Actively Recruiting

Phase Not Applicable
Age: 14Years - 21Years
All Genders
NCT06395467

Integrated Treatment for Enhancing Growth in Recovery During Adolescence

Led by Massachusetts General Hospital · Updated on 2026-03-06

294

Participants Needed

2

Research Sites

183 weeks

Total Duration

On this page

Sponsors

M

Massachusetts General Hospital

Lead Sponsor

N

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a Phase II parallel group randomized controlled trial with 294 adolescents (age: 14-21 years) with alcohol and other drug \[AOD\] use disorder (hereafter substance use disorder), that compares two different active psychosocial interventions designed to address adolescent substance use disorder. Participants are recruited from our clinical settings and the community at two sites: one in the metro Boston, Massachusetts (MA) area and the other in the metro Farmington, Connecticut (CT), area. Study aims and hypotheses are as follows: 1. To extend the evidence for the initial efficacy of Integrated Treatment for Enhancing Growth in Recovery During Adolescence (InTEGRA), which integrates 12-Step Facilitation (TSF) with Motivational Enhancement Therapy/Cognitive Behavioral Therapy (MET/CBT) relative to gold standard MET/CBT alone (N = 294). It is hypothesized that youth assigned to InTEGRA will have greater 12-step participation during and following treatment, higher abstinence rates, and fewer substance-related negative consequences. 2. Investigate the personal recovery capital (PRC) and social recovery capital (SRC) mechanisms of behavior change through which InTEGRA may confer benefits dynamically over time (e.g., PRC: motivation, self-efficacy, coping; SRC: 12-step involvement; social network changes). 3. Investigate moderators of InTEGRA's effects on outcomes across one-year follow-up (e.g., effect of age, network support for AOD use; psychiatric severity; age composition of 12-step meetings on substance use and substance-related consequences). It is hypothesized that higher network support for AOD use, abstinence motivation, and greater AOD severity, will have a better response to InTEGRA. 4. Explore barriers and facilitators to InTEGRA adoption and implementation across providers and system administrators within the context of a type I hybrid effectiveness-implementation research design.

CONDITIONS

Official Title

Integrated Treatment for Enhancing Growth in Recovery During Adolescence

Who Can Participate

Age: 14Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 14 and 21 years
  • Diagnosis of substance use disorder according to DSM-5
  • Able to read and understand English at a 5th-grade level
  • Reside in Eastern time zone states including CT, DE, FL, GA, IN, KY, ME, MD, MA, MI, NH, NJ, NY, NC, OH, PA, RI, SC, TN, VT, VA, and WV
  • Any alcohol or other drug use in the past 90 days or in the 90 days before being in a controlled environment
  • Meet criteria for outpatient (level I) treatment
  • Participant and family member or guardian (if under 18) agree to sign consent forms
  • Participant and family member or guardian available to provide contact information for follow-up
Not Eligible

You will not qualify if you...

  • Suicidal thoughts with a plan, suicidal behavior, plans to harm self or others, or self-injury history in past 30 days
  • Lifetime diagnosis of schizophrenia
  • Current medical or psychiatric condition preventing outpatient treatment attendance
  • Inability or unwillingness to identify a contact person for follow-up
  • Currently attending another substance use disorder treatment program or receiving conflicting psychotherapy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 2 locations

1

UConn Health

Farmington, Connecticut, United States, 06032

Actively Recruiting

2

MGH Department of Psychiatry

Boston, Massachusetts, United States, 02114

Actively Recruiting

Loading map...

Research Team

A

Alexandra W Abry, BA

CONTACT

J

Jenny B O'Connor, BA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here