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Insomnia clinical trials

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NCT ID: NCT02513017 Completed - Clinical trials for Cardiovascular Disease

Insomnia and Cardiovascular Diseases: Influence of Behavioral Treatments and Preferences

Start date: February 2009
Phase: N/A
Study type: Interventional

Research has shown that persons who have trouble sleeping and experience stress are at risk of developing heart diseases. Two treatments, called stimulus control instructions and sleep efficiency treatment, that do not involve sleeping pills, have been found effective in managing trouble sleeping. This study will be undertaken to find out if the two treatments are effective in improving sleep, and reducing stress and the risk of heart diseases. Persons with trouble sleeping may have a preference for either treatment. It is believed that if persons get the treatment they prefer, then they will be satisfied with the treatment and comply with it, and experience improvement in their sleep. This study will also examine the extent to which giving persons the treatment of their choice, as compared to giving persons treatment based on chance, will lead to higher satisfaction and compliance with treatment, and improved sleep. About 300 persons who experience trouble sleeping will be included in the study. They will be requested to complete a questionnaire and a sleep diary before and after they receive treatment, as well as 6 month and one year later.

NCT ID: NCT02508129 Completed - Hypertension Clinical Trials

Hypertension With Unsatisfactory Sleep Health

HUSH
Start date: August 2015
Phase: N/A
Study type: Interventional

Insomnia and hypertension are common health problems that often occur together and influence each other. This practical, low-cost, clinical trial will evaluate two behavioral treatments for insomnia (a brief intervention with therapist contact and a self-guided Internet intervention) compared to usual care. Participants will be recruited using the electronic health record in their primary care physicians' offices, and will be evaluated for sleep, blood pressure, and health outcomes after 9 weeks, 6 months, and 12 months.

NCT ID: NCT02495155 Completed - Breast Cancer Clinical Trials

Initial Assessment of an Internet-based Symptom Management Intervention in Early Stage Breast Cancer

PROSPECT
Start date: June 2015
Phase: N/A
Study type: Interventional

In order to determine the acceptability of a breast cancer-specific cognitive behavioral therapy intervention, as well as to obtain preliminary data to assess efficacy in managing symptoms, the investigators will ask 45 breast cancer survivors with moderate insomnia, fatigue, and/or pain to use the investigators' internet-based intervention for 8 weeks and to complete patient-reported outcomes assessments before and after the 8 week intervention.

NCT ID: NCT02478593 Withdrawn - Anxiety Clinical Trials

Impact of Patient Education on Benzodiazepine Use in the Elderly

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

The overall goal of this research is to develop and test strategies to decrease potentially inappropriate medication use among the elderly.

NCT ID: NCT02464046 Completed - Insomnia Clinical Trials

Study to Evaluate Efficacy, Safety and Tolerability of JNJ-42847922 in Participants With Insomnia Disorder Without Psychiatric Comorbidity

Start date: July 27, 2015
Phase: Phase 2
Study type: Interventional

The primary purpose of this study is to investigate the effect of JNJ-42847922 (change versus placebo) on sleep efficiency (SE) measured by polysomnography (PSG) after single and multiple dose administration to participants with insomnia disorder without psychiatric comorbidity.

NCT ID: NCT02463461 Withdrawn - Insomnia Clinical Trials

Comparison Between Multiple Wrist-worn Actigraphy Devices and Polysomnography

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

The primary objective of the proposed study is to investigate the agreement levels of modern and well-established actigraphy devices against PSG in healthy as well as patient populations for multiple sleep parameters across two study sites (Qatar and New York City).

NCT ID: NCT02455271 Completed - Insomnia Clinical Trials

Investigation of the Safety and Efficacy of Long Term Administration of Eszopiclone in Insomnia Patients

Start date: October 1, 2012
Phase:
Study type: Observational

To investigate the safety and efficacy of administration of eszopiclone for 6 months in insomnia participants.

NCT ID: NCT02452684 Completed - Insomnia Clinical Trials

Investigation of the Safety and Efficacy of Eszopiclone in Insomnia Patients

Start date: October 1, 2012
Phase:
Study type: Observational

To investigate the safety and efficacy of administration of eszopiclone for 4 weeks in insomnia patients.

NCT ID: NCT02445378 Completed - Depression Clinical Trials

Aromatherapy and Essential Oils in Improving Insomnia and Other Symptoms in Patients With Newly Diagnosed Acute Leukemia Undergoing Chemotherapy

Start date: December 28, 2014
Phase: N/A
Study type: Interventional

This randomized clinical trial studies aromatherapy and essential oils in improving insomnia and other symptoms in patients with newly diagnosed acute leukemia. Aromatherapy and essential oils may help improve insomnia and other complications caused by chemotherapy.

NCT ID: NCT02444026 Recruiting - Insomnia Clinical Trials

Feasibility and Efficacy of Internet-delivered CBT for Insomnia in a National Cohort of Danish Breast Cancer Survivors

Start date: December 2014
Phase: N/A
Study type: Interventional

The aim is, in a randomized controlled trial, to test the feasibility and evaluate the efficacy of an internet-based treatment for insomnia, previously tested in a group of 28 US cancer patients, in a large sample of Danish breast cancer survivors who are experiencing significant sleep problems 0-3 years after treatment. The investigators aim to test the following hypotheses: That a group receiving Internet-delivered cognitive-behavioral therapy (CCBT) for insomnia (CCBT-I) will experience reduced sleep latency, more hours of sleep, fewer awakenings during the night, improved sleep efficiency, increased subjective sleep quality, and improved quality of life after the intervention, when compared to a waiting list control group. The investigators also aim to explore a number of possible moderators of the effect (comorbidity, depression, fear of cancer recurrence tendency to ruminate) and mediating mechanisms (changes in sleep habits and sleep-related lifestyle factors).