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临床试验/NCT03057119
NCT03057119已完成不适用

Feasibility of Screening, Brief Intervention, Referral to Treatment With Peer Navigation (SBIRT-PN) for Underserved HIV+ Adults 50+ in Primary Care Settings.

Florida State University6 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2018年2月12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
86
试验地点
6
主要终点
Number of Participants Ranking Intervention as Acceptable

研究概览

简要总结

Substance misuse is a common problem among HIV+ individuals. Research suggests that a Screening, Brief Intervention, and Treatment (SBIRT) model can be effective in reducing substance misuse in the general older adult population; however these findings have not been verified in the more vulnerable HIV+ older adult population. The present study seeks to address the problem of substance misuse in older HIV+ adults by piloting a SBIRT model for older HIV+ adults in a in a primary care setting. Individual reductions in alcohol and drug use can have significant effects on public health and safety when observed over a large population at risk for substance use problems. With wider dissemination statewide, a relatively low-cost intervention such as SBIRT could offer demonstrated benefits in this population.

详细描述

The current project will pilot SBIRT with a peer navigator (SBIRT-PN) versus treatment at usual (TAU) to increase substance use treatment engagement among HIV-positive adults aged 50 years and older. The investigators will recruit patients from the Southern HIV and Alcohol Research Consortium (SHARC) HIV primary care clinic network.

In order to develop effective substance use intervention models for HIV care settings the specific aims of the current project are:

Aim1: Examine the feasibility of the SBIRT-PN model at the UF Health Infectious Disease-Medical Specialties Clinic. The investigators hypothesize that the SBIRT-PN model will demonstrate high feasibility within the UF Health Infectious Disease - Medical Specialties Clinic.

Aim2a: Assess the acceptability of SBIRT-PN. The investigators hypothesize that SBIRT-PN will demonstrate high acceptability among patients enrolled in this condition.

Aim2b: Assess the acceptability of SBIRT-PN among HIV-positive individuals by age cohort (younger vs older). The investigators hypothesize that SBIRT-PN will demonstrate higher acceptability among older HIV-positive patients enrolled in this condition.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Receiving care at an Infectious disease Medical Clinic
  • HIV-positive (seropositive confirmed by medical records)
  • have a substance misuse screening score indicating moderate or high risk.

排除标准

  • lack fluency in English
  • are unwilling to provide information for follow-up
  • plan to leave the area within 6 months
  • already have a referral to treatment from another provider
  • unable to provide informed consent due to cognitive impairment.

结局指标

主要结局

Number of Participants Ranking Intervention as Acceptable

时间窗: 30 Days

To examine ratings of acceptability, the investigators will use the overall acceptability score and percentage of acceptability. Overall acceptability will be assessed by summing ratings from the 10-item questionnaire to provide a total intervention acceptability score for the intervention, such that acceptability scores for the intervention could range from 10 (low acceptability) to 50 (high acceptability). The intervention will be considered to have acceptability if 80% of the participants rank the intervention as acceptable (i.e., 4 or higher) on 80% or more of the scale items. The investigators will then examine each question of the Acceptability Questionnaire separately to determine strengths and weaknesses of the intervention.

次要结局

  • Number of Participants Who Used Different Types of Substances (Self-Reported)(6 Months)
  • Number of Participants Who Obtained Formal Substance Use Treatment(6 Months)
  • Number of Participants Who Used Different Types of Substances (Biologically Confirmed Via Urinalysis)(6 Months)

研究者

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

Nicole Ennis

Associate Professor

Florida State University

研究点 (6)

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