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Nutritional Supplementation in Cognitive Aging
This study has been completed.
Sponsors and Collaborators: University of Cincinnati
Welch Foods Incorporated
Information provided by: University of Cincinnati
ClinicalTrials.gov Identifier: NCT00599508
  Purpose

To evaluate the effect of supplemented fruit juice on memory function in older adults


Condition Intervention
Age-Related Memory Decline
Dietary Supplement: purple grape juice
Dietary Supplement: wild blueberry juice
Dietary Supplement: placebo juice

MedlinePlus related topics: Dietary Supplements Memory
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Nutritional Supplementation in Cognitive Aging

Further study details as provided by University of Cincinnati:

Primary Outcome Measures:
  • memory performance [ Time Frame: at the end of the intervention ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • cortisol [ Time Frame: at the end of the intervention ] [ Designated as safety issue: No ]

Estimated Enrollment: 33
Study Start Date: June 2006
Study Completion Date: June 2008
Primary Completion Date: June 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
A: Experimental
purple grape juice.
Dietary Supplement: purple grape juice
Several ounces three times a day for 12 weeks. Specific dosage determined by subject's weight.
B: Active Comparator
wild blueberry juice
Dietary Supplement: wild blueberry juice
Several ounces of juice consumed three times a day for 12 weeks; dosage determined according to subject's weight.
C: Placebo Comparator
placebo juice
Dietary Supplement: placebo juice
several ounces consumed three times a day for 12 weeks; dosage determined according to subject's weight

  Eligibility

Ages Eligible for Study:   64 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Mild Cognitive Impairment

Exclusion Criteria:

  • Diabetes
  • Weight of under 120 or over 200 pounds
  • Chronic use of pain medication
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00599508

Locations
United States, Ohio
University of Cincinnati
Cincinnati, Ohio, United States, 45267-0559
Sponsors and Collaborators
University of Cincinnati
Welch Foods Incorporated
Investigators
Principal Investigator: Robert Krikorian, Ph.D. University of Cincinnati
  More Information

Responsible Party: Welch Foods Incorporated ( Pam Gardner )
Study ID Numbers: 06-03-20-08
Study First Received: January 10, 2008
Last Updated: July 28, 2008
ClinicalTrials.gov Identifier: NCT00599508  
Health Authority: United States: Institutional Review Board

Keywords provided by University of Cincinnati:
memory
aging

ClinicalTrials.gov processed this record on January 14, 2009