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Recruiting NCT07503067

Identifying Substance Use Consequences

Observational Substance Use Disorder (SUD)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: none, there is no intervention in this study.
Who it may be relevant to
Registry conditions: Substance Use Disorder (SUD). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Development and Validation of a Measure of Substance-Related Consequences: A Novel Clinical Outcome Assessment for Substance Use Disorder Trials

Overview

The goal of this study is to develop a new tool for measuring substance use disorder treatment outcome. We will start by interviewing people and gathering advisory groups to develop the items for this new tool.

Interventions

  • Other none, there is no intervention in this study
    this is not an intervention study

Primary outcome measures

  • Extracted Themes [Time frame: same-day, single session]
  • Thematic analysis [Time frame: single-session, same day]

Eligibility criteria

Inclusion criteria

  • (1) ability to read and provide informed consent in English, and at least one of the following 2a) currently providing direct care to patients with substance use disorders, 2b) current or past treatment for an substance use disorder, or 2c) self-report of a close friend or family member who currently or previously received treatment for a substance use disorder.

Exclusion criteria

  • 1\) major psychiatric or medical condition that would interfere with participation (e.g., acute psychosis, severe withdrawal); 2) current intoxication (positive breath alcohol test or behavioral evidence of other substance intoxication).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • McLean Hospital — Belmont

Identifiers

NCT: NCT07503067 · 2025P000636 · UG3DA062906

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗