ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Biological CVD Risk Factors in Older Depressed Patients

This study has been completed.

Sponsored by: Stanford University
Information provided by: Stanford University
ClinicalTrials.gov Identifier: NCT00318864
  Purpose

The purpose of this study is to determine if improvements in mood will ameliorate autonomic dysregulation, HPA dysfunction and typical (e.g. lipids) and atypical risk factors in depressed patients with elevated cardiovascular risk (CVD). Up to 70, depressed participants with elevated cardiovascular risk factors were randomized to a cognitive behavioral intervention (CBT) or a waiting list control (WLC) condition. Twenty non-depressed age and risk-matched controls will also recruited. Traditional risk factors (e.g. lipids, blood pressure, heart rate), atypical risk factors (endothelial function, asymmetric dimethylarginine, C-reactive protein) will be measured pre and post treatment six months later Subjects will undergo a psychophysiological stress test while cardiovascular physiology was measured. Salivary cortisol will be measured during the day and during the psychological stress test. Depressed subjects will be randomized to a 16 week cognitive behavior therapy intervention or to a wait-list control. It is hypothesized that reduction in mood will be associated with reduction in typical and atypical risk factors.


Condition Intervention
Depression
Hypertension
Hypercholesterolemia
Behavioral: Cognitive behavioral therapy

Genetics Home Reference related topics:   hypercholesterolemia   

MedlinePlus related topics:   Cholesterol    Depression    High Blood Pressure    Stress   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Active Control, Single Group Assignment, Bio-equivalence Study
Official Title:   Stress, the HPA and Health in Aging

Further study details as provided by Stanford University:

Primary Outcome Measures:
  • Change in depression

Secondary Outcome Measures:
  • Change in typical and atypical risk factors

Estimated Enrollment:   70
Study Start Date:   June 2002
Estimated Study Completion Date:   July 2005

Show detailed description  Show Detailed Description

  Eligibility
Ages Eligible for Study:   55 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • age > 55 years, hypertensive or hypercholesterolemic, depressed

Exclusion Criteria:

  • suicidal
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00318864

Locations
United States, California
Stanford Medical Center    
      Stanford, California, United States, 94305

Sponsors and Collaborators
Stanford University

Investigators
Principal Investigator:     Craig B Taylor     Stanford Medical Center    
  More Information


Study ID Numbers:   CBarrTaylor, 5 p01 AG18784-02
First Received:   April 25, 2006
Last Updated:   April 25, 2006
ClinicalTrials.gov Identifier:   NCT00318864
Health Authority:   United States: Institutional Review Board

Keywords provided by Stanford University:
depression  
cardiovascular risk  
mechanisms  

Study placed in the following topic categories:
Depression
Hyperlipidemias
Metabolic Diseases
Vascular Diseases
Stress
Depressive Disorder
Behavioral Symptoms
Mental Disorders
Mood Disorders
Metabolic disorder
Hypercholesterolemia
Dyslipidemias
Hypertension
Lipid Metabolism Disorders

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on October 06, 2008




Links to all studies - primarily for crawlers