Clinical Trials for Sleep Disorders

Currently registered clinical trials for Sleep Disorders from ClinicalTrials.gov. 20 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Sleep Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 20
  • Active, not recruiting: 2
  • Completed: 17
  • Other: 11

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT05508971 — Treatment of Obstructive Sleep Apnea With Personalized Surgery in Children With Down Syndrome (TOPS-DS)

StatusRecruiting
PhaseN/A
SponsorOregon Health and Science University
Enrollment304
Study TypeINTERVENTIONAL
ConditionsObstructive Sleep Apnea; Down Syndrome
Interventions;

The overall objective of this randomized clinical trial is to test the effectiveness of a personalized approach to the surgical treatment of OSA in children with Down syndrome (DS).The estimated prevalence of obstructive sleep apnea (OSA) in children with DS ranges from 45-83%, compared to 1-6% in the general pediatric population. Untreated OSA in children has been associated with daytime sleep…

NCT07685262 — Morning Bright Light Therapy and Daytime Functioning in University Students

StatusRecruiting
PhaseN/A
SponsorThe Hong Kong Polytechnic University
Enrollment153
Study TypeINTERVENTIONAL
ConditionsSleep; Circadian Rhythm; Daytime Sleepiness; Mood; Cognition
Interventions

This study tests whether a week of morning bright light therapy changes how well healthy young adults sleep and how alert, positive, and mentally sharp they feel during the day.

Morning light is the body’s main signal for keeping its internal clock and sleep-wake timing on track. Many university students keep irregular hours and spend most of the day indoors, where light is far dimmer than day…

NCT06258837 — Treatment of Obstructive Sleep Apnea With Personalized Surgery in Children With Small Tonsils

StatusRecruiting
PhaseN/A
SponsorOregon Health and Science University
Enrollment175
Study TypeINTERVENTIONAL
ConditionsOtolaryngological Disease; Obstructive Sleep Apnea
Interventions;

The purpose of this study is to compare the effectiveness of a novel personalized surgical approach to the standard AT in children with small tonsils (ST). This will be accomplished by randomizing children with ST and OSA to one of these two treatments and comparing outcomes after 6 months. It is the investigators’ central hypothesis that a personalized drug-induced sleep endoscopy (DISE)-direc…

NCT06661759 — Clinic-based and Technology-Supported Sleep Intervention for Pediatric Epilepsy

StatusRecruiting
PhaseN/A
SponsorNational Taiwan University Hospital
Enrollment150
Study TypeINTERVENTIONAL
ConditionsEpilepsy
Interventions

Sleep problems are more common and more severe in children with epilepsy. The purpose of this study is to develop and evaluate the effect of a clinic-based and technology-supported sleep intervention for improving sleep and health in children with epilepsy and their parents.

NCT06720090 — Light Therapy for Obsessive-compulsive Disorder (OCD)

StatusRecruiting
PhaseEarly Phase 1
SponsorWashington University School of Medicine
Enrollment40
Study TypeINTERVENTIONAL
ConditionsOCD
Interventions

The goal of this clinical trial is to test whether light therapy is effective for reducing symptoms in young adults with OCD and late bedtimes (1am or later). The main question[s] it aims to answer are:

Does light therapy reduce OCD symptoms? Does light therapy advance the circadian clock? If there is a comparison group: Researchers will compare a higher dose of light therapy to a lower dose…

NCT06192615 — Minimizing ICU Neurological Dysfunction With Dexmedetomidine-induced Sleep (MINDDS II)

StatusRecruiting
PhasePhase 3
SponsorMassachusetts General Hospital
Enrollment1800
Study TypeINTERVENTIONAL
ConditionsDelirium
Interventions; ;

This is a pragmatic phase III, randomized, blinded, double placebo-controlled, three-arm trial of elderly patients following cardiac surgery to assess the relationship between nighttime intravenous (IV) and sublingual dexmedetomidine on postoperative delirium and functional outcomes after surgery.

NCT07613710 — A Trial to Test the Safety and Tolerability of Lu AH69593 in Adults That Are Healthy or Have Narcolepsy

StatusRecruiting
PhasePhase 1
SponsorH. Lundbeck A/S
Enrollment104
Study TypeINTERVENTIONAL
ConditionsNarcolepsy
Interventions;

The purpose of the trial is to determine if Lu AH69593 is safe and well tolerated. The trial will also look at how the body processes Lu AH69593 with and without food.

NCT06188923 — A New Intervention to Improve Function in Veterans With Anxiety and Depression

StatusRecruiting
PhasePhase 2
SponsorVA Office of Research and Development
Enrollment84
Study TypeINTERVENTIONAL
ConditionsAnxiety and Depression
Interventions;

Anxiety and depression symptoms occur at high rates in Veteran populations and can significantly impact function, compromising the ability to work and to successfully form and maintain valued relationships. Several other symptoms commonly occur with anxiety and depression, including poor sleep quality and chronic pain. Since all these symptoms frequently occur together, they may have a common u…

NCT07119268 — SPARK Healthy Sleep

StatusRecruiting
PhaseN/A
SponsorIndiana University
Enrollment115
Study TypeINTERVENTIONAL
ConditionsSchizophrenia and Related Disorders; Sleep Disturbance
Interventions

SPARK-Healthy Sleep is a digital mental health intervention designed to help college students who may be at risk for psychosis and experience sleep problems. About 1 in 4 college students report psychotic-like experiences (such as hearing voices or feeling paranoid), and these students often have poor sleep quality, which can worsen their mental health symptoms.

This study tests whether a sing…

NCT07283289 — Prevalence of Obstructive Sleep Apnea in Patients With Peripheral Arterial Occlusive Disease

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment295
Study TypeOBSERVATIONAL
ConditionsPeripheral Artery Disease

Obstructive sleep apnea syndrome (OSAS) is characterized by partial (hypopnea) or complete (apnea) obstruction of the upper airways, leading to intermittent hypoxemia and sleep fragmentation. Peripheral arterial occlusive disease (PAOD) is a chronic condition defined by the narrowing or occlusion of arteries in the lower limbs, often resulting in ischemia of downstream tissues. This disease is …

NCT07284342 — A Study to Assess Change in Sleep Disturbances of Adult Participants With Advanced Parkinson’s Disease Receiving Subcutaneous Foslevodopa/Foscarbidopa

StatusRecruiting
PhaseN/A
SponsorAbbVie
Enrollment103
Study TypeOBSERVATIONAL
ConditionsAdvanced Parkinson’s Disease

Parkinson’s disease (PD) is a neurological condition, which affects the brain. Some symptoms of PD are tremors, stiffness, and slowness of movement. This study will assess change in sleep disturbances of adult participants with advanced Parkinson’s disease receiving subcutaneous Foslevodopa/Foscarbidopa under routine clinical practice.

Foslevodopa/Foscarbidopa is an approved drug for the treat…

NCT06532773 — Mindfulness Intervention for Sleep Disturbance and Symptom Management in Hematologic Cancer Patients During and After Inpatient Treatment

StatusRecruiting
PhaseN/A
SponsorDuke University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsHematologic Malignancy
Interventions

People with hematologic cancer often have sleep disturbance and symptoms of fatigue, stress, and pain. This study is being done to test a mindfulness intervention for sleep disturbance and symptom management in patients with hematologic cancer during and after inpatient treatment (Nite2Day+). Participants will complete a baseline survey online, using a mobile application, or paper/pencil. Once …

NCT07363720 — A Trial of TAK-861 for the Treatment of Narcolepsy With Cataplexy

StatusRecruiting
PhasePhase 3
SponsorTakeda
Enrollment88
Study TypeINTERVENTIONAL
ConditionsNarcolepsy Type 1 (NT1); Narcolepsy With Cataplexy
Interventions;

The main aim of this study is to assess how effective TAK-861 is for treating narcolepsy type 1 and if this effect is maintained over time. Participants will take TAK-861 for a few months and if they meet certain criteria, they will be randomly assigned (by chance, like flipping a coin) to continue taking TAK-861 or take placebo (fake medicine) for up to 4 weeks to see if their narcolepsy sympt…

NCT07369011 — A Study of Eloralintide (LY3841136) in Participants With Obstructive Sleep Apnea and Obesity or Overweight

StatusRecruiting
PhasePhase 3
SponsorEli Lilly and Company
Enrollment800
Study TypeINTERVENTIONAL
ConditionsSleep Apnea, Obstructive; Obesity; Overweight
Interventions;

The purpose of the studies is to evaluate the efficacy and safety of eloralintide in participants with moderate-to-severe obstructive sleep apnea and obesity or overweight. YDAO is a master protocol designed to support two independent studies: YSA1 and YSA2. Study YSA1 will include participants who are unable or unwilling to use Positive Airway Pressure (PAP) therapy and study YSA2 will include…

NCT06642246 — Sleep Promotion and Pediatric Hypertension

StatusRecruiting
PhaseN/A
SponsorChildren’s Hospital of Philadelphia
Enrollment10
Study TypeINTERVENTIONAL
ConditionsInsufficient Sleep; Hypertension
Interventions

Determine the effectiveness and feasibility of a mobile health sleep extension approach in the pediatric nephrology setting, to increase sleep duration and reduce systolic and diastolic blood pressure.

NCT07270406 — Healthy Behaviors for Insomnia Prevention in People With HIV and Ongoing Pain

StatusRecruiting
PhaseN/A
SponsorWashington University School of Medicine
Enrollment200
Study TypeINTERVENTIONAL
ConditionsChronic Pain; Insomnia; HIV
Interventions;

The purpose of this research study is to test whether Brief Behavioral Treatment for Insomnia (BBTI) delivered over the phone or Brief Mindfulness Training (BMT) delivered over the phone is better able to improve the symptoms of insomnia, reduce chronic pain, and slow the pace of biological aging in individuals with HIV and Chronic Pain.

NCT07213219 — PET-MRI of Reward System in Parkinson’s Disease With RBD

StatusRecruiting
PhaseN/A
SponsorUniversity Hospital, Clermont-Ferrand
Enrollment44
Study TypeINTERVENTIONAL
ConditionsParkinson's Disease (PD)
Interventions

Impulse control disorders (ICDs) are frequently observed in Parkinson’s disease (PD) and can have a major functional impact on the quality of life of both the patient and their entourage. The primary risk factor for the emergence of ICDs in PD is long-term dopaminergic treatment, but other risk factors, such as rapid eye movement sleep behavior disorder (RBD), have recently been identified. The…

NCT07552714 — Thread Embedding Plus Auricular Acupressure for Non-Organic Insomnia Based on Traditional Medicine Pattern Differentiation

StatusRecruiting
PhaseN/A
SponsorUniversity of Medicine and Pharmacy at Ho Chi Minh City
Enrollment70
Study TypeINTERVENTIONAL
ConditionsInsomnia, Nonorganic
Interventions; ;

Non-organic insomnia is a prevalent disorder that significantly impairs quality of life, characterized by difficulty initiating or maintaining sleep alongside daytime functional decline. This condition is particularly common among adults facing chronic stress, which increases the risk of chronic diseases and dysregulates the Microbiota-Gut-Brain Axis (MGBA)-a bidirectional communication system …

NCT07540897 — A Study to Evaluate the Efficacy, Safety and Tolerability of ALKS 2680 in Adults With Narcolepsy Type 1 (Brilliance NT1 - 304)

StatusRecruiting
PhasePhase 3
SponsorAlkermes, Inc.
Enrollment150
Study TypeINTERVENTIONAL
ConditionsNarcolepsy Type 1
Interventions; ;

The purpose of this study is to measure decreases in daytime sleepiness, cataplexy (sudden loss of muscle tone), and disease symptoms in participants with NT1 when taking ALKS 2680 tablets compared with placebo tablets.

NCT07346014 — Sleep and Circadian Interventions for College Students at High Risk of Suicide

StatusRecruiting
PhaseN/A
SponsorUniversity of Pittsburgh
Enrollment90
Study TypeINTERVENTIONAL
ConditionsSleep Disturbance; Sleep; Depression; Suicide
Interventions; ;

The purpose of this study is to examine the extent to which delivering sleep and circadian focused interventions in addition to evidenced based psychiatric care for depression and suicide risk may contribute to decreasing suicide risk among high risk young adults. Investigators will evaluate three interventions targeting sleep in acutely suicidal college students enrolled in intensive outpatien…

Active, Not Recruiting

NCT04057716 — Project REST: Regulation of Eating and Sleep Topography

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Pittsburgh
Enrollment120
Study TypeINTERVENTIONAL
ConditionsObesity, Childhood; Binge Eating; Sleep; Self-regulation
Interventions;

Overweight/obesity and inadequate sleep are prevalent, and frequently co-occurring, health risks among children, both of which are associated with serious medical and psychosocial health complications including risk for cardiovascular disease. Although the investigator’s data suggest that disrupted or shortened sleep may be causally associated with increased energy intake and weight gain in chi…

NCT07406620 — Entropy-based Physiological Signal Analysis in Patients With Obstructive Sleep Apnoea

StatusActive, not recruiting
PhaseN/A
SponsorKing’s College London
Enrollment139
Study TypeOBSERVATIONAL
ConditionsObstructive Sleep Apnoea (OSA)
Interventions

This observational study is being undertaken as a part of a Master of Research (MRes) in Clinical Research programme.

Its goal is to learn about how continuous positive airway pressure (CPAP) therapy changes the complexity of body signals in adults with obstructive sleep apnoea (OSA). The main question it aims to answer is:

- How does the complexity of physiological signals (specifically oxy…

Not Yet Recruiting

NCT07688603 — Level 3 Validation Study

StatusNot yet recruiting
PhaseN/A
SponsorWindsor Sleep Disorders Clinic
Enrollment80
Study TypeINTERVENTIONAL
ConditionsObstructive Sleep Apnea (OSA)
Interventions;

This study will compare the output of a new Level 3 polysomnography system against in-laboratory polysomnography.

NCT07688798 — Mentalization and Social Cognition in Adolescents After Suicide Attempt

StatusNot yet recruiting
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment82
Study TypeINTERVENTIONAL
ConditionsViolent Suicide Attempts in Adolescents
Interventions;

This study investigates the risk of violent suicide attempts in adolescents, with a particular focus on social cognition and sleep disturbances, to better understand the cognitive and behavioral mechanisms involved and to inform more targeted prevention strategies.

Violent suicide attempts are defined as the use of methods with a high immediate lethal potential. They are associated with distin…

NCT07684417 — Impact of Short and Mistimed Sleep on Adolescents With ADHD: The Adolescent Attention and Circadian Timing Study

StatusNot yet recruiting
PhaseN/A
SponsorChildren’s Hospital Medical Center, Cincinnati
Enrollment50
Study TypeINTERVENTIONAL
ConditionsADHD
Interventions;

Many adolescents go to bed late and wake up early for school. Science is only beginning to understand how sleep schedules can affect them. The investigators are interested in whether changing adolescents’ sleep patterns affects their functioning, attention, and how they feel. The investigators are especially interested in the effects of changing both how much sleep adolescents get and when that…

NCT07680114 — Overnight Thalamic TES-TI to Modulate Sleep Spindles in Individuals With Schizophrenia Spectrum Disorders and Matched Healthy Controls

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Wisconsin, Madison
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSchizophrenia
Interventions;

This study to find out whether a type of non-invasive electrical brain stimulation called transcranial electrical stimulation with temporal interference (TES-TI) can temporarily change brain activity during sleep-especially sleep spindles (brain rhythms in the ~8-16 Hz range). The investigators are focusing on the thalamus, a deep brain region that helps coordinate brain activity during non-RE…

NCT06579183 — Pilot Trial for Health Products on Mood and Sleep Quality

StatusNot yet recruiting
PhaseN/A
SponsorThe University of Hong Kong
Enrollment60
Study TypeINTERVENTIONAL
ConditionsSleep Disturbance; Emotional Disturbance
Interventions; ;

This is a pilot, single-site clinical trial that will follow a randomized, double-blinded, parallel-group, placebo-controlled design. A total of 60 participants aged 18-65 will be recruited for a 12-week intervention, followed by a 4-week observational phase and a post-intervention visit at week 16. Participants will attend five scheduled visits at 4-week intervals (baseline, weeks 4, 8, 12, an…

NCT07686731 — Suvorexant 3 - PE-PC

StatusNot yet recruiting
PhasePhase 4
SponsorNorthern California Institute of Research and Education
Enrollment142
Study TypeINTERVENTIONAL
ConditionsPTSD - Post Traumatic Stress Disorder; Insomnia; TBI (Traumatic Brain Injury)
Interventions; ;

The goal of this clinical trial is to learn if combining suvorexant (a sleep medication) with a shorter form of prolonged exposure therapy called PE-PC works to treat PTSD symptoms and improve sleep in Veterans and military personnel with PTSD and insomnia, with and without mild-to-moderate traumatic brain injury (TBI). The main questions it aims to answer are:

Does suvorexant, when combined w…

NCT07683442 — The Optimal One-Month Dosing of Lemborexant for Moderate Obstructive Sleep Apnea (OSA) Patients With Low Arousal Threshold

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorChulalongkorn University
Enrollment36
Study TypeINTERVENTIONAL
ConditionsOSA - Obstructive Sleep Apnea
Interventions; ;

The goal of this clinical trial is to investigate the 1-month treatment effects of different dose of lemborexant in moderate OSA adult patients (18-65 years of age) with low arousal threshold.

The main questions it aims to answer are:

Primary outcome measure: Apnea/hypopnea index (AHI)

Secondary outcome measure:

  1. Polysomnography parameters

    • Mean and nadir oxygen saturation
    • Sleep…

NCT07679984 — Evaluating the Effects of a Mindfulness Intervention on Health Outcomes in Individuals With Hypertension

StatusNot yet recruiting
PhaseN/A
SponsorOhio State University
Enrollment140
Study TypeINTERVENTIONAL
ConditionsHypertension; Essential (Primary) Hypertension
Interventions

The purpose of this study is to evaluate the effectiveness of adding the Mindfulness in Motion (MIM) program to usual primary care for people with high blood pressure. MIM is a facilitated, 8-week online program that teaches simple ways to manage stress using mindfulness practices. The program also includes the use of a companion smartphone app throughout the 12-month study period. In this stud…

Enrolling by Invitation

NCT07685925 — Intern Health Study 2026

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of Michigan
Enrollment1000
Study TypeINTERVENTIONAL
ConditionsDepression / Major Depressive Disorder; Mood; Sleep; Physical Activity
Interventions

The aim of this study is to evaluate the efficacy of using a reinforcement learning algorithm to determine the optimal content of a mobile health intervention (message delivered via smartphone) for improving the mood, physical activity, and sleep of medical interns.

NCT07566871 — Effect of Non-Invasive Vagus Nerve Stimulation in Burn Patients

StatusEnrolling by invitation
PhaseN/A
SponsorFenerbahce University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBurn Injury
Interventions;

This study will evaluate the effects of non-invasive vagus nerve stimulation (nVNS) in adults with burn injuries. Burn patients may experience anxiety, poor sleep quality, pain, itching, and changes in autonomic nervous system function during recovery.

Participants will be randomly assigned to one of two groups. The intervention group will receive conventional physiotherapy plus nVNS, and the …

NCT07566923 — Effects of Non-Invasive Vagus Nerve Stimulation in Adolescent Burn Patients

StatusEnrolling by invitation
PhaseN/A
SponsorFenerbahce University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBurn Injury
Interventions;

This study will evaluate the effects of non-invasive vagus nerve stimulation in adolescents aged 12 to 18 years who have burn injuries. The study will include patients who have completed the acute phase after burn injury and who have symptoms such as anxiety, sleep problems, pain, or itching.

Participants will be randomly assigned to one of two groups. One group will receive conventional physi…

Completed Trials

NCT00097474 — Effects of Hydrocortisone, Melatonin, and Placebo on Jet Lag

StatusCompleted
PhasePhase 2
SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Enrollment57
Study TypeINTERVENTIONAL
ConditionsJet Lag
Interventions; ;

This study will examine the effects of cortisol (hydrocortisone), melatonin, a combination of cortisol and melatonin, and placebo (an inactive substance) on jet lag symptoms. Jet lag is a term used to describe symptoms people commonly experience after rapid travel across several time zones. The cause of jet lag is not known, but various hormones, including cortisol and melatonin, have a day-to-…

NCT02181569 — Sleep Disturbance and Relapse in Individuals With Alcohol Dependence: An Exploratory Mixed Methods Study

StatusCompleted
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment198
Study TypeOBSERVATIONAL
ConditionsAlcoholism

Despite research establishing the relationship between sleep disturbances and alcohol use, there is no clear understanding or model for what occurs once individuals who seek inpatient alcoholism treatment are discharged from rehabilitation facilities and attempt to integrate back into their homes and communities. The purpose of this investigation will be to characterize sleep patterns, percepti…

NCT02669225 — Brain Amyloid- Retention During Wakefulness and Following Emergence From Sleep in Healthy People

StatusCompleted
PhaseEarly Phase 1
SponsorNational Institute on Alcohol Abuse and Alcoholism (NIAAA)
Enrollment22
Study TypeINTERVENTIONAL
ConditionsNormal Physiology
Interventions

Background:

Brain activity creates waste products. The body s glymphatic system removes this waste, especially during sleep. One brain waste product is amyloid-beta (Ab). It plays a role in Alzheimer s disease. Researchers want to study the effect of sleep on Ab in the brain.

Objective:

To see if sleep affects the amount of waste product removed from the brain.

Eligibility:

Healthy people …

NCT04792697 — Experimental Manipulation of Sleep and Circadian Rhythms and the Role Played on Reward Function in Teens

StatusCompleted
PhaseN/A
SponsorUniversity of Pittsburgh
Enrollment115
Study TypeINTERVENTIONAL
ConditionsDelayed Sleep Phase Syndrome
Interventions; ;

Adolescence is a time of heightened reward sensitivity and greater impulsivity. On top of this, many teenagers experience chronic sleep deprivation and misalignment of their circadian rhythms due to biological shifts in their sleep/wake patterns paired with early school start times. Many studies find that this increases the risk for substance use (SU). However, what impact circadian rhythm and …

NCT07685379 — A Study Comparing Real and Sham Repetitive Transcranial Magnetic Stimulation in Adults With Fibromyalgia, Assessing Effects on Pain, Fatigue, Sleep, Mood, Quality of Life, Cognition, and Walking Under Usual and Dual-task Conditions

StatusCompleted
PhaseN/A
SponsorInstitute of Rheumatology, Serbia
Enrollment30
Study TypeINTERVENTIONAL
ConditionsFibromyalgia Syndrome
Interventions;

Fibromyalgia is a chronic condition that causes widespread pain and is often accompanied by fatigue, poor sleep, mood symptoms, memory and concentration difficulties, and reduced quality of life. Many adults with fibromyalgia also experience limitations in daily physical functioning. These limitations may include slower or less stable walking, reduced walking endurance, and greater difficulty w…

NCT05397353 — Sleep Treatment for Teens

StatusCompleted
PhaseN/A
SponsorRutgers, The State University of New Jersey
Enrollment12
Study TypeINTERVENTIONAL
ConditionsSleep Problem; Suicidal Ideation; Suicide, Attempted
Interventions

The purpose of this research study is to test a brief (6-session), empirically supported, and highly disseminable version of digital (i.e., smartphone or web-based) cognitive behavioral therapy for insomnia (dCBT-I), called SleepioTM, in suicidal adolescents with co-occurring insomnia during the high-risk post-hospitalization period. Suicide is the 2nd leading cause of death among adolescents. …

NCT06094751 — An ACT Website for College Students With Insomnia

StatusCompleted
PhaseN/A
SponsorUtah State University
Enrollment79
Study TypeINTERVENTIONAL
ConditionsInsomnia
Interventions

College students experience higher rates of insomnia compared the general population, and accessibility and availability for the appropriate intervention is difficult due limited resources available to them in a college environment. Theorefore, it is vital to offer an intervention that can be just as effective yet more accessible than other available treatments targeting insomnia. That is why t…

NCT05950646 — Mini-dose Dexmedetomidine-Esketamine Infusion and Perioperative Sleep Quality

StatusCompleted
PhasePhase 4
SponsorPeking University First Hospital
Enrollment154
Study TypeINTERVENTIONAL
ConditionsOld Age; Knee Replacement Surgery; Hip Replacement Surgery; Dexmedetomidine; Esketamine
Interventions; ;

Sleep disturbances are prevalent in older patients with osteoarthrosis or fracture who are scheduled for knee or hip replacement surgery. The occurrence of sleep disturbances is associated with worse outcomes including increased risk of delirium and cardiac events, and worsened functional recovery. Dexmedetomidine is a highly selective α2-adrenergic agonist with sedative, anxiolytic, and analge…

NCT06094608 — IBD-Sleep: A Pilot Study Looking at Changes in Sleep Timing and IBD Symptoms

StatusCompleted
PhaseN/A
SponsorUniversity of Michigan
Enrollment64
Study TypeINTERVENTIONAL
ConditionsInflammatory Bowel Diseases; Ulcerative Colitis; Crohn Disease
Interventions;

This research study is testing whether changes in sleep timing and morning light treatment may have an impact on symptoms related to inflammatory bowel disease.

NCT07668609 — Storybook App vs Cognitive Behavioral Therapy for Child Sleep and Attachment

StatusCompleted
PhaseN/A
SponsorUniversidad Católica de Cuenca
Enrollment60
Study TypeINTERVENTIONAL
ConditionsPediatric Sleep Problems; Sleep Hygiene; Parent-Child Attachment
Interventions;

This completed randomized controlled trial compared two caregiver-delivered interventions for sleep in young children: a multimodal mobile health intervention delivered through the Storybook mobile application and a face-to-face psychoeducational intervention based on cognitive behavioral therapy principles. The study was conducted in Azuay Province, Ecuador.

Children aged 12 to 84 months were…

NCT06404112 — RECOVER-SLEEP: Platform Protocol, Appendix_B (CPSD)

StatusCompleted
PhasePhase 2
SponsorDuke University
Enrollment469
Study TypeINTERVENTIONAL
ConditionsLong COVID; Long COVID-19; Sleep Disturbance
Interventions; ;

The platform protocol is designed to be flexible so that it is suitable for a range of study settings and intervention types. Therefore, the platform protocol provides a general protocol structure that can be shared by multiple interventions and allows comparative analysis across the interventions. For example, objectives, measures, and endpoints are generalized in the platform protocol, but in…

StatusCompleted
PhaseN/A
SponsorZentrela Inc.
Enrollment21
Study TypeOBSERVATIONAL
ConditionsDandruff
Interventions

The goal of this clinical trial is to learn whether regular use of Nizoral® Daily Prevent shampoo and conditioner can improve scalp comfort, sleep experiences, mood, and overall well-being in adults who have scalp discomfort and difficulty sleeping. The main questions it aims to answer are:

  1. Does using the shampoo and conditioner improve scalp comfort and reduce the impact of scalp discomfor…

NCT07258485 — A Study to Evaluate Sleep Electroencephalogram (EEG) Features (Brain Activity While Sleeping) in Participants With Major Depressive Disorder (MDD)

StatusCompleted
PhaseN/A
SponsorJanssen Research & Development, LLC
Enrollment94
Study TypeOBSERVATIONAL
ConditionsDepressive Disorder, Major

The purpose of this study is to evaluate sleep in participants with Major Depressive Disorder with moderate to severe insomnia symptoms (MDDIS) or MDD with no or mild insomnia symptoms (non-MDDIS), using an at-home sleep Electroencephalogram (EEG; a device that records brain activity during sleep). The study also aims to examine the association between objective sleep EEG features (measured usi…

NCT07264114 — Aquatic High-Intensity Interval Training for Parkinson’s Disease

StatusCompleted
PhaseN/A
SponsorPardis Specialized Wellness Institute
Enrollment56
Study TypeINTERVENTIONAL
ConditionsParkinson Disease
Interventions

This randomized, single-center, parallel-group superiority trial will evaluate the effect of an 8-week aquatic High-Intensity Interval Training (HIIT) program on balance, physical function, and sarcopenia-related outcomes in individuals with Parkinson’s disease (PD). The intervention aims to deliver Tabata-style aquatic HIIT (3 sessions/week) in a therapeutic pool to determine adherence and pre…

NCT07511465 — Development, Sensory Profile, and Sleep Quality in Preschool Children Across Different Caregiving Models

StatusCompleted
PhaseN/A
SponsorFenerbahce University
Enrollment60
Study TypeOBSERVATIONAL
ConditionsChild Development; Sensory Processing; Sleep Quality; Caregiving Models

This observational study aims to examine developmental status, sensory processing, and sleep quality in preschool children aged 3 to 6 years across different caregiving models. Children raised primarily by first-degree relatives, second-degree relatives, caregivers, or in daycare settings will be compared. Data will be collected using the Denver II Developmental Screening Test, the Dunn Sensory…

NCT07396779 — Cognitive Task-Based Walking Effects on Cognition, Mood, Sleep, and Quality of Life in Older Adults With Brain Fog

StatusCompleted
PhaseN/A
SponsorMedipol University
Enrollment90
Study TypeINTERVENTIONAL
ConditionsBrain Fog; Cognitive Impairment; Geriatric Population
Interventions;

This randomized controlled trial aims to investigate the effects of cognitive task-based walking exercise on cognitive function, depressive symptoms, sleep quality, and quality of life in older adults experiencing brain fog. Eligible participants will be randomly assigned to either a cognitive task-based walking exercise group or a walking-only exercise group. The intervention will be conducted…

NCT07495592 — The Acute Effects of Onnit Alpha Brain on Cognition and Mood States

StatusCompleted
PhaseN/A
SponsorApplied Science & Performance Institute
Enrollment32
Study TypeINTERVENTIONAL
ConditionsCognitive; Mood and Cognitive Performance; Sleep Deprivation; Executive Function (Cognition); Fatigue
Interventions; ;

The purpose of this randomized, double-blind, placebo-controlled crossover study is to evaluate the efficacy of the acute effects of an investigational supplement (Alpha Brain or Alpha Brain 2.0) on improving cognitive performance, vigilance, and subjective mood in healthy adults compared to placebo during a period of acute sleep deprivation under conditions of controlled sleep deprivation.