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临床试验/NCT01347437
NCT01347437已完成不适用

Improving Antiretroviral Medication Adherence Among HIV-infected Youth: Phase II

Fenway Community Health6 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2011年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
17
试验地点
6
主要终点
Electronically monitored (MEMS) antiretroviral medication adherence

研究概览

简要总结

HIV is increasing among adolescents and young adults in the US. Antiretroviral medications, when taken correctly (≥ 90% of prescribed doses taken), can vastly improve life expectancy. However, adherence among HIV-infected young people is suboptimal, and few interventions are available to help adolescents adhere to treatment.

The study is a randomized controlled trial (RCT) pilot trial of Positive STEPS (the adapted form of the Life-Steps behavioral intervention) to improve medication adherence among HIV-infected youth. The study will allow us to demonstrate participant acceptance, ability to recruit, feasibility of intervention delivery with study counselors and all study procedures, and initial clinically significant improvement in medication adherence via MEMS caps. This research will lay the groundwork for a federal grant application for a multi-site randomized controlled intervention trial.

详细描述

Aims:

  1. To conduct a randomized controlled pilot test of a behavioral adherence intervention to improve medication adherence among HIV-infected youth aged 13-24. Feasibility of all study procedures and participant acceptability will be assessed.
  2. To explore whether the intervention leads to improved medication adherence among youth who receive the intervention, compared to a control group of youth who do not.

40 HIV-infected adolescents will be recruited for a RCT pilot of the Positive STEPS intervention at Fenway Health and Children's Hospital Boston. Participants will be randomized into one of two arms (half and half). Randomization for all participants will occur after the beginning of the week 2 study visit. The duration of the study is 3 months

Randomization:

The investigators will conduct block randomization based on two categories of electronic adherence: 85% or above versus < 85%. All participants will have exhibited some non-adherence in order to be eligible for the study, although they may vary in the extent of non-adherence. Because insufficient information is known about the range of non-adherence in the population to determine the most valid non-adherence cut-off points, the investigators may need to reconsider adherence categories over the course of the pilot study. The investigators will regularly examine the data to determine whether finer adherence categories are needed, and the investigators will adjust the categories if such a determination is made.

研究设计

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

入排标准

年龄范围
13 Years 至 24 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Age 13 to 24 years
  • HIV-infected
  • Currently taking antiretroviral therapy or prescribed medication for HIV
  • Self-reported difficulties adhering to HIV medications in the past 3 months (i.e., <95% compliant)
  • If 18-24: Willing and able to provide informed consent
  • If 13-17: Parent/guardian willing and able to provide parental permission and participant willing and able to provide assent
  • Willing to attend all study visits

排除标准

  • If 18-24:Unwilling or unable to provide informed consent
  • If 13-17: Parent/guardian unwilling or unable to provide parental permission and participant willing and able to provide assent
  • Has severe mental illness requiring immediate treatment (e.g. active psychotic episode) or a mental illness that would limit your ability to participate (e.g. dementia)
  • Has severe cognitive limitation that would limit your ability to comprehend the informed consent or assent (see Decisional Capacity Determination SOP)
  • Unwilling to attend all study visits

结局指标

主要结局

Electronically monitored (MEMS) antiretroviral medication adherence

时间窗: 3 months

The primary outcome will be antiretroviral medication adherence. Adherence will be measured through the medication event monitoring device(MEMS).

次要结局

未报告次要终点

研究者

发起方
Fenway Community Health
申办方类型
Other
责任方
Principal Investigator
主要研究者

Matthew Mimiaga

Research Scientist

Fenway Community Health

研究点 (6)

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