Clinical Trials Logo

Clinical Trial Summary

Objectives:

1. To investigate the effectiveness of adjuvant with aripiprazole to methylphenidate for disruptive mood dysregulation disorder (DMDD) in youths with attention-deficit/hyperactivity disorder (ADHD)

2. To investigate the neural basis of chronic irritability in youths with functional magnetic resonance imaging (fMRI)

3. To compare the clinical characteristics of youths with comorbid ADHD and DMDD to youths with ADHD only


Clinical Trial Description

Background:

Disruptive mood dysregulation disorder (DMDD) in children and adolescents with attention-deficit/hyperactivity disorder (ADHD) is a common clinical challenge and leads to severe impact and burden on both the patients and their family. Although methylphenidate (MPH) showed good efficacy in the treatment of ADHD, there is still lack of well-established pharmacological treatment for DMDD. Furthermore, little research focuses on the effect of pharmacological treatment on neural correlates of chronic irritability. Previous literature suggested the potential role of atypical antipsychotics in the treatment of DMDD. Therefore, this study aimed to investigate the effectiveness of adjuvant of aripiprazole (APZ) to MPH in patients with comorbid ADHD and DMDD. In addition, the investigators explored the clinical manifestation and neural basis of DMDD using inventories, neuropsychological tests and neuroimaging studies.

Methods:

The investigators enrolled patients with ADHD+DMDD (n = 31) and ADHD only (n = 27). Those subjects were evaluated with inventories of emotional and behavioral problems, neuropsychological tests, as well as fMRI with challenging tests which aimed to induce frustration at baseline assessment. Then, subjects of ADHD+DMDD group received 6 weeks' combination treatment of MPH+ APZ with flexible dosage according to clinical judgment. All the initial evaluations were administered again after treatment. The comparison of clinical characteristics and neuroimaging findings between ADHD+DMDD group and ADHD only group will be conducted. In addition, the effectiveness of treatment will be analyzed. The effects of pharmacological treatment on neural correlates of chronic irritability will also be investigated. ;


Study Design


Related Conditions & MeSH terms

  • Disruptive Mood Dysregulation Disorder

NCT number NCT03358277
Study type Interventional
Source Tri-Service General Hospital
Contact
Status Completed
Phase N/A
Start date November 19, 2014
Completion date August 12, 2017

See also
  Status Clinical Trial Phase
Completed NCT03669289 - Enhanced Support for Behavioral Barriers to Learning: An Evaluation of the SCHOOL STARS Program N/A
Active, not recruiting NCT05049356 - Symptoms and Mechanisms of Child Psychiatric Disorders
Completed NCT02281825 - Correlating Real and Virtual World Behavioral Fluctuations in Adolescence N/A
Completed NCT01862549 - Adapting DBT for Children With DMDD: Pilot RCT N/A
Recruiting NCT04820946 - Evolution of DMDD Children and Adolescent
Recruiting NCT03944083 - Children With ADHD and Emotional Dysregulation
Withdrawn NCT05357495 - Characterization and Brain Mechanisms of Frustration in Youth With Severe Irritability or Attention Deficit Hyperactivity Disorder (ADHD) N/A