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临床试验/NCT02766751
NCT02766751已完成不适用

Treating Comorbid Pain and Depression in HIV+ Individuals

Butler Hospital8 个研究点 分布在 1 个国家目标入组 187 人开始时间: 2016年11月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
187
试验地点
8
主要终点
pain interference

研究概览

简要总结

This study is designed to look at two different programs that may help people who are HIV+ and have pain and depression. The investigators are trying to understand how to help people learn to live better lives even with these chronic illnesses.

详细描述

The primary aim of this RCT is to evaluate the HIVPass intervention. HIV+ participants (n=236) with chronic pain and depression will be recruited at primary care HIV Clinics through posted advertisements in the waiting rooms of the PCP offices and by physician referral. After an initial phone study screen, research staff will meet with interested individuals in their PCP offices for informed consent, baseline interview and randomization into one of two study groups (Health Education or HIVPass Counseling). Seven intervention sessions (HE or HIVPASS) will occur during the first 3 months of study participation. For all participants, the first session is a collaborative in-person joint session with the participant, his/her PCP and the study BHS. Session 2 is conducted immediately after this collaborative session, and is also in-person. Sessions 3-7 are conducted by phone. Follow-up assessment interviews will be at months 1, 2, 3 (post-intervention), 4, 6, 9 and 12.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Chronic Pain (pain duration for at least six months with a mean score of greater than 3.5 on the BPI Pain Interference Scale)
  • Pain severity > or equal to 4 on a Numeric Rating Scale indicating "average pain in the last week"
  • At least one trial of PCP-recommended medication (i.e. acetaminophen, NSAIDS, muscle relaxants) judged through interviews with patients and PCPs
  • Quick Inventory of Depression Symptoms (QIDS) score of ≥ 9 (depression severity)
  • Stable dose of an antidepressant, if using, for the previous 1 months
  • Age > or equal to 18
  • Planning to live in the area for the next 6 months
  • Access to a telephone that is typically working.

排除标准

  • In psychotherapy or a multidisciplinary pain management program
  • Planned surgery in the next 6 months
  • Pain thought due to cancer
  • Current mania
  • Past year chronic psychotic condition
  • Excessive substance use (Use of cocaine, heroin, or non-prescribe opioids 15 days per month or more; binge alcohol use 4 days per month or more)
  • Suicidality requiring immediate attention
  • Pregnancy or planned pregnancy in the next 6 months

结局指标

主要结局

pain interference

时间窗: 3 months

Brief pain inventory, interference scale

次要结局

  • depression(3 months; 12 months)
  • activity level(3 months; 12 months)
  • anxiety(3 months; 12 months)
  • viral load(3 months, 12 months)
  • perception of global improvement(3 months, 12 months)
  • health related quality of life(3 months, 12 onths)
  • ART adherence(3 months, 12 months)
  • pain interference(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael Stein, MD

Principal Investigator

Butler Hospital

研究点 (8)

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