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Research and Evaluation of Link-Up, DCR in Brussels

Research and Evaluation of Link-Up, Drug Consumption Room in Brussels

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07452926
Enrollment
250
Registered
2026-03-05
Start date
2026-03-01
Completion date
2026-09-01
Last updated
2026-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance Use (Drugs, Alcohol)

Brief summary

Link-Up is the second Safer Consumption Room (SCMR) to open in the Brussels-Capital Region. SCMRs are public health facilities designed for people who use drugs mainly in public places. They are hygienically safe spaces where users can safely consume the products they have acquired elsewhere without moral judgment, under the supervision of specially trained professional staff. It is a risk reduction facility. Before Link-Up, two other SCMRs were opened in Belgium, including one, GATE, in the Brussels region. These first two SCMRs are currently undergoing scientific evaluation as part of the REVE-DROOM project (approved by the CEHF (2024/28MAI/276, on 06/18/2024) of the "Drugs" research program funded by BELSPO (Federal Science Policy). The present project aims to replicate the study of the effects associated with the use of SCMRs on users, as implemented in the evaluation system currently underway at GATE in the new SCMR, Link-Up, with a view to also evaluating its effects. The RELINK study is being conducted at the request of Iriscare, the bicommunal social protection OIP (Public Interests Organization) of the Brussels-Capital Region. It is a study based on a natural experiment (i.e., all Link-Up users who agree to participate in the study will be included) and measures various indicators concerning them. The measured indicators primarily concern risky consumption practices (injection, consumption in public spaces, reuse and/or sharing of consumption equipment, and other practices that endanger the health of people who use drugs). As secondary effects, the measures concern the sociodemographic and socioeconomic characteristics of the user population, drug-use profiles, level of social integration, quality of life, level of personal recovery, and care needs. The analysis of these various indicators will make it possible to describe the profile of Link-up SCS users and to compare it with that of GATE users. In addition, the study design allows for an extension to conduct a cohort follow-up and, therefore, to measure changes associated with the use of the SCS service. The current study aims for a sample of at least 250 people recruited within the service. Indicator measurement is carried out using a questionnaire administered with the assistance of the research team and supported by SCS staff. The questionnaire consists of various scales validated in the scientific literature and already used in the REVE-DROOM study. Given the similarity of the proposed Link-Up system with the one implemented at GATE, the results of the two Brussels SCSs will be the subject of a comparative analysis.

Interventions

OTHERSelf-reported questionnaire to monitor the consumption behaviors and sociodemographic characteristics

Participants will complete a unique questionnaire covering different aspects: * risky consumption practices: injection, consumption in public spaces, reuse and/or sharing of consumption equipment, and other practices that endanger the health of people who use drugs * sociodemographic and socioeconomic characteristics * drug-use profiles * level of social integration * quality of life * level of personal recovery * care needs

Sponsors

Université Catholique de Louvain
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* user of the DCR Link-Up in Bruxelles * agree to participate * sufficient command of either French or Dutch

Exclusion criteria

* Refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Risky consumption behavioursThroughout the entire study, during approximately 6 monthsThe questionnaire concerns different aspects of consumption behaviors (consumption mode, in public spaces, reuse and/or sharing of consumption equipment,...) and also sociodemographic and socioeconomic characteristics of the user population, level of social integration, quality of life, level of personal recovery, and care needs

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026