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Emotional Dysregulation in Adult ADHD.

Emotional Dysregulation and Cyclothymia in Adult Patients With ADHD: Cohort Follow-up of Patients in Two Referral Centers

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03494478
Acronym
EMO-TDA
Enrollment
120
Registered
2018-04-11
Start date
2019-10-30
Completion date
2023-06-30
Last updated
2023-04-18

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

Conditions

Adult ADHD

Keywords

Cohort study, Emotion dysregulation, Questionnaires, Actimetry, Neuropsychology

Brief summary

Attention deficit disorder in adults with or without hyperactivity (ADHD) is a common disorder, affecting around 3% of the population. ADHD increases the risk of psychiatric disorders (mood disorders, sleep disorders, personality disorders, addictive behavior), risky behaviors, and vocational difficulties. Emotional dysregulation (ED) constitute a major hindrance in the daily life of subjects, with a great impact on the general functioning and the quality of life of the patients. The investigators want to determine the characteristics of patients with each type of ED (impulsivity, exacerbated emotional intensity, cyclothymia, borderline personality traits), and study the stability of these traits over time. Since circadian rhythms influence mood and circadian rhythms frequently occur in patients with ADHD, the investigators want to determine if there is a link between ED and instability in circadian rhythms. Finally, they would like to observe whether the ED evolves and according to whether or not treatment is taken

Interventions

OTHERNeuropsychological testing

The assessment will will be done at the time of the initial evaluation (undiagnosed / untreated patients), then at one year of follow-up

The assessment will will be done at the time of the initial evaluation (undiagnosed / untreated patients), then at one year of follow-up.

OTHERSelf-questionnaires on emotional topics

The assessment will will be done at the time of the initial evaluation (undiagnosed / untreated patients), then at one year of follow-up.

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female aged ≥ 18 years * diagnosis of adult ADHD prior to inclusion * Affiliated to a social health insurance * Subject having dated and signed informed consent * Subject having been informed of the results of the prior medical examination

Exclusion criteria

* Mobility project preventing follow-up for 1 year (planned move) * impossibility to give the subject information enlightened (subject in emergency situation, difficulties in understanding the subject, mental retardation, illiteracy or insufficient command of the French language ...) * Subject under the protection of justice * Subject under guardianship or curatorship * Pregnancy * Breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Characterization of emotional dysregulation (descriptive analysis of different scales assessing emotional dysregulation)At inclusionScore of cyclothymia (TEMPS-A scale)

Secondary

MeasureTime frameDescription
Association between emotional dysregulation, cognitive deficits and circadian instabilityAt inclusionCorrelation between emotional dysregulation and executive and attentional dysfunction measured with the TAP test. Correlation between emotional dysregulation and instability index of circadian rhythms measured by actimetry.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026