Substance Use Disorder (SUD)DIS-SUDNCT07875361
Disease Intervention Specialist (DIS) for SUD
An observational study of Substance Use Disorder (SUD) and Opioid Use Disorder, run by Ohio State University at 1 site in United States.
Trial summary
This prospective observational study evaluates three Disease Intervention Specialist service models designed to proactively identify and support adults at risk for substance use disorder. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Substance Use Disorder (SUD), Opioid Use Disorder, Alcohol Use Disorder (AUD)
- How many people
- 1,200 participants
- Where
- 1 siteUnited States
- Study dates
- Dec 2026to 29 Sep 2030
- Phase
- Observational
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: * Columbus Public Health DIS programs * Emergency Department referrals * Community Agencies * Social-network outreach
Who may be able to join
- age: must be 18 years or older at the time of screening
- language: must be English-Speaking
- Capacity and willingness to participate
- SUD risk or diagnosis
- Not already in SUD care
Who cannot join
- Non-English Speaking
- Currently engaged in formal substance use disorder treatment at the time of initial DIS contact
- Low risk or does not have a current substance use disorder diagnosis
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
The Ohio State University Wexner Medical Center
Columbus, Ohio, 43210
About this study
Official title: Adapting the Public Health Disease Intervention Specialist (DIS) Model for Proactive Substance Use Disorder (SUD) Intervention
This prospective observational study evaluates three Disease Intervention Specialist service models designed to proactively identify and support adults at risk for substance use disorder. The models include substance use screening, motivational interviewing, case management, treatment referral, and optional peer support. The study will compare participant outcomes across the service models, including substance use severity, treatment engagement, overdose, service utilization, and satisfaction.
Read the detailed description
There is a critical need to intervene with individuals affected by substance use disorder (SUD) earlier in their trajectory, even before they present to a location where screening or care could be possible. Rapid diagnosis and linkage to treatment (secondary prevention) is a cornerstone of any epidemic response but often very delayed for SUD. For communicable infectious diseases (ID), health departments employ disease intervention specialists (DIS) skilled in outreach to underserved and disproportionately affected populations identified via social contacts, who once located, disclose their own contacts, yielding "snowball" chain-referral for the most direct, rapid, and proactive approach to identify affected, but undetected, populations. SUD also exists within social networks and substance exposure spreads like contagion, but the DIS paradigm has not been adapted to the problem of SUD. We will (AIM 1): Develop and implement promising operational models for adapting the conventional ID DIS model to provide secondary SUD prevention: In close collaboration with health department partners, we will create three service models: 1) Overlay of SUD intervention on current ID DIS: systematically screen clients (already being identified by ID diagnosis or exposure) for concurrent SUD; 2) SUD DIS: SUD specific DIS elicit social contacts with potential SUD from index clients with SUD who are identified in collaboration with other local service agencies; and 3) SUD DIS with peer-support: Peers embedded with the SUD DIS team. Model 1 will be operated separately from the SUD DIS program. In all 3 models, DIS will provide secondary prevention to those SUD screen+ (i.e., high risk score on NIDA-Modified ASSIST) and not already in care. (AIM 2): Rigorously evaluate models for incorporating SUD prevention into DIS programs. We will compare program-level outcomes using (i) data from DIS records, (ii) summary intake counts from regional SUD treatment centers, (iii) time and motion observations of DIS activities, and (iv) qualitative interviews with stakeholders (clients and staff) about the DIS program. We will also prospectively observe clients (n=400 each DIS program, for total n=1200) receiving DIS intervention who consent to research to enable comparison of the effectiveness of SUD secondary prevention provided by the different DIS program models. Assessment: Self-report at baseline (0),1, and 6 months, complemented by review of health records (via release of information) and vital statistics (i.e., mortality). Primary Outcome: severity of drug use at 6 months post initial DIS interview. Key Secondary Outcomes: participant characteristics; healthcare/service utilization; alcohol use; and overdose. This innovative, high-impact investigation will be the first to use this well-established public health approach, capitalizing on social networks, to offer early and more specifically targeted secondary prevention for SUD. Results will vastly improve public health practice, program planning, policy, and future intervention.
- Conditions
- Substance Use Disorder (SUD), Opioid Use Disorder, Alcohol Use Disorder (AUD), Drug Use, Overdose
- Keywords
- substance use disorder, disease intervention specialist, public health, contact tracing, peer navigation, substance use treatment, public health outreach
- Medical subject headings
- Substance-Related Disorders, Opioid-Related Disorders, Alcoholism, Drug Overdose
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Model 1: Integrated Infectious Disease DIS+SUD Intervention | Participants receive services through an existing infectious disease DIS program in which substance use disorder (SUD) screening, motivational interviewing, case management, referral to treatment, and social network outreach are integrated into routine infectious disease investigation activities. | |
| Model 2: SUD Specific DIS Intervention | Participants receive services through a DIS program dedicated specifically to substance use disorder prevention and intervention. Services include SUD screening, motivational interviewing, case management, referral to treatment providers, and social network-based outreach. | |
| Model 3: SUD DIS Intervention with Peer Support | Participants receive the same SUD-focused DIS intervention as Model 2, with the addition of trained peer support specialists. Peer navigators assist with outreach, rapport building, appointment support, treatment navigation, reminders, and overcoming barriers to care. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Severity of Drug Use
Change in substance use severity among participants receiving DIS-based SUD interventions
-substance use severity will be assessed using the NIDA-Modified ASSIST (NM-ASSIST)
Measured: 6 months post initial DIS interview
Secondary outcomes (5)
Linkage to Substance Use Disorder Treatment
After DIS based intervention, the number of participants who initiate treatment with SUD treatment provider
-assessed through study self-report follow-up survey and referral tracking records
Measured: Within 3 months of initial DIS interview
Retention in SUD treatment
Participants who remain engaged in SUD treatment services following successful linkage to care
-self reported treatment services utilization and treatment engagement records
Measured: 6 months after initial DIS interview
Number of Social Contacts Elicited per Index Participant
Count of social contacts (number of named individuals) elicited from each index participant during DIS contact elicitation interviews. Unit of measure: number of contacts per index participant.
-Measured by abstraction of DIS social network and case management records documenting elicited contacts
Measured: During DIS intervention period (up to 3 months)
Number of Healthcare and Substance Use Treatment Encounters
Number of self-reported healthcare and SUD treatment encounters, including emergency department visits, hospital admissions, outpatient medical visits, and SUD treatment visits, reported for the follow-up period. Unit of measure: number of encounters per participant in each category.
-Measured using a study-developed healthcare utilization questionnaire administered at the 1-month and 6-month follow-up surveys, with verification by health record review as available
Measured: From baseline through 6 months post-initial DIS interview
Percentage of Participants Attending at Least One SUD Treatment Visit
Percentage of participants who attend at least one substance use disorder treatment visit during follow-up, compared between participants receiving SUD DIS services with embedded peer support (Model 3) and those receiving SUD DIS services without peer support (Model 2). Unit of measure: percentage of participants.
-Measured by self-report at follow-up and treatment engagement records
Measured: 6 months post-initial DIS interview
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Oct 2026
- Study startDec 2026 (estimated)
- Primary completionSep 2029 (estimated)
- Study completion29 Sep 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Substance Use Disorder (SUD)Studies of the same condition, open and under way.
- More trials run by Ohio State UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ohio State University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Brittany Punches, Ohio State University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07875361
- Sponsor's protocol ID
- STUDY20252142
- Other IDs
- U01CE003823
- Acronym
- DIS-SUD
- Status last verified
- Sep 2026
- First submitted
- 23 Sep 2026
- Last updated
- 15 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided