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Age, Risk Factors for CVD and Cognitive Functioning

This study has been completed.
Study NCT00007397.   Last updated on December 21, 2005.   Information provided by National Heart, Lung, and Blood Institute (NHLBI)

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Descriptive Information Fields
Brief Title  Age, Risk Factors for CVD and Cognitive Functioning
Official Title 
Brief Summary

To relate cardiovascular disease (CHD) risk factors to cognitive performance among middle-aged and elderly men and women over a 10 year longitudinal study period.

Detailed Description

BACKGROUND:

The Framingham Heart Study is a major epidemiological investigation of prospective relationships between risk factors for the development of cardiovascular disease (CVD risk factors) and CVD risk factor outcomes. The Framingham Study and other large, prospective studies have resulted in an extensive literature on the impact of CVD risk factors (including age) and CVD outcomes. Comparatively, there have been many fewer studies of the impact of CVD risk factors on cognitive functioning, and possibly no studies of the effect of objectively measured, competing risk factors on cognitive functioning.

DESIGN NARRATIVE:

Dr. Elias and colleagues used cardiovascular risk factor data from the Framingham Heart Study (N= 2,123) in a prospective design allowing them to relate CVD risk factors (including age and gender) to two outcome measures: (1) level of cognitive performance and (2) change in cognitive performance over a 10 year longitudinal study period. The overall goals were to determine the best multivariate combination of biological and psychosocial risk factors for the prediction of lowered cognitive ability in middle-aged and elderly men and women, and to evaluate the relative impact of age, gender, and other biological and psychosocial risk factors on cognitive functioning.

Study Phase
Study Type  Observational
Study Design  Natural History, Longitudinal, Defined Population
Primary Outcome Measure 
Secondary Outcome Measure 
Condition  Cardiovascular Diseases
Heart Diseases
Neurologic Manifestations
Intervention 
MEDLINE PMIDs 12587008,   14726556,   15673620
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment 
Start Date  February 2000
Completion Date January 2004
Eligibility Criteria 

No eligibility criteria

Gender Both
Ages
Accepts Healthy Volunteers No
Contacts ††
Location Countries 
Administrative Information Fields
NCT ID  NCT00007397
Organization ID 958
Secondary IDs ††
Study Sponsor  National Heart, Lung, and Blood Institute (NHLBI)
Collaborators ††
Investigators 
Investigator:     Merrill Elias     Boston University    
Information Provided By National Heart, Lung, and Blood Institute (NHLBI)
Verification Date December 2005
First Received Date  December 19, 2000
Last Updated Date December 21, 2005

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




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