跳至主要内容
临床试验/NCT01751594
NCT01751594已完成不适用

Testing a Secondary Prevention Intervention for HIV-Positive Black Young Men Who Have Sex With Men

University of North Carolina, Chapel Hill5 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2012年4月1日最近更新:
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
92
试验地点
5
主要终点
Finalize and manualize a critical consciousness based intervention for HIV positive B-YMSM

研究概览

简要总结

The proposed research study aims to conduct a culturally-based secondary prevention intervention targeted toward HIV-positive Black young men who have sex with men (B-YMSM) to explore (1) feasibility and acceptability (Trial 1 and Trial 2) and (2) evidence of potential efficacy (Trial 2). The primary outcomes will be health promotion behaviors (i.e., treatment adherence, sexual risk reduction, reduction in substance use behaviors, and HIV status disclosure). Psychosocial factors (i.e. self-esteem, critical consciousness, and socio-political awareness) will be examined as secondary outcomes.

详细描述

First, the protocol team will finalize the development and manualization of Health 4 Life (H4L) a comparison intervention, which will serve as the basis of comparison for Mobilizing Our Voices for Empowerment (MOVE), the treatment intervention. H4L will be a health promotion and life skills intervention to account for time and attention. Following this the protocol team will then implement Trial 1. In this trial, the intervention specialist and a "peer buddy" (intervention co-facilitator) from one AMTU will conduct one wave of both MOVE and H4L. The team will then conduct an analysis of the process data and revise the two interventions (MOVE and H4L). Upon revising the interventions, the protocol team will implement Trial 2. In this trial, the protocol co-chairs and the interventionist from Trial 1 will train interventionists and peer buddies from four new AMTUs; these interventionists and peer buddies will run the revised MOVE and H4L interventions. Each site will be designated as either a treatment or comparison site, and they will conduct two waves of their assigned intervention. The team at that time will conduct data analyses and then modify and manualize the final version of MOVE and H4L.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
16 Years 至 24 Years(Child, Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •To be considered eligible for enrollment into Trial 1 and Trial 2, an individual must meet the criteria listed below:
  • •Receives services at one of the selected AMTU sites or one of their community partners;
  • •Biological male at birth and self identifies as male gender at the time of consent;
  • •Self identifies as "Black" (including Black/African-American, Black Latino, Black/Afro-Caribbean, Black/African immigrant, or any self-identified member of the African Diaspora);
  • •HIV-infected as documented by medical record review or verification with referring medical professional;
  • •Between the ages of 16-24 years, inclusive, at the time of consent;
  • •HIV-infected through sexual behavior;
  • •At least one sexual encounter involving oral or anal sex with a male partner in the past year;
  • •Ability to understand both written and spoken English;
  • •Willingness to participate in a group-based intervention with other HIV-positive B-YMSM and agree to respect the privacy of other group members;
  • •Willingness and ability to attend the first group session on any of the date chosen by the site staff and;
  • •Willingness to provide signed informed consent or assent with parental/legal guardian permission as applicable.
  • •To be considered eligible for enrollment, an individual must not meet any of the criteria listed below.
  • •Active psychiatric condition that in the opinion of the site personnel would interfere with the ability to give true informed consent and to adhere to the study requirements;
  • •Visibly distraught and/or visibly emotionally unstable (i.e., exhibiting suicidal, homicidal, or violent behavior);
  • •Active drug or alcohol use or dependence that, in the opinion of the site personnel, would interfere with the ability to give true informed consent and to adhere to the study requirements;
  • •Acute illness that, in the opinion of the treating clinician, would interfere with the participant's ability to adhere to the protocol requirements and/or interfere with the protocol objectives.
  • •Previous participation in ATN 090, "Development of a Secondary Prevention Intervention Targeting HIV-Positive Black Young Men Who have Sex with Men." (NOTE: YAB members from ATN090 cannot participate in ATN 104)
  • •Previous participation in Trial 1 of ATN104 and;
  • •Current enrollment in any other behavioral intervention study or program. Any cases that are uncertain require Protocol Team approval.

排除标准

  • 未提供

研究组 & 干预措施

H4L Comparison Intervention

Active Comparator

干预措施: H4L Comparison Intervention (Behavioral)

MOVE Intervention

Experimental

干预措施: MOVE Intervention (Behavioral)

结局指标

主要结局

Finalize and manualize a critical consciousness based intervention for HIV positive B-YMSM

时间窗: 2 years

To finalize and manualize Mobilizing Our Voices for Empowerment (MOVE) resulting in an intervention with evidence of potential efficacy in reducing sexual risk and substance use behaviors and promoting treatment adherence and HIV status disclosure, as well as self-esteem, critical consciousness, and socio-political awareness. At the same time a non-critical consciousness intervention Health 4 Life (H4L) which will be used as comparison will also be finalized and manualized. H4L is primarily a health promotion and life skills intervention for HIV-positive B-YMSM.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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