A Stage 2 Cognitive-behavioral Trial: Reduce Alcohol First in Kenya Intervention (RAFIKI)
Primary Purpose
Hazardous Drinking, Binge Drinking, HIV-infected
Status
Completed
Phase
Phase 1
Locations
Kenya
Study Type
Interventional
Intervention
cognitive behavioral group therapy
health education group
Sponsored by

About this trial
This is an interventional treatment trial for Hazardous Drinking focused on measuring CBT, alcohol, HIV, Kenya, paraprofessional
Eligibility Criteria
Inclusion Criteria:
- minimum age 18
- HIV infected outpatient enrolled in 1 of 5 AMPATH clinics
- drank alcohol in past month
- hazardous or binge drinker (AUDIT-C)
- lives within an hour of Eldoret HIV clinic
- verbal working knowledge of Kiswahili
Exclusion Criteria:
- active psychosis, suicidality or severe cognitive impairment
- physically unable to attend session
- previous participation in CBT study
Sites / Locations
- Moi University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
cognitive behavioral group therapy
health education group
Arm Description
Outcomes
Primary Outcome Measures
Timeline Followback alcohol use (percent drinking days)
The Timeline Followback is a well-established, reliable and valid retrospective calendar-based measure employing memory cues to assess alcohol use. The primary hypothesis is that CBT will be more effective than HL in reducing alcohol use (percent drinking days) from baseline (past 30 days) through the 6-week active treatment phase. The secondary hypothesis is that CBT will be more effective than HL in reducing alcohol use (percent drinking days) from baseline through the 9-month post-intervention follow-up. Results will be analyzed in a longitudinal model.
Secondary Outcome Measures
Full Information
NCT ID
NCT01503255
First Posted
December 16, 2011
Last Updated
July 13, 2017
Sponsor
Brown University
Collaborators
Moi University, Syracuse University, Indiana University, Yale University
1. Study Identification
Unique Protocol Identification Number
NCT01503255
Brief Title
A Stage 2 Cognitive-behavioral Trial: Reduce Alcohol First in Kenya Intervention
Acronym
RAFIKI
Official Title
A Stage 2 Cognitive-behavioral Trial: Reduce Alcohol First in Kenya Intervention
Study Type
Interventional
2. Study Status
Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
July 2012 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brown University
Collaborators
Moi University, Syracuse University, Indiana University, Yale University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will determine whether a group cognitive-behavioral therapy intervention that demonstrates preliminary evidence of reducing alcohol use among HIV-infected outpatients in western Kenya is effective when compared against a group health education intervention in a large sample over a longer period of time. It will be delivered by paraprofessionals, individuals with limited formal education and little or no relevant professional experience. This approach is consistent with successful cost-effective models of service delivery in resource-limited settings in which paraprofessionals (e.g., clinical officers, traditional birth attendants and peer counselors) are trained.
Detailed Description
Hazardous and binge drinking have been associated with increased risky sexual behavior, poor adherence to antiretroviral therapy (ARVs) and toxicity from ARVs among those with HIV infection. As such, hazardous and binge drinking (score of e3 on the Alcohol Use Disorders Test - Consumption (AUDIT-C), or e6 drinks per occasion at least monthly) have a major impact on HIV transmission and disease progression. Prevalence rates of hazardous drinking are particularly high among HIV (53%) and general medicine (68%) outpatients in western Kenya, in part due to the wide availability of potent traditional brew. Growing evidence suggests that heavy drinking is an obstacle to successful sexual risk reduction approaches. This team recently completed a Stage 1 trial of a group cognitive-behavioral therapy (CBT) intervention delivered by paraprofessionals to reduce alcohol use among 74 HIV-infected Kenyans (R21AA017884). Results demonstrated feasibility, acceptability and estimated a large treatment effect at post-treatment. Investigators now propose a large Stage 2 efficacy trial of the CBT alcohol intervention. The goal is to evaluate the efficacy of the Reduce Alcohol First in Kenya Intervention (RAFIKI) in its ability to reduce alcohol use within a larger Stage 2 trial that includes an active control and a longer follow-up period. Rafiki means friend in Kiswahili, the national language of Kenya. The trial will be conducted by the Kenya Health Behavior Study (KHBS) team, an experienced group of Kenyan and U.S. behavioral scientists, physicians, substance users in recovery and persons infected with HIV. KHBS expands on well-established ties between the Academic Model for Providing Access to Healthcare (AMPATH) and the Brown University Medical School, which has been an active AMPATH partner since 1997. AMPATH currently treats more than 75,000 HIV-infected patients in 25 clinics in western Kenya. As part of these efforts, investigators have ready locally adapted training, treatment and fidelity rating manuals, a successful paraprofessional intervention delivery model, clinical assessment tools, and an experienced local team of trainers and supervisors. The specific aims are to: 1) To examine the efficacy of a same-sex group CBT intervention in a randomized clinical trial of 336 HIV-infected Kenyan outpatients who report hazardous or binge drinking, when compared to a time-matched group Healthy Lifestyles education intervention; 2) To conduct analyses to examine the mechanisms of intervention effects; and 3) To conduct exploratory analyses to examine the relationship between intervention condition and sexual risk behaviors. Completion of these objectives, which are consistent with NIAAA's mission to reduce both alcohol use and HIV risk in vulnerable populations, will provide a robust test of efficacy of the paraprofessionally led group CBT and potentially provide a sustainable and transportable intervention for other settings in sub-Saharan Africa.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hazardous Drinking, Binge Drinking, HIV-infected
Keywords
CBT, alcohol, HIV, Kenya, paraprofessional
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
614 (Actual)
8. Arms, Groups, and Interventions
Arm Title
cognitive behavioral group therapy
Arm Type
Experimental
Arm Title
health education group
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
cognitive behavioral group therapy
Intervention Description
6 weekly 90-minute group sessions
Intervention Type
Behavioral
Intervention Name(s)
health education group
Intervention Description
6 weekly 90-minute group sessions
Primary Outcome Measure Information:
Title
Timeline Followback alcohol use (percent drinking days)
Description
The Timeline Followback is a well-established, reliable and valid retrospective calendar-based measure employing memory cues to assess alcohol use. The primary hypothesis is that CBT will be more effective than HL in reducing alcohol use (percent drinking days) from baseline (past 30 days) through the 6-week active treatment phase. The secondary hypothesis is that CBT will be more effective than HL in reducing alcohol use (percent drinking days) from baseline through the 9-month post-intervention follow-up. Results will be analyzed in a longitudinal model.
Time Frame
longitudinal alcohol use from baseline (past 30 days) to 9 month post-intervention follow up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
minimum age 18
HIV infected outpatient enrolled in 1 of 5 AMPATH clinics
drank alcohol in past month
hazardous or binge drinker (AUDIT-C)
lives within an hour of Eldoret HIV clinic
verbal working knowledge of Kiswahili
Exclusion Criteria:
active psychosis, suicidality or severe cognitive impairment
physically unable to attend session
previous participation in CBT study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rebecca Papas, PhD
Organizational Affiliation
Brown University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Moi University
City
Eldoret
Country
Kenya
12. IPD Sharing Statement
Citations:
PubMed Identifier
28351364
Citation
Galarraga O, Gao B, Gakinya BN, Klein DA, Wamai RG, Sidle JE, Papas RK. Task-shifting alcohol interventions for HIV+ persons in Kenya: a cost-benefit analysis. BMC Health Serv Res. 2017 Mar 28;17(1):239. doi: 10.1186/s12913-017-2169-4.
Results Reference
derived
Learn more about this trial
A Stage 2 Cognitive-behavioral Trial: Reduce Alcohol First in Kenya Intervention
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