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
- Are there results?
- Not yet: the study is under way
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
Study at a glance
From the registry record, last updated by the sponsor on 15 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Adapting the Public Health Disease Intervention Specialist (DIS) Model for Proactive Substance Use Disorder (SUD) Intervention
- ClinicalTrials.gov ID
- NCT07875361
- Acronym / sponsor ID
- DIS-SUD / STUDY20252142
- 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
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 1,200 participants (estimated)
- Lead sponsor
- Ohio State UniversityUniversity, hospital or other
- Study start
- Dec 2026 (estimated)
- Primary completion
- Sep 2029 (estimated)
- Study completion
- 29 Sep 2030 (estimated)
- First posted
- 15 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| 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. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- * Columbus Public Health DIS programs * Emergency Department referrals * Community Agencies * Social-network outreach
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (3 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Severity of Drug Use
Time frame: 6 months post initial DIS interview
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)
5 secondary outcomes
Linkage to Substance Use Disorder Treatment
Time frame: Within 3 months of initial DIS interview
Retention in SUD treatment
Time frame: 6 months after initial DIS interview
Number of Social Contacts Elicited per Index Participant
Time frame: During DIS intervention period (up to 3 months)
Number of Healthcare and Substance Use Treatment Encounters
Time frame: From baseline through 6 months post-initial DIS interview
Percentage of Participants Attending at Least One SUD Treatment Visit
Time frame: 6 months post-initial DIS interview
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Oct 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Substance Use Disorder (SUD) and Opioid Use Disorder, run by Ohio State University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 15 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Severity of Drug Use (time frame: 6 months post initial DIS interview). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Oct 2026.