ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  Related Studies  
Brain Aging Project--Kansas University

This study is currently recruiting participants.
Information provided by National Institute on Aging (NIA)

This Tabular View shows the required WHO registration data elements as marked by

Descriptive Information Fields
Brief Title  Brain Aging Project--Kansas University
Official Title  KU Brain Aging Project
Brief Summary

The purpose of this study is to determine the effects of exercise and cardiorespiratory fitness on age-related brain changes.

Detailed Description

The mission of the KU Brain Aging Project is to promote healthy brain aging. How the brain changes with age is not well-characterized and even less is known about the factors influencing the rate of brain aging. Thus, we are using MRI scans to examine the structure of the brain in relation to important lifestyle factors. This will allow us to better understand the processes influencing the brain as it ages. In turn, this will help identify specific ways to promote healthy brain aging and, perhaps, prevent the onset of Alzheimer's disease.

Participants complete 4 visits over several months. The first visit entails a clinical evaluation and memory testing involving the use of paper and pencil testing. The second visit is an MRI brain scan which lasts approximately one hour. The third visit involves drawing blood for laboratory testing and blood banking for future lab studies, lasting roughly 4 hours. The glucose tolerance test is administered. The fourth and final visit is an assessment of the participant's metabolism and exercise testing. This visit lasts approximately two hours.

Study Phase
Study Type  Observational
Study Design  Longitudinal, Defined Population, Prospective Study
Primary Outcome Measure 
Secondary Outcome Measure 
Condition  Alzheimer's Disease
Intervention 
MEDLINE PMIDs
Links KU Brain Imaging Project This link exits the ClinicalTrials.gov site
Recruitment Information Fields
Recruitment Status  Recruiting
Enrollment  120
Start Date  November 2004
Completion Date
Eligibility Criteria 

Inclusion Criteria:

  • Age 65 years or older
  • Healthy male or female
  • Normal control volunteers and early Alzheimer's disease patients
  • Clinical Dementia Rating of 0, 0.5, or 1.0
  • On stable doses of medications

Exclusion Criteria:

  • Unstable angina
  • Schizophrenia
  • Clinical signs of depression; major depression; mental health disorder; nervous system disorder
  • Significant visual/auditory impairment
  • Significant system illness; cancer
  • Pacemaker/metal
  • Thyroid problems
  • Kidney dialysis
  • Organ transplant
  • Alcoholism
  • Heart surgery
  • Insulin
Gender Both
Ages 65 Years and older
Accepts Healthy Volunteers Yes
Contacts ††
Contact: M. Pat Laubinger, MPA, BSN     913-588-0685     plaubinger@kumc.edu    
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00267124
Organization ID IA0089
Secondary IDs †† 1R03AG026374-01
Study Sponsor  National Institute on Aging (NIA)
Collaborators †† University of Kansas
Investigators 
Principal Investigator:     Jeffrey Burns, MD     University of Kansas Medical Center, Landon Center on Aging    
Information Provided By National Institute on Aging (NIA)
Verification Date September 2007
First Received Date  December 16, 2005
Last Updated Date September 19, 2007

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




Links to all studies - primarily for crawlers