Clinical Trials Logo

Problem Behavior clinical trials

View clinical trials related to Problem Behavior.

Filter by:

NCT ID: NCT01244854 Completed - Schizophrenia Clinical Trials

Life Goals Behavioral Change to Improve Outcomes for Veterans With Serious Mental Illness

Start date: October 1, 2010
Phase: N/A
Study type: Interventional

Persons with serious mental illness are at increased risk of cardiovascular disease. The goals of this study are to test a treatment, Life Goals Collaborative Care to help promote health behavior change and to get feedback from patients and providers on what is needed to help better coordinate and physical and mental health care of these patients.

NCT ID: NCT01178554 Completed - Depression Clinical Trials

The Clinic Treatment Project

CTP
Start date: June 2005
Phase: N/A
Study type: Interventional

The Clinic Treatment Project tested two alternative methods of delivering evidence-based practices within public community-based mental health clinics, using training and supervision procedures designed for the settings and users.

NCT ID: NCT01116726 Completed - Clinical trials for Early Childhood Dental Caries

Promoting Behavioral Change for Oral Health in American Indian Mothers and Children

Start date: August 2011
Phase: N/A
Study type: Interventional

A program of motivational interviewing plus enhanced community services in prevention of early childhood caries vs. enhanced community services alone for American Indian mothers and their children will reduce the childrens' decayed, missing, and filled tooth surfaces measure over a 3-year period.

NCT ID: NCT01085305 Completed - Conduct Disorder Clinical Trials

The Effectiveness of Parent-Child Interaction Therapy (PCIT)

Start date: September 2006
Phase: N/A
Study type: Interventional

The purpose of this study was to investigate whether a type of parent-based intervention, Parent-Child Interaction Therapy will lower symptoms of behavior problems in young children more than treatment as usual.

NCT ID: NCT00997425 Completed - Problem Behavior Clinical Trials

Home Evaluation of Exit Barriers in Wandering

HEEBW
Start date: October 2009
Phase: N/A
Study type: Interventional

Main hypothesis. Floor and door visual exit barriers will decrease exit-seeking wandering (exit door approaches) proximal to exit doorways by persons with dementia who wander.

NCT ID: NCT00889538 Completed - Autism Clinical Trials

Study of Glutathione, Vitamin C and Cysteine in Children With Autism and Severe Behavior Problems

Start date: April 2009
Phase: N/A
Study type: Interventional

This is a double-blind, placebo-controlled crossover study to evaluate the safety and efficacy of glutathione alone or glutathione, vitamin C and NAC treatment in children with autism who also have severe behavior problems. The investigators hypothesis is that children with autism will show improvement in both learning capabilities and behavior with either glutathione, or glutathione, vitamin C and NAC therapy.

NCT ID: NCT00794040 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

A Controlled Trial of Serotonin Reuptake Inhibitors Added to Stimulant Medication in Youth With Severe Mood Dysregulation

Start date: November 17, 2008
Phase: Phase 2
Study type: Interventional

Severe mood dysregulation (SMD) is a very common syndrome in children. Its symptoms include very severe irritability, including persistent anger and frequent outbursts, as well as distractibility, hyperactivity, and other symptoms of attention deficit hyperactivity disorder (ADHD). Many children with SMD receive the diagnosis of bipolar disorder (BD) in the community, although they do not have clear manic episodes (with symptoms such as extreme happiness and decreased need for sleep). Because SMD has not been studied in depth, we do not know which medications are most helpful to those with SMD. This study will evaluate the effectiveness of the stimulant medication methylphenidate (MPH, more commonly known as Ritalin ) when combined (or not combined) with the antidepressant citalopram (Celexa ) in treating symptoms of SMD in children and adolescents. This study will provide information about how to treat SMD in youth. This study will include approximately 80 patients between 7 and 17 years of age with SMD. The patient s symptoms must have started before age 12. The study will consist of four phases carried out over 4 to 5 months. During Phase 1, the patient will undergo blood and urine tests, and will gradually taper off his or her medication. The duration of this phase depends on the patient s medication before starting the study. In Phase 2, the patient remains off all medication for 1 week. In Phase 3, the patient will be treated with MPH for 2 weeks, and then will be randomly assigned to receive either MPH plus citalopram or MPH plus a placebo for a further 8 weeks. In Phase 4, the researchers will evaluate the effectiveness of the medications taken, and begin an open treatment phase using medications that they deem appropriate for that patient (this may include MPH with citalopram and/or other medication combinations). Most patients will be admitted to the Pediatric Behavioral Health Unit at the National Institutes of Health Clinical Center during the medication withdrawal part of the study (Phases 1 and 2). From Phase 3 on, a patient may participate as an inpatient, outpatient, or in day treatment, depending on what is in his or her best interests. ...

NCT ID: NCT00399373 Terminated - Chronic Illness Clinical Trials

Structuring the Integration of Care Management Services For Medicaid Enrollees Recipients With Chronic Illness, Substance Abuse Problems and Possible Psychiatric Disorders

Start date: November 2005
Phase: N/A
Study type: Observational

The study seeks to measure the effect of increased coordination of care on medical costs, treatment utilization and selected clinical indicators among a Medicaid population with chronic medical conditions and substance abuse problems? We shall address this question by conducting a demonstration project consisting of the provision of integrated care management (somatic and behavioral) to Medicaid enrollees living on the Eastern Shore of Maryland and who have both chronic medical conditions and problems with substance abuse. A specific component of the study will be the participation of Maryland's Mental Health Administration (MHA) and MAPS, the administrator of psychiatric services for the Medicaid enrollees in Maryland. We shall compare the results of the integrated care management for the study sample on the Eastern Shore with a control group from the counties of western Maryland.

NCT ID: NCT00292058 Completed - Clinical trials for Psychiatric Disorders

Comparing Telepsychiatry and In-person Outcomes

Start date: August 2001
Phase: N/A
Study type: Interventional

Psychiatric consultation and short-term follow-up will produce equivalent clinical outcomes and be less costly when provided via videoconferencing (telepsychiatry) than when provided in-person.

NCT ID: NCT00218114 Completed - Marijuana Abuse Clinical Trials

Divalproex Sodium (Depakote) for Explosive Tempers in Adolescents and Adults

Start date: February 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness of divalproex sodium (Depakote) versus placebo in treating disruptive behavior disorder and explosive tempers in adolescents and adults.