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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.

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Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

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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
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

Other trials in United States

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.

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 groups in NCT07875361
Study groupRoleWhat they receive
Model 1: Integrated Infectious Disease DIS+SUD InterventionParticipants 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 InterventionParticipants 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 SupportParticipants 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.

  1. 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)
  1. 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

  2. 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

  3. 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)

  4. 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

  5. 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.

  1. First posted15 Oct 2026
  2. Study startDec 2026 (estimated)
  3. Primary completionSep 2029 (estimated)
  4. Study completion29 Sep 2030 (estimated)

Resources

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)
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

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