HIV Infections
Conditions
Brief summary
Despite decades of traditional prevention efforts based on behavior change and condom use, Ontario has seen over 700 new HIV infections annually over the past 10 years. Post-exposure prophylaxis (PEP) is one such approach, in which uninfected persons use 28 days of antiretroviral medications (ARVs) shortly after an HIV exposure to minimize the risk of acquiring HIV. PEP is highly efficacious, is considered a standard of care intervention based on medical and ethical grounds, and is supported by treatment guidelines. Yet several implementation challenges have limited its clinical and public health impact in Ontario, where no formal PEP policy exists. Our proposal seeks to optimize two aspects of delivering PEP for sexual exposures (nPEP). Results will inform the development of a standardized approach to nPEP both province-wide and elsewhere. Thus study has pragmatic, multicenter randomized controlled trial using a 2x2 factorial design to determine whether the proportion of nPEP patients that successfully complete follow-up: 1. is higher among those receiving mobile phone-based text messaging support than among those receiving standard care; and 2. is non-inferior among those receiving care from a sexual health clinic nurse compared to those receiving hospital-based physician care. The prospective, randomized, non-blinded, 2x2 factorial trial that will enroll 318 study participants in Toronto. In Intervention A, we will randomize half of study participants to a text messaging support service ('WelTel'), in which a trained, community-based counselor provides standardized weekly 'check-in' messages during their 12-week course of PEP follow-up. The other half will receive standard care, which does not include any form of active outreach or reminders outside of scheduled appointments. In Intervention B, we will randomize half of participants to receive nurse-led care for PEP follow-up at a local sexual health clinic; the other half will receive standard care by a hospital-based ID physician. The specific activities for each follow-up visit will be clearly defined in a medical directive. In keeping with Ontario legislation on medical directives, nurses will review cases with their authorizing physician or nurse practitioner on a routine basis.
Interventions
DRUGnPEP
Participants will receive Bictegravir/emtricitabine/tenofovir alafenamide 50/200/25mg (Biktarvy®) one tablet once daily as study drug to complete a 28 day course of PEP.
BEHAVIORALText Messaging Support
Text messaging support service ('WelTel'): community-based counselors will provides standardized weekly 'check-in' messages during the participants 12-week course of nPEP follow-up. Participants in the text-message arm will also have the option of receiving generic non-specific automated text reminders of their upcoming appointments in the form of Don't forget about tomorrow.
OTHERNurse-Led nPEP
nPEP follow-up is provided by nurse-led care at a local sexual health clinic instead of a hospital-based ID physician.
Sponsors
Canadian Institutes of Health Research (CIHR)
CIHR Canadian HIV Trials Network
Unity Health Toronto
Study design
Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Be 18 years or older 2. Be known or presumed to be HIV-uninfected at baseline 3. Be initiated on PEP by a healthcare provider in the past six days for a sexual exposure to a known or suspected HIV-infected source 4. STAGE 1 only: Own a mobile phone with text messaging capabilities on which they are willing to potentially receive messages from the text messaging service 5. Be capable of communicating verbally and via text in English 6. Be planning to continue their follow-up locally or be willing to have follow-up study visits conducted remotely; either by telephone or via an encrypted video conferencing system (such as Zoom for healthcare). 7. Be referred to a sexual assault center and provided with necessary counselling and support services if presented for nPEP following sexual assault.
Exclusion criteria
1. Creatinine clearance \<30 mL/min (using Cockcroft-Gault formula) 2. Enrolled in any other clinical trial of an HIV prevention intervention 3. Prior participation in this clinical trial for a previous episode of nPEP 4. Known co-infection with chronic hepatitis B at enrollment 5. Current or planned pregnancy or breastfeeding 6. Use of a medication whose co-administration with Biktarvy is contraindicated (dofetilide, carbamazepine, oxcarbazepine, phenobarbital, phenytoin, rifampin, rifampicin, rifabutin, rifapentine, modafinil, dexamethasone, metformin, St. John's Wort) 7. Concomitant use of HIV pre-exposure prophylaxis (PrEP) 8. Stage 2 only: Concomitant use of any non-prescription medication, supplement, vitamin or natural remedy which the patient is unwilling to discontinue during Biktarvy® administration
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Self-reported completion of a full course of PEP medications and receipt of a final HIV test result from their nPEP provider 12 weeks after the index exposure | 12 weeks | Determined by patient completion of acceptability questionnaire and evidence of HIV test result |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Numbers and types of linkages made by PEP providers to other forms of healthcare | Week 12 | 1. Number of participants referred to psychiatry/mental health services and 2. Number of participants referred to addictions/substance services |
| Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability of TAF/FTC/ELV/cobi-based nPEP] | 12 weeks | Collection of adverse events |
| Completion of each scheduled follow-up activity (blood tests and clinic visits) | 12 weeks | Measured by study visit attendance on CRFs |
| Diagnosis of incident HIV | 12 weeks | Determined through laboratory analysis of blood, urine and mucosal swab samples |
| Self-reported sexual risk-taking behaviour | 12 weeks | The following activities will be captured in a questionnaire: number of unprotected vaginal/anal sex acts, and for men who have sex with men, score on a HIV risk index (based on the validated HIRI-MSM) |
| Patient satisfaction with their PEP experience | 12 weeks | Collected using a patient survey |
| Inquiries from participants to the PEP provider outside of scheduled follow-up | 12 weeks | the number of times participants contacted their healthcare provider outside of scheduled follow-up |
| PEP-related referrals for physician consultation | 12 weeks | Number of times a participant randomized to the nurse-led arm had to be referred to a physician; captured on the sexual health clinic documentation. |
| Sexually transmitted infections (gonorrhea, chlamydia, syphilis, hepatitis B and C) | 12 weeks | Determined through laboratory analysis of blood sample |
Other
| Measure | Time frame | Description |
|---|---|---|
| Assessment of cost on heathcare system | Week 12 | Prospective collection of cost data during the trial to inform a future health economic analysis from the perspective of the healthcare system. |
Countries
Canada
Contacts
Primary ContactDarrell HS Tan, MD, FRCPC, PhD
Backup ContactAttia Qamar, BME
Outcome results
None listed