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NCT07102914

Brief Intervention at Adult Education

Enrolling by Invitation
NAAges 17+InterventionalScreening
Yale University
~340 participants
Updated 2026-03-27 on ClinicalTrials.gov
What's tested:Screening, Brief Intervention and Referral for Treatment (SBIRT)

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Patient-Reported Outcomes Measurement Information System (PROMIS) - Depression
Measured over pre-intervention, day 1; 3; 6 months
+5 more outcomes measured

Conditions

Behavioral Health Challenges

Explore related trials

AngerAnxietyBehavioral Health ChallengesDepressionSubstance Use

NCT07102914

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • New Haven Adult Education Center

    New Haven, Connecticutno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Derrick Gordon, Ph.D. · PRINCIPAL_INVESTIGATOR · Yale University

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

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Eligibility criteria

Inclusion

≥ 17 years and currently enrolled either the High School Credit or General Educational Development programs.
All eligible staff will be invited to participate in this study

Exclusion

students with acute psychosis or intoxication, low intellectual functioning.
Not a staff at New Haven Adult Education

What this trial measures

  • Patient-Reported Outcomes Measurement Information System (PROMIS) - Depressionpre-intervention, day 1; 3; 6 months

    Behavioral measure of depression symptoms, Mild symptoms (T-score of 55\<\>60), moderate (T-score of 60\<\>65), and severe (T-score of 66\<) clinical thresholds

  • Patient-Reported Outcomes Measurement Information System (PROMIS) - Anxietypre-intervention, day 1; 3; 6 months

    Behavioral health measure, Mild symptoms (T-score of 55\<\>60), moderate (T-score of 60\<\>65), and severe (T-score of 66\<) clinical thresholds

  • Patient-Reported Outcomes Measurement Information System (PROMIS) - Angerpre-intervention, day 1; 3; 6 months

    Behavioral Health Screening and Tracking measure, Mild symptoms (T-score of 55\<\>60), moderate (T-score of 60\<\>65), and severe (T-score of 66\<) clinical thresholds

  • Patient-Reported Outcomes Measurement Information System (PROMIS) - Smokingpre-intervention, day 1; 3; 6 months

    Behavioral Health measure, Mild symptoms (T-score of 55\<\>60), moderate (T-score of 60\<\>65), and severe (T-score of 66\<) clinical thresholds

  • Patient-Reported Outcomes Measurement Information System (PROMIS) - Substance Usepre-intervention, day 1; 3; 6 months

    Behavioral Health measure, Mild symptoms (T-score of 55\<\>60), moderate (T-score of 60\<\>65), and severe (T-score of 66\<) clinical thresholds

  • Patient-Reported Outcomes Measurement Information System (PROMIS) - Alcohol Usepre-intervention, day 1; 3; 6 months

    Behavioral Health measure, Mild symptoms (T-score of 55\<\>60), moderate (T-score of 60\<\>65), and severe (T-score of 66\<) clinical thresholds