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Depression Therapy to Improve Cardiovascular Risk in HIV

Primary Purpose

Depression, HIV

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Beating the Blues
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Indiana University Health University Hospital, Indiana Clinical Research Center
  • Infectious Diseases Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Cognitive Behavioral Therapy (CBT)

Usual Care

Arm Description

Those assigned to the CBT arm will undergo therapy with the Beating the Blues (BtB) computerized intervention.

No specific depression care will be provided through this study for those assigned to this arm. However, the participant's caregiver may choose to provide depression treatment outside of this trial.

Outcomes

Primary Outcome Measures

Change in Brachial Artery Flow-mediated Dilation From Baseline to Week 12
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 Outcome Measures

Changes in Circulating IL-6 From Baseline to Week 12
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.
Change in hsCRP From Baseline to Week 12
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.
Change in D-dimer From Baseline to Week 12
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.

Full Information

First Posted
December 3, 2014
Last Updated
July 2, 2020
Sponsor
Indiana University
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1. Study Identification

Unique Protocol Identification Number
NCT02309372
Brief Title
Depression Therapy to Improve Cardiovascular Risk in HIV
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
April 2015 (Actual)
Primary Completion Date
April 2019 (Actual)
Study Completion Date
April 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, HIV

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive Behavioral Therapy (CBT)
Arm Type
Experimental
Arm Description
Those assigned to the CBT arm will undergo therapy with the Beating the Blues (BtB) computerized intervention.
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
No specific depression care will be provided through this study for those assigned to this arm. However, the participant's caregiver may choose to provide depression treatment outside of this trial.
Intervention Type
Behavioral
Intervention Name(s)
Beating the Blues
Intervention Description
Computerized depression treatment intervention
Primary Outcome Measure Information:
Title
Change in Brachial Artery Flow-mediated Dilation From Baseline to Week 12
Description
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.
Time Frame
Baseline and Week 12 of participation
Secondary Outcome Measure Information:
Title
Changes in Circulating IL-6 From Baseline to Week 12
Description
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.
Time Frame
Baseline and 12 weeks
Title
Change in hsCRP From Baseline to Week 12
Description
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.
Time Frame
12 weeks
Title
Change in D-dimer From Baseline to Week 12
Description
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.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samir K Gupta, MD
Organizational Affiliation
Indiana University School of Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jesse C Stewart, PhD
Organizational Affiliation
Indiana University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indiana University Health University Hospital, Indiana Clinical Research Center
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Infectious Diseases Research Center
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

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Depression Therapy to Improve Cardiovascular Risk in HIV

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