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Parasomnias clinical trials

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NCT ID: NCT04808232 Completed - Hot Flashes Clinical Trials

The Effect of Health Education and Progressive Muscle Relaxation Exercise on Vasomotor Symptoms and Sleep Problems With Perimenopausal Women

Start date: February 17, 2019
Phase: N/A
Study type: Interventional

This study aims to determine the effect of health education and progressive muscle relaxation exercise (PMRE) on vasomotor symptoms and sleep problems in women with perimenopausal period; a randomized, pretest-posttest is a randomized controlled, factorial group experimental study. The research was conducted in a family health center. The required institutional permission and ethics committee approval was received. The sample consisted of 90 women totally, 30 of whom in the PMRE + health education group, 30 of whom in the PMRE group and 30 of whom in the control group. The data was collected using personal information form, Visual Analog Scale for Vasomotor Symptoms (VAS), Women's Health Initiative Insomnia Rating Scale-WHIIRS, vasomotor symptom diary, progressive muscle relaxation exercise follow-up schedule, and health education practice follow-up schedule. The data were stored in the SPSS 24 program. In the analysis of the data, ANOVA test, Repeated Measures test, Kruskal-Wallis H test, Friedman test and χ2 test statistics were used.

NCT ID: NCT04804176 Enrolling by invitation - Parkinson Disease Clinical Trials

Study on the Mode and Mechanism of Ultra-low Frequency rTMS for Sleep Disorders in Patients With Parkinson's Disease

Start date: December 20, 2019
Phase: N/A
Study type: Interventional

The study by giving a sleep disorder Parkinson's disease patients with different patterns of ultra-low frequency transcranial magnetic stimulation or sham stimulation, scale for assessment of the patients were observed, hematology and imaging changes before and after therapy, clear ultra-low frequency transcranial magnetic stimulation for sleep disorder Parkinson's disease treatment, to explore the mechanism of action, compare the difference between different modes.

NCT ID: NCT04800653 Completed - Clinical trials for Stellate Ganglion Block

The Effect of Stellate Ganglion Block on Postoperative Sleep Disturbance and Cognitive Function in Elderly Surgical Patients

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

Postoperative delirium is an acute state of confusion, which is characterized by changes in attention and cognitive functions and fluctuations in consciousness; postoperative cognitive dysfunction is a common central nervous system complication in elderly patients after surgery, often manifested as memory, Obstacles in abstract thinking and orientation are accompanied by a decline in social activity ability. Postoperative delirium and cognitive dysfunction can prolong hospital stay, increase medical expenses, affect postoperative functional recovery, and even increase postoperative mortality. Sleep disorders are a group of diseases that affect the ability to sleep well regularly and cause severe impairment of social and occupational functions. Stellate ganglion block is a selective sympathetic ganglion block, in which a local anesthetic is injected into the loose connective tissue of the neck including the stellate ganglion. There are complex connections between stellate ganglia and multiple brain regions in the brain, which can improve postoperative delirium, cognitive function and sleep disturbance to a certain extent, and have certain guiding significance for postoperative rehabilitation of elderly patients.

NCT ID: NCT04786899 Completed - Sleep Disturbance Clinical Trials

Sleep & Postoperative Delirium in Hispanic/ Latino Patients After Cardiothoracic Surgery

Start date: February 12, 2021
Phase:
Study type: Observational

The purpose of this research is to study pre-operative sleep problems and delirium in Hispanic/Latino patients after heart and lung surgery.

NCT ID: NCT04780893 Withdrawn - Insomnia Clinical Trials

Electrical Vestibular Nerve Stimulation (VeNS) as a Method of Sleep Management in People With PTSD

Start date: February 1, 2022
Phase: N/A
Study type: Interventional

This double blind randomized controlled study will enroll 20 subjects and will be conducted remotely. The study will be randomized for an 8-week period with a 1:1 active to sham device allocation. Primary endpoint analysis will be performed at 4 weeks.

NCT ID: NCT04771234 Completed - Chronic Insomnia Clinical Trials

Digital Psychological Self-care for Sleep Problems

Start date: February 25, 2021
Phase: N/A
Study type: Interventional

In this non-randomized treatment feasibility pilot we want to explore if a simplified version of CBT-i as a non-therapist-guided digital tool can work; if the digital tool is perceived as user friendly and if participants' insomnia severity is improved following four weeks of treatment.

NCT ID: NCT04771104 Completed - Liver Cirrhosis Clinical Trials

The Effect of Induced Hyperammonaemia on Sleep and Melanopsin-mediated Pupillary Light Response in Patients With Liver Cirrhosis

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

Sleep disturbances are common among patients with liver cirrhosis, but the reasons are not well understood. In this project the investigators evaluated whether an increase in blood ammonia in patients with cirrhosis had an impact on sleep quality and the function of retinal ganglion cells measured by pupillary response to blue light.

NCT ID: NCT04767997 Completed - Sleep Disturbance Clinical Trials

Probiotics on Sleep Among Adults Study

Start date: October 12, 2021
Phase: Phase 2
Study type: Interventional

The aim of this study is to determine the impact of a probiotic formulation on subjective sleep patterns. It is hypothesized that participants given the probiotics will improve their sleep patterns compared to participants receiving placebo.

NCT ID: NCT04759651 Recruiting - Lung Cancer Clinical Trials

Sleep Disorders in Patients With Suspected Lung Cancer Before and After Thoracic Surgery

Start date: June 1, 2021
Phase:
Study type: Observational

The main aim of this study is to prospectively evaluate the occurrence of sleep disorders in patients undergoing thoracic surgery due to the preliminary diagnosis of lung cancer. Secondary aims include anxiety, depressive mood and functional outcomes before and 3 months after the intervention.

NCT ID: NCT04751019 Completed - Insomnia Clinical Trials

The Use of Amber Glasses in Improving Sleep

Start date: March 11, 2019
Phase: N/A
Study type: Interventional

The use of amber glasses will aid the patient to fall asleep without the need for the use of hypnotic medication.