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Parasomnias clinical trials

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NCT ID: NCT00993850 Completed - Bipolar Disorder Clinical Trials

Sleep Disturbance and Bipolar Disorder

Start date: October 2009
Phase: Phase 3
Study type: Interventional

The study aims to evaluate a psychological intervention for individuals who suffer from sleep disturbance and bipolar disorder. We are hoping that this treatment will: (1) improve the quality of life of individuals with bipolar disorder who are suffering from sleep disturbance and (2) reduce the risk of, or help prevent, episodes.

NCT ID: NCT00992160 Completed - Sleep Disorders Clinical Trials

Vestipitant 28-day Tolerance Study

Start date: May 2009
Phase: Phase 2
Study type: Interventional

This study is a 28-day polysomnographic and subjective assessment of oral Vestipitant 15mg/day for treatment of Primary Insomnia in adults outpatients.

NCT ID: NCT00990106 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Augmentation Trial of Prazosin for Post-Traumatic Stress Disorder (PTSD)

Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether prazosin will: - reduce the incidence of nightmares and sleep disturbance - increase functioning and sense of well being in combat-trauma exposed Operation Iraqi Freedom/Operation Enduring Freedom (OIF/OEF) Veterans.

NCT ID: NCT00989976 Completed - Diabetes Clinical Trials

Individual Differences in Diabetes Risk: Role of Sleep Disturbances

Start date: February 2009
Phase: N/A
Study type: Interventional

The hypothesis for this study is that some individuals may be at much higher risk to develop type 2 diabetes and that the individual diabetes risk will be predicted by the individual level of slow wave sleep activity (SWA).

NCT ID: NCT00988104 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Preventing Long Term Psychiatric Disability Among Those With Major Burn Injuries

SMART
Start date: October 16, 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a newly developed, brief cognitive behavioral intervention, relative to supportive counseling, is effective in reducing acute stress disorder (ASD) and preventing post traumatic stress disorder (PTSD) and depression.

NCT ID: NCT00969540 Completed - Insomnia Clinical Trials

Trial on the Effect of Optically Modified Fiber Mattress Covers on Sleep Disturbances in Patients With Chronic Back Pain

Start date: June 2009
Phase: N/A
Study type: Interventional

Sleep quantity and quality can be influenced by the type of mattress used. This study is being done to see if a mattress cover with optically active particles can help back pain and improve sleep quality.

NCT ID: NCT00946803 Completed - Pain Clinical Trials

A Patient-Controlled Cognitive-Behavioral Intervention for Cancer Symptoms

Start date: July 2009
Phase: N/A
Study type: Interventional

Patients receiving treatment for advanced cancer often experience co-occuring pain, fatigue, and sleep disturbance that are not relieved with medications. Brief cognitive-behavioral coping strategies such as relaxation or imagery have been shown to be useful for these symptoms individually and may be effective for the cluster of co-occuring pain, fatigue, and sleep disturbance. Because single cognitive-behavioral strategies don't work equally well for all persons, providing training in multiple cognitive-behavioral strategies is necessary. However, oncology nurses report having insufficient time and are often not available to deliver the interventions exactly when patients experience symptom exacerbation. This application proposes a patient-controlled cognitive-behavioral (PC-CB) intervention, using an MP3 player to deliver recorded cognitive-behavioral strategies. The PC-CB intervention would allow patients to select from a variety of cognitive-behavioral strategies based on their personal preferences, and facilitate self-administration of those strategies at whatever time and place the symptoms occur, without increasing burden on nursing staff. Primary aims are (1) to explore acceptability and patterns of use of the recorded cognitive-behavioral strategies and (2) to pilot test efficacy of the PC-CB intervention compared to a waitlist control.

NCT ID: NCT00945230 Completed - Pain Clinical Trials

Actigraphic Measurement of a Neurosurgical Procedure

Start date: March 2009
Phase: N/A
Study type: Interventional

The study examines and illustrates the utility of utilizing actigraphic measurements to assess treatment response.

NCT ID: NCT00942253 Completed - Clinical trials for End Stage Renal Disease

Exercise Training in Dialysis Patients With Restless Legs Syndrome (RLS)

HDRLS
Start date: September 2006
Phase: Phase 2
Study type: Interventional

Uremic etiology Restless legs syndrome (RLS) has been associated with poorer quality of life (QoL) compared to RLS-free counterparts mainly due to sleep deprivation factors. Exercise training in hemodialysis (HD) patients with RLS has been proven to be a safe approach in temporally ameliorating RLS symptoms similarly to the use of pharmacological treatment with dopamine agonists. However it not known whether the exercise anabolic stimulus and the dopamine agonist treatment could act synergistically for the improvement of physical functioning and muscle performance as well as in the amelioration of augmentation symptoms in hemodialysis patients with RLS.

NCT ID: NCT00940589 Completed - Alzheimer's Disease Clinical Trials

Efficacy of Circadin® 2 mg in Patients With Mild to Moderate Alzheimer Disease Treated With AChE Inhibitor

Start date: September 2009
Phase: Phase 2
Study type: Interventional

The aim of this exploratory randomized, placebo controlled study is to evaluate the efficacy of Circadin® 2mg in patients with mild to moderate Alzheimer Disease (AD) treated with the acetylcholinesterase (AChE) inhibitor. The effects of add-on Circadin® 2mg vs. placebo on the decline in cognitive skills and global functioning, as well as on daytime somnolence and will be assessed.