will receive a placebo. Participants will take 1 serving of placebo/day.
InterventionInterventionParticipants will receive the dietary intervention. Participants will take 1 serving of blueberries/day.
Primary Outcome Measures
NameTimeMethod
Change in cerebral blood flow (CBF)Change from baseline to 3 months

Measure of CBF with a 3 T MRI scanner

Change in brain glutathione (GSH) levelsChange from baseline to 3 months

Measure of brain GSH with a 3 T MRI scanner

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Kansas Medical Center

🇺🇸

Kansas City, Kansas, United States

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