Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06852170

Supporting Data-driven Decision-Making to Support Substance Use Service Expansion Policies and to Prevent Overdoses

Led by Chestnut Health Systems · Updated on 2026-03-16

341

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

C

Chestnut Health Systems

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research focuses on supporting decision makers across various sectors in Oregon, such as community service providers, public health officials, justice system members, advocates, and payers, to improve substance use services and reduce overdoses. Oregon faces significant challenges with opioid and methamphetamine use and limited access to services. The study aims to provide these leaders with relevant, easy-to-use data to guide evidence-informed policies and actions that enhance substance use prevention and treatment statewide. The study evaluates a novel strategy called Co-Design Sessions (CDS), which engages decision makers in collaboratively identifying and refining data products tailored to their needs. Counties are randomly assigned to either participate in CDS and receive customized data products or to receive standardized data products later. CDS uses methods like Liberating Structures, Group Model Building, and human-centered design to create reports, dashboards, and other tools that support policy decisions. The study also includes an extension phase where all counties eventually receive data products. Participants will engage in surveys and assessments at multiple time points over approximately 42 months to measure community engagement, collaboration networks, trust in data, and the usability of data products. Researchers will monitor how these data tools influence policy decisions, substance use service availability, and overdose prevention efforts. The study ensures ongoing evaluation through these measurements and aims to develop sustainable methods for data sharing to support state-wide substance use service improvements.

CONDITIONS

Brief Title

Data2Action Oregon Project: Supporting Data-driven Decision-Making for Substance Use Services, Policy, and Overdose Prevention

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old
  • Has decision-making authority related to substance use service delivery or policy within their professional role
  • Includes leadership (e.g., executive directors), middle managers (e.g., case managers, supervisors), frontline workers, or advisors (e.g., legislative staff, data analysts)
  • Works in organizations involved in behavioral health, public health, health payment, first response, or health advocacy
Not Eligible

You will not qualify if you...

  • None

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or virtual) for eligibility assessment

Co-Design Sessions

Duration - Up to 2 years depending on wedge assignment

Participants in the CDS group will participate in 4 co-design sessions to collaborate and tailor data products for substance use service decision-making.

4 sessions (in-person or virtual)

Data Product Dissemination

Duration - Up to 2 years depending on wedge assignment

Participants receive data products, either fully tailored through CDS or standardized, to inform their daily decision-making related to substance use services and policy.

Data products provided at key timepoints (T3 or T4)

Long-term Monitoring

Duration - Approximately 42 months post-baseline

Participants are observed through surveys and assessments measuring community engagement, collaboration, trust in data, and usability of data products over multiple timepoints.

Surveys at baseline, 15, 18, 30, and 42 months post-baseline; annual usability assessments for up to 2 years after data product release

Trial Site Locations

Total: 1 location

1

Chestnut Health Systems

Eugene, Oregon, United States, 97401

Actively Recruiting

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Research Team

G

Gracelyn Cruden, PhD, MA

J

Jessica Harrison, MS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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