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Study identifier: NCT06858527 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Deficit Hyperactivity Disorder / Substance Use Disorder Comorbidity in Integrated Treatment

Condition: Attention Deficit Hyperactivity Disorder (ADHD) · Substance-related Disorder  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseNA
Planned participants132
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Attention Deficit Hyperactivity Disorder (ADHD) and Substance Use Disorders (SUDs) is a highly common comorbid condition associated with serious medical and psychosocial consequences. However, and despite the international consensus recommending integrated treatment for this comorbidity, few studies tested the efficacy of specific psychotherapeutic treatment for this comorbidity. The aim of this study is to test the efficacy of a specific group Cognitive and Behavioral Therapy (CBT) for the treatment of adults with this comorbidity. This is a longitudinal, randomized controlled intervention study utilizing a crossover design between the intervention and treatment-as-usual (TAU) waitlist condition, aimed at testing the effectiveness of an integrated psychotherapeutic group treatment for adults with comorbid Attention Deficit Hyperactivity Disorder (ADHD) and Substance Use Disorders (SUDs).

This description comes directly from the study's public registry record.

Talk to the study team

Norman Therribout, PhD  ·  +33140054464  ·  norman.therribout@aphp.fr

Romain Icick, MD, PhD  ·  +33140054275  ·  espace.murger.lrb@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Hôpital Fernand Widal, Assistance-Publique - Hôpitaux de ParisParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06858527