Substance Use Disorders in HIV People of Cameroon

February 15, 2015 updated by: Jean Joel R. Bigna, Goulfey Health District Unit

Prevalence, Socio-demographic Correlates of Substance Use Disorders Among HIV-infected Adults in Cameroon, and Their Influence on Adherence to Antiretroviral Therapy and Immunological Feature: Study Protocol for a Retrospective Cohort Study

Background:

Data are scarce concerning injecting drug use (IDU) and alcohol consumption among HIV-infected people on highly active antiretroviral treatment (HAART) in Cameroon. The aim of this study is to determine the prevalence of alcohol consumption and IDU among HIV-infected people on HAART; to determine sociodemographic factors associated with alcohol abuse and IDU among people on HAART; and to determine impact of alcohol consumption and IDU on adherence to HAART.

Methods/Design:

The investigators will conduct a cross sectional study at the Yaoundé Central Hospital in Cameroon, from February to August 2015. Using a self-report questionnaire, the investigators will include at least 1,000 HIV-infected adults (18 years or more) on HAART for at least one month coming for HIV care. The investigators will exclude pregnant women. Data collection will include sociodemographic and economic profile, alcohol consumption using Alcohol Use Disorders Identification Test, injecting drug use, adherence to HAART using visual analog scale and self-rate report. The investigators will perform sub-analysis for sex group and area of habitation. A p value < 0.05 will be considered statistically significant.

Discussion:

There is a critical need of accurate estimates of the amplitude and the distribution of IDU and alcohol consumption among HIV-infected adults, in order to inform health policies maker for curbing burden of both injecting drug use and alcohol consumption among people living with HIV.

Study Overview

Status

Unknown

Conditions

Detailed Description

  1. Introduction

    1.1. Background

    In low and middle income countries, 28.6 million people were eligible for antiretroviral therapy (ART) based on 2013 guidelines and only around 10 million were currently on ART. Cameroon is a lower-middle-income country with a prevalence of human immunodeficiency virus (HIV) infection in adults of 4.3% in 2011. In the same year, coverage for antiretroviral therapy in adults and children was 49.6%, demonstrating the immensity of the work to be done to achieve the goals of good ART coverage. The considerable expansion of access to HIV treatment in the world has changed the epidemic of HIV infection. The importance of ART is well established. Life expectancy of adults receiving ART is approximately 80% of the normal life expectancy. The preventive effect of ART is increasingly evident, even in cases where the HIV epidemic is concentrated.

    There exists the link between alcohol consumption and infectious diseases, with the deleterious effect of alcohol on disease progression. In Cameroon, in general population, adult (15+ years) per capita alcohol consumption was 13.74 litters of pure alcohol. Heavy episodic drinking is 8.4% and 2.1% respectively among males and females in Cameroon in general population. Alcohol binge drinking was found in 11.6% of people living with HIV on ART and in 20.6% of those who were interrupted their treatment. Binge drinking was defined for male as consumption of 5 or more drinks, for female as consumption of 4 or more drinks, in about 2 hours. Alcohol use disorders screened with cutting down, annoyance by criticism, guilty feelings, eye-openers (cage) questionnaire are present among 17% of adults HIV-infected in Cameroon.

    In Cameroon, the prevalence of non-adherence to ART was 22.5% based on the Community Programs for Clinical Research on AIDS index and 34.9% based on the Centre for Adherence Support Evaluation index. Alcohol is one of the main factors of ART interruption and ART non-adherence. The consumption of alcohol being on ART decrease response to highly active ART, and decrease health related quality of life.

    In general, health data, including HIV prevalence data, are less robust for key populations than for general populations due to complexities in sampling (and lack of size estimation data), legal concerns and issues of stigma and discrimination. To date, studies on injecting drug user in Cameroon, and even in sub-Sahara Africa are scarce among HIV-infected people. The estimation showed that in 2012 worldwide about 12.7 million people had recently injected drugs and that, of these, 13.1% was living with HIV.

    1.2. Study rationale

    With this demonstrated burden so harmful of alcohol consumption and injecting drug use (IDU) among people living with HIV, it is necessary to measure the weight of alcohol consumption and IDU among HIV-infected adult on HAART; to understand why HIV-infected people consume alcohol and use injecting drug being on HAART in Cameroon, sub-Saharan Africa country; and to assess the impact of alcohol consumption and IDU on adherence to ART.

  2. Study objectives

    The aim of this study is (1) to determine and describe the prevalence of alcohol consumption and IDU among HIV-infected people on HAART; (2) to determine sociodemographic factors associated with alcohol consumption and IDU among people on HAART; (3) and to determine impact of alcohol consumption and IDU on adherence to HAART.

  3. Methods

    3.1. Design

    The investigators will use cross-sectional design. The recruitment of participants will be conducted from January to June 2015. Socio-demographic data, adherence to ART, alcohol consumption will be self-reported by the patients with a questionnaire, but patient will can ask more clarifications if he/she not understood a question. The investigators will follow STROBE guidelines for the report this study.

    3.2. Setting

    Cameroon is a sub-Saharan central Africa country, divided in ten region and with a population of 19,406,100 inhabitants in 2011. The adult prevalence rate of HIV in the country is 4.3%. In Yaoundé, capital of Cameroon, site of recruitment, the adult prevalence rate of HIV infection is 6.4% (3.6% for men and 8.9% for women). Subjects were recruited at Day Hospital in Yaoundé Central Hospital. It is the largest HIV clinic in the country. This is an urban center in the heart of Yaoundé city.

    3.3. Participants

    The investigators will include in this study subjects who are aged 18 years or above and who were on HAART for at least one month. The investigators will exclude pregnant women. Informed consent will be a prerequisite for participating in the study, and will be provided verbally.

    3.4. Data collection

    3.4.1. Sociodemographic profile

    The investigators will collect age, gender, sexual orientation, last level of education, monthly household income, area of habitation, number or person in household, mode of healthcare payment, marital status, employment status, probable route of HIV infection and when, and disclosure of HIV status.

    3.4.2. Alcohol consumption

    The investigators will use the Alcohol Use Disorders Identification Test (AUDIT) to identify subjects with at-risk, hazardous, or harmful drinking. AUDIT has a possible range from 0 to 40. A score ≤ 7 is classified as no current problem (low risk drinking), a score range between 8 - 15 is classified as probable current problem drinking (risky or hazardous drinking), a score range between 16 - 19 is classified as high risk or harmful drinking, and a score ≥ 20 as define harm and likely to be alcohol dependent. The investigators prefer to use self-reported questionnaire vs. interview questionnaire because it may produce more accurate answers, but patients who will not well understand a question, could ask more clarifications. The investigators will therefore use AUDIT screening instrument test to classify current drinkers as problem or non-problem drinkers at cut-off ≥ 8. Sensitivity and specificity of AUDIT is respectively 51%-97% and 78%-96%. The investigators will define as current drinkers, all patients who had consumed alcohol in the last 12 months.

    3.4.3. Adherence to antiretroviral therapy

    The investigators will use several methods to measure adherence to ART: a linear visual analogue scale (VAS) on the past month and self-rate of adherence to ART in the last month using scale from '1 - very good' to '5 - very bad'.

    3.4.4. Injecting drug use

    Patients will report if Yes or No, they have already used an injectable drug. If yes, they will give frequency and last time of use.

    3.5. Statistical analysis

    3.5.1. Sample size

    The sample calculation was based on alcohol consumption, because there is no data for IDU in Cameroon among HIV-infected people. The investigators assume that alcohol abuse among adults HIV-infected is 17%. With a 95% confidence interval (95%CI), acceptable difference of 5%; the minimal required sample size was 217 adult HIV-infected on ART. The investigators have used Windows Program for Epidemiologist (WinPepi, version 11.43) to estimate required sample size. Because the investigators will use self-reported questionnaire, the investigators suppose 20% for missing data. Therefore, the minimal required sample size will 272 for male and 272 for female because alcohol consumption was different between both sex (14). The investigators hope to have a sample of about 1,000 patients to have a high powered study.

    3.5.2. Statistical method

    Data will be coded, entered, and analyzed using the Statistical Package for Social Science version 20.0 for Windows (IBM Corp. Released 2011. IBM SPSS Statistics for Windows, Version 20.0. Armonk, New York: IBM Corp.). The investigators will describe continuous variables using means with standard deviations or using median with interquartile range, and categorical variables using their frequencies and percentages. For all tests, we will use 2-sided p-values with alpha < 0.05 level of significance. The investigators used χ² test or equivalents for categorical variables, Student T test for means, and Mann-Whitney U test for medians. Null hypothesis of no difference was rejected if the 95% CI of odds ratio (OR) estimates excluded 1. All regression analyses will be conducted with stepwise forward method with entry in model if p value ≤ 0.2. Multiple imputation will be used to handle missing data, creating a new data set which was the average of five data sets of imputed values. The investigators will only impute socio-demographic data for regression analysis.

  4. Ethical considerations

    The study will be conducted in accordance with Helsinki Declaration. Prior to enrolment, all eligible participants will provide verbal consent. Patients with alcohol consumption, injecting drug use and/or non-adherence to ART will receive a counseling to address this problem according WHO recommendations.

  5. Discussion

The expansion of the use of ART helped make HIV infection as a chronic disease. One of the major challenges to overcome is the effective use of ARVs to improve the outcome of people living with HIV. Consumption of alcohol and injecting drug by patients on HAART may be obstacles. The scientific evidence is already done for the first for its negative effect on antiretroviral therapy in others people than Africa but very few studies on the IDU are done, particularly in Africa. Even if there are data on alcohol consumption being on antiretroviral therapy exist in Africa, very few studies have a large sample size. More and to the best of our best knowledge, there are almost no studies on the prevalence of injecting drug use among HIV infected people in Africa, particularly in Cameroon.

With this study, the gap in knowledge about injecting drugs and alcohol and their effects on adherence to antiretroviral therapy may be addressed. This will guide future research. This knowledge can also provide to clinicians and policy makers of health, a light on the implementation of guidelines to improve the outcomes of people living with HIV in our context.

One of the limitations that might emerge during the implementation of this study is the presence of missing data, particularly related to data collection of the study by patients themselves. It is nonetheless necessary to use this form of data collection, since we will collect data on adherence to ARV treatment, on alcohol consumption, and on injecting drug use. In general, people tend to underestimate their alcohol consumption and overestimate adherence to treatment when a third party ask them a question about. In addition, the use of drugs is prohibited by law. Some patients may therefore deny its consumption. This is why no name or contact will be asked, no signature or written consent for participation in the study will be required for this study. We will thus use verbal consent.

The final report of this study in the form of scientific paper will be published in peer-reviewed journals. Findings will further be presented at conferences and submitted to relevant health authorities.

Study Type

Observational

Enrollment (Anticipated)

1000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

HIV infected people

Description

Inclusion Criteria:

  • aged 18 years or older
  • being for at least one month on highly active antiretroviral therapy

Exclusion Criteria:

  • pregnant women

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Adherence to antiretroviral therapy
Time Frame: All days up to 180 days
The investigators will measure adherence to antiretroviral therapy using a linear visual analogue scale on the past month as primary method of measure
All days up to 180 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-rate of adherence to antiretroviral therapy
Time Frame: All days up to 180 days
The investigators will measure adherence to antiretroviral therapy using self-rate by following scale: '1 - very good' to '5 - very bad'
All days up to 180 days

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Alcohol consumption
Time Frame: All days up to 180 days
The investigators will use the Alcohol Use Disorders Identification Test (AUDIT) to identify subjects with at-risk, hazardous, or harmful drinking. AUDIT has a possible range from 0 to 40. A score ≤ 7 is classified as no current problem (low risk drinking), a score range between 8 - 15 is classified as probable current problem drinking (risky or hazardous drinking), a score range between 16 - 19 is classified as high risk or harmful drinking, and a score ≥ 20 as define harm and likely to be alcohol dependent. The investigators prefer to use self-reported questionnaire vs. interview questionnaire because it may produce more accurate answers, but patients who will not well understand a question, could ask more clarifications. The investigators will therefore use AUDIT screening instrument test to classify current drinkers as problem or non-problem drinkers at cut-off ≥ 8.
All days up to 180 days
Injecting drug use
Time Frame: All days up to 180 days
Patients will report if Yes or No, they have already used an injectable drug. If yes, they will give frequency and last time of use.
All days up to 180 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Goulfey Health District Unit

Collaborators

NYU Langone Health
Yaounde Central Hospital
University of Yaounde 1
Edea Regional Hospital

Investigators

  • Principal Investigator: Jean Joel R Bigna, MD, Goulfey Health District Unit

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2015

Primary Completion (Anticipated)

December 1, 2015

Study Completion (Anticipated)

December 1, 2015

Study Registration Dates

First Submitted

December 24, 2014

First Submitted That Met QC Criteria

February 4, 2015

First Posted (Estimate)

February 5, 2015

Study Record Updates

Last Update Posted (Estimate)

February 18, 2015

Last Update Submitted That Met QC Criteria

February 15, 2015

Last Verified

February 1, 2015

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ASSIST-HIV

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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