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Primary Insomnia clinical trials

View clinical trials related to Primary Insomnia.

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NCT ID: NCT05420090 Completed - Primary Insomnia Clinical Trials

The Effects of Milk and Banana as a Night Meal to Primary Insomnia on Sleep Quality, BDNF and Appetite Mechanism

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

The aim of this study to determine the impact of banana and milk on sleep and appetite

NCT ID: NCT05416346 Completed - Primary Insomnia Clinical Trials

Digital Cognitive Behavioral Therapy for Insomnia in China

Start date: April 12, 2021
Phase: N/A
Study type: Interventional

Digital cognitive behavioral therapy for insomnia (dCBT-i) is found to be effective but is rarely used in China. Hence, the investigators developed an automated Chinese dCBT-i program and examined its feasibility, acceptability, and preliminary effectiveness in individuals with insomnia symptoms.

NCT ID: NCT03542396 Completed - Depression Clinical Trials

Evaluation of a Group Therapeutic Exercise Program

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

Moderate to vigorous physical activity can reduce symptoms of mental disorders like major depression, anxiety disorders, insomnia, and ADHD. However, in Germany there are no group therapeutical exercise programs for psychotherapy patients in an outpatient context. The current study aims to examine the effectiveness of a manualized exercise program, named ImPuls, which consists of a supervised and non-supervised endurance training in moderate to vigorous intensity and behaviour change techniques.

NCT ID: NCT03314441 Completed - Primary Insomnia Clinical Trials

Effects of Regular Practice of Yoga on Subjective and Objective Sleep Quality in Primary Insomnia

Start date: November 8, 2017
Phase: N/A
Study type: Interventional

The purpose of the study is to assess the effects of regular Viniyoga in patients suffering from primary insomnia.

NCT ID: NCT02832804 Completed - Primary Insomnia Clinical Trials

Effect of Transcranial Direct-current Stimulation Therapy on Primary Chronic Insomnia Patients

Start date: February 2016
Phase: N/A
Study type: Interventional

To evaluate the clinical efficacy and safety of neuromodulation by transcranial direct current stimulation (tDCS) in the patients with primary chronic insomnia .

NCT ID: NCT02443649 Completed - Primary Insomnia Clinical Trials

Improving Sleep Quality in People With Insomnia

Start date: January 2015
Phase: N/A
Study type: Interventional

Insomnia is a significant problem affecting 10 to 20% of US population. Long-term pharmacological treatments are not recommended due to side effects, with therapy and sleep hygiene education often employed as alternatives. Use of mind-body approaches for insomnia is increasing. One of the most promising mind-body approaches for alleviating sleep problems is hypnosis. Research indicates significant beneficial effects of hypnosis on sleep, but sleep was rarely assessed as primary outcome and studied populations were diverse. Further, it remains unclear who the best candidates for benefitting from hypnosis are. To address some of the gaps in the current knowledge, the study evaluates whether 1) an addition of hypnotic suggestion for sleep improvement to the optimizing sleep hygiene (OSH) program increases the effectiveness of the OSH using objective and subjective assessments and 2) determines characteristics associated with hypnotic responsiveness.To address these goals a randomized controlled trial (RCT) with 3 laboratory visits (baseline, intervention, and 1 month follow-up) will be conducted with 50 adults meeting criteria for primary insomnia and allocated to one the two groups: 1) experimental group receiving during the intervention visit a combination of the Optimizing Sleep Hygiene (OSH) program and a hypnosis session for sleep improvement and 2) a control group receiving at the intervention visit the OSH only. Hypnosis session for sleep improvement for the control group will be offered at the end of the follow-up study visit (conducted after 4 weeks post-intervention) after completing all follow-up measures. Each study visit will last for 2-3 hours. During the visits sleep, personality traits and daily function of the participants will be assessed. Further, after the baseline and one week before the follow-up visit subjects will wear a watch-like actigraphic device monitoring their sleep patterns at home and will complete sleep diary. The knowledge gained from this study will inform the literature and clinicians about usefulness of hypnosis for insomnia sufferers and will help identify the population of insomnia sufferers most likely benefit from use of hypnosis for sleep

NCT ID: NCT02290405 Completed - Insomnia Clinical Trials

Impact of Hyperarousal on Simple and Complex Cognitive Task Performance Among Insomnia Sufferers

Start date: October 1, 2014
Phase:
Study type: Observational

The purpose of this study is to learn more about people with insomnia disorder and cognitive impairment. Cognitive impairment is difficulty with mental abilities such as thinking, knowing and remembering.

NCT ID: NCT02087488 Completed - Primary Insomnia Clinical Trials

Auricular Acupuncture for Primary Insomnia

AAPI
Start date: March 2014
Phase: N/A
Study type: Interventional

This double-blind RCT will evaluate the therapeutic effectiveness and safety of auricular acupuncture(AA) for primary insomnia(PI) .

NCT ID: NCT01960452 Completed - Primary Insomnia Clinical Trials

A High Density EEG Comparison of Sleep Patterns in Insomnia

Start date: October 2013
Phase: N/A
Study type: Observational

Insomnia, defined as a subjective report of difficulty initiating sleep, maintaining sleep, and/or non-restorative sleep, leads to significant daytime dysfunction and increased health risks. A commonly held hypothesis is that insomnia is caused by a state of hyperarousal, but the neurobiological mechanisms of hyperarousal in insomnia are poorly understood, in part because of limitations in our ability to image the brain during normal human sleep with sufficient temporal resolution. Furthermore, the efficacy of insomnia treatment is judged by subjective report of the patient and demonstration of changes in sleep latency and/or sleep amount which are generally small in magnitude; there are currently no data to demonstrate that insomnia treatments correct any functional abnormalities in the sleep process that likely contribute to neurobehavioral abnormalities and health risks. The goals of the proposed study are to use high density EEG to define abnormalities in specific aspects of sleep in insomnia patients compared to healthy sleeping control subjects to define biomarkers that will both increase our understanding of the pathophysiology of insomnia as well as provide targets to assess treatments for insomnia.

NCT ID: NCT01957111 Completed - Primary Insomnia Clinical Trials

Metabolomics of Insomnia-Related Hyperarousal

Start date: October 2013
Phase: N/A
Study type: Observational

Individuals with insomnia have been shown to have higher overall metabolic rates compared to good sleepers, but it is not known which metabolic processes are involved. The goal of this study is to compare a wide array of metabolic processes in 15 people with insomnia and 15 good sleepers. We hypothesize that there will be distinct metabolic processes that are functioning differently in those with insomnia.