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Sleep clinical trials

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NCT ID: NCT01159652 Completed - Sleep Clinical Trials

Hypnotic Medications and Memory: Effect of Drug Exposure During the Night

Start date: October 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of two hypnotic medications, zolpidem extended release and zaleplon, on memory. It is expected that a hypnotic with shorter drug duration will allow greater memory consolidation than a hypnotic with longer drug duration.

NCT ID: NCT01149577 Completed - Schizophrenia Clinical Trials

Effect of Olanzapine on Sleep Electroencephalogram (EEG) in Schizophrenia Patients

Start date: August 2007
Phase: Phase 4
Study type: Interventional

Acute and sub-chronic administration of olanzapine has shown a favourable effect on the sleep disturbances in previously medicated schizophrenia patients with predominantly negative symptoms. The present study will be carried out to clarify the effect of olanzapine on polysomnographic profiles of schizophrenia patients in an acute phase of illness after controlling for the drug effects.

NCT ID: NCT01142258 Completed - Alzheimer's Disease Clinical Trials

Trazodone for Sleep Disorders in Alzheimer's Disease

Start date: March 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether trazodone is effective in the treatment of sleep disorders in Alzheimer's disease (AD).

NCT ID: NCT01123993 Completed - Sleep Clinical Trials

The Effect of Thai Traditional Music on Cognitive Function, Psychological Health and Quality of Sleep Among Thai Older Individuals With Dementia

Start date: February 2010
Phase: Phase 3
Study type: Interventional

To determine the effect of Thai traditional music on cognitive function, psychological health and quality of sleep among Thai older individuals with dementia.

NCT ID: NCT01118273 Completed - Sleep Clinical Trials

Evaluate Analgesic/Sedative Efficacy of Naproxen Sodium and Diphenhydramine

Start date: January 2008
Phase: Phase 4
Study type: Interventional

The objectives of the study are to evaluate the analgesic and hypnotic efficacy of naproxen sodium and diphenhydramine combination when compared to naproxen sodium, diphenhydramine, and an ibuprofen and diphenhydramine combination

NCT ID: NCT01102842 Completed - Sleep Clinical Trials

Unattended In-home Sleep Recording: A Pilot Study

Start date: April 2010
Phase: N/A
Study type: Observational

Laboratory studies have found that insufficient sleep duration and impaired sleep quality are associated with disease risk, including obesity, diabetes and heart disease. The limitation to the laboratory studies is that they are conducted in artificial environments that do not reflect real-world behavior. Although the epidemiologic studies do reflect habitual behavior, the vast majority of them rely on self-reported measures of sleep, which are only moderately correlated with objective measures of sleep.. The next logical step in the examination of sleep's role in cardiometabolic health is to conduct objective, detailed measures of sleep in people's homes. This project is a pilot study that will develop ideal methodologies for recording sleep in the home environment. Because there is currently is a gap between laboratory models of sleep loss and real world conditions, the ultimate goal of this research is to expand our work on sleep and cardiometabolic health outside of the laboratory. Given the strong evidence for a link between impaired and insufficient sleep and increased disease risk, it is critical that we understand how people sleep in their daily lives and what factors can impact sleep. This project will record sleep in people's homes using ambulatory polysomnography recordings and wrist actigraphy.

NCT ID: NCT01092845 Completed - Healthy Clinical Trials

Study To Establish The Effects Of PF-04457845 On Sleep In Healthy Volunteers

Start date: April 2010
Phase: Phase 1
Study type: Interventional

PF-04457845 has been shown to temporarily decrease the dream (REM) period of sleep in rats, which suggests that PF-04457845 is active in rat's brains. This study is designed to see whether this is also the case in man.

NCT ID: NCT01064700 Completed - Depression Clinical Trials

Bright Light: A Novel Treatment for Anxiety

Start date: October 2006
Phase: Phase 1
Study type: Interventional

The primary aim of this research was to examine the influence of bright light on anxiety in high-anxious young adults. In an acute exposure study, participants were randomly assigned to 45 min of either (1) bright light (3,000 lux) or (2) a placebo inactivated negative ion generator. Treatments were initiated ≤1 hr after awakening. At 10 min before and 30 min after the treatments, state anxiety, mood, and blood pressure were assessed. Following the acute exposure study, participants performed a 5-week study. Following a a 1-week baseline, participants were randomly assigned to four weeks of daily exposure to either (1) bright light (45 min/day; 3,000 lux) or (2) placebo inactivated negative ion generator, which were initiated ≤1 hr after awakening. Before and after the experiment, clinical ratings were conducted with the Hamilton Anxiety Scale, the Hamilton Depression Scale, and the Clinical Global Impressions scale (CGI). Following baseline, and following each week of treatment, blood pressure, as well as questionnaires for state anxiety, depression, mood, sleep, and side effects were assessed.

NCT ID: NCT01062295 Completed - Sleep Clinical Trials

Efficacy and Safety of the Device Siesta-SystemTM for Inducing Objective Sleep and re Rest

Start date: November 2008
Phase: N/A
Study type: Interventional

NTRODUCTION: The investigators have developed a new device to help passengers of vehicles to rest, sleep, and to avoid cervical injuries due to sleepiness postures while travelling. The device is attached to the headrest and is based in a new concept called "dynamic vertical holding of the head and neck". It could also provide some help in avoiding accidents by allowing a sleeping time for a secondary driver while the main one is driving. Several studies have shown that up to 30% of car crashes are related to sleepiness. AIM: To estimate the efficacy and safety of a new device in "patent pending" phase to facilitate the sleep and rest in the passenger. METODOLOGY: DESIGN: Prospective, cross-over and open clinical assay, comparing the results of 40 different passengers during a journey after using both systems, that is the new device and the standard headrest. MEASUREMENTS: A) Standard polysomnography for 3 and a half hours during the night; B) Anthropometric and clinical variables; C) Sleepiness scale and Epworth sleepiness; D) Questionnaires of sleep, health and quality of life. E) Evaluation of the neck posture in recorded images. ANALYSIS: To compare the results of questionnaires of sleep quality, comfort and safety as well as the images recorded and polysomnographic variables of objective sleep variables obtained by the device Siesta-SystemTM and the conventional headrest.

NCT ID: NCT01050699 Completed - Critical Illness Clinical Trials

Sleep Intervention During Acute Lung Injury

Start date: August 2009
Phase: Phase 4
Study type: Interventional

The central purpose of this proposal is to study the short-term effects of sedation with sympatholysis, using α2 adrenergic agent Dexmedetomidine, on sleep and inflammation in critically ill patients with Acute Lung Injury and Acute Respiratory Disorder Syndrome (ALI/ARDS). An additional objective is to determine the effect of Dexmedetomidine sedation on the in-vitro production of sleep-modulating inflammatory cytokines by peripheral blood mononuclear cells of critically ill patients with ALI/ARDS.