Addiction, Hepatitis, HIV/AIDS, Opioid Dependence, Tuberculosis
Conditions
Keywords
prison
Brief summary
The purpose of this study is to conduct empiric studies of tuberculosis (TB) among people in prison with and without a history of opioid dependence. A RCT of latent TB infection prevention strategies among HIV+ and HIV- prisoners with high prevalence of hepatitis C (HCV) using standard 40-week daily isoniazid (40H) vs short-course weekly isoniazid + rifapentine (12HR). Investigators will also use this data, and publicly available data to complete agent-based modeling for comparative and cost-effectiveness of various TB screening and treatment strategies among prisoners.
Detailed description
Screening: All newly admitted prisoners (80-120 new inmates on admission days) undergo a complete assessment, including a brief exam and mandatory rapid HIV test by the prison medical unit. Each prisoner waiting to be evaluated will be invited for participation in TB screening activities (not currently part of standard care). If they verbally assent to wanting to learn more in a group session, their names and ID will be recorded and then invited for informed consent privately, followed by a brief survey, WHO symptom assessment, tuberculin skin testing (TST) with reading after 72 hours, sputum induction on 2 consecutive mornings for AFB smear, TB culture (results back 6-8 weeks using the BACTEC MGIT 960 liquid culture gold standard), and point-of care (POC) Gene Xpert. Each person will have phlebotomy for HBV and HCV Ab, LFTs, and if HIV+, CD4 testing (all of these are POC using Alere™). For those with CD4\<50, they will undergo POC low-cost, urinary TB-LAM lateral flow testing (sensitivity=67%) (Alere™ Determine) to identify disseminated TB. Additional demographic, drug use, and TB risks will also be assessed along with prison data (release date, previous incarcerations, type of offense). Participants will then undergo CXR testing. A TB specialist will review all patients and results, ensuring that patients with suspected TB initiate treatment. All suspected or confirmed cases active TB cases in HIV+ prisoners will have ART initiated after 2 weeks of TB treatment initiation (if CNS TB not suspected) if CD4\<50 and within 8 weeks for all others. Trial: All HIV+ and HIV- prisoners with latent TB infection (LTBI) (TST reaction 10 mm or greater) from screening will be asked to participate in the trial. Enrolled participants will undergo block stratified randomization, stratifying on three factors: a) CD4\<350; b) HCV Ab status; and c) ART status. After randomization and allocation to 12HR or 40H, participants will be provided 12HR weekly (12 weeks) and INH daily (26 weeks) as directly observed therapy. Every 4 weeks, patients will be monitored for AST/ALT and adverse side effects. Premature treatment discontinuation will occur for any DAIDS Grade 4 toxicity or patient refusal to continue. The focus of this registration is the RCT. Outcomes measures were updated to match most recent protocol March 2025.
Interventions
Participants will be randomized to receive standard INH as TB preventative treatment
Participants will be randomized to receive short course INH + RIF as TB preventative treatment
Sponsors
Study design
Eligibility
Inclusion criteria
Inclusion Criteria (screening): * Age ≥ 18 years * Newly admitted inmate at Kajang Prison Inclusion Criteria (Trial): * Age ≥ 18 years HIV-1 seropositivity * Confirmed LTBI (TST ≥ 5mm if HIV+; TST ≥ 10 mm if HIV-) * Meets DSM-V criteria for opioid dependence * \>9 months before release (to ensure treatment completion in prison) * AST/ALT \< 3x upper limit normal
Exclusion criteria
* Unable to provide informed consent * On a protease inhibitor * Women who are pregnant or are planning on becoming pregnant
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| TB Treatment Completion Rates in Prison | 3 to 6 months | TB treatment completion in prison will be verified using medical records. All TB treatment in prison will be administered under directly observed therapy (DOTs), and treatment administration will be recorded in the participant's prison medical record. Data presented here is the number of participants that completed TB treatment of those that initiated treatment. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| TB Treatment Adherence | monthly for up to 6 months | TB treatment adherence in prison will be verified using medical records. All TB treatment in prison will be administered under directly observed therapy (DOTs), and treatment administration will be recorded in the participant's prison medical record. Data presented here is the number of participants that adhered to TB treatment of those that initiated treatment. |
| Discontinuation Due to Experiencing an Adverse Event | up to 6 months | The number of participants that discontinued the trial due to experiencing an Adverse Event |
| Acceptability of Starting the Trial | Day 1 | Acceptability defined as the number of eligible participants that agreed to consent |
Countries
Malaysia
Contacts
Yale University
University of Malaya
Yale University
Participant flow
Pre-assignment details
Of 327 eligible participants, 316 participants consented, 4 participants were excluded prior to randomization, and 312 randomized
Baseline characteristics
| Characteristic | — |
|---|---|
| Age, Continuous | 42 years |
| Education level Primary school and below | 52 Participants |
| Education level secondary school | 100 Participants |
| Education level Tertiary school | 4 Participants |
| Elevated (>4) Alcohol Use Disorders Identification Test (AUDIT) C score | 18 Participants |
| Employed prior to incarceration | 119 Participants |
| Homelessness | 28 Participants |
| Marital Status Married | 33 Participants |
| Marital Status Single/partner | 180 Participants |
| Marital Status Widowed/Divorced | 34 Participants |
| Median Body Mass Index (BMI) | 21.51 kg/m² |
| Median days since prison entry | 76.5 days |
| Median number of prior incarcerations | 9 incarcerations |
| Number of Participants previously prescribed ART | 26 Participants |
| Positive Hepatitis C | 69 Participants |
| Positive Rapid Opioid Dependence Screen (RODS) (≥3) on enrollment | 112 Participants |
| Previous diagnosis of HIV | 17 Participants |
| Previous intravenous drug use (IVDU) | 67 Participants |
| Previously incarcerated | 294 Participants |
| Previously taking ART prior to prison entry | 6 Participants |
| Previous Opioid Use | 130 Participants |
| Previous TB disease | 10 Participants |
| Race/Ethnicity, Customized Chinese | 34 Participants |
| Race/Ethnicity, Customized Indian | 39 Participants |
| Race/Ethnicity, Customized Malay | 104 Participants |
| Race/Ethnicity, Customized Other | 1 Participants |
| Region of Enrollment Malaysia | 312 participants |
| Sex: Female, Male Female | 0 Participants |
| Sex: Female, Male Male | 156 Participants |
| Total people with HIV | 18 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 156 | 0 / 156 |
| other Total, other adverse events | 112 / 156 | 84 / 156 |
| serious Total, serious adverse events | 0 / 156 | 0 / 156 |