MAKASI Intervention for African and Caribbean Migrants' Empowerment in Sexual Health in Paris Greater Area (MAKASI)

MAKASI. An Intervention for African and Caribbean Migrants' Empowerment in Sexual Health in Order to Reduce Their Social and Health Vulnerabilities in Paris Greater Area

Background. Immigrants from Sub-Saharan Africa are the second group most affected by HIV in France. Part of these HIV infections occurred after arrival in France, in relation to social hardships. Immigrants coming from the non-French Caribbean islands face similar difficulties. Many actors strive for an easier access to healthcare services for immigrants; however the mere supply of knowledge and medicalised solutions is not enough to make persons adopt prevention behaviours. It seems necessary to act upon empowerment to bring resources to individuals and communities in order to improve their autonomy and action capacity. Civil Society Organisations and researchers join forces in the MAKASI interventional research which aims at reinforcing immigrants' empowerment in sexual health in order to reduce their exposure to sexual risks.

Objectives : The MAKASI intervention consists in a unique Empowerment interview based on the principles of motivational interviewing, using an Active Referral system to social or sanitary services relevant to the person's needs. Our hypothesis is that this intervention is going to reinforce four dimensions of empowerment in sexual health among immigrants: the capacity to express their needs, competencies in sexual, self-esteem, awareness of exposure to HIV and STIs. The proposed research aims at measuring the efficacy of the intervention on these four dimensions, and at evaluating its processes and efficiency (cost-efficacy).

Methods: The intervention is delivered within the mobile units of Afrique Avenir in the public spaces where African and Caribbean populations live and work. The evaluation uses integrated mixed-method approach, combining a quantitative evaluation of impact and a qualitative research on processes. The measure of impact will be done by comparing indicators on the four dimensions of empowerment in sexual health and indicators of exposure to sexual risks, between an arm where the intervention is immediate and an arm where the intervention is differed by 3 months (control arm). The qualitative evaluation of the intervention processes will be based upon an ethnographic approach of the intervention and the participants' experience.

Perspectives: This project will demonstrate the efficacy and the efficiency of an innovative intervention aiming at reducing Sub-Saharan and Caribbean immigrants' exposure to risks in sexual health.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Migrants from Sub-Saharan Africa are the second group most affected by HIV epidemic in France. Previous study established that part of HIV infections among Sub-Saharan migrants occurred after arrival in France, and that the exposure to sexual risks was linked both to social hardships and structural difficulties experienced during the settlement period in France. Many actors strive for an easier access to healthcare services for migrants, however the mere supply of knowledge and medicalised solutions is not enough to make persons adopt protection or healthcare practices. It seems necessary to work for the individual and community empowerment in order to bring resources to individuals and communities so they can more easily take action in the new and complex context of a host country.

To improve the prevention of sexual risks in this population coming from Sub-Saharan Africa, local charities and researchers join forces in order to propose an interventional research which aims at enabling Sub-Saharan migrants to appropriate prevention and healthcare means, especially in the area of sexual health, to reinforce their autonomy, their capacity and power to take action and to protect their health against the disruption caused by migration and the difficulty in accessing rights and fundamental needs.

The pilot phase of this research has made it possible to build an empowerment intervention which consists of a single individual interview based on the principles of motivational maintenance, articulated with an active orientation towards adequate social or health services, possibly accompanied when necessary. Our hypothesis is that this intervention will strengthen four dimensions of empowerment in sexual health among immigrants:

  • Ability to express needs: Ability to talk about sexuality or sexual health to peers or professionals
  • sexual health skills: know the different tools of combined prevention, know where to go for screening, gynaecology or sexual health consultation
  • self-esteem: knowing your rights, having the material means (housing, administrative situation, financial resources) to refuse a situation of sexual constraint and avoid being exposed to violence, feeling that you can act on your own situation (sense of personal effectiveness)
  • awareness of HIV exposure and its determinants: being informed about the epidemiology of HIV, the fact that it is possible to be infected in France, and risk factors

Objectives

To strengthen the sexual health empowerment of immigrants from sub-Saharan Africa and the Caribbean, we propose to act on the four dimensions of sexual empowerment with the following specific objectives:

Ability to express needs:

  • Speaking up
  • Reduce social isolation

Sexual Health Skills:

  • Improve knowledge of health and social resources
  • Improve access to screening
  • Improve access to sexual health services (Contraception, condoms, Prep)
  • Improve ownership of combined prevention

Self-esteem:

  • Improve people's autonomy in social processes (housing, paper)
  • Improving Mental Health: Reducing Psychological Distress and Suffering
  • Improve personal efficiency

Awareness of HIV and STI exposure

• Improve perception of HIV and STI exposure, effectiveness of antiretroviral treatment and preventive strategies.

The research aims to measure the effectiveness of the intervention against all of these indicators, as well as to conduct an evaluation of the processes and efficiency (cost-effectiveness).

Methods:

The intervention is part of the action already carried out by the mobile team of Afrique Avenir, which offers in strategic places of passage (markets, squares, RER stations, etc.) an awareness of sexual health through cultural mediation and a TROD offer. The MAKASI intervention involves identifying immigrants in precarious situations and exposed to HIV in these awareness-raising places, offering them a personalized interview with a health mediator to help them prioritize their needs, and guide them through the health and welfare system.

To assess this complex intervention, we will use an integrated mixed-method approach. A quantitative impact assessment and a qualitative assessment of the processes will be conducted in parallel to establish, by integrating these data, the causal attribution of the effects of the intervention.

Quantitative assessment of impact:

To measure the impact of the intervention, we propose a two-arm diagram: an intervention arm and a control arm. However, for ethical reasons, in order to offer help to all identified people with social or health needs, we will compare an arm where the intervention is immediate, and an arm where it is delayed by 3 months (control arm). The comparison of what happens in the first three months will measure the short-term effect of the intervention, and establish a causal link between the intervention and the observed changes. All people, in both arms, will be followed six months to observe the evolution of the indicators in the medium term. The impact assessment of the intervention will be made possible both by comparison between the immediate intervention arm and the control arms in the first three months, and by comparison before/after the intervention in both arms). Individuals will be randomly allocated to the immediate or delayed intervention arm after an initial interview to identify social and health needs. The goal is to include 1200 people (600 in each arm).

Qualitative assessment of processes and effects:

The qualitative analysis of the processes aims to highlight and analyse the successes, failures and limitations of the intervention, with particular regard to the implementation and its effects. It will also be necessary to produce knowledge on the conditions of reproduction or the extension of the intervention. This analysis will be based on an ethnographic approach to the intervention and the participants' journey, with a work of observation of the different stages and in-depth and repeated semi-directive interviews.

Cost collection will measure the efficiency of the response.

Expected results :

This project will demonstrate the effectiveness and efficiency of an innovative intervention to reduce exposure to sexual health risks among immigrants from sub-Saharan Africa and the Caribbean, and will highlight the conditions of its reproduction or extension. It is closely linked to the initiative towards Paris without AIDS, which develops the collective dimensions of empowerment through different approaches in the communities concerned.

Study Type

Interventional

Enrollment (Anticipated)

1200

Phase

  • Not Applicable

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

      • Paris, France, 75003
        • Recruiting
        • Afrique Avenir Mobile Unit
        • Contact:
          • Romain Mbiribindi

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

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Be aged at least 18
  • HIV negative
  • Born in sub-Saharan Africa or the non-French Carribean
  • At least one of the eight vulnerability criteria: no stable house, no job, food deprivation, no papers, feeling isolated, not knowing where to go to to the doctor, no health insurance, experiencing violence

Exclusion Criteria:

  • Does not speak French or English
  • Persons whose rapid HIV or HCV test is reactive
  • Persons who are not able to give an informed consent: bad mental health, persons who are on drugs

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

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: IMMEDIATE
People who are included in the Immediate Arm receive the Makasi intervention right away or in a six-week time if they are not available on the spot

The Makasi intervention consists in a unique Empowerment interview, based on motivational interviewing techniques. Is is made of three components:

  • Listening and building trust
  • Active referral to structures that answers sanitary and social needs
  • Sexual Health Prevention

Materials used are: referral letters, bilingual health guides, adapted maps of the the neighborhoods with useful addresses.

The Makasi intervention is proposed and delivered in an outreach setting: health mediators propose information on general health and rapid HIV and HCV testing. They screen the people attending and propose Makasi to eligible persons.

OTHER: DIFFERED
People who are included in the Differed Arm receive the Makasi intervention three months after inclusion

The Makasi intervention consists in a unique Empowerment interview, based on motivational interviewing techniques. Is is made of three components:

  • Listening and building trust
  • Active referral to structures that answers sanitary and social needs
  • Sexual Health Prevention

Materials used are: referral letters, bilingual health guides, adapted maps of the the neighborhoods with useful addresses.

The Makasi intervention is proposed and delivered in an outreach setting: health mediators propose information on general health and rapid HIV and HCV testing. They screen the people attending and propose Makasi to eligible persons.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of unprotected sex
Time Frame: 0, 3 months, 6 months after inclusion
Declare unprotected sex at least once during the last three months (percent)
0, 3 months, 6 months after inclusion
Change of transactional sex
Time Frame: 0, 3 months, 6 months after inclusion
Declare Transactional sex at least once during the last three months (percent)
0, 3 months, 6 months after inclusion
Change of Forced sex
Time Frame: 0, 3 months, 6 months after inclusion
Declare having forced to have sex at least once during the last three months (percent)
0, 3 months, 6 months after inclusion

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Empowerment - Social Isolation
Time Frame: 0, 3 months, 6 months after inclusion
Feeling to be alone (percent)
0, 3 months, 6 months after inclusion
Empowerment - Ability to talk
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - Perception of ability to talk about one's situation with a professional (percent)
0, 3 months, 6 months after inclusion
Empowerment - Health insurance
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - having a health insurance (percent)
0, 3 months, 6 months after inclusion
Empowerment - HIV test
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - Has been HIV tested
0, 3 months, 6 months after inclusion
Empowerment - TASP knowledge
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - Knowledge that HIV treatment prevents from transmitting HIV
0, 3 months, 6 months after inclusion
Empowerment - mental health score
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - PHQ 9 (Patient Health Questionnaire in 9 items) score : from 0 (good mental health) to 9 (very bad mental health)
0, 3 months, 6 months after inclusion
Empowerment - self-efficacy
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - feeling of control over the decisions that affect its life (percent)
0, 3 months, 6 months after inclusion
Empowerment - HIV risk awareness
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - knowing that the risk of being HIV infected concerns everyone (percent)
0, 3 months, 6 months after inclusion
Empowerment - access to healthcare structure
Time Frame: 0, 3 months, 6 months after inclusion
Empowerment - having had access to a health structure when needed, in the last 3 months (percent)
0, 3 months, 6 months after inclusion

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Annabel Desgrées du Loû, PhD, French Institute for Sustainable Developement (IRD)

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.

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 (ACTUAL)

February 1, 2019

Primary Completion (ANTICIPATED)

January 31, 2021

Study Completion (ANTICIPATED)

January 31, 2021

Study Registration Dates

First Submitted

June 26, 2020

First Submitted That Met QC Criteria

July 8, 2020

First Posted (ACTUAL)

July 13, 2020

Study Record Updates

Last Update Posted (ACTUAL)

July 13, 2020

Last Update Submitted That Met QC Criteria

July 8, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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