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Descriptive Epidemiology of a Specialized Consultation on ADHD in Adults at the Strasbourg University Hospital

Descriptive Epidemiology of a Specialized Consultation on Attention Deficit Hyperactivity Disorder in Adults at the Strasbourg University Hospital, and Evolution Analysis at One Year

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03601858
Acronym
Stras-TDA
Enrollment
300
Registered
2018-07-26
Start date
2018-06-01
Completion date
2019-06-30
Last updated
2018-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit and Hyperactivity Disorder

Keywords

Attention deficit, hyperactivity disorder, Adult, Epidemiology, Evolution, treatment

Brief summary

The main objective of this study is to carry out a descriptive study of the clinical and demographic characteristics of patients having consulted for a specialized opinion about ADHD in adults of the psychiatric service of the Strasbourg University Hospital. The characteristics of patients were collected during the first consultation, by the psychiatrist, and analyzed retrospectively. The secondary objective is to evaluate the evolution at one year in terms of follow-up, maintenance under medical treatment and perceived effects of it. The patients who had a prescription for pharmacological treatment of ADHD were contacted between 9 and 15 months after the first consultation and responded to a questionnaire assessing the evolution.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age \> 18 * Having a specialized consultation about ADHD in adults in the psychiatric service of the Strasbourg University Hospital * Agree with the use of medical files from the consultation for medical research

Exclusion criteria

* Disgree with the use of medical files from the consultation for medical research

Design outcomes

Primary

MeasureTime frameDescription
Hyperactivity DisorderBetween 9 and 15 months after the first consultation, contact of patients and collection of data for the evolution at one year analyzeMeasuring from the medical files of patients and questionnaire

Countries

France

Contacts

Primary ContactSébastien Weibel, MD
sebastien.weibel@chru-strasbourg.fr33 3 88 11 51 57

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026