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Problem Behavior clinical trials

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NCT ID: NCT03264560 Completed - Clinical trials for Psychiatric Disorder

Comparison of Asynchronous Telepsychiatry vs. Synchronous Telepsychiatry in Skilled Nursing Facilities

CATeleST
Start date: June 27, 2017
Phase: N/A
Study type: Interventional

There is a critical shortage of psychiatric services to people with mental illness who live in Skilled Nursing Facilities (SNFs), especially those in rural settings. Although real-time video conferencing psychiatric consultation, termed Synchronous Telepsychiatry (STP), has been around for almost 3 decades, its adaptation is met with logistic and other challenges. In this context, the investigators investigate a novel method of psychiatric consultation termed Asynchronous Telepsychiatry (ATP). The main hypotheses are that that ATP will be as clinically effective as STP, and that it will be acceptable to patients. This study aims to evaluate the comparative clinical effectiveness of ATP vs. STP in SNF population, in a 12-month non-inferiority, randomized, controlled trial.

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: NCT03260725 Completed - Conduct Disorder Clinical Trials

Evaluating the Feasibility of Internet-delivered PCIT

Start date: April 4, 2011
Phase: N/A
Study type: Interventional

The present study is leveraging a randomized-controlled design to evaluate an Internet-based format for the delivery of Parent-Child Interaction Therapy (I-PCIT). Drawing on videoteleconferencing technology, this format affords real-time interactions for the provision of care traditionally delivered in person, regardless of a family's geographic proximity to a mental health facility. Moreover, drawing on technological innovation to deliver interventions directly to families in their natural settings may extend the ecological validity of PCIT, as treatment is delivered in the very context in which child problems occur. Families seeking treatment for early child disruptive behavior problems (N=40) are being randomly assigned to either receive Internet-delivered PCIT or clinic-based PCIT. Outcomes and feasibility/acceptability will be assessed across the treatment phase as well as at post-treatment and 6-month follow-up.

NCT ID: NCT03260296 Not yet recruiting - Addiction Clinical Trials

Smartphones Addiction in Assiut University Students

Start date: October 2018
Phase: N/A
Study type: Observational

Smartphones have become a part of our daily life, the number of people using smartphones is increasing day after day. Easy access to internet is the main advantage of smartphones in comparison to traditional mobile phones, so they are considered as handheld convenient substitutes to computers. People use smartphones for many different purposes such as communication, entertainment, browsing for information, education or business facilitation. Unfortunately the excessive use of smartphones makes people 'addicted' to that type of technology. Past research has shown that older people have less positive attitudes towards a variety of technologies and they are less likely than younger people to embrace new technology, so It seems that the problem of smartphones addiction is most likely to affect young people who are fascinated with new technologies.

NCT ID: NCT03216941 Completed - Clinical trials for Psychiatric Disorder

Randomised Trial Ketiapine Olanzapine Fast Sedation Agitated Patients Emergency Ward

IM-OK-FAST
Start date: January 1, 2015
Phase: Phase 4
Study type: Interventional

comparison of intramuscular olanzapine and ketamine efficacy as first medication for fast sedation of patients with agitation and aggressive behavior. Five hundred patients with agitation caused by psychiatric disorder were randomly assigned under double-blind conditions to receive olanzapine or ketiapine. The Overt Agitation Severity Scale, Overt Aggression Scale and Ramsay Sedation Scale will be applied within 12 hours after the first dosage.

NCT ID: NCT03207633 Completed - Clinical trials for Psychiatric Disorder

Low Frequency TMS on DLPFC and OFC in OCD Patients

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

This study aims to evaluate the therapeutic effect of low frequency rTMS over the right DLPFC, versus right OFC versus Sham group of obsessive-compulsive disorder (OCD) patients. Sixty patients will be recruited from the out-patient psychiatric clinic of a university hospital, and randomized into three equal groups. The 1st group will receive 10 sessions of low frequency rTMS targeting right DLPFC by means of a butterfly coil, 120% RMT, 1 Hz, 3 trains, each of 500 pulses with a 40 seconds inter-train interval allowing the coil to cool. The 2nd group will receive 10 sessions of low-frequency rTMS over the right orbitofrontal cortex (OFC), the international 10-20 EEG system will be used to position the coil over the right OFC, at the right frontopolar 2 (Fp2) electrode site, using the following parameters: 120% motor threshold, 1 Hz, 3 trains, each of 500 pulses with a 40 seconds inter-train interval allowing the coil to cool. The 3rd group will receive sham stimulations with the same pulse delivery as the other groups but with the coil placed perpendicular to the scalp. The resting motor threshold (RMT) and cortical silent period (CSP) at different intensities from 110 % to 150 % will be measured before and after the end of sessions. All assessments like (Y-BOCS), (HAM-A), Beck Depression Inventory, (CGI-S), (MoCA) will be performed before and after end of the sessions and 3 months later.

NCT ID: NCT03153904 Completed - Depression Clinical Trials

Connecticut Child STEPs

Start date: October 2013
Phase: N/A
Study type: Interventional

Connecticut Child STEPS is a randomized controlled trail investigating the effectiveness of MATCH-ADTC in treating anxiety, depression, trauma, and/or behavioral problems in children seeking services at four Department of Children and Families (DCF) funded clinics in the state of Connecticut. The study will evaluate child outcomes following two forms of therapist training in the MATCH model.

NCT ID: NCT03151187 Recruiting - Disruptive Behavior Clinical Trials

Evaluation of a Teaching Curriculum on Disruptive Behaviour Disorders

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

The investigators have initiated an education program for residents on the diagnosis and management of disruptive behavior disorders in children. These will be presented as two 2-hour modules to be delivered at an academic half-day for pediatric trainees across Canada. We plan to evaluate the effectiveness of the curriculum by administering a pre and post test. Pediatric residents in Canada all participate in a practical assessment of their skills (an Observed Structured Clinical Examination or OSCE). The investigators plan to develop on OSCE station which assesses the curriculum and randomize programs to do the curriculum either before or after the OSCE. This will help us determine how effective the curriculum is at teaching about disruptive behaviours.

NCT ID: NCT03125083 Completed - Clinical trials for Psychiatric Disorders

Role of Inflammation in Psychiatric Disorders in Patients With Cutaneous Lupus

RIP-LC
Start date: May 5, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the role of inflammation in the high prevalence of psychiatric disorders in skin-restricted lupus (SRL) patients. SRL is an inflammatory disease. Inflammation can lead to a decrease in the synthesis of neurotransmitters via the activation of the IDO enzyme and to induce the synthesis of neurotoxic molecules (kynurenin pathway). This leads to the development of psychiatric disorders. Investigator therefore want to compare inflammation and neurotransmitter synthesis in SRL patients according to the presence or absence of psychiatric disorders. Investigator expect a decrease in neurotransmitter synthesis and activation of the kynurenin pathway in patients with a psychiatric disorder.

NCT ID: NCT03124342 Completed - Clinical trials for Intensive Care Unit Syndrome

Vanderbilt ICU Recovery Program Pilot Trial

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

Every year, millions of Americans are admitted to the intensive care unit. Due to advances in critical care, mortality rates are decreasing, increasing the number of ICU survivors. Survivors of critical illness, however, often face physical, functional, and cognitive deficits that place them at risk for a cycle of re-hospitalization that frequently culminates in premature death. Moreover, post-ICU interventions may be resource-intensive and may be most cost-effective only in a subgroup of patients at highest risk. Whether a multi-disciplinary program to facilitate recovery from critical illness can prevent hospital readmission and improve quality of life among high-risk ICU survivors remains unknown. The primary aim of this pilot is to examine the feasibility of implementing a multidisciplinary ICU Recovery Program and the influence of such a program on process measures including contact with the ICU recovery team and attendance of ICU recovery clinic. The secondary aims are to compare the effect of an ICU Recovery Program on 30-day same-hospital readmission and other clinical outcomes.