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Enhancing Uptake of Needle and Syringe Programs in Canadian Federal Prisons

Enhancing Uptake of Needle and Syringe Programs in Canadian Federal Prisons

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07122219
Enrollment
548
Registered
2025-08-14
Start date
2024-10-01
Completion date
2029-09-30
Last updated
2025-12-29

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

Conditions

Hepatitis C Virus (HCV), HIV

Keywords

Needle-Exchange Programs, Prisons, Health Services for Prisoners, Blood-Borne Pathogens, HIV, Hepatitis C

Brief summary

This study is focused on improving the implementation of Prison Needle Exchange Programs (PNEPs) in Canadian federal prisons, with the goal of increasing the uptake of these programs among people who inject drugs in prison. The study is being conducted in nine federal prisons, including five women's prisons, where a higher proportion of incarcerated individuals report a history of injection drug use. This study aims to improve PNEP adoption and sustainability by identifying barriers and facilitators and implementing evidence-based strategies to enhance program engagement.

Detailed description

Using a step-wedge design, we will conduct a Type 2 hybrid implementation trial to assess the extent to which PNEP uptake is improved over 24 months of observation using the Network for the Improvement of Addiction Treatment (NIATx) implementation strategy bundle. Nine prisons were non-randomly\* allocated to one of three groups, with the groups receiving the intervention (i.e., NIATx) over 24 months at staggered time intervals (every 6 months). This will be followed by an additional 12 month post-intervention period, when sustainability will be assessed. \*Originally randomized; allocation was modified due to logistical constraints

Interventions

BEHAVIORALNIATx

The Network for the Improvement of Addiction Treatment (NIATx) model uses a bundle of implementation tools that include expert facilitation (coaching) and quality process improvement specifically for behavioural healthcare settings to improve access and retention in treatment.

Sponsors

Yale University
CollaboratorOTHER
Burnet Institute
CollaboratorOTHER
Kirby Institute
CollaboratorOTHER_GOV
McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Hybrid type 2 stepped-wedge implementation trial. All sites will receive the intervention (NIATx); the order in which they receive the intervention was non-randomized\*. \*Originally randomized; allocation was modified due to logistical constraints

Eligibility

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

Inclusion criteria

* All people incarcerated at a study site during the intervention period

Exclusion criteria

\- None (site level intervention)

Design outcomes

Primary

MeasureTime frameDescription
EffectivenessFrom start to end of intervention period (24 months)Number of participants on the PNEP

Secondary

MeasureTime frameDescription
Bloodborne virus cascade of careFrom start to end of intervention period (24 months)Number of HIV and hepatitis C virus screenings/tests, diagnoses, and treatment initiations, among the total prison population
Enrollment in opioid agonist therapyFrom start to end of intervention period (24 months)The number of people who inject drugs who access opioid agonist therapy among the total prison population

Countries

Canada

Contacts

Primary ContactNadine Kronfli
nadine.kronfli@mcgill.ca514-934-1934

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026