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NCT ID: NCT04063384 Recruiting - Bipolar Disorder Clinical Trials

Acute Alcohol Response In Bipolar Disorder: a fMRI Study

BACS
Start date: July 22, 2019
Phase: N/A
Study type: Interventional

Alcohol use disorders (AUDs) affect up to 60% of individuals with bipolar disorder during their lifetime-a rate 3 to 5 times higher than what occurs in the general population. The mechanisms that contribute to elevated rates of comorbidity are not known. Early identification in individuals with bipolar disorder who are at risk for AUDs could inform novel intervention strategies and improve life-long outcomes. The primary objective of this protocol is to use alcohol administration procedures and functional MRI techniques to investigate subjective response to alcohol, compared to placebo, and relationship with functional responses of, and connectivity among, brain regions in ventral prefrontal emotional networks in young adults with bipolar disorder and healthy comparison young adults. Baseline clinical and structural MRI assessments will be completed in 30 bipolar and 30 healthy young adults (21-26 years of age, 50% women). Then, following standard beverage administration procedures, participants will complete within-person, counter-balanced, fMRI scans and complete measures of subjective response to alcohol while under the influence of alcohol or placebo. Specifically, individual differences in the experience of stimulating, sedative, and anxiolytic effects of alcohol (measured with self-report surveys) and individual differences in neural responses to alcohol within ventral prefrontal emotional networks will be investigated and differences in bipolar disorder compared to healthy participants assessed. Functional MRI scans during a continuous performance task with emotional and neutral distractors (CPT-END) and at rest will be collected while under the influence of alcohol and placebo and compared. Experience of stimulating, sedative, and anxiolytic effects of alcohol from self-report survey data and neural responses to emotional stimuli while under the influence of alcohol compared to placebo will be the primary data outcomes assessed. Additionally, associations between subjective and neural response to alcohol and drinking patterns will be explored (secondary outcomes). The primary endpoint of the study will be after completion of both alcohol and placebo beverage conditions.

NCT ID: NCT04059432 Recruiting - Clinical trials for Musculoskeletal Disorder

CHAIN1 : Dental Wear and Musculoskeletal Disorders - Association?

Start date: March 1, 2019
Phase:
Study type: Observational [Patient Registry]

This study aims to explore the relationships between tooth wear (TW) and musculoskeletal disorders (MSDs). The null hypothesis is that TW is not associated to MSDs. It also explores the influence of bruxism signs, life habits and stress on TW and MSDs.

NCT ID: NCT04048603 Recruiting - Clinical trials for REM Sleep Behavior Disorder

Search for Biomarkers of Neurodegenerative Diseases in Idiopathic REM Sleep Behavior Disorder

Start date: May 15, 2019
Phase:
Study type: Observational

This study is a prospective study with a mean of 7-year follow-up interval, aims to monitor the progression of α-synucleinopathy neurodegeneration by the evolution of prodromal markers and development of clinical disorders in patients with idiopathic REM Sleep Behavior Disorder (iRBD) and healthy controls.

NCT ID: NCT04043351 Recruiting - Clinical trials for Autism Spectrum Disorder

Diagnostic Performance of Exome Sequencing in Autism Spectrum Disorders

REDIA
Start date: June 12, 2019
Phase:
Study type: Observational

Evaluation of the diagnostic performance of exome sequencing in a prospective series of patients with autism spectrum disorders (ASD).

NCT ID: NCT04042038 Recruiting - Clinical trials for Obsessive-Compulsive Disorder (OCD)

Neural Predictors and Neural Changes Associated With Cognitive Behavior Therapy for Obssesive Compulsive Disorder

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

The goals of the project are 1) to understand what are the neural mechanisms involved in the psychological treatment of obsessive-compulsive disorder (OCD) in children/adolescents and adults, 2) to assess potential differences in the neural mechanisms involved in the psychological treatment of OCD between children/adolescents and adults, and 3) to assess the effectiveness of intensive CBT for children/adolescents and adults with OCD.

NCT ID: NCT04035798 Recruiting - Bipolar II Disorder Clinical Trials

add-on Low Dose Memantine in Middle-to-old Aged Bipolar II Disorder Patients

Start date: August 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators hypothesized that add-on memantine (MM) 5 mg/day may reduce chronic inflammation, and subsequently improve neuro-progression process and cognitive function in middle-to-old aged bipolar II disorder (BP-II) patients. In current proposal, the investigators will conduct a randomized double-blind placebo-controlled study. The investigators will recruit 100-120 patients with BP-II who are older than 40 years old in three years, and allocate them to add-on MM or placebo plus standard valproic acid treatment in a 1: 1 ratio. The investigators will follow up the participants for 12 weeks and measure the severity of mood symptoms, neuropsychological tests and inflammatory markers to evaluate the therapeutic effects of add-on MM.

NCT ID: NCT04034576 Recruiting - Depressive Disorder Clinical Trials

Mindfulness and Relaxation Interventions in Individual Psychotherapies for Children and Adolescents

MARS-CA
Start date: April 30, 2019
Phase: N/A
Study type: Interventional

The study 'Mindfulness and Relaxation interventions in Individual Training Psychotherapies for Children and Adolescents' (MARS-CA) aims to examine the effects of short session-introducing interventions with mindfulness elements (SIIME) on juvenile patients' psychopathological symptomatology and therapeutic alliance at the beginning of the first 24 therapy sessions.

NCT ID: NCT04026815 Recruiting - Healthy Aging Clinical Trials

Health Status and Its Socio-economic Covariates of the Older Population in Poland - the Nationwide PolSenior2 Survey.

PolSenior2
Start date: January 1, 2018
Phase:
Study type: Observational

The PolSenior2 survey is aimed to characterise health status of old and very-old adults in Poland.

NCT ID: NCT04015596 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

Trial of Naproxen Sodium for the Treatment of OCD in Children With PANDAS

Start date: October 20, 2020
Phase: Phase 4
Study type: Interventional

This project aims to rigorously evaluate a potential treatment for inflammation-related Obsessive-Compulsive Disorder (OCD) symptoms in children. To accomplish this goal, the investigators will conduct a double-blind, randomized, placebo-controlled trial of Naproxen Sodium, a nonsteroidal anti-inflammatory drug (NSAID) in participants diagnosed with Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal infections (PANDAS). This research fills a gap in the empirical evidence base for the treatment of PANDAS, and will add to a growing literature of empirically-derived practices for PANDAS.

NCT ID: NCT04010838 Recruiting - Clinical trials for Disorder of Consciousness

Spinal Cord Stimulation in Patients With Disorders of Consciousness

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Disorders of consciousness(DOC) is the most serious complications and has been widely paid attention to by the government. DOC patients cause large social and economic burden to our society for there has no effective cure so far. Spinal cord stimulation(SCS) for wake-promoting therapy has aroused scholars' attention and become a hot area recently. There was much debate about the effectiveness of SCS therapy, but because of the limitation of our understanding of consciousness and the uncertainty of parameters of the stimulation, So, to figure out the indications and effectiveness of neuromodulation therapy should be the first step, and finding individual treatment and parameter may have important implications for DOC patients.