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Parasomnias clinical trials

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NCT ID: NCT01442610 Completed - Sleep Disturbances Clinical Trials

Effects of Rasagiline on Sleep Disturbances in Parkinson's Disease

RaSPar
Start date: October 2011
Phase: Phase 4
Study type: Interventional

As the MAO-B inhibitor rasagiline is able to improve motor skills it might have positive effects on sleep disruption by reducing nocturnal akinesia. As it was reported to cause only minor sleep disruption in PD Patients, it might be able to improve sleep architecture. The investigators thus study the effects of Rasagiline on sleep disturbances measured by polysomnographic (PSG) evaluation of sleep efficacy and PDSS-2. Secondary measures are other sleep variables measured by PSG, sleep quality and daytime sleepiness assessed by standardized scales as well as cognitive function, depression and QoL index.

NCT ID: NCT01429636 Completed - Hot Flashes Clinical Trials

Applied Relaxation (AR) Technique Versus Its Modified Version for Treating Menopausal Symptoms

Start date: August 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate better efficacy and effectiveness of modified applied relaxation technique over its original version for treating menopausal symptoms.

NCT ID: NCT01427192 Completed - Clinical trials for Pulmonary Hypertension

Treatment of Sleep Related Breathing Disorders in Patients With Pulmonary Hypertension

CSRPH
Start date: November 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to study the differential short-term effect of nocturnal oxygen, acetazolamide tablets and nocturnal non-invasive positive pressure ventilation on symptoms, exercise capacity and nocturnal breathing disturbances in subjects with pulmonary hypertension and sleep related breathing disorders - Trial with medicinal product

NCT ID: NCT01419314 Completed - Pain Clinical Trials

Lower Extremity Splinting to Manage Pain and Sleep Disturbances Associated With HIV/AIDS Related Peripheral Neuropathy

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

WHAT IS THE PURPOSE OF THIS STUDY? The investigators want to know if wearing a pair of splints at night works to bring the pain down and help you sleep better (in people living with HIV/AIDS related neuropathy). HOW MANY PEOPLE WILL PARTICIPATE? About 58 to 88 people will take part in this study at the Harris County Hospital District (HCHD). WHAT WILL HAPPEN DURING THIS STUDY? As a participant, you will be assigned to one of two treatment groups. In one group, you will be asked to wear leg splints at night and the other you will wear the liners of the splints only. You will be asked to answer questions about how well you sleep, how long you sleep, and about your discomfort at the legs. The researcher will be there to help, but the investigators want you to answer the questions on your own if you can. You will be asked to reach forwards standing next to a wall and to walk for 6 minutes after that. The tests will de done in random order. The sessions will be done at the beginning, at week three and week six. You should finish all of the testing and questionnaires in an hour or less, for a total of three hours over six weeks in the investigators clinic. You will receive instructions on how to use the splints with liners or the liners alone at home. You will be asked to wear them at night only for the next 6 weeks. Finally, the principal investigator will contact you weekly by phone, to discuss issues of comfort and your ability to adhere to the instructions provided.

NCT ID: NCT01405313 Recruiting - Periodic Breathing Clinical Trials

Modified Adaptive Servoventilation (ASV) Compared to Conventional ASV

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

This study will determine if modified adaptive servoventilation (ASV) is as effective as the conventional ASV in treating periodic breathing. The study will determine if the modified ASV reacts appropriately to reduce apneas and hypopneas and provides suitable levels of positive airway pressure compared to conventional ASV.

NCT ID: NCT01404286 Completed - Clinical trials for SLEEP DISTURBANCES Nec in ICD9CM

Resistance Training and Sleep in the Elderly

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

Purpose: The objective of this study was to evaluate the influence of a session of resistance training on the sleep patterns of elderly people. Methods: Forty men aged 65 to 80 years, sedentary and clinically healthy were divided into two groups: the control group (n=18) and the resistance group (n=22). Both groups underwent two polysomnography tests, one at baseline and another after either a resistance training session (One Repetition Maximum - Strength Test, resistance group) or without physical exercise (control group).

NCT ID: NCT01402570 Completed - Depression Clinical Trials

Glutathione and Health With Post-Polio Syndrome

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

In this study, people who have symptoms of post polio will take oral glutathione supplements for three months. Their levels of fatigue, physical function, sleep disturbance, impairment and emotional distress will be measured with both subjective and objective measures.

NCT ID: NCT01383369 Completed - Clinical trials for Postoperative Cognitive Abilities

Postoperative Sleep Disturbances Role in Cognitive Test Results After Fast-track Hip and Knee Arthroplasty

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

The purpose of this study is to evaluate sleep cycle before and after fast-track arthroplasty (3 days before and 10 days after) combined with cognitive testing preoperatively, on postoperative day 1,2,10.

NCT ID: NCT01371669 Completed - Sleep Disorders Clinical Trials

Screening for Sleep Hypoxemia in Pulmonary Arterial Hypertension

Sommeil_HTAP
Start date: June 2010
Phase: N/A
Study type: Observational

In the investigators study, and regarding results of small cohorts in the literature, the investigators hypothesize that hypoxemia is frequent in IPAH and CPEPH. The investigators will explore these patients with a one night polysomnography and transcutaneous capnography, searching for hypoxemia and hypercapnia and by determining its physiopathologic mechanisms.

NCT ID: NCT01366677 Completed - Depression Clinical Trials

Yoga for Persons With Severe Visual Impairment

RPY
Start date: August 2010
Phase: N/A
Study type: Interventional

This study aims to provide novel information on the feasibility of yoga interventions for secondary symptoms related to severe vision loss, such as sleep disturbances, negative mood states, fall risk and balance. This information will be important for determining safe, cost-effective and reliable practices for the benefits of yoga as an alternative means for improved health and well-being. A yoga intervention that is integrative and evidence-based will benefit the blind population through effective treatments and prevention of secondary symptoms as well as serve to inform rehabilitation specialists, educators, and clinicians in the future.