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Aggression clinical trials

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NCT ID: NCT02618434 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder (ADHD)

Treatment of Impulsive Aggression in Subjects With ADHD in Conjunction With Standard ADHD Treatment (CHIME 2)

Start date: February 16, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the efficacy, safety, and tolerability of SPN-810 in the treatment of impulsive aggression in patients with Attention-Deficit/Hyperactivity Disorder (ADHD) in conjunction with standard ADHD treatment. Approximately 297 subjects aged 6 to 12 years with ADHD and comorbid impulsive aggression will be recruited in this study. The frequency of impulsive aggression behaviors will be assessed as a primary outcome. Additionally, the severity and improvement in impulsive aggression and quality of life measures for the subject and caregiver will be assessed using validated scales.

NCT ID: NCT02618408 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder (ADHD)

Treatment of Impulsive Aggression in Subjects With ADHD in Conjunction With Standard ADHD Treatment (CHIME 1)

Start date: January 25, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the efficacy, safety, and tolerability of SPN-810 in the treatment of Impulsive Aggression (IA) in subjects with Attention-Deficit/Hyperactivity Disorder (ADHD) in conjunction with standard ADHD treatment. Approximately 426 subjects aged 6 to 12 years with ADHD and comorbid impulsive aggression will be recruited in this study. The frequency of impulsive aggression behaviors will be assessed as a primary outcome. Additionally, the severity and improvement in impulsive aggression and quality of life measures for the subject and caregiver will be assessed using validated scales.

NCT ID: NCT02563145 Completed - Aggression Clinical Trials

Real-time fMRI for the Treatment of Aggressive Behavior in Adolescents

Start date: October 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether real-time fMRI feedback is effective in the treatment of aggressive behavior problems in adolescents with high callous unemotional traits when compared to treatment as usual.

NCT ID: NCT02552147 Completed - Clinical trials for Autism Spectrum Disorder

Nicotinic Cholinergic Modulation as a Novel Treatment Strategy for Aggression Associated With Autism

Start date: September 2015
Phase: Phase 1
Study type: Interventional

Some individuals with autism spectrum disorders (ASD) also demonstrate irritability or aggression, which can interfere with functioning. The purpose of this pilot study is to test whether transdermal nicotine is effective for irritability and/or aggression in adults with ASD using a double-blind, placebo-controlled clinical trial. Subjects will participate in three visits. At the first visit, subjects are screened for eligibility and enrolled. Baseline measures include rating scales and a frustrative computerized task. They will then wear seven days of transdermal nicotine or placebo. Visit two is on day seven and the study measures are repeated, vital signs and side effects monitored. Subjects will return for a third and final visit on day 21 to repeat the study measures performed during visit two.

NCT ID: NCT02506088 Completed - Violence Clinical Trials

Preventing Sexual Aggression Among High School Boys

Start date: September 2015
Phase: N/A
Study type: Interventional

The present research creates a partnership between researchers and a community agency to evaluate whether a sexual assault prevention program for high school students reduces perpetration of sexual violence among high school boys.

NCT ID: NCT02503488 Completed - Depression Clinical Trials

Decreasing Youth Involvement in Violence in Burundi

Start date: May 2015
Phase: N/A
Study type: Interventional

The purpose of the current study is to examine the psychological well-being of youth within the context of participation in political violence during the 2015 election period in Burundi. In detail, the investigators are interested in fostering improved outcomes in a peace-building initiative aimed at youth in Burundi by reducing the mental health-related stress of the initiative's most severely affected participants. In addition, the investigators are interested in learning more about the youth experience of involvement in the Burundian political system in an effort to understand the links between youth engagement in political violence and past experiences of traumatic events.

NCT ID: NCT02498106 Completed - Clinical trials for Psychiatric Hospitalization

Diet and Aggression: Reducing Aggression Among Chronic Psychiatric Inpatients Through Dietary Supplementation

Start date: May 2015
Phase: N/A
Study type: Interventional

The overall goal of this study is to investigate whether the daily administration of multivitamins, minerals and n-3 fatty acids will reduce aggression in long-term psychiatric inpatients and will thereby reduce costs of care.

NCT ID: NCT02495519 Completed - Fibromatosis Clinical Trials

A Trial of Imatinib for Patients With Aggressive Desmoid Tumor (Aggressive Fibromatosis)

Start date: April 2014
Phase: Phase 2
Study type: Interventional

Aggressive fibromatosis (AF, also known as desmoid tumor) is a fibroproliferative neoplasm that typically arises in the abdomen but can develop at other anatomic sites, most commonly in the extremities. These tumors have a relatively high local failure rate after primary treatment using surgery and/or radiotherapy, and although rarely giving rise to distant metastases, can be multifocal and, therefore, not surgically resectable. Moreover, tumor may recur adjacent to the site of surgical resection, underscoring the limitations of surgery in the palliative setting. Therefore, effective medical therapies for AF are needed to maintain quality of life and prolong survival.The goal of the current study was to better define the activity of imatinib in the treatment of AF and to determine the molecular basis for response/nonresponse

NCT ID: NCT02485587 Completed - Aggression Clinical Trials

Arousal-Biofeedback for the Treatment of Aggressive Behavior in Children and Adolescents

Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether individualized biofeedback of arousal (skin conductance) is effective in the treatment of aggressive behavior problems in children and adolescents with either predominantly impulsive (reactive) and/or high callous unemotional traits (proactive) subtypes of aggression when compared to treatment as usual (TAU), and induces normalization when compared to a group of typically developing children receiving no intervention.

NCT ID: NCT02471911 Completed - Clinical trials for Diffuse Large B-Cell Lymphoma

KPT-330 Plus RICE for Relapsed/Refractory Aggressive B-Cell Lymphoma

KPT-330+RICE
Start date: December 11, 2015
Phase: Phase 1
Study type: Interventional

This study evaluates the addition of selinexor (KPT-330) to RICE chemotherapy in the treatment of relapsed and refractory aggressive B-Cell Lymphoma, with the goal of improved response rates (as compared to RICE chemotherapy alone).