- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05942937
National Prisons Hepatitis Education Project: Research Evaluation (HepPEd)
The National Prisons Hepatitis Education Program (HepPEd Program) is a national, prison-based hepatitis C health literacy education program for healthcare providers, correctional officers, and people in prison. The HepPEd Program aims to improve the public health literacy of the prison sector regarding hepatitis C in prisons.
The HepPEd: Research Evaluation aims to evaluate the impact of the HepPEd Program on HCV testing and treatment uptake amongst people incarcerated in Australian prisons, as well as changes in knowledge, attitudes, and capabilities of healthcare providers, correctional officers, and people in prison. The study is a controlled before and after study being conducted in 3-6 correctional centres in Australia.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The National Prisons Hepatitis Education Program (HepPEd Program) is a national, prison-based hepatitis C health literacy education program for healthcare providers, correctional officers, and people in prison.
The broad goal of HepPEd: Research Evaluation is to measure the impact of a prison-specific hepatitis C (HCV) education program (the HepPEd Program) on enhancing HCV testing and treatment rates in Australian prisons. The HepPEd Program aims to improve HCV testing and treatment rates by enhancing the public health literacy of the prison sector regarding HCV in the prisons (that is the knowledge, attitudes and behaviours), and specifically targets the three key audience groups from the prison setting: healthcare providers, correctional officers, and people in prison.
The study will be conducted as a prison-level, controlled before-and-after trial with a primary objective of evaluating the impact of the HepPEd Program on HCV treatment uptake amongst people incarcerated in Australian prisons. Three to six Australian correctional centres will be selected to participate in the 9-month study. Each correctional centre will have a 3-month period of pre-intervention surveillance, involving monthly observation of HCV treatment uptake under existing operations. This will be followed by a three-month period of education delivery of the HepPEd Program (the 'education intervention'). The monthly surveillance data collection will continue during the intervention period. Finally, each correctional centre will have another 3-month period of post-intervention surveillance, again involving monthly surveillance of HCV treatment rates. Surveys will be conducted with members from each target audience group before and after the education intervention and dried blood spot testing will be conducted with members from the people in prison group to assess baseline HCV prevalence before the education intervention.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Andrew Lloyd
- Phone Number: 02 9385 2534
- Email: a.lloyd@unsw.edu.au
Study Contact Backup
- Name: Yumi Sheehan
- Phone Number: 02 9385 0375
- Email: ysheehan@kirby.unsw.edu.au
Study Locations
-
-
Queensland
-
Rockhampton, Queensland, Australia, 4702
- Recruiting
- Capricornia Correctional Centre
-
Contact:
- Tahnee Gardiner
-
-
Tasmania
-
Hobart, Tasmania, Australia, 7016
- Recruiting
- Risdon Prison Complex
-
Contact:
- Deb Siddall
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
All healthcare providers, correctional officers, and people in prison at the participating prison sites are anticipated to be exposed to the various HepPEd Program resources during the 3 month education intervention phase.
Participating prison sites must meet the following inclusion criteria to be eligible to participate in the study. Participating prison sites must have:
- a prisoner population of 400-600 inmates (assumed mean 500); and
- an existing prison-based hepatitis service undertaking both HCV testing and treatment.
Prisoners must meet the following inclusion criteria to be eligible to participate as peer educators. Prisoners must:
- be currently incarcerated in a participating correctional centre;
- anticipate being in the participating correctional centre for >12 months;
- be considered as capable and willing, and well-respected amongst their peers; and
- have approval from custodial authorities to participate as a peer educator.
Correctional officers must meet the following inclusion criteria to be eligible to participate as peer champions. Correctional officers must:
- be currently working in a participating correctional centre; and
- be considered as capable and willing, and well-respected amongst their peers.
Prisoners must meet the following inclusion criteria to be eligible to participate in the interview-style survey and dried blood spot (DBS) testing component:
- be over the age of 18 years;
- be currently incarcerated in a participating correctional centre;
- have sufficient English comprehension skills to understand the survey questions; and
- be willing and able to provide written informed consent.
Healthcare providers and correctional officers must meet the following inclusion criteria to be eligible to participate in the survey component:
1) be currently working in a participating correctional centre.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Whole-of-prison education intervention
The HepPEd Program will saturate the entire prison during a 3-month intervention phase.
|
All healthcare providers, correctional officers, and people in prison (HepPEd Program target audience groups) at each participating site are anticipated to be exposed to the HepPEd Program over the course of the three-month education intervention phase. The HepPEd Program involves a suite of multi-modal resources targeting each target audience group and a peer education program (for correctional officer and people in prison groups only). The HepPEd Program resources will be delivered in an informal, mass education-style, as well as in peer to peer format. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The change in the proportion of prisoners treated for HCV before and after the education intervention.
Time Frame: 9 months from baseline
|
This will be measured by calculating the change in HCV treatment rates before and after the education intervention.
|
9 months from baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The proportion of prisoners tested for HCV before and after the education intervention.
Time Frame: 9 months from baseline
|
This will be measured by calculating the change in HCV testing rates before and after the education intervention.
|
9 months from baseline
|
|
The health literacy (knowledge, attitudes, and capabilities) amongst target audience groups (healthcare providers, correctional officers, and people in prison) before and after the education intervention.
Time Frame: 9 months from baseline
|
This will be measured by assessing the change in health literacy before and after the education intervention.
|
9 months from baseline
|
|
The acceptability, utility, and impact of the HepPEd Program.
Time Frame: 9 months from baseline
|
This is measured by surveys, before and after the education intervention.
|
9 months from baseline
|
|
The dose, reach, and fidelity of the HepPEd Program.
Time Frame: 9 months from baseline
|
This is measured by surveys, before and after the education intervention.
|
9 months from baseline
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- VISP2101
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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