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Depression Therapy to Improve Cardiovascular Risk in HIV

2020年7月2日 更新者:Samir K Gupta, MD, MS、Indiana University

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

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.

研究概览

地位

完全的

详细说明

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).

研究类型

介入性

注册 (实际的)

54

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Indiana
      • Indianapolis、Indiana、美国、46202
        • Infectious Diseases Research Center
      • Indianapolis、Indiana、美国、46202
        • Indiana University Health University Hospital, Indiana Clinical Research Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

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

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Cognitive Behavioral Therapy (CBT)
Those assigned to the CBT arm will undergo therapy with the Beating the Blues (BtB) computerized intervention.
Computerized depression treatment intervention
无干预:Usual Care
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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Brachial Artery Flow-mediated Dilation From Baseline to Week 12
大体时间: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.
Baseline and Week 12 of participation

次要结果测量

结果测量
措施说明
大体时间
Changes in Circulating IL-6 From Baseline to Week 12
大体时间: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.
Baseline and 12 weeks
Change in hsCRP From Baseline to Week 12
大体时间: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.
12 weeks
Change in D-dimer From Baseline to Week 12
大体时间: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.
12 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Samir K Gupta, MD、Indiana University School of Medicine
  • 首席研究员:Jesse C Stewart, PhD、Indiana University School of Medicine

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2015年4月1日

初级完成 (实际的)

2019年4月1日

研究完成 (实际的)

2019年4月1日

研究注册日期

首次提交

2014年12月3日

首先提交符合 QC 标准的

2014年12月4日

首次发布 (估计)

2014年12月5日

研究记录更新

最后更新发布 (实际的)

2020年7月14日

上次提交的符合 QC 标准的更新

2020年7月2日

最后验证

2020年7月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • R01HL126557 (美国 NIH 拨款/合同)

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

Beating the Blues的临床试验

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