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Clinical Trials/NCT01615094
NCT01615094CompletedNot Applicable

BNP and Neuroimmune Characteristics of CHF and Depression (Competing Renewal)

University of California, San Diego0 sites456 target enrollmentStarted: January 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
456
Primary Endpoint
Rate of dysphoria

Study Overview

Brief Summary

The study is designed to find out more about how mood and the nervous system affect the body's immune system. The investigators plan to study this in people who have been identified by their physician as being at-risk for the development of heart failure. There will be approximately 525 individuals participating in this study at UCSD and at the VASDHS. Individuals who will be asked to take part in this study will have a functional or structural heart problem apparent on an echocardiogram, or a previous heart attack, but no symptoms of heart failure. Some individuals will only complete one assessment (consisting of psychological questionnaires and interview, walk test, blood draw, and body measurements), whereas others deemed "high-risk" on the basis of a laboratory test, will be asked to complete that same assessment every 6 months for the duration of the study.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age range 18 years or older
  • ACC/AHA classification Stage B HF patients
  • Receiving optimal treatment according to their cardiologist and/or internists
  • An echocardiogram within the past 12 months
  • Ejection fraction: as described below in Initial Screening and Identification of Stage B Patients
  • Men and women of all ethnicities and races
  • Ability and physician clearance to perform mild exercise
  • With and without depressive symptoms and DSM-IV MDD
  • Ability to fully understand all elements of and sign the written informed consent before initiation of the study

Exclusion Criteria

  • History of recent myocardial infarction (3 months)
  • Significant aortic or mitral stenosis, angina not adequately managed with nitrates
  • Coronary revascularization, mitral valve repair or any other cardiac surgery or implantation of a biventricular pacemaker within the past 2 months
  • Hypertension >180/110 mm Hg
  • Recent stroke or significant cerebral neurological impairment
  • Severe COPD, patients who require mechanical ventilation, with cardiogenic shock, volume depletion
  • Subjects with high suicide risk
  • Immune-related disorders including infectious diseases and autoimmune and inflammatory disorders
  • Morbid Obesity: BMI > 40 due to likelihood of inability to perform exercise
  • Women who are pregnant or nursing
  • Major mental illness as determined by referring provider

Outcomes

Primary Outcomes

Rate of dysphoria

Time Frame: up to 4 years

In high-risk (BNP ≥ 65pg/ml) Stage B patients, characterize rates of clinically significant depressed mood (BDI ≥10) and MDD (SCID) and determine prospective relationships with transition to Stages C and/or D HF and clinical outcomes during an average follow-up time of 30 months.

Secondary Outcomes

  • Neuroimmune activation(up to 4 years)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Paul J. Mills

Professor IR

University of California, San Diego

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