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Clinical Trials/NCT01969461
NCT01969461
Unknown
Not Applicable

Comparing the Effectiveness of Two Alcohol+Adherence Interventions for HIV+ Youth

Wayne State University1 site in 1 country400 target enrollmentJuly 2014
ConditionsHIV

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV
Sponsor
Wayne State University
Enrollment
400
Locations
1
Primary Endpoint
Change in Alcohol Use from Baseline to 9 months post intervention
Last Updated
9 years ago

Overview

Brief Summary

Alcohol use among persons with HIV exacerbates health problems and accelerates HIV disease progression. Antiretroviral therapy (ART) is the single most important treatment for people living with HIV. However, ART adherence is suboptimal among adolescents and young adults living with HIV, the age group with the fastest growing rates of HIV infection, and great risk of engaging in risky behaviors such as alcohol use. The proposed study will compare the effectiveness of home-based versus clinic-based "Healthy Choices", a brief, 4- session intervention using Motivational Enhancement Therapy (MET) to address alcohol use, medication adherence, and health outcomes in youth living with HIV (YLH) using a repeated measures design. Unlike previous trials, Healthy Choices will be tested in a "real world" clinical setting and be delivered by community health workers (CHW: already members of the HIV care team). The study population will consist of YLH, ages 16-24, who are current patients at 5 ATN sites. Site staff will recruit potential participants. Youth will be randomized to receive Healthy Choices, either clinic-based or home-based delivered by the same CHW in both conditions. Outcomes are measured at baseline, 4-, 7-, and 13-months. Data collection for biological measures will be through medical record extraction, and self-reported measures will occur using a brief Web-based CASI (computer-administered self-interviewing) survey on an iPad. All intervention sessions will be audio-recorded for MITI fidelity coding, and investigators will support local supervisors during the active intervention phase. We will conduct qualitative interviews with CHWs, supervisors and organization leaders at the end of the trial to obtain information about barriers and facilitators of implementation. Thus, the proposed trial will allow us to use a Type 1 Effectiveness-implementation hybrid design to pilot a sustainable model of MI implementation in real-world youth care settings towards the goals of 1) examining the effectiveness, cost-effectiveness, and scalability of an efficacious behavioral intervention when delivered by CHWs in real-world adolescent HIV care settings; 2) gathering information about who responds under what contexts; and 3) increasing our understanding of the barriers and facilitators for future implementation. The primary hypothesis is that YLH receiving home-based MET will have greater improvements in alcohol use and viral load than YLH receiving clinic-based MET.

Registry
clinicaltrials.gov
Start Date
July 2014
End Date
December 2018
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sylvie Naar-King

Professor

Wayne State University

Eligibility Criteria

Inclusion Criteria

  • HIV-infected
  • Ability to speak and understand English
  • Prescribed antiretroviral therapy
  • Detectable viral load in the last month

Exclusion Criteria

  • Not fluent in English
  • History of sever learning disability, mental retardation, major psychiatric disorders (e.g., schizophrenia, bipolar disorder, major depression with psychotic features, etc).
  • Participation in another adherence intervention trial
  • On ART due to pregnancy

Outcomes

Primary Outcomes

Change in Alcohol Use from Baseline to 9 months post intervention

Time Frame: Baseline, 4-, 7-, and 13-months

We will use multiple methods of assessing use including calendar-based interview, biomarker, and self-report questionnaire.

Change in Viral Load from Baseline to 9 months post intervention

Time Frame: Baseline, 4-, 7-, and 13-months

Viral load will be extracted from medical records, though we have budgeted to collect a percentage of viral loads for youth who drop out of care or transfer to a care setting where records are not available.

Secondary Outcomes

  • Change in Sexual Risk from Baseline to 9 months post intervention(Baseline, 4-, 7-, and 13-months)
  • Change in Medication Adherence from Baseline to 9 months post intervention(Baseline, 4-, 7-, and 13-months)
  • Change in Other Substance Use (not alcohol use) from Baseline to 9 months post intervention(Baseline, 4-, 7-, and 13-months)

Study Sites (1)

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