Epilepsy and Mood Regulation Disorder in Children

NCT02568813 | Unknown

• 1 other identifier: 2013-834
• Study Type: interventional
• Target: 300
• Locations: 1 country
• Sites: 1

Brief Summary

Epilepsy is a multifaceted disorder and a major public health problem. In addition to recurrent and unpredictable seizures, abnormalities in psychiatric status, cognition and social-adaptive behaviors are potential major sources of disability in children and adults with epilepsy disorders. Recent studies have unequivocally documented raised psychiatric comorbidities in children with epilepsy, particularly emotional regulation disorders such as depression and anxiety, as compared to both the general population and the children with other medical disorders, neurological and non-neurological. A prevalence of 12% to 35% has been reported, compared to 3-8% in the general population. Major advances have begun to uncover the potential mediators of emotional regulation disorders and social comorbidities in epilepsy, but important gaps remain in the early detection, treatment and prevention of these disorders. A very small number of investigations have examined children with epilepsy at or near the time of diagnosis. This is a time during which the effects of chronic epilepsy, potential averse social effects of epilepsy, and other complicating aetiological effects are minimized. Epilepsy syndromes provide a useful framework for considering the risk and type of emotional dysregulation comorbidities. But variability within and across syndromes needs to be taken into account thus requiring a strict phenotyping by specialists in the filed of pediatric epileptology. Retrospective studies, usually including patients with chronic epilepsies and suffering from a mixed spectrum of epilepsy syndromes introduce biases leading to rather disparate findings. Are such disorders the result of common physiopathological mechanisms, which precede the development of the epilepsy? The link between an underlying brain disorder and psychiatric comorbidities has emerged in recent literature, with evidence based on studies in adults, suggesting bidirectional relations between epilepsy and neurobehavioural comorbidities. Emotional regulation disorders can follow the onset of epilepsy, but they can also precede it, thus serving as a possible risk factor. The clinical implication of such a bidirectional association is that neurobehavioural comorbidities might be present at diagnosis and even before epilepsy onset. There is a need for greater understanding of the causes of these conditions in younger people. The degree to which specific epilepsy syndromes are associated with the relative risk of emotional dysregulation disorders in children with new- or recent-onset (within six months prior to enrolment) has rarely been comprehensively examined and represents the focus of the current investigation. The investigators study will be based on a prospectively recruited cohort of 280 children/adolescents with recently diagnosed epilepsy. All participating centres dispose of the necessary competences for a precise diagnosis of the epilepsy syndromes and the tools for a per case appropriate aetiology screening. Following a first seizure children are usually first examined at hospital based emergency departments. Prompt referral to the epilepsy teams participating at the present study will significantly reduce the population biases and shortcuts encountered in studies that recruited patients with chronic epilepsy followed in tertiary care epilepsy units. The investigators expect their results to provide a greater understanding of both the shared and the unique features of emotional regulation disorders, in relation to specific epilepsy categories defined on the basis of the underlying physiopathological mechanisms. Such knowledge will also assist clinicians and families in the planning of both diagnosis and management resources.

Conditions

Epilepsy

Keywords

epilepsy; depression; mood disorder; anxiety; cyclothymia; Behavioral neuropsychiatric features

Outcome Measures

Primary Outcomes (1)

• Number of children with new- or recent-onset epilepsy with a pathological score in a least one of the 3 scales

  The 3 scales are MDI-C ; R-CMAS and Kochman scale : * A standard score of \>66 for MDI-C (Multiscore Depression Inventory for Children) indicating a depressive disorder; * A standard score of \>60 or \<40 for R-CMAS (Revisited Children's Manifest Anxiety Scale) indicating an anxiety disorder; * A score of \>12 for Kochman indicating a cyclothymia disorder

  18 months

Secondary Outcomes (2)

• Correlate pathological scores obtained with the type of epilepsy

  18 months

• Correlate pathological scores with the progression of epilepsy disease

  18 months

Study Arms (1)

Scales passation

EXPERIMENTAL

Behavioral: Multiscore Depression Inventory for Children scale

Interventions

Multiscore Depression Inventory for Children scale BEHAVIORAL

Also known as: Revisited Children's Manifest Anxiety Scale, Kochman indicating a cyclothymia disorder Scale, Weschler Intelligence Scale for Children - 4th Edition

Scales passation

Eligibility Criteria

• Age: 6 Years - 15 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17)

You may qualify if:

• one of the following 3 epilepsy categories (focal structural epilepsy, with or without (MRI-negative) detectable cerebral lesion; focal idiopathic (genetic) epilepsy; generalized idiopathic (genetic) epilepsy).
• Onset of epilepsy within the 6 months from enrolment.
• Patients whose eventual antiepileptic drug treatments were not modified in the months preceding the neuropsychological and psychiatric evaluations.
• Patients who give their consent to participate in the study and whose legal guardians have agreed to sign the written consent form.

You may not qualify if:

• Patients younger than 5 years and 11 months or older than 15 years and 6 months.
• Patients with a diagnosis of epilepsy, other than the types defined above.
• Cognitive impairment, defined as a score of \<70, based on WISC-IV verbal comprehension and perceptual reasoning scales.
• Children with a confirmed diagnosis of a psychiatric disorder, other than those studied.

Sponsors & Collaborators

• Hospices Civils de Lyon: lead

Study Sites (1)

Hôpital Femme Mère Enfant

Bron, Rhône, 69500, France

RECRUITING

MeSH Terms

Conditions

Epilepsy; Depression; Mood Disorders; Anxiety Disorders; Cyclothymic Disorder

Condition Hierarchy (Ancestors)

Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Behavioral Symptoms; Behavior; Mental Disorders

Central Study Contacts

Alexis ARZIMANOGLOU, Pr

CONTACT

(0)4 27 85 77 04; aarzimanoglou@orange.fr

Agathe LAURENT,, PhD

CONTACT

(0)6 61 60 11 30; agathelaurent1977@gmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 30, 2015
• First Posted: October 6, 2015
• Study Start: March 30, 2015
• Primary Completion: April 30, 2022
• Study Completion: April 30, 2022
• Last Updated: September 13, 2019

Record last verified: 2019-09

Locations

FR (1)