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Dyssomnias clinical trials

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NCT ID: NCT03154697 Recruiting - Clinical trials for Sleep Disturbances in Smith-Magenis Syndrome

Development of Clinical Database of Individuals With Smith-Magenis Syndrome and Sleep Disturbances

Start date: January 2016
Phase:
Study type: Observational

This database will be used to better understand the sleep problems of people with SMS. This clinical database will be a part of a larger Smith-Magenis Patient Registry used to create an awareness campaign around SMS and the sleep disturbances that are characteristic of the disorder.

NCT ID: NCT03150433 Completed - Pain Clinical Trials

Sleep and Pain in Sickle Cell Disease

Start date: November 5, 2017
Phase: N/A
Study type: Interventional

This is a study testing the effects of behavioral sleep interventions on pain and brain function in sickle cell disease.

NCT ID: NCT03144531 Completed - Asthma Clinical Trials

Sleep Intervention for Kids and Parents: A Self-Management Pilot Study

SKIP
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Behavioral intervention for 6-11 year children with persistent asthma and sleep disturbance and a parent with sleep disturbance.

NCT ID: NCT03136575 Recruiting - Clinical trials for Head and Neck Cancer

The Impact of Qigong on Quality of Life and Sleep Disturbance in Head and Neck Patients Undergoing Radiotherapy

Start date: March 28, 2016
Phase: N/A
Study type: Interventional

This study aimed to observe how a six week qigong program influence patients with head and neck cancer during active radiotherapy treatment course. The quality of life, sleep dysfunction or depression and shoulder and neck function will be accessed by questionnaire, and ANS function will be objectively investigated using heart rate variability measurement.

NCT ID: NCT03125967 Recruiting - Stroke Clinical Trials

Daily Light Exposure for Sleep Disturbance, Fatigue, and Functional Outcomes in Acute Brain Injury

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of daily morning exposure to colored light in patients receiving acute inpatient rehabilitation services for stroke, traumatic brain injury, or non-traumatic brain injury with sleep disturbances such as poor nighttime sleep and/or excessive daytime sleepiness.In a two-arm randomized placebo-controlled study with pre-exposure and post-exposure assessments, we are comparing the effects of daily morning exposure to either blue light or red light on objective sleep quality, subjective sleep quality, functional rehabilitation outcomes, cognitive symptoms, fatigue, and neurological symptoms.

NCT ID: NCT03116841 Completed - Reflux Esophagitis Clinical Trials

Vonoprazan Study of Investigating the Effect on Sleep Disturbance Associated With Reflux Esophagitis- Exploratory Evaluation

VISTAEXE
Start date: August 2, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to exploratorily evaluate the effect of vonoprazan 20 mg on sleep disturbance of patients with reflux esophagitis, who have heartburn and/or regurgitation and ≥ 6.0 in the Pittsburgh Sleep Quality Index (PSQI) global score despite the maintenance treatment with PPI other than vonoprazan.

NCT ID: NCT03114189 Completed - Sleep Disturbance Clinical Trials

Kneipp Water Applications for Insomnia

KWAI
Start date: November 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to ascertain whether warm footbathes are effective on sleep disturbances in women before climacteric.

NCT ID: NCT03114072 Active, not recruiting - Sleep Disturbance Clinical Trials

Blocking Blue Light in Pregnancy, Effects on Melatonin Profile and Sleep

Start date: June 6, 2017
Phase: N/A
Study type: Interventional

Sleep disturbances are common in pregnancy, and the incidence increases during the third trimester. Light and specially the blue wavelengths of light, is affecting sleep and the circadian rhythm. The main aim of this randomized controlled study is to investigate the effect of Blue-blocking glasses (BB-glasses) used in the evening and night on sleep and mood in pregnant women in the third trimester. The outcome measures assess sleep variables, alertness, melatonin level, sleepiness (subjectively), mood and symptoms of anxiety and depression. In addition we want to measure the pregnancy related sleep problems, alcohol intake, physical activity and perceives stress in the study population, and the association with daily/nightly light exposure.

NCT ID: NCT03112824 Completed - Obesity Clinical Trials

Functional Assessment of Ashwagandaha Root Extract During Weight Loss

Start date: October 5, 2017
Phase: N/A
Study type: Interventional

Patients who are involved in a clinical protocol driven 12 week medical weight loss intervention will be randomized to receive either a placebo or 600 mg of an ashwagandha root extract. The study endpoints are primarily the patients self-reported perception of life stress and sleep quality. The working hypothesis of this study is that the addition of aschwagandha to .the medical weight loss program will improve the self-reported perception of life stress and sleep quality

NCT ID: NCT03108599 Recruiting - Fatigue Clinical Trials

Tech4Rest Trial With Team Truck Drivers

Tech4Rest
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The current project is a safety and health intervention focused on sleep and fatigue among truck driver teams (pairs), where one driver sleeps in a moving vehicle while the other partner drives. This study is conducted within the Oregon Healthy Workforce Center (OHWC), a NIOSH Center of Excellence in Total Worker Health. We will evaluate engineering and behavioral interventions to improve sleep, reduce fatigue, and impact Total Worker Health. An enhanced cab intervention will alter whole body vibrations during driving and sleep periods, and includes a therapeutic mattress system and an active suspension seat. The enhanced cab will be evaluated alone and in combination with a behavioral sleep intervention adapted from our effective SHIFT (Safety &Health Involvement For Truckers) program. The interventions prioritize hazard reduction according to the hierarchy of controls, and will be evaluated with a randomized controlled design.