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Behavioral Interventions to Reduce Heavy Drinking Among MSM in HIV Primary Care

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Brown University

Status

Completed

Conditions

HIV
Alcohol Drinking

Treatments

Behavioral: Brief Advice
Behavioral: Interactive text messaging
Behavioral: Motivational intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02709759
P01AA01907

Details and patient eligibility

About

The purpose of the present study is to conduct a fully-crossed 2 X 2 X 2 factorial randomized controlled trial with a diverse sample of 224 MSM recruited from 2 urban HIV primary care clinics (one in the Northeast and one in the South). The first study factor will compare brief advice (BA) vs. a motivational intervention (MI) that contains detailed personalized normative and HIV-specific feedback. The second factor compares an interactive text messaging (ITM) intervention vs. no text messaging. The final factor compares intervention of low intensity and duration (two sessions over 1 month) to extended intervention (EI) entailing 5 sessions over 9 months.

Full description

Heavy drinking in HIV-infected patients can lead to low antiretroviral therapy adherence and poor virologic control, greater sexual risk taking, increased risk of liver disease, and decreased cognitive function. Therefore, reductions in drinking may have particularly positive and widespread effects in HIV-infected patients. Men who have sex with men (MSM) continue to represent the majority of new HIV infections, and HIV-infected MSM have rates of hazardous drinking as high as 33%. Therefore, developing and testing interventions to reduce heavy drinking in HIV-infected MSM is a very high public health priority. There have been relatively few alcohol interventions tested that focus on MSM, and only two have addressed drinking in HIV-infected MSM. Although recent studies indicate that behavioral interventions can reduce heavy drinking in HIV-infected patients, much remains unknown about the efficacy of different approaches to behavioral intervention and their unique and combined effects. The purpose of the present study is to conduct a fully-crossed 2 X 2 X 2 factorial randomized controlled trial with a diverse sample of 224 MSM recruited from 2 urban HIV primary care clinics (one in the Northeast and one in the South). The first study factor will compare brief advice (BA) vs. a motivational intervention (MI) that contains detailed personalized normative and HIV-specific feedback. The second factor compares an interactive text messaging (ITM) intervention vs. no text messaging. The final factor compares intervention of low intensity and duration (two sessions over 1 month) to extended intervention (EI) entailing 5 sessions over 9 months. BA and MI will be delivered by a core set of interventionists from a central location using a webcam-enabled telemedicine system, which can facilitate larger-scale implementation. The design will allow us to test the hypothesis that MI compared to BA, ITM compared to no ITM, and EI compared to no EI, will result in significantly greater reductions in number of alcoholic drinks consumed and number of heavy drinking days at 6- and 12-month follow-ups. Secondary outcomes include engagement in unprotected anal intercourse, ART adherence and viral suppression, CD4 cell count, liver function tests, and neurocognitive function. We also will test the hypothesis that the effects of MI, ITM, and EI on drinking will be moderated by alcohol use disorder status and readiness to change drinking such that these interventions will be relatively more efficacious in those with a current disorder and those with low readiness. The study will provide crucial evidence regarding which intervention approaches, alone or in combination, are likely to be most efficient to implement on a large scale in HIV care settings.

Enrollment

210 patients

Sex

Male

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • be at least 18 years of age
  • drink heavily at least once per month on average (≥5 drinks) or drink have drunk more than 14 drinks per week over the past 3 months
  • have a confirmed diagnosis of HIV
  • be a biological male who identifies as male
  • report having had sex (oral or anal) with a male partner in the past 12 months and/or, identify as gay or bisexual.
  • For those on ART, they must be stabilized on their current regimen for at least 3 months prior to study enrollment.

Exclusion criteria

  • report past 3 month intravenous drug use
  • are currently psychotic, suicidal, or manic
  • being treated or have been treated in the past 3 months for an HIV-related opportunistic infection
  • currently receiving treatment for an alcohol or drug problem.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

210 participants in 8 patient groups

MI
Active Comparator group
Description:
Motivational interviewing focused on reducing alcohol use, delivered by videoconferencing.
Treatment:
Behavioral: Motivational intervention
BA
Active Comparator group
Description:
Brief Advice to reduce drinking delivered by videoconferencing
Treatment:
Behavioral: Brief Advice
MI + ITM
Active Comparator group
Description:
Motivational intervention to reduce drinking, delivered by videoconferencing, plus Interactive text messaging around alcohol use
Treatment:
Behavioral: Motivational intervention
Behavioral: Interactive text messaging
BA + ITM
Active Comparator group
Description:
Brief Advice to reduce drinking, delivered by videoconferencing, plus Interactive text messaging around alcohol use
Treatment:
Behavioral: Interactive text messaging
Behavioral: Brief Advice
MI + ITM + EI
Active Comparator group
Description:
Participants in this arm receive MI delivered by videoconferencing and ITM over 9 months rather than 1
Treatment:
Behavioral: Motivational intervention
Behavioral: Interactive text messaging
BA + ITM + EI
Active Comparator group
Description:
Participants in this arm receive BA delivered by videoconferencing and ITM over 9 months rather than 1
Treatment:
Behavioral: Interactive text messaging
Behavioral: Brief Advice
BA + EI
Active Comparator group
Description:
Participants in this arm receive BA delivered by videoconferencing over 9 months rather than 1
Treatment:
Behavioral: Interactive text messaging
Behavioral: Brief Advice
MI + EI
Active Comparator group
Description:
Participants in this arm receive MI delivered by videoconferencing over 9 months rather than 1
Treatment:
Behavioral: Motivational intervention
Behavioral: Interactive text messaging

Trial documents
1

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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