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Sleep Deprivation clinical trials

View clinical trials related to Sleep Deprivation.

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NCT ID: NCT01989741 Completed - Sleep Deprivation Clinical Trials

Effect of Sleep Restriction on Decision Making and Inflammation

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

- hypothesis: sleep restriction in healthy subject trigger alteration of decision making associated with immuno-inflammatory changes - inclusion criterias: healthy subjects, men, under 35 years, BMI<26, no sleep troubles, intermediate chronotype - design: 12 subjects, longitudinal study 2 days of baseline, 7 night of sleep restriction (4h sleep/night), recovery (1, 2, 3 and 9 normal sleep nights). - parameters: decision making tests, reaction time, wakefulness test, biological parameters (cathecholamines, pro-inflammatory cytokines...), heart rate, blood pressure - control of sleep restriction: continuous polysomnographic survey

NCT ID: NCT01828320 Completed - Eveningness/Sleep Clinical Trials

Triple Vulnerability? Circadian Tendency, Sleep Deprivation and Adolescence

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

There is an urgent need to identify modifiable mechanisms contributing to risk and vulnerability among youth. The investigators test the hypothesis that eveningness, the tendency to go to sleep late and wake late, is an important contributor to, and even cause of, vicious cycles that escalate vulnerability and risk among youth. This study seeks to determine whether two interventions to reduce eveningness can reduce risk and confer resilience in critical aspects of health, development and functioning in youth.

NCT ID: NCT01800253 Completed - Sleep Clinical Trials

The Effects of Acute Total Sleep Deprivation Versus Normal Sleep on Metabolism

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

The study proposes to investigate whether acute total deprivation affects metabolism as measured through blood and peripheral tissues. Its aim is also to investigate how acute total sleep deprivation affects neurodegenerative markers, as well as hormones, memory performance and aspects of appetite regulation.

NCT ID: NCT01794689 Completed - Pain Clinical Trials

Mechanisms of Sleep Disruption Hyperalgesia

ESP2
Start date: May 2013
Phase: N/A
Study type: Interventional

Twenty percent of Americans suffer from chronic pain. Sleep disturbance is similarly prevalent and among the most common and disabling neurobehavioral problems associated with chronic pain. This research is designed to evaluate the effects of disrupted sleep patterns on mood, inflammation, the perception of pain, and pain relief. This study will help researchers understand the relationship between sleep and pain, and how sleep disturbance might influence chronic pain conditions.

NCT ID: NCT01791296 Completed - Delirium Clinical Trials

Does Nightly Dexmedetomidine Improve Sleep and Reduce Delirium in ICU Patients?

SKY-DEX
Start date: January 2011
Phase: Phase 4
Study type: Interventional

Specific Aims 1. Establish the feasibility of larger trial by implementing a sleep protocol in the ICU at 2 different sites. Specifically will be estimating the recruitment rates of patients and the compliance with both interventions. 2. Measure the safety and tolerance of adding night-time sedation with dexmedetomidine using adverse effects and withdrawal rates as indicators. 3. Measure the effect of nocturnal dexmedetomidine on pertinent clinical outcomes and use this outcome data to plan a larger, multicenter trial in this area. The goal of this study is to determine whether a night-time protocol that incorporates a pharmacologic intervention associated with improved sleep (i.e. dexmedetomidine) will improve sleep quality and reduce the incidence of delirium and sub-syndromal delirium in critically ill patients.

NCT ID: NCT01786564 Completed - Diabetes Clinical Trials

Home Sleep and Circadian Phase: Mediators of Diabetes Risk

Start date: December 6, 2011
Phase:
Study type: Observational

The purpose of this study is to determine if deficient sleep and/or disruption with the body's internal clock ("circadian rhythms") are associated with diabetes risk. This study is being done to look at the possible relationships between sleep and risk of diabetes by examining sleep in the home and diabetes risk in the laboratory.

NCT ID: NCT01651429 Completed - Sleep Deprivation Clinical Trials

Predicting Cognitive Resilience Against Sleep Loss

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

Resilience is the ability to cope effectively and adapt to a wide range of stressful environmental challenges. Sleep loss has been shown to reduce activity in the brain regions responsible for resilience. The ability to resist the effects of sleep loss appears to be a stable, trait-like quality. This study will attempt to predict individuals' trait-resistance to sleep loss based on their neurobiology.

NCT ID: NCT01648062 Completed - Insomnia Clinical Trials

Sleep Self-Regulation Using Mental Imagery

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

This randomised controlled trial assessed the efficacy of four mental imagery techniques for improving sleep and its related behaviour: (1) imagery focused on reducing arousal levels; (2) imagery incorporating implementation intentions (a strategy designed to link specified behaviour with the anticipated context) for sleep-related behaviour; (3) a combination of imagery using arousal reduction and implementation intention strategies; or (4) a condition where participants were asked to imagine their typical post work activities.

NCT ID: NCT01623674 Completed - Clinical trials for Effect of Sleep Deprivation

Laparoscopic Skills and Cognitive Function Are Not Affected by Night Shifts in Surgeons

Start date: December 2011
Phase: N/A
Study type: Observational

The aim of the study was to asses the effect of sleep deprivation during nightshift by monitoring 30 surgeons in unit of surgical gastroenterology in 4 consecutive days. The first day was pre call= day 1, second day was on call= day 2, third day was the first post call day = day 3 and fourth day was the second post call= day 4. The surgeons were monitored in order to asses how performance was on call compared to pre call and post call. The hypothesis was that they would perform worse on call than pre call, and again slightly worse post call.

NCT ID: NCT01606020 Completed - Healthy Volunteers Clinical Trials

Sleep Deprivation : Effects on Driving Performance and Central Fatigue

PrivSom
Start date: September 2011
Phase: N/A
Study type: Interventional

The effects of sleep deprivation (SD) on performance, while contradictory at first glance, are in reality rather clear when exercise duration is considered, i.e. intense/supramaximal versus prolonged exercises. This latter type of exercise leads to the most important performance decrements after SD.