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PRe-Exposure Prophylaxis Acceptability & Readiness Assessments for Toronto gaY, Bisexual and Other Men Who Have Sex With Men-5 (PREP-5)

Primary Purpose

HIV, Human Immunodeficiency Virus

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Tenofovir/emtricitabine
Sponsored by
Unity Health Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV focused on measuring HIV, Pre-Exposure Prophylaxis, PrEP, Human Immunodeficiency Virus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Self-identified man who has sex with men
  • Age 18 years or older
  • Able to communicate in both written and oral english
  • HIRI-MSM score greater than or equal to 10
  • At least one self-reported unprotected receptive anal sex act over the preceding 6 months
  • Creatinine clearance greater than or equal to 60mL/min by Modified Diet in Renal Disease (MDRD) formula
  • HIV un-infected at screening using standard ELISA and Western Blot testing

Exclusion Criteria:

  • Clinical signs or symptoms suggestive of an HIV seroconversion illness within the last 3 months in the opinion of the investigator
  • Use of pre- or post-exposure prophylaxis within the last 3 months
  • Use of concomitant nephrotoxic drugs
  • Use of concomitant immune modulatory drugs
  • Hepatitis B surface antigen positivity
  • Any condition or concomitant medication portending an increased risk of osteoporosis
  • Enrollment in any other HIV prevention program or trial

Sites / Locations

  • St. Michael's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tenofovir/emtricitabine

Arm Description

MSM receiving once daily TDF/FTC-based (Truvada®) pre-exposure prophylaxis

Outcomes

Primary Outcome Measures

Participants' self-reported overall acceptability of PrEP
Participants' self-reported overall acceptability of PrEP over the full one-year follow-up period (including the use of the medication, clinic visits, and their impact on the participant's life) will be quantified using a Likert scale.
The level of community interest in PrEP
The level of community interest in PrEP will be measured by quantifying the volume, rate and HIV risk levels of patient referrals to the PrEP clinic from each key referral source

Secondary Outcome Measures

Adherence to daily TDF/FTC-based PrEP
Adherence will be measured by self-report, pill count, and intra-RBC tenofovir diphosphate levels.
Time required by the patient, physician and research coordinator for each type of study visit.
The time required by the patient, physician and research coordinator will be measured for each type of study visit.
HIV infection
HIV infection will be detected using point-of-care tests, standard serology and HIV RNA testing.
Sexually transmitted infections
Testing will be performed at each study visit to screen for gonorrhea, chlamydia and syphilis infection, including pharyngeal swab cultures, rectal swab cultures and urine NAAT tests.
Burden of syndemic health problems
The burden of specific syndemic health problems (depression, social anxiety, substance abuse, sexual addiction, childhood sexual abuse, partner violence) will be quantified using standardized, validated psychometric tools.
Change in estimated glomerular filtration rate
Estimated by the Modified Diet in Renal Disease (MDRD) formula
Percentage change in bone mineral density at the lumbar spine and total hip
Adverse events
Adverse events will be assessed at each visit via clinical assessment and laboratory monitoring (CBC, phosphate, urinalysis).
Pilot testing study instruments
Outcomes related to pilot testing study instruments will include numbers of minutes required and participant-reported acceptability for each procedure

Full Information

First Posted
May 12, 2014
Last Updated
October 14, 2016
Sponsor
Unity Health Toronto
Collaborators
Hassle Free Clinic, Maple Leaf Research, Toronto Metropolitan University, AIDS Committee of Toronto, Canadian AIDS Treatment Information Exchange, Gilead Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02149888
Brief Title
PRe-Exposure Prophylaxis Acceptability & Readiness Assessments for Toronto gaY, Bisexual and Other Men Who Have Sex With Men-5
Acronym
PREP-5
Official Title
A Pilot Study of Daily TDF/FTC-based PrEP Among High-risk Toronto MSM:The PREPARATORY-5 Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Unity Health Toronto
Collaborators
Hassle Free Clinic, Maple Leaf Research, Toronto Metropolitan University, AIDS Committee of Toronto, Canadian AIDS Treatment Information Exchange, Gilead Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Canada continues to see an unrelenting stream of new HIV diagnoses, with a disproportionate burden among gay, bisexual, and other MSM in major centers such as Toronto. Pre-exposure prophylaxis (PrEP) with oral, daily tenofovir/emtricitabine (TDF/FTC, Truvada®) is a novel biomedical approach to HIV prevention shown in the iPrEx trial to be safe and efficacious in reducing HIV acquisition by 44% among MSM, when provided in a comprehensive package of HIV prevention interventions including counseling, testing/treatment of sexually transmitted infections (STIs), and condoms. There is now widespread mobilization to assess the feasibility of PrEP roll-out worldwide, with urgent calls for 'demonstration projects' addressing real-world PrEP implementation issues. PREPARATORY-5 is Canada's first PrEP demonstration project, and will examine real-world PrEP implementation issues including acceptability, effectiveness, impact on sexually transmitted infections, and strategies for supporting adherence outside the clinical trial setting. The investigators have also established a comprehensive community-based research program investigating the role of community-based organizations in PrEP implementation and delivery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Human Immunodeficiency Virus
Keywords
HIV, Pre-Exposure Prophylaxis, PrEP, Human Immunodeficiency Virus

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tenofovir/emtricitabine
Arm Type
Experimental
Arm Description
MSM receiving once daily TDF/FTC-based (Truvada®) pre-exposure prophylaxis
Intervention Type
Drug
Intervention Name(s)
Tenofovir/emtricitabine
Other Intervention Name(s)
Truvada®
Intervention Description
Once daily Tenofovir/emtricitabine (Truvada®)
Primary Outcome Measure Information:
Title
Participants' self-reported overall acceptability of PrEP
Description
Participants' self-reported overall acceptability of PrEP over the full one-year follow-up period (including the use of the medication, clinic visits, and their impact on the participant's life) will be quantified using a Likert scale.
Time Frame
12 months
Title
The level of community interest in PrEP
Description
The level of community interest in PrEP will be measured by quantifying the volume, rate and HIV risk levels of patient referrals to the PrEP clinic from each key referral source
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Adherence to daily TDF/FTC-based PrEP
Description
Adherence will be measured by self-report, pill count, and intra-RBC tenofovir diphosphate levels.
Time Frame
12 months
Title
Time required by the patient, physician and research coordinator for each type of study visit.
Description
The time required by the patient, physician and research coordinator will be measured for each type of study visit.
Time Frame
12 months
Title
HIV infection
Description
HIV infection will be detected using point-of-care tests, standard serology and HIV RNA testing.
Time Frame
12 months
Title
Sexually transmitted infections
Description
Testing will be performed at each study visit to screen for gonorrhea, chlamydia and syphilis infection, including pharyngeal swab cultures, rectal swab cultures and urine NAAT tests.
Time Frame
12 months
Title
Burden of syndemic health problems
Description
The burden of specific syndemic health problems (depression, social anxiety, substance abuse, sexual addiction, childhood sexual abuse, partner violence) will be quantified using standardized, validated psychometric tools.
Time Frame
12 months
Title
Change in estimated glomerular filtration rate
Description
Estimated by the Modified Diet in Renal Disease (MDRD) formula
Time Frame
12 months
Title
Percentage change in bone mineral density at the lumbar spine and total hip
Time Frame
12 months
Title
Adverse events
Description
Adverse events will be assessed at each visit via clinical assessment and laboratory monitoring (CBC, phosphate, urinalysis).
Time Frame
12 months
Title
Pilot testing study instruments
Description
Outcomes related to pilot testing study instruments will include numbers of minutes required and participant-reported acceptability for each procedure
Time Frame
12 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Self-identified man who has sex with men Age 18 years or older Able to communicate in both written and oral english HIRI-MSM score greater than or equal to 10 At least one self-reported unprotected receptive anal sex act over the preceding 6 months Creatinine clearance greater than or equal to 60mL/min by Modified Diet in Renal Disease (MDRD) formula HIV un-infected at screening using standard ELISA and Western Blot testing Exclusion Criteria: Clinical signs or symptoms suggestive of an HIV seroconversion illness within the last 3 months in the opinion of the investigator Use of pre- or post-exposure prophylaxis within the last 3 months Use of concomitant nephrotoxic drugs Use of concomitant immune modulatory drugs Hepatitis B surface antigen positivity Any condition or concomitant medication portending an increased risk of osteoporosis Enrollment in any other HIV prevention program or trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Darrell Tan, MD FRCPC PhD
Organizational Affiliation
Unity Health Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B 1W8
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
30530721
Citation
Tan DHS, Schnubb A, Lawless J, Szadkowski L, Grennan T, Wilton J, Fowler S, Hart TA, Maxwell J, Raboud JM. Acceptability and tolerability of and adherence to HIV preexposure prophylaxis among Toronto gay and bisexual men: a pilot study. CMAJ Open. 2018 Dec 10;6(4):E611-E617. doi: 10.9778/cmajo.20180068. Print 2018 Oct-Dec.
Results Reference
derived
PubMed Identifier
29486737
Citation
Wilton J, Noor SW, Schnubb A, Lawless J, Hart TA, Grennan T, Fowler S, Maxwell J, Tan DHS. High HIV risk and syndemic burden regardless of referral source among MSM screening for a PrEP demonstration project in Toronto, Canada. BMC Public Health. 2018 Feb 27;18(1):292. doi: 10.1186/s12889-018-5180-8.
Results Reference
derived

Learn more about this trial

PRe-Exposure Prophylaxis Acceptability & Readiness Assessments for Toronto gaY, Bisexual and Other Men Who Have Sex With Men-5

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