R01DA057608
Project Grant
Overview
Grant Description
Treating Polysubstance Use in Methadone Maintenance: Application of Novel Digital Technology - Abstract
Methadone is a highly effective treatment for opioid use disorder (OUD), but many patients leave treatment prematurely, placing them at high risk of relapse and overdose. Extensive research shows that comorbid cocaine use is associated with poor retention in methadone treatment.
The proposed study will examine a novel intervention designed to improve methadone treatment retention and other outcomes among people with opioid and cocaine polysubstance use. The design is a 2-arm randomized controlled trial conducted over a one-year period following methadone treatment entry.
Retention (primary) and drug use (secondary) outcomes for methadone treatment as usual (TAU, N=120) will be compared with the addition of the DynamiCare Health Contingency Management App (TAU+DCM, N=120). DCM is a personal digital therapy tool provided as an app on the patient's smartphone. Its central feature is the delivery of evidence-based contingency management therapy in a convenient, remote, and fully automated fashion that ensures validity of target behaviors and immediacy of reward delivery.
Two target behaviors relevant to retention will be the primary focus of the DCM program: 1) abstinence from opiates and cocaine as verified via remote oral fluid testing, and 2) medication pickup from the methadone program as verified by clinic records. Participants in the TAU+DCM arm will receive financial rewards for achieving these pre-determined behavioral targets over a 48-week intervention period.
Comprehensive assessment of all participants will be conducted at baseline, 3-, 6-, and 12-months.
Aim 1: To determine the relative effectiveness of TAU+DCM compared to TAU alone in improving methadone treatment retention through 12-months post-treatment entry.
Aim 2: To determine the relative effectiveness of TAU+DCM compared to TAU alone in terms of [Aim 2A] reducing opioid use and cocaine use; and [Aim 2B] improving other secondary outcomes including non-targeted substance use and quality of life through 12-months post-treatment entry.
Aim 3: To explore app use patterns, acceptability, and perceived value of the personalized treatment intervention through 12-months post-treatment entry.
Innovation lies in the platform and structure of CM delivery that ensures treatment fidelity with automation of remote behavioral monitoring and reward delivery without involvement of clinical staff. This project represents a novel application of digital therapeutics to enhance the effectiveness of OUD treatment with polysubstance use.
Findings from this project can improve the public health impact of methadone treatment by identifying an effective and scalable approach to address polysubstance use among patients at heightened risk of treatment dropout.
Methadone is a highly effective treatment for opioid use disorder (OUD), but many patients leave treatment prematurely, placing them at high risk of relapse and overdose. Extensive research shows that comorbid cocaine use is associated with poor retention in methadone treatment.
The proposed study will examine a novel intervention designed to improve methadone treatment retention and other outcomes among people with opioid and cocaine polysubstance use. The design is a 2-arm randomized controlled trial conducted over a one-year period following methadone treatment entry.
Retention (primary) and drug use (secondary) outcomes for methadone treatment as usual (TAU, N=120) will be compared with the addition of the DynamiCare Health Contingency Management App (TAU+DCM, N=120). DCM is a personal digital therapy tool provided as an app on the patient's smartphone. Its central feature is the delivery of evidence-based contingency management therapy in a convenient, remote, and fully automated fashion that ensures validity of target behaviors and immediacy of reward delivery.
Two target behaviors relevant to retention will be the primary focus of the DCM program: 1) abstinence from opiates and cocaine as verified via remote oral fluid testing, and 2) medication pickup from the methadone program as verified by clinic records. Participants in the TAU+DCM arm will receive financial rewards for achieving these pre-determined behavioral targets over a 48-week intervention period.
Comprehensive assessment of all participants will be conducted at baseline, 3-, 6-, and 12-months.
Aim 1: To determine the relative effectiveness of TAU+DCM compared to TAU alone in improving methadone treatment retention through 12-months post-treatment entry.
Aim 2: To determine the relative effectiveness of TAU+DCM compared to TAU alone in terms of [Aim 2A] reducing opioid use and cocaine use; and [Aim 2B] improving other secondary outcomes including non-targeted substance use and quality of life through 12-months post-treatment entry.
Aim 3: To explore app use patterns, acceptability, and perceived value of the personalized treatment intervention through 12-months post-treatment entry.
Innovation lies in the platform and structure of CM delivery that ensures treatment fidelity with automation of remote behavioral monitoring and reward delivery without involvement of clinical staff. This project represents a novel application of digital therapeutics to enhance the effectiveness of OUD treatment with polysubstance use.
Findings from this project can improve the public health impact of methadone treatment by identifying an effective and scalable approach to address polysubstance use among patients at heightened risk of treatment dropout.
Awardee
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
Baltimore,
Maryland
212015633
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 09/29/25 to 07/31/27 and the total obligations have increased 34% from $2,254,579 to $3,027,776.
Friends Research Institute was awarded
Digital Contingency Management Polysubstance Use in Methadone Treatment
Project Grant R01DA057608
worth $3,027,776
from National Institute on Drug Abuse in September 2022 with work to be completed primarily in Baltimore Maryland United States.
The grant
has a duration of 4 years 10 months and
was awarded through assistance program 93.279 Drug Abuse and Addiction Research Programs.
The Project Grant was awarded through grant opportunity HEAL Initiative: Understanding Polysubstance Use and Improving Service Delivery to Address Polysubstance Use (R01 Clinical Trial Optional).
Status
(Ongoing)
Last Modified 8/6/25
Period of Performance
9/30/22
Start Date
7/31/27
End Date
Funding Split
$3.0M
Federal Obligation
$0.0
Non-Federal Obligation
$3.0M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01DA057608
Additional Detail
Award ID FAIN
R01DA057608
SAI Number
R01DA057608-3199651070
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75N600 NIH National Insitute on Drug Abuse
Funding Office
75N600 NIH National Insitute on Drug Abuse
Awardee UEI
YM5EKEVEGB75
Awardee CAGE
3D0E6
Performance District
MD-07
Senators
Benjamin Cardin
Chris Van Hollen
Chris Van Hollen
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) | $2,254,579 | 100% |
Modified: 8/6/25