Deficit Hyperactivity Disorder / Substance Use Disorder Comorbidity in Integrated Treatment
Launched by ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS · Feb 27, 2025
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at how effective a specific type of therapy called group Cognitive Behavioral Therapy (CBT) is for adults who have both Attention Deficit Hyperactivity Disorder (ADHD) and Substance Use Disorders (SUDs). Many people with ADHD also struggle with substance use, which can lead to serious health and social problems. The goal of the study is to see if this special group therapy can help improve the lives of those dealing with both conditions.
To be eligible for the trial, participants need to be 18 years or older, currently receiving treatment for a substance use disorder (except tobacco), and diagnosed with ADHD. They should also be able to understand and communicate in French and provide consent to participate. Those who join the study can expect to take part in group therapy sessions, where they will learn skills to manage their ADHD and substance use together. It's important to note that this trial is not currently recruiting participants, so if someone is interested, they will need to wait until the study begins.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18 or older ;
- • Suffer from at least one moderate to severe SUD regarding the DSM-5 (tobacco excluded) ;
- • Being currently treated for a SUD by a physician of a psychologist ;
- • Being diagnosed with an ADHD according to the DIVA 2.0 of DIVA-5 ;
- • Being affiliated to a health insurance ;
- • Understanding and being able to express himselves in French
- • Signed consent
- Exclusion Criteria:
- • Age under 18;
- • Pregnant or breastfeeding women;
- • Not having sign the consent form;
- • Major difficulties in understanding and/or expressing themselves in french;
- • Severe cognitive impairment;
- • Acute medical condition making assessment impossible and/or contraindicating participation in group intervention;
- • Substance use disorder in a protected environment, currentlu or in the last 15 days, or expected during the study;
- • No substance use disorder other than tobacco use disorder;
- • Persons under guardianship;
- • Participant deprived of liberty or under penal care orders;
- • Participation in another group psychotherapeutic intervention throughout the duration of the intervention
About Assistance Publique Hôpitaux De Paris
Assistance Publique - Hôpitaux de Paris (AP-HP) is a leading public hospital system in France, renowned for its commitment to healthcare excellence and innovative medical research. As a prominent clinical trial sponsor, AP-HP plays a pivotal role in advancing medical knowledge and improving patient care through rigorous scientific investigations across a wide range of therapeutic areas. With a focus on collaboration and interdisciplinary approaches, AP-HP leverages its extensive network of hospitals and expert clinicians to facilitate high-quality clinical trials that adhere to the highest ethical and regulatory standards, ultimately aiming to translate research findings into tangible health benefits for diverse patient populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Paris, , France
Patients applied
Trial Officials
Norman Therribout, PhD
Principal Investigator
Paris-Nanterre University, UR-4430 CLIPSYD ; Paris-Cité University, UMR-S-1144 INSERM; Fernand-Widal Hospital AP-HP
Romain Icick, MD, PhD
Study Director
Paris-Cité University, UMR-S-1144 INSERM; Fernand-Widal Hospital AP-HP
Lucia Romo, MD, PhD
Study Director
Paris-Nanterre University, UR-4430 CLIPSYD
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported