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Attention Deficit Disorder With Hyperactivity (ADHD)JUSTICE-TDAHNCT07487155

Unified Junction of Care, Integrated Treatments and Team Coordination for ADHD in Prison Settings With Substance Use Disorder

A study testing Workshop in people with Attention Deficit Disorder With Hyperactivity (ADHD) and Substance Use Disorder (SUD), run by University Hospital, Brest at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

Substance use disorders (SUD) and attention deficit disorder with or without hyperactivity (ADHD) are frequently co-morbid, particularly among people under court supervision. The coexistence of these disorders increases the social and legal vulnerability of individuals. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Workshop
Could I receive a placebo?
No, everyone receives an active treatment
How many people
39 participants
Where
1 siteFrance
Study dates
3 Aug 2026to 1 Jan 2028
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adult, under the supervision of the justice system or monitored by a correctional facility
  • Diagnosis of Substance Use Disorder (SUD)
  • Diagnosis of Attention Deficit Hyperactivity Disorder (ADHD)
  • No objection from the patient
  • Affiliated with a Social Security system

Who cannot join

  • Severe or decompensated psychiatric disorders
  • Severe cognitive impairment
  • Lack of understanding of the French language
  • Refusal to participate

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • CHU Brest

    Brest, 29200

    Morgane GUILLOU LANDREAT, MD, 029822342348, morgane.guillou@chu-brest.fr

    Morgane GUILLOU LANDREAT, MD

    Recruiting

Other trials in France

About this study

Substance use disorders (SUD) and attention deficit disorder with or without hyperactivity (ADHD) are frequently co-morbid, particularly among people under court supervision. The coexistence of these disorders increases the social and legal vulnerability of individuals. Better identification of ADHD in vulnerable people with SUD is essential to improving their care. This project aims to provide appropriate support for this at-risk population.

Being tested
Workshop
Medical subject headings
Attention Deficit Disorder with Hyperactivity, Substance-Related Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • WorkshopOther

    Assess the 5 workshops, co-constructed by the scientific committee and thanks to feedback from the qualitative study

Study groups in NCT07487155
Study groupRoleWhat they receive
WorkshopsExperimentalWorkshops with a small group of patients.
Receives: Other: Workshop

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 80% of patients participated in the workshops

    The primary outcome measure is the acceptability of the program to participants in the pilot workshops, gathered through:

    • Semi-structured pre- and post-intervention interviews
    • A Likert scale
    • Workshop participation rate (at least 80%)

    Measured: From enrollment to the end of wordshop at 6 months

Secondary outcomes (1)
  1. SF-12 quality of life

    The secondary outcome measure will be measured by the SF-12 quality of life, before and after the 5 workshops. The SF-12 is a self-reported outcome measure assessing the impact of health on an individual's everyday life.

    Measured: From enrollment to the end of wordshop at 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Mar 2026
  2. Study start3 Aug 2026
  3. Primary completion1 Jan 2028 (estimated)
  4. Study completion1 Jan 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
39 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07487155
Sponsor's protocol ID
29BRC25.0324 - JUSTICE-TDAH
Other IDs
IDRCB
Acronym
JUSTICE-TDAH
Status last verified
Aug 2026
First submitted
12 Mar 2026
Last updated
11 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All collected data that underlie results in a publication

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