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Completed

NCT Number: NCT02309372

Depression Therapy to Improve Cardiovascular Risk in HIV

This trial will determine if depression treatment will reduce cardiovascular risk in HIV-infected patients already receiving HIV treatments. Half of the participants will undergo a specific computerized depression treatment with the other half receiving usual care from their HIV providers.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Indiana University Health University Hospital, Indiana Clinical Research Center, Indianapolis, Indiana, United States

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About this study

The objectives of this study will be met by performing a 24-week, randomized, controlled, single-blinded, two-arm, parallel group, pilot trial at a single center. A total of 200 subjects may be screened to identify 110 participants to be enrolled and randomized. These participants will be ≥ 18 years old, have been receiving antiretroviral therapy for at least one year with an HIV viral load < 75 copies/mL at screening, and have major depression using the PHQ-9 questionnaire. These participants will be randomized 1:1 to either depression treatment with the Beating-the-Blues cognitive behavioral therapy program (N=55) or usual care (N=55).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV-1 infection, documented by both: (1) any licensed rapid HIV test or HIV enzyme test kit at any time prior to study entry and (2) by at least one detectable HIV-1 antigen or at least one detectable plasma HIV-1 RNA viral load
  • Age equal to or greater than 18 years
  • Receipt of antiretroviral therapy of any kind for at least 360 days prior to screening

Note: Interruptions in ART of up to 14 days total during the 360 days prior to screening are allowed

  • HIV-1 RNA level < 75 copies/mL at screening

NOTE: There are no CD4 cell count eligibility criteria for this trial

  • For women who are still of reproductive potential, a negative urine pregnancy test
  • Depression as defined by having a score ≥ 10 on the PHQ-9 questionnaire

Exclusion criteria

  • Inability to complete written, informed consent
  • Incarceration at the time of any study visit
  • Active suicidality, as determined by the patient's HIV provider or social worker following a positive response (1, 2, or 3) to PHQ-9 Item #9 and a positive response (yes) to one or more of the three questions on the Patient Suicidality Form (with last suicide attempt within the past ten years)
  • Diagnosed vascular disease (documented history of angina pectoris, coronary disease, peripheral vascular disease, cerebrovascular disease, aortic aneurysm, or otherwise known atherosclerotic disease)
  • History of congestive heart failure, even if currently compensated
  • Diagnosed disease or process, besides HIV infection, associated with increased systemic inflammation (including, but not limited to, systemic lupus erythematosis, inflammatory bowel diseases, other collagen vascular diseases)

Note: Hepatitis B or C co-infections are NOT exclusionary

  • Known or suspected malignancy requiring systemic treatment within 180 days of screening

NOTE: Localized treatment for skin cancers is not exclusionary

  • History of Raynaud's phenomenon
  • History of cardiac arrhythmias or cardiomyopathy
  • Uncontrolled hyperthyroidism or hypothyroidism, defined as TSH values outside of the local reference range on most recent clinical assessment
  • History of carotid bruits
  • Systolic blood pressure > 160 mmHg or diastolic blood pressure > 110 mmHg at screening
  • Screening estimated glomerular filtration rate (eGFR) < 50 mL/min/1.732 (using the 2009 CKD-EPI equation) using a serum creatinine level measured at screening
  • Screening glucose ≥ 140 mg/dL or hemoglobin A1c > 8.0%
  • Screening total cholesterol > 240 mg/dL
  • Therapy for serious medical illnesses within 14 days prior to screening

Note: Therapy for serious medical illnesses that overlaps with a main study visit will result in postponement of that study visit until the course of therapy is completed; postponement outside of the allowed study visit timeframe will result in study discontinuation

  • Pregnancy or breastfeeding during the course of the study
  • Receipt of investigational agents, cytotoxic chemotherapy, systemic glucocorticoids (of any dose), or anabolic steroids at screening

Note: Physiologic testosterone replacement therapy or topical steroids is not exclusionary. Inhaled/nasal steroids are not exclusionary as long as the participant is not also receiving HIV protease inhibitors

  • Active drug use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements
  • History of schizophrenia or bipolar disorder

Treatment and study plan

Beating the Blues

Behavioral

Computerized depression treatment intervention

Primary outcomes

  1. Change in Brachial Artery Flow-mediated Dilation From Baseline to Week 12

    Time frame: Baseline and Week 12 of participation

    Changes in flow-mediated dilation of the brachial artery from baseline to week 12. This is calculated by the FMD value at Week 12 minus the FMD value at baseline.

Secondary outcomes

  1. Changes in Circulating IL-6 From Baseline to Week 12

    Time frame: Baseline and 12 weeks

    Interleukin-6 (IL-6) is a measure of systemic inflammation. This is calculated by the IL-6 value at Week 12 minus the IL-6 value at baseline.

  2. Change in hsCRP From Baseline to Week 12

    Time frame: 12 weeks

    hsCRP (high sensitivity C-reactive protein) is a measure of systemic inflammation. This is calculated by the hsCRP value at Week 12 minus the hsCRP value at baseline.

  3. Change in D-dimer From Baseline to Week 12

    Time frame: 12 weeks

    D-dimer is a measure of systemic coagulation. This is calculated by the D-dimer value at Week 12 minus the D-dimer value at baseline.

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Registry information

Official study title

A Randomized, Controlled Pilot Trial Assessing the Utility of Cognitive Behavioral Therapy to Improve Endothelial Function and Reduce Inflammation in Depressed, Virologically-Suppressed, Antiretroviral-Treated, HIV-infected Adults

Important dates

Study start
2015
Primary completion
2019
Study completion
2019
First posted
Dec 5, 2014
Registry last updated
Jul 14, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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