Clinical Trials Logo

Disease clinical trials

View clinical trials related to Disease.

Filter by:

NCT ID: NCT01978392 Completed - Clinical trials for Chronic Physical Health Conditions

MANAGE AT WORK: Addressing the Challenge of Chronic Physical Health Conditions in the Workplace

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

The specific aim of the study is to evaluate the health benefits of a series of group workshops designed for workers with chronic physical health conditions. The facilitated workshops apply principles of pain and illness self-management to help workers deal with health-related challenges while at work. The workshops address issues of pain management, physical job demands, pacing of work, communication, problem solving, and coping. Half of the participants in the study will be randomly assigned to attend workshop sessions (10 hours total), and all study participants will be followed for one year. The primary hypothesis is that workers who participate in these workshops will show improvements in work engagement and reductions in work limitation in the subsequent 12 months.

NCT ID: NCT01977521 Recruiting - Clinical trials for Stress Disorders, Post-Traumatic

Transcranial Direct Current Stimulation as Treatment for Auditory Hallucinations

tDCS
Start date: April 2014
Phase: N/A
Study type: Interventional

The present study aims to examine the efficacy of transcranial direct current stimulation on the severity of auditory hallucinations.

NCT ID: NCT01977248 Completed - Clinical trials for Autism Spectrum Disorder

Sensorimotor Affect Relationship-based Therapy (SMART) for Children With Autism Spectrum Disorders Ages 2-12

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

The SMART Program at Nationwide Children's Hospital is an interdisciplinary social skills group that teaches children with autism spectrum disorders (ASD) ages 2-12 the fundamental social skills necessary to build and maintain relationships. The manualized curriculum addresses skills such as joint attention, eye contact, play, and peer engagement. Currently individual goals are set for each child who participates and this is documented in the daily treatment note. In order to research group outcomes, the investigators will use parent questionnaires (an addition to current clinical practices) to measure changes in behavior after each 12 week session for up to one year of treatment. The investigators hypothesize that maladaptive behaviors will decrease and adaptive behaviors will increase in children with ASD after participation in the SMART program.

NCT ID: NCT01976975 Completed - Clinical trials for Major Depressive Disorder

Brain Mechanisms of Human Motivation

Start date: October 2013
Phase:
Study type: Observational

This study aims to investigate reward learning across the mood disorder spectrum and to investigate the predictive validity of reward learning for subsequent symptom severity.

NCT ID: NCT01974973 Withdrawn - Clinical trials for Autism Spectrum Disorders

Stem Cell Therapy in Autism Spectrum Disorders

Start date: August 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study was to study the effect of stem cell therapy on common symptoms in patients with autism spectrum disorders

NCT ID: NCT01974583 Completed - Clinical trials for Wound Healing Disturbance of

Wound-healing Improvement by Resurfacing Split-Thickness Skin Donor Sites With Thin Split-thickness Grafting

Start date: January 2002
Phase: N/A
Study type: Observational [Patient Registry]

Split-thickness skin grafting remains fundamental treatment of patients with deep burns and other traumatic injuries. However, the split-thickness skin graft (STSG) donor site dressing has been controversial until now. Our study here aimed to assess patient comfort and wound-healing efficacy with the application of thin split-thickness grafting on STSG donor sites.

NCT ID: NCT01973478 Completed - Clinical trials for Major Depressive Disorder

Deep Brain Stimulation in Patients With Chronic Treatment Resistant Depression

STHYM
Start date: June 3, 2014
Phase: N/A
Study type: Interventional

Major depressive disorders are real public health issues in terms of diagnosis and treatment. Some forms of depression are chronic and resistant to treatment (TRD). In these forms suicide risk is important. Patients with TRD are potential candidates for neurosurgical interventions to treat depression. However, psychosurgery interventions based upon lesions, showed their limitations related to 1. the large variability in neurosurgical gestures, 2. their side effects, and of course 3. the irreversible damage caused by the surgery. Thus, deep brain stimulation (DBS) could represent an opportunity for patients suffering from TRD. Our preliminary study based upon the stimulation of the accumbens nucleus showed encouraging results. The investigators have thus planned a randomized controlled trial versus sham stimulation to confirm the therapeutic value of nucleus accumbens DBS.

NCT ID: NCT01973283 Completed - Clinical trials for Major Depressive Disorder

Antidepressant Response in the Treatment of Depressive Symptoms and Frailty Characteristics in Older Adults

Start date: February 19, 2014
Phase: Phase 4
Study type: Interventional

The goal of this open-administration treatment study of citalopram (or duloxetine) is to evaluate the effect of antidepressant medication on treating the syndrome of "frailty" in older adults with depressive symptoms. Patients with significant depressive symptoms (defined as CES-D (Center for Epidemiological Studies - Depression scale) > 10) and 1 or more symptoms of the frailty syndrome (exhaustion, decreased energy, weight loss, decreased grip strength, and slow/unsteady gait) will be evaluated and treated with citalopram (or duloxetine) for 8 weeks to test whether antidepressant medication improves both the syndrome of frailty and depressive symptoms. Patients evaluated at the Adult and Late Life Depression clinic and eligible to participate in the study will be treated with an antidepressant medication and assessed on the primary outcome variables (characteristics of frailty, depressive symptoms) as well as on secondary variables which include cognition (global cognition, episodic memory, executive function), and function (physical mobility, instrumental activities of daily living, and social functioning) prior to treatment initiation and following 8-weeks of treatment. The hypotheses for this protocol predict that we will discover a significant improvement on both frailty characteristics and depressive symptoms in this clinical population when treated with antidepressant medication (citalopram or duloxetine).

NCT ID: NCT01972074 Completed - Clinical trials for Autism Spectrum Disorder

Behavioral and Neural Response to Memantine in Adolescents With Autism Spectrum Disorder

Start date: February 17, 2015
Phase: Phase 3
Study type: Interventional

This study is a 12-week, randomized-controlled trial of memantine hydrochloride (Namenda) for the treatment of social impairment in adolescents with autism spectrum disorder (ASD). The investigators will also conduct pre- and post-treatment neuroimaging (functional magnetic resonance imaging [fMRI] and hydrogen magnetic resonance spectroscopy [HMRS]) to assess neural functional deficits in adolescents with autism spectrum disorder compared to healthy volunteer adolescents. This pre- and post-neuroimaging will also be used to assess any effects of memantine therapy on neural function in adolescents with autism spectrum disorder. The investigators hypothesize that short-term memantine monotherapy will be safe, well-tolerated, and effective in improving the core symptoms of autism spectrum disorder in adolescents with autism spectrum disorder. Additionally, the investigators hypothesize that following memantine therapy, adolescents with autism spectrum disorder will exhibit a decrease in glutamate (Glu) concentration in the anterior cingulate cortex (ACC) and a change towards normalization in altered functional connectivity of the anterior cingulate cortex and medial temporal lobes, consistent with improvement in social impairments in autism spectrum disorder. The investigators hypothesize that compared to healthy volunteer participants, participants with autism spectrum disorder will significantly differ on neuroimaging measures at baseline but that following memantine therapy, the difference between autism spectrum disorder and healthy volunteer neuroimaging data will decrease.

NCT ID: NCT01971827 Enrolling by invitation - Obesity Clinical Trials

Effectiveness of a Physical Activity Intervention to Prevent Obesity and Improve Academic Performance

MOVI-KIDS
Start date: September 2013
Phase: N/A
Study type: Interventional

Coordinated project whose objectives are: a) to test the effectiveness of a promotion of physical activity intervention (MOVI-KIDS) on preventing obesity; and b) to improve the academic performance in both children with and without attention deficit hyperactivity disorder (ADHD)