search
Back to results

Connecting Resources for Urban Sexual Health (CRUSH)

Primary Purpose

HIV, Sexually Transmitted Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Testing and linkage to care for Y/MSM
Engagement and retention for HIV-positive Y/MSM in care
Engagement and retention for HIV-negative Y/MSM in sexual health services
Stribild PEP Substudy
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for HIV

Eligibility Criteria

18 Years - 29 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Men between the ages of 18-29 who are ever sexually active with men;
  • Transgender females (M2F) between the ages of 18-29 who are sexually active with men; Transgender males (F2M) between the ages of 18-29 who are sexually active with men; and
  • Any HIV-negative person aged 18-29, male or female, who has at least one known HIV positive (i.e. serodiscordant) sexual partner.

Exclusion Criteria:

  • None.

For the PEP substudy the inclusion criterion is at least one episode in the 72 hours prior to presentation of unprotected receptive anal intercourse with a partner known or suspected to be HIV positive and the following are the substudy exclusion criteria:

  • Known kidney disease
  • Dipstick proteinuria >1+
  • eGFR < 70 ml/min/1.73m2
  • Known metabolic bone disease
  • Signs or symptoms of acute HIV infection
  • Concomitant use of nephrotoxic drug or medication contraindicated with Stribild®

Sites / Locations

  • Downtown Youth Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Study intervention

Arm Description

Outcomes

Primary Outcome Measures

The proportion of young men who have sex with men (YMSM) of color who test positive for HIV at partner agencies and the proportion of positive and negative YMSM who are tested for HIV and linked to care on a quarterly and annual basis.
Expanding the investigators currently successful HIV testing strategy-collaborations and systems of referral of new cases of HIV from existing partners-so that referrals are also received for high risk negatives to receive sexual health services. Implementing two new strategies: social network testing and a youth outreach corps working with partner agencies; it is hypothesized that social network testing will increase the proportion of positive test results.
The proportion of HIV-positive enrolled YMSM who are retained, on therapy, and who have achieved viral suppression within one year of entering care.
Optimizing current HIV care and treatment services at DYC by adding three new components: a patient peer mentoring component, a linkage and retention specialist, and psychosocial support for program staff.
The proportion of HIV-uninfected YMSM participants who are retained, receive sexually transmitted infection (STI) testing, and receive non-occupational post-exposure-prophylaxis (nPEP) and/or PrEP.
Integrating sexual health services for HIV-uninfected young MSM of color into an HIV care setting, including PrEP, warm-hand offs for high risk negatives, nPEP, risk reduction counseling, frequent HIV and STI testing, and youth-focused programming.
Substudy Primary Outcome: To evaluate the tolerability and acceptability of a 28 day course of Stribild® given as post-exposure prophylaxis (PEP) to prevent sexual acquisition of HIV-1.
Regimen completion at 28 days.

Secondary Outcome Measures

Substudy Secondary Outcome: To assess the renal safety of Stribild® PEP.
Change from baseline in serum creatinine and eGFR.
Substudy Secondary Outcome: To assess the renal safety of Stribild® PEP.
Markers of proximal tubulopathy (glycosuria, proteinuria > 1+).
Substudy Secondary Outcome: To document any HIV-1 seroconversions occurring while on Stribild® PEP.
HIV-1 seroconversion.
Substudy Secondary Outcome: To document the side effect profile of Stribild® given as PEP
Frequency of adverse events.
Substudy Secondary Outcome: To assess adherence to Stribild® PEP.
Self-reported adherence and reasons for non-adherence.
Substudy Secondary Outcome: To assess adherence to Stribild® PEP.
Changes from baseline in quality of life.
Substudy Secondary Outcome: To assess adherence to Stribild® PEP.
Early cessation of regimen.

Full Information

First Posted
May 6, 2014
Last Updated
November 17, 2017
Sponsor
University of California, San Francisco
search

1. Study Identification

Unique Protocol Identification Number
NCT02183909
Brief Title
Connecting Resources for Urban Sexual Health
Acronym
CRUSH
Official Title
Connecting Resources for Urban Sexual Health
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
May 2013 (Actual)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
August 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall goal of the CRUSH project is to enhance and extend a response to the local HIV/AIDS epidemic in Alameda County with a set of innovative, evidence-based interventions across the continuum of HIV prevention and care, targeting individuals and communities most vulnerable to HIV. The East Bay AIDS Center, in partnership with the University of California San Francisco's Center for AIDS Prevention Studies, the Gladstone Institutes, and several key community-based organizations, are engaging in a participatory partnership to enhance and implement HIV services which target the East Bay's highest risk population- young men who have sex with men (Y/MSM). Specifically, the CRUSH Project is designed to evaluate a combination of program approaches to address the sexual health care needs of young gay men of color and their sexual partners by enhancing the current program activities of the Downtown Youth Clinic (DYC). We hypothesize that we can reduce the impact of HIV among Y/MSM by expanding the current DYC services structure in two ways. We intend to expand HIV testing, and linkage to and retention in care for youth who test HIV positive, providing them with intensive risk-reduction counseling and antiretroviral treatment, and thereby ultimately reducing the risk of further HIV transmission. And we intend for the first time to offer a comprehensive combination package of preventive services to HIV-negative youth, including routine accesses to HIV/STI screening and treatment, and access to HIV pre-exposure prophylaxis (PrEP). The CRUSH Project will also have a substudy that will enroll HIV-negative participants who are eligible to receive PEP. The substudy will evaluate the tolerability and acceptability of a 28 day course of Stribild® given as post-exposure prophylaxis (PEP) to prevent sexual acquisition of HIV-1 in Y/MSM of color.
Detailed Description
The CRUSH Project (Connecting Resources for Urban Sexual Health) is a demonstration project at Alta Bates Summit Medical Center's East Bay AIDS Center (EBAC) and Downtown Youth Clinic (DYC) offering interventions aimed at reducing HIV-1 incidence among young MSM of color in the East Bay region. CRUSH has two major components: Providing enhanced testing and linkage to care (TLC+) for HIV positives, aimed at increasing the proportion of HIV positive Y/MSM who are in care, virologically suppressed, and receiving intensive risk reduction counseling. Providing comprehensive sexual health services to high risk HIV-negatives, including but not limited to the provision of PrEP and PEP when clinically appropriate. In addition, the CRUSH Project will offer a substudy of CRUSH, and will enroll HIV negative CRUSH participants who are eligible to receive PEP. Stribild® is a single-tablet, four-drug, once-daily complete regimen that is FDA-approved for the treatment of HIV-1 infection in treatment-naïve HIV-infected adults with estimated glomerular filtration rate ≥70ml/min/1.73m2. Because of limited data, no antiretroviral drug or combination of drugs has been approved for PEP. Current PEP guidelines generally call for using a 28-day course of a 3-drug regimen that has been approved for the treatment of HIV-1 infection

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Sexually Transmitted Infections

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
380 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study intervention
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Testing and linkage to care for Y/MSM
Intervention Description
Implementation of strategies to enhance testing and linkage to care of Y/MSM, including social network testing and a youth outreach corps working with existing and new community partner agencies.
Intervention Type
Behavioral
Intervention Name(s)
Engagement and retention for HIV-positive Y/MSM in care
Intervention Description
Optimizing current HIV care and treatment services at DYC by implementing a patient peer mentoring component, a linkage and retention specialist, and psychosocial support for program staff.
Intervention Type
Other
Intervention Name(s)
Engagement and retention for HIV-negative Y/MSM in sexual health services
Intervention Description
Offering a highly effective combination HIV prevention strategy, including PrEP; warm-hand offs for high-risk negatives, nPEP; risk reduction counseling; frequent HIV and STI testing, including testing a highly sensitive method of detecting early HIV infection; and youth-focused programming.
Intervention Type
Drug
Intervention Name(s)
Stribild PEP Substudy
Intervention Description
A substudy of 28 days of once-daily Stribild® initiated within 72 hours of a high risk sexual exposure for HIV post-exposure prophylaxis (PEP).
Primary Outcome Measure Information:
Title
The proportion of young men who have sex with men (YMSM) of color who test positive for HIV at partner agencies and the proportion of positive and negative YMSM who are tested for HIV and linked to care on a quarterly and annual basis.
Description
Expanding the investigators currently successful HIV testing strategy-collaborations and systems of referral of new cases of HIV from existing partners-so that referrals are also received for high risk negatives to receive sexual health services. Implementing two new strategies: social network testing and a youth outreach corps working with partner agencies; it is hypothesized that social network testing will increase the proportion of positive test results.
Time Frame
1 year
Title
The proportion of HIV-positive enrolled YMSM who are retained, on therapy, and who have achieved viral suppression within one year of entering care.
Description
Optimizing current HIV care and treatment services at DYC by adding three new components: a patient peer mentoring component, a linkage and retention specialist, and psychosocial support for program staff.
Time Frame
1 year
Title
The proportion of HIV-uninfected YMSM participants who are retained, receive sexually transmitted infection (STI) testing, and receive non-occupational post-exposure-prophylaxis (nPEP) and/or PrEP.
Description
Integrating sexual health services for HIV-uninfected young MSM of color into an HIV care setting, including PrEP, warm-hand offs for high risk negatives, nPEP, risk reduction counseling, frequent HIV and STI testing, and youth-focused programming.
Time Frame
1 year
Title
Substudy Primary Outcome: To evaluate the tolerability and acceptability of a 28 day course of Stribild® given as post-exposure prophylaxis (PEP) to prevent sexual acquisition of HIV-1.
Description
Regimen completion at 28 days.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Substudy Secondary Outcome: To assess the renal safety of Stribild® PEP.
Description
Change from baseline in serum creatinine and eGFR.
Time Frame
1 year
Title
Substudy Secondary Outcome: To assess the renal safety of Stribild® PEP.
Description
Markers of proximal tubulopathy (glycosuria, proteinuria > 1+).
Time Frame
1 year
Title
Substudy Secondary Outcome: To document any HIV-1 seroconversions occurring while on Stribild® PEP.
Description
HIV-1 seroconversion.
Time Frame
1 year
Title
Substudy Secondary Outcome: To document the side effect profile of Stribild® given as PEP
Description
Frequency of adverse events.
Time Frame
1 year
Title
Substudy Secondary Outcome: To assess adherence to Stribild® PEP.
Description
Self-reported adherence and reasons for non-adherence.
Time Frame
1 year
Title
Substudy Secondary Outcome: To assess adherence to Stribild® PEP.
Description
Changes from baseline in quality of life.
Time Frame
1 year
Title
Substudy Secondary Outcome: To assess adherence to Stribild® PEP.
Description
Early cessation of regimen.
Time Frame
1 year

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
29 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men between the ages of 18-29 who are ever sexually active with men; Transgender females (M2F) between the ages of 18-29 who are sexually active with men; Transgender males (F2M) between the ages of 18-29 who are sexually active with men; and Any HIV-negative person aged 18-29, male or female, who has at least one known HIV positive (i.e. serodiscordant) sexual partner. Exclusion Criteria: None. For the PEP substudy the inclusion criterion is at least one episode in the 72 hours prior to presentation of unprotected receptive anal intercourse with a partner known or suspected to be HIV positive and the following are the substudy exclusion criteria: Known kidney disease Dipstick proteinuria >1+ eGFR < 70 ml/min/1.73m2 Known metabolic bone disease Signs or symptoms of acute HIV infection Concomitant use of nephrotoxic drug or medication contraindicated with Stribild®
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeff Burack, MD
Organizational Affiliation
East Bay AIDS Center (EBAC)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Robert Grant, MD, MPH
Organizational Affiliation
Gladstone Institutes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Janet Myers, PhD
Organizational Affiliation
UCSF Center for AIDS Prevention
Official's Role
Principal Investigator
Facility Information:
Facility Name
Downtown Youth Clinic
City
Oakland
State/Province
California
ZIP/Postal Code
94609
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21091279
Citation
Grant RM, Lama JR, Anderson PL, McMahan V, Liu AY, Vargas L, Goicochea P, Casapia M, Guanira-Carranza JV, Ramirez-Cardich ME, Montoya-Herrera O, Fernandez T, Veloso VG, Buchbinder SP, Chariyalertsak S, Schechter M, Bekker LG, Mayer KH, Kallas EG, Amico KR, Mulligan K, Bushman LR, Hance RJ, Ganoza C, Defechereux P, Postle B, Wang F, McConnell JJ, Zheng JH, Lee J, Rooney JF, Jaffe HS, Martinez AI, Burns DN, Glidden DV; iPrEx Study Team. Preexposure chemoprophylaxis for HIV prevention in men who have sex with men. N Engl J Med. 2010 Dec 30;363(27):2587-99. doi: 10.1056/NEJMoa1011205. Epub 2010 Nov 23.
Results Reference
background
PubMed Identifier
22784037
Citation
Baeten JM, Donnell D, Ndase P, Mugo NR, Campbell JD, Wangisi J, Tappero JW, Bukusi EA, Cohen CR, Katabira E, Ronald A, Tumwesigye E, Were E, Fife KH, Kiarie J, Farquhar C, John-Stewart G, Kakia A, Odoyo J, Mucunguzi A, Nakku-Joloba E, Twesigye R, Ngure K, Apaka C, Tamooh H, Gabona F, Mujugira A, Panteleeff D, Thomas KK, Kidoguchi L, Krows M, Revall J, Morrison S, Haugen H, Emmanuel-Ogier M, Ondrejcek L, Coombs RW, Frenkel L, Hendrix C, Bumpus NN, Bangsberg D, Haberer JE, Stevens WS, Lingappa JR, Celum C; Partners PrEP Study Team. Antiretroviral prophylaxis for HIV prevention in heterosexual men and women. N Engl J Med. 2012 Aug 2;367(5):399-410. doi: 10.1056/NEJMoa1108524. Epub 2012 Jul 11.
Results Reference
background
PubMed Identifier
22784038
Citation
Thigpen MC, Kebaabetswe PM, Paxton LA, Smith DK, Rose CE, Segolodi TM, Henderson FL, Pathak SR, Soud FA, Chillag KL, Mutanhaurwa R, Chirwa LI, Kasonde M, Abebe D, Buliva E, Gvetadze RJ, Johnson S, Sukalac T, Thomas VT, Hart C, Johnson JA, Malotte CK, Hendrix CW, Brooks JT; TDF2 Study Group. Antiretroviral preexposure prophylaxis for heterosexual HIV transmission in Botswana. N Engl J Med. 2012 Aug 2;367(5):423-34. doi: 10.1056/NEJMoa1110711. Epub 2012 Jul 11.
Results Reference
background
Links:
URL
http://www.altabatessummit.org/clinical/aids_scvs.html
Description
East Bay AIDS Center Website

Learn more about this trial

Connecting Resources for Urban Sexual Health

We'll reach out to this number within 24 hrs