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临床试验/NCT00103532
NCT00103532已完成不适用

Motivational Enhancement to Promote Health and Reduce Risk in HIV-Infected Youth

University of North Carolina, Chapel Hill12 个研究点 分布在 1 个国家目标入组 225 人开始时间: 2005年3月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
225
试验地点
12
主要终点
Determine the efficacy of a motivational enhancement intervention

研究概览

简要总结

Risk behaviors and their associated adverse health outcomes are becoming increasingly problematic among HIV-infected youth. This study is being conducted to test whether a brief motivational enhancement (ME) intervention will help reduce health risk behaviors (drug and alcohol use, sexual risk behavior, poor adherence to medications) among HIV+ youth.

详细描述

Healthy Choices is a randomized clinical trial examining the efficacy of motivational enhancement in reducing risk and promoting healthy behaviors. This study will use a sample of 225 youth (180 after attrition), ages 16-24, of whom 90 will receive the intervention, referral, and standard care, and 90 will receive referral plus standard care. The sample will be drawn from five study sites. Using parallel screening, recruitment will target 100 youth with an adherence problem, 100 youth with a substance use problem, and 25 youth with a sexual risk problem. A repeated measures design will be used for the proposed study. Primary outcome measures are drug and alcohol use, condom use, and HIV medication adherence. Youth will complete an initial data collection session (baseline) during which questionnaire and interview measures will be administered. Blood specimens for viral load and CD4+ count will also be obtained.

Randomization procedures will take place after completion of the baseline assessment. Participants who are randomized to the intervention group will participate in four sessions for approximately 3 months and will also receive standard care plus individualized referrals. The control group will receive standard care and individualized referrals. All five sites offer comprehensive, multidisciplinary care including social work and case management services and access to mental health services. Participants will receive a three-month post-test designed to coincide with ME completion. Subsequent post-tests will occur at 6, 9, 12, and 15 months after baseline data collection (3, 6, 9, and 12 months after ME completion).

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
16 Years 至 24 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • HIV infection as documented by professional referral and medical record review. HIV+ participants who are self-referred and not in medical care will be required to provide documentation of test results.
  • Males or females between the age of 16 years and 0 days and 24 years and 364 days at the time of study enrollment.
  • Reports having ever engaged in at least 2 of the following 3 behaviors based on screening questionnaire:
  • taken prescribed antiretroviral medications, OR been told by his/her physician that he/she should be on antiretroviral medications (whether he/she takes them or not);
  • vaginal or anal sex, OR
  • alcohol or drug use.
  • At least one of the 3 aforementioned behaviors are currently at a problem level, based on screening questionnaire:
  • taking currently prescribed antiretroviral medications <90 % of the time in the last month,
  • having unprotected intercourse within the last 3 months,
  • demonstrating problem level alcohol and/or drug use as measured during screening.
  • Able to understand spoken and written English sufficiently to provide consent/assent and be interviewed and participate in study intervention.
  • Not intending to relocate out of the current geographical area for the duration of study participation.

排除标准

  • History of any psychiatric thought disorder (e.g., schizophrenia, schizoaffective disorder).
  • Currently involved in behavioral research (assessment or intervention) targeting adherence, sexual risk, or alcohol and/or drug substance abuse OR currently involved in a substance abuse treatment program.

研究组 & 干预措施

Healthy Choices - Motivational Enhancement Intervention

Experimental

Motivational enhancement intervention

干预措施: Healthy Choices - Motivational Enhancement Intervention (Behavioral)

Standard Care

Active Comparator

Standard care/individualized referrals

干预措施: Standard care (Behavioral)

结局指标

主要结局

Determine the efficacy of a motivational enhancement intervention

时间窗: 15 months

The primary objective is to determine the efficacy of a motivational enhancement intervention in reducing health risk behaviors (drug and alcohol use, sexual risk behavior, poor adherence to medications) among HIV+ youth.

次要结局

  • Determine secondary intervention effects(15 months)
  • Determine the mediators and moderators of the intervention(15 months)
  • Determine if intervention effects are maintained(15 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (12)

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