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Parasomnias clinical trials

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NCT ID: NCT01534338 Completed - Inflammation Clinical Trials

Effect of Mindfulness Training on Sleep and Inflammation Among Older Adults With Sleep Problems

MAPS
Start date: February 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The primary aim of the study is to test the effect of mindfulness training on sleep parameters among older adults with insomnia symptoms The secondary aims are to examine if changes in mindfulness meditation practice (daily log) and level of mindfulness (self-report) are associated with changes in sleep parameters, and to determine if mindfulness training is associated with in vitro biological markers of peripheral inflammation

NCT ID: NCT01534130 Completed - Clinical trials for Chronic Fatigue Syndrome

Acupuncture for the Sleep Disorder of Chronic Fatigue Syndrome

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

The investigators will conduct acupuncture for participants with chronic fatigue syndrome(CFS). Firstly the investigators aim to figure out the characteristic of sleep structure of CFS and the changes caused by acupuncture. Secondly the investigators seek to investigate the characteristic of sleep-wake rhythm, slow wave sleep(SWS)-rapid eye movement(REM)sleep rhythm, and REM sleep rhythm of CFS and the readjusting of acupuncture for it. Thirdly the investigators want to know the efficacy of acupuncture for relieving the fatigue, reducing accompanying symptoms and for improving the life quality of CFS.

NCT ID: NCT01528462 Completed - Stroke Clinical Trials

Sleep Disorders Managed and Assessed Rapidly in Transient Ischemic Attack (TIA) and In Early Stroke

SMARTIES
Start date: October 2011
Phase:
Study type: Observational

The aim of the investigators was to determine whether the immediate management of any detected sleep disorders can improve outcomes in patients who have had a transient ischemic attack (TIA) or minor stroke. This group of patients is at high risk for having a recurrent stroke or TIA, and the investigators would like to investigate new ways of preventing potentially avoidable events. The treatment of sleep disorders immediately after a stroke or TIA may prove to be a novel method of avoiding future strokes and improving outcomes.

NCT ID: NCT01519544 Completed - Clinical trials for High-altitude Sleep Disturbance

Comparison of Temazepam and Acetazolamide to Treat Difficulty Sleeping at High Altitude

Start date: March 2012
Phase: N/A
Study type: Interventional

More than 70% of visitors to high altitude suffer poor sleep. The present study seeks to answer the question: Which medication is associated with better sleep at high altitude: temazepam or acetazolamide? The investigators hypothesis is that one medication will be associated with higher subjective sleep scores than the other. The study will compare the sleep quality of 100 subjects as they take either temazepam or acetazolamide during a visit to high altitude.

NCT ID: NCT01489215 Not yet recruiting - Sleep Disorder Clinical Trials

Interventions for Sleep Problems in Early Childhood

Start date: February 2012
Phase: N/A
Study type: Interventional

This study will inform the field about underlying mechanisms associated with infant sleep problems and will deepen the understanding of the intervention process. The study will provide detailed information on the intervention process itself and will explore how behavioral sleep interventions affect broader infant outcome.

NCT ID: NCT01468038 Completed - Sleep Disorder Clinical Trials

A Double-blind Placebo Controlled Trial of Sentra PM, a Medical Food

Start date: April 2008
Phase: Phase 3
Study type: Interventional

This is a double blind placebo controlled study of one hundred and four subjects which will be randomized for treatment with Sentra PM alone, Sentra PM with trazadone, trazadone alone and placebo alone. Twenty -six subjects will be randomly placed in one of the four groups. Each of the one hundred and four subjects will undergo baseline examination to include a sleep study questionnaires and 24- hour electrocardiographic recording. The one hundred and four subjects will then be randomly placed in one of the four groups.

NCT ID: NCT01466270 Completed - Breast Cancer Clinical Trials

Study of Donepezil in Female Breast Cancer Survivors With Cognitive Dysfunction

Start date: July 2012
Phase: Phase 2
Study type: Interventional

RATIONALE: Donepezil hydrochloride may help lessen cognitive dysfunction caused by chemotherapy. PURPOSE: This phase II trial is studying donepezil hydrochloride in treating cognitive dysfunction after chemotherapy in female breast cancer survivors.

NCT ID: NCT01465971 Completed - Clinical trials for Cheyne-Stokes Respiration

Monitoring of the Cerebral Tissue Oxygenation and Perfusion in the Adapting Climber During Sleep in High Altitude

PerOxySleep
Start date: May 2011
Phase: N/A
Study type: Observational

One of the major challenges in adapting to high altitudes is that with increasing altitude sleeping quality declines rapidly. Thus, the night sleep can only provide limited to none regeneration. It usually takes a prolonged stay at a constant altitude to adapt sufficiently to the altitude and to have a refreshing night sleep. 1975 Reit et. al showed in their EEG-recordings that the sleep architecture (the regular succession of the particular sleep phases) is disturbed by repeating arousals which occur due to an irregularity in the breathing rhythm. The purpose of this study is to create a better understanding of the underlying mechanisms that lead to failed acclimatization and AMS, due to sleep disturbance.

NCT ID: NCT01463839 Completed - Sleep Disorder Clinical Trials

Sleep Disorder and Oral Habits in Children

SOHab
Start date: September 2010
Phase: N/A
Study type: Observational

Sleep is a vital physiological function for the maintenance of health and quality of life. Harmful, non-nutritive and parafunctional oral habits are believed to have a negative effect on adequate rest at night. The aim of the present study was to determine associations between quality of sleep and harmful oral habits among children aged three to six years. Fifty children from a private school in São Paulo (Brazil) were evaluated using two questionnaires on sleep quality and harmful oral habits. The data were submitted to descriptive analysis. The chi-square test was employed for the categorical variables and analysis of variance (ANOVA) was carried out to compare mean values. The Student's t-test was used for all analyses, with the significance level set at 5%. The SPSS 12.0 program for Windows was used to analyze the results.

NCT ID: NCT01446588 Withdrawn - Depression Clinical Trials

Ocular Hypertension And Yoga Study

OHAYS
Start date: June 2012
Phase: N/A
Study type: Interventional

The investigators aim to pilot test the efficacy of a yoga intervention designed specifically for individuals with ocular hypertension. The investigators would like to find out if a combination of breathing, postures and meditation may help to reduce intraocular pressure in the short term after each yoga session, and also long-term across an 8-week program. Subjects will participate in the yoga intervention sessions led by Dr. Pamela Jeter once a week at the investigators center, and will be asked to practice at home at least twice a week using a audio CD.