R01DA056883
Project Grant
Overview
Grant Description
Saia-Prep: A Systems Analysis and Improvement Approach to Optimize Prep Implementation in Syringe Service Programs - Abstract
For the first time in decades, HIV incidence is increasing among people who inject drugs (PWID). Pre-exposure prophylaxis (Prep) is a safe, effective, evidence-based HIV prevention strategy recommended for at-risk PWID. However, despite the acceptability of Prep among PWID, access remains low, and uptake has lagged far behind that observed in other vulnerable populations.
Our preliminary research demonstrates that syringe service programs (SSPs) are uniquely poised to improve Prep access, and many already provide some services along the Prep delivery cascade, including Prep education, HIV testing, and linkage to onsite and external medical services. Despite being ideal venues for improving Prep access among PWID, our data demonstrate that these agencies need additional support to optimally implement the SSP-based Prep delivery cascade.
This novel randomized controlled trial (RCT) uses an interrupted time series design to test whether an evidence-based, organization-level intervention, the Systems Analysis and Improvement Approach (Saia), can improve the delivery of Prep services among 32 SSPs located in Ending the HIV Epidemic priority jurisdictions. After a 3-month run-in period, SSPs will be randomized to receive Saia (n=16) versus treatment as usual (n=16).
Saia will be delivered by trained specialists through five cyclical steps over 12 months: (1) analyze SSPs' Prep delivery cascade to identify priority areas for system improvements, (2) map processes and build consensus around programmatic modifications to address priority areas, (3) implement programmatic modifications, (4) assess effects of programmatic modifications on delivery of cascade services, and (5) repeat steps 1-4 as needed.
SSPs will use an electronic data collection system to report on outcomes including numbers of SSP clients receiving (1) Prep education, (2) HIV testing, (3) Prep linkage, and (4) Prep initiation verification. Data will be collected during the 3-month run-in period prior to randomization, and then for an additional 24 months, allowing us to identify initial impacts of Saia after 12 months (Aim 1) and sustained impacts at 24 months (Aim 2).
Outcomes will be disaggregated by sex and race/ethnicity to allow for process monitoring of programmatic changes to address equity in service delivery. We will also estimate the cost and cost-effectiveness of Saia relative to treatment as usual using an activity-based costing approach (Aim 3).
To our knowledge, this will be the first RCT of an organizational-level intervention to optimize the SSP-based Prep delivery cascade. If successful, Saia could be disseminated to the =430 SSPs nationally and in global settings, carrying the potential for exceptional impact amidst persistent HIV transmission in PWID.
For the first time in decades, HIV incidence is increasing among people who inject drugs (PWID). Pre-exposure prophylaxis (Prep) is a safe, effective, evidence-based HIV prevention strategy recommended for at-risk PWID. However, despite the acceptability of Prep among PWID, access remains low, and uptake has lagged far behind that observed in other vulnerable populations.
Our preliminary research demonstrates that syringe service programs (SSPs) are uniquely poised to improve Prep access, and many already provide some services along the Prep delivery cascade, including Prep education, HIV testing, and linkage to onsite and external medical services. Despite being ideal venues for improving Prep access among PWID, our data demonstrate that these agencies need additional support to optimally implement the SSP-based Prep delivery cascade.
This novel randomized controlled trial (RCT) uses an interrupted time series design to test whether an evidence-based, organization-level intervention, the Systems Analysis and Improvement Approach (Saia), can improve the delivery of Prep services among 32 SSPs located in Ending the HIV Epidemic priority jurisdictions. After a 3-month run-in period, SSPs will be randomized to receive Saia (n=16) versus treatment as usual (n=16).
Saia will be delivered by trained specialists through five cyclical steps over 12 months: (1) analyze SSPs' Prep delivery cascade to identify priority areas for system improvements, (2) map processes and build consensus around programmatic modifications to address priority areas, (3) implement programmatic modifications, (4) assess effects of programmatic modifications on delivery of cascade services, and (5) repeat steps 1-4 as needed.
SSPs will use an electronic data collection system to report on outcomes including numbers of SSP clients receiving (1) Prep education, (2) HIV testing, (3) Prep linkage, and (4) Prep initiation verification. Data will be collected during the 3-month run-in period prior to randomization, and then for an additional 24 months, allowing us to identify initial impacts of Saia after 12 months (Aim 1) and sustained impacts at 24 months (Aim 2).
Outcomes will be disaggregated by sex and race/ethnicity to allow for process monitoring of programmatic changes to address equity in service delivery. We will also estimate the cost and cost-effectiveness of Saia relative to treatment as usual using an activity-based costing approach (Aim 3).
To our knowledge, this will be the first RCT of an organizational-level intervention to optimize the SSP-based Prep delivery cascade. If successful, Saia could be disseminated to the =430 SSPs nationally and in global settings, carrying the potential for exceptional impact amidst persistent HIV transmission in PWID.
Funding Goals
TO SUPPORT BASIC AND CLINICAL NEUROSCIENCE, BIOMEDICAL, BEHAVIORAL AND SOCIAL SCIENCE, EPIDEMIOLOGIC, HEALTH SERVICES AND HEALTH DISPARITY RESEARCH. TO DEVELOP NEW KNOWLEDGE AND APPROACHES RELATED TO THE PREVENTION, DIAGNOSIS, TREATMENT, ETIOLOGY, AND CONSEQUENCES OF DRUG ABUSE AND ADDICTION, INCLUDING HIV/AIDS. TO SUPPORT RESEARCH TRAINING AND RESEARCH SCIENTIST DEVELOPMENT. TO SUPPORT DISSEMINATION OF RESEARCH FINDINGS. SMALL BUSINESS INNOVATION RESEARCH (SBIR) LEGISLATION IS INTENDED TO EXPAND AND IMPROVE THE SBIR PROGRAMS TO EMPHASIZE AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF TECHNOLOGY DEVELOPED THROUGH FEDERAL SBIR RESEARCH AND DEVELOPMENT, INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN THE SBIR PROGRAM. THE LEGISLATION INTENDS THAT THE SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
La Jolla,
California
92093
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 298% from $858,690 to $3,418,213.
San Diego University Of California was awarded
Saia-Prep: Optimizing Prep Implementation in Syringe Service Programs
Project Grant R01DA056883
worth $3,418,213
from National Institute on Drug Abuse in September 2022 with work to be completed primarily in La Jolla California United States.
The grant
has a duration of 3 years 9 months and
was awarded through assistance program 93.279 Drug Abuse and Addiction Research Programs.
The Project Grant was awarded through grant opportunity PrEP for HIV Prevention among Substance Using Populations (R01 - Clinical Trial Optional).
Status
(Ongoing)
Last Modified 7/21/25
Period of Performance
9/1/22
Start Date
6/30/26
End Date
Funding Split
$3.4M
Federal Obligation
$0.0
Non-Federal Obligation
$3.4M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01DA056883
Transaction History
Modifications to R01DA056883
Additional Detail
Award ID FAIN
R01DA056883
SAI Number
R01DA056883-1885477789
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75N600 NIH National Insitute on Drug Abuse
Funding Office
75N600 NIH National Insitute on Drug Abuse
Awardee UEI
UYTTZT6G9DT1
Awardee CAGE
50854
Performance District
CA-50
Senators
Dianne Feinstein
Alejandro Padilla
Alejandro Padilla
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Institute on Drug Abuse, National Institutes of Health, Health and Human Services (075-0893) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,837,085 | 100% |
Modified: 7/21/25