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Disruptive Behavior clinical trials

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NCT ID: NCT03510156 Completed - Fragile X Syndrome Clinical Trials

Treatment of Disruptive Behaviors in Fragile X Syndrome

Start date: July 2016
Phase: N/A
Study type: Interventional

Disruptive behaviors such as self-injury, aggression, and property destruction pose significant health-related issues to children diagnosed with fragile X syndrome (FXS), impacting the child's quality of life and causing significant distress to families. Access to appropriate treatment for families is severely limited by factors such as cost of care, shortages of qualified treatment providers, and geographic spread of children with FXS across the country. To address these potential issues, the effectiveness of administering a standardized function-based behavioral treatment for problem behaviors in FXS will be evaluated using telemedicine. The proposed study intervention therefore offers a tremendous step forward in clinical research both in the field of FXS and in the field of developmental disabilities more broadly, and thus will have a significant impact on public health.

NCT ID: NCT03499600 Completed - Disruptive Behavior Clinical Trials

Improving Satisfaction, Engagement and Outcomes Among Traditionally Underserved Children Through Cultural Formulation

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The project at the center of this proposal will leverage a pilot randomized design to examine initial feasibility and preliminary effects of augmenting usual mental health evaluation procedures with a structured person-centered assessment tool that specifically considers the cultural context of patient mental health problems (i.e., the Cultural Formulation Interview; CFI) on parent satisfaction, engagement and clinical child outcomes in the treatment of early child behavior problems. Additional analyses will explore whether traditional barriers (e.g., stigma, ethnic identity, and daily stress) moderate the effects of the CFI on satisfaction, engagement and treatment outcomes.

NCT ID: NCT03378245 Completed - Dementia Alzheimers Clinical Trials

Telemedicine-based, Multidisciplinary-team, Intervention to Reduce Unnecessary Hospitalizations

TeleNH
Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the use of telemedicine-based intervention at urban and rural skilled nursing facilities to recommend multidisciplinary dementia care to residents with dementia who are at risk for unnecessary hospitalization due behavioral or neuropsychiatric symptoms and/or complications as well as caregivers and facility staff. The multidisciplinary team is comprised of trained behavioral neurologists, social workers, advanced practice providers, primary medical team and nurse coordinators.

NCT ID: NCT03260816 Completed - Developmental Delay Clinical Trials

Advancing Child Competencies by Extending Supported Services (ACCESS) for Families Program

ACCESS
Start date: March 16, 2016
Phase: N/A
Study type: Interventional

The Advancing Child Competencies by Extending Supported Services (ACCESS) for Families Program is a study funded by the National Institutes of Health to explore behavior and developmental problems among young children aging out of Early Steps (Part C). All families will participate in five evaluations in their home to learn more about their child's behavior and development. Families also may receive treatment designed to help change their child's behaviors that will be conducted over the Internet using a tablet.

NCT ID: NCT01965184 Completed - Aggression Clinical Trials

Cognitive-Behavioral Therapy for Disruptive Behavior in Children and Adolescents

RDoC-CBT
Start date: November 14, 2013
Phase: N/A
Study type: Interventional

This is a randomized controlled study of cognitive-behavioral therapy (CBT) for disruptive behavior such as irritability, anger and aggression in children and adolescents. CBT will be compared to Supportive Psychotherapy (SPT) and participants of this study will be randomly assigned (like the flip of a coin) to receive CBT or SPT. Participants will be also asked to complete functional magnetic resonance imaging (fMRI) and electrophysiological (EEG) tasks (recordings/images of brain activity) before and after treatment.