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Sleep clinical trials

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NCT ID: NCT05683483 Recruiting - Surgery Clinical Trials

WEsleep Trial: Improving Sleep in Hospitalized Patients

WEsleep
Start date: April 11, 2023
Phase: N/A
Study type: Interventional

In the WEsleep study, the investigators will perform a cluster randomized controlled trial. 3 surgical and 3 medical departments will be randomized to implement low-cost and simple interventions aimed at improving sleep in admitted patients. Another 3 surgical and 3 medical departments will be randomized to function as control groups. Subjective sleep quality and sleep-wake timing will be assessed in adult medical and surgical patients admitted into one of 12 participating wards, using questionnaires and a sleep diary. In addition, in a subset of participants, objective sleep measures will be assessed in with an EEG headband and a sleep mat.

NCT ID: NCT05677412 Recruiting - Sleep Clinical Trials

Sleep, Pain and Stress in Adolescents With Persistent Pain

PedPainSleep
Start date: May 23, 2023
Phase: N/A
Study type: Interventional

The main aim is the gain information of sleep structures in adolescents with persistent pain. Also to study simple interventions to support their sleep and pain management. The main aim of this study is to test the efficacy and feasibility of suggestive presleep relaxation technique in improving sleep quality and sleep-related emotional memory processing.

NCT ID: NCT05673213 Completed - Sleep Clinical Trials

Preterm Infants Physiological Parameters and Sleep-Wakefulness Status

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

This research was carried out between December 2021 and May 2022 as a randomized controlled experimental design. In the study, between 28-35 weeks of gestation preterm infants were divided into two groups as the experimental group (n=30) and the control group (n=30). The block randomization method was used to ensure that the infants were similar in terms of both weeks and weight due to the large interval between the weeks and to ensure the balance between the groups. Infants in the control group were followed in the routine prone position of the neonatal intensive care unit, while infants in the experimental group were followed in the prone position with three-stair positioning pillows.

NCT ID: NCT05663034 Recruiting - Depression Clinical Trials

CBT-I vs. MBTI for Traumatic Brain Injury (TBI)-Related Insomnia and Post-Traumatic Stress Symptoms

Start date: May 10, 2024
Phase: N/A
Study type: Interventional

This study is a prospective two-arm, single blind randomized controlled trial design to compare the clinical effectiveness of telemedicine-delivered, 6-session, standardized cognitive behavioral therapy for insomnia (CBT-I) and mindfulness-based treatment for insomnia (MBTI) in treating insomnia symptoms and ameliorating depressive symptoms in persons with mild to moderate TBI and comorbid Post-Traumatic Stress Symptoms (PTSS) and insomnia symptoms in a 360 patients. Participants will undergo assessment (psychosocial questionnaires, neurocognitive testing, sleep monitoring) at baseline, at the end of treatment, and at 6- and 12-weeks post-treatment. The primary outcome is sleep as measured by the Insomnia Severity Index (ISI).

NCT ID: NCT05658783 Completed - Pain Clinical Trials

Effect of Footbath on Pain Severity and Sleep Quality

Start date: October 5, 2021
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to examine the effect of hot water foot bath on the patients' pain severity and sleep quality levels on the night of the lumbar degenerative disc surgery. The main hypotheses are: - H1=Pain severity of the patients who applied footbath is lower than the patients who did not. - H2=The sleep quality of the patients who applied footbath is higher than the patients who did not. Participants will be asked to keep their feet in 42oC hot water for 20 minutes on the night of the day of surgery. If there is a comparison group: Researchers will compare control group to see if there is any difference on the pain severity and sleep quality of the patients.

NCT ID: NCT05657808 Completed - Sleep Clinical Trials

Radicle Rest 2: A Study of Health and Wellness Products on Sleep and Health Outcomes

Start date: January 9, 2023
Phase: N/A
Study type: Interventional

A randomized, blinded, placebo-controlled direct-to-consumer study assessing the impact of health and wellness products on sleep and other health outcomes.

NCT ID: NCT05656768 Enrolling by invitation - Hypertension Clinical Trials

Sleep and Circadian Contributions to Nighttime Blood Pressure

SCN-BP
Start date: June 1, 2023
Phase: N/A
Study type: Interventional

Broadly, this study (SCN-BP) seeks to examine sleep and circadian factors that contribute to blood pressure levels at night.

NCT ID: NCT05652829 Recruiting - Sleep Clinical Trials

Sleep Duration and Quality in Children

Sleep-FAST
Start date: February 1, 2022
Phase:
Study type: Observational

Obesity in children is a priority of public health initiatives, and reliable obesity prevalence and severity assessments are needed for policy decisions and study directions. Obesity in childhood raises the risk of insulin resistance, type 2 diabetes, and cardiovascular diseases in later life. To develop preventive strategies, it is essential to identify modifiable lifestyle habits linked to childhood obesity. The four main modifiable lifestyle behaviors affecting body weight are physical activity, sleep, screen time, and eating patterns. Among these factors, sleep is a neglected issue for clinicians, and recent research has shown that sleep patterns can predict BMI and macronutrient intake. Getting enough sleep is essential to a person's physical and mental well-being and development. This study aims to determine the sleep duration and quality of children aged 9-12 during the school year and how sleep impacts food intake and choice. Also, determining any relationships between the sleep and food intake outcomes and screen time, physical activity, and anthropometric indicators.

NCT ID: NCT05641194 Recruiting - Sleep Clinical Trials

EaseAlert: Tactile Firefighter Alerting System

Start date: August 26, 2023
Phase: N/A
Study type: Interventional

The purpose of this research is to test a commercially viable Fire Fighter Altering System (FFAS) comprised of proprietary wearables and optional bed shakers called BunkAlerts; collectively "personal alerting devices" as an alternative approach to the traditional fire alarm system used in fire stations. Participants (fire fighters) will be asked to take part in the study to investigate the impact of the new FFAS on cardiovascular response and sleep. This study includes three phases: 1) baseline, 2) implementation of EaseAlert FFAS with traditional alarm, and 3) implementation of EaseAlert FFAS without traditional alarm. Participants will be asked to wear an Actigraph wGT3x-BT and Polar H10 device to record sleep and heart rate data for 12 days at work in addition to EaseAlert FFAS device for 8 out of the 12 days at work. They will also be asked to complete a questionnaire and complete daily journal entries.

NCT ID: NCT05635578 Completed - Sleep Clinical Trials

The Effect of Reiki Applicatıon on Sleep and Qualıty of Life in Epılepsy Patıents

Start date: November 15, 2022
Phase: N/A
Study type: Interventional

After the general period of positive social adjustments, epilepsy is in a high life cycle to control seizures. During seizures in epilepsy, patients' quality of life and antiepileptic life span can be seen in daily life such as daily life and daily awakenings. Reiki, which has been proven by studies in health problems such as fatigue and pain; an energy that can be unblocked or applied in a non-applicable way can benefit from a therapy that can be applied by touch or remotely, without negative effects. In the literature, reiki applied to epilepsy patients has sleep and quality of life. This thesis is planned to do research on sleep and living areas of reiki applied to epilepsy patients.