Attention Deficit Hyperactivity Disorder (ADA)

N

Nantes University Hospital (NUH)

Status

Not yet enrolling

Conditions

Behavior Hyperactive
Attention Deficit Hyperactivity Disorder
Behavior Disorders

Treatments

Other: Patients suffering from the co-occurrence of ADHD and addiction(s)

Study type

Interventional

Funder types

Other

Identifiers

NCT06232226
RC23_0074

Details and patient eligibility

About

The ADA cohort aims for the systematic and standardized collection of sociodemographic, clinical and neuropsychological data, during 2 visits (inclusion and 12 months), from patients suffering from the co-occurrence of ADHD (Attention Deficit Hyperactivity Disorder) and addiction(s), in addition to the treatment as usual adapted to each situation.

Full description

Information on the study and diagnosis of ADHD will be carried out during a medical evaluation consultation, as part of routine care. The two research visits (inclusion and at 12 months) will be added by the research and will each include: A structured clinical interview with a research professional (traceability of oral consent, administration of structured interviews, collection of self-questionnaires, collection of care from the medical record) A neuropsychological assessment with a neuropsychologist

Enrollment

60 estimated patients

Sex

All

Ages

15 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria :

  • Patients aged over 15 years and 3 months
  • For whom a diagnosis of ADHD has been confirmed less than 6 weeks ago
  • For whom the diagnosis of one or more addictive disorder(s) (substance use disorder or behavioral addiction) has been confirmed
  • Meeting the indication for treatment with MPH according to European recommendations (Kooij et al., 2019)
  • For patients who can actually benefit from MPH: who have not yet started taking MPH
  • Social security affiliates

Exclusion Criteria :

  • Presenting disorders of higher cognitive functions (at the discretion of the referring clinician or the investigator making the inclusion), making data collection impossible
  • Presenting difficulties in reading or writing the French language making data collection impossible
  • Unable to commit to being available for the 2 visits planned as part of the cohort
  • Under guardianship or legal protection

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

Neuropsychological assessment
Other group
Description:
Determination of the neuropsychological profile
Treatment:
Other: Patients suffering from the co-occurrence of ADHD and addiction(s)

Trial contacts and locations

1

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Central trial contact

Clémence CABELGUEN, PH

Data sourced from clinicaltrials.gov

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