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)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Oregon Health and Science University |
| Enrollment | 304 |
| Study Type | INTERVENTIONAL |
| Conditions | Obstructive 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The Hong Kong Polytechnic University |
| Enrollment | 153 |
| Study Type | INTERVENTIONAL |
| Conditions | Sleep; 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Oregon Health and Science University |
| Enrollment | 175 |
| Study Type | INTERVENTIONAL |
| Conditions | Otolaryngological 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Taiwan University Hospital |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Epilepsy |
| 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)
| Status | Recruiting |
| Phase | Early Phase 1 |
| Sponsor | Washington University School of Medicine |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | OCD |
| 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)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Massachusetts General Hospital |
| Enrollment | 1800 |
| Study Type | INTERVENTIONAL |
| Conditions | Delirium |
| 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
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | H. Lundbeck A/S |
| Enrollment | 104 |
| Study Type | INTERVENTIONAL |
| Conditions | Narcolepsy |
| 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
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | VA Office of Research and Development |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Anxiety 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Indiana University |
| Enrollment | 115 |
| Study Type | INTERVENTIONAL |
| Conditions | Schizophrenia 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer |
| Enrollment | 295 |
| Study Type | OBSERVATIONAL |
| Conditions | Peripheral 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AbbVie |
| Enrollment | 103 |
| Study Type | OBSERVATIONAL |
| Conditions | Advanced 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Hematologic 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
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Takeda |
| Enrollment | 88 |
| Study Type | INTERVENTIONAL |
| Conditions | Narcolepsy 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
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 800 |
| Study Type | INTERVENTIONAL |
| Conditions | Sleep 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Children’s Hospital of Philadelphia |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Insufficient 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Washington University School of Medicine |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Clermont-Ferrand |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson'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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Medicine and Pharmacy at Ho Chi Minh City |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Insomnia, 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)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Alkermes, Inc. |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Narcolepsy 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Sleep 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
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity, 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
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | King’s College London |
| Enrollment | 139 |
| Study Type | OBSERVATIONAL |
| Conditions | Obstructive 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Windsor Sleep Disorders Clinic |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Obstructive 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 82 |
| Study Type | INTERVENTIONAL |
| Conditions | Violent 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Children’s Hospital Medical Center, Cincinnati |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | ADHD |
| 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Wisconsin, Madison |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Schizophrenia |
| 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | The University of Hong Kong |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Sleep 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
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Northern California Institute of Research and Education |
| Enrollment | 142 |
| Study Type | INTERVENTIONAL |
| Conditions | PTSD - 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
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Chulalongkorn University |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | OSA - 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:
Polysomnography parameters
- Mean and nadir oxygen saturation
- Sleep…
NCT07679984 — Evaluating the Effects of a Mindfulness Intervention on Health Outcomes in Individuals With Hypertension
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ohio State University |
| Enrollment | 140 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension; 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
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | University of Michigan |
| Enrollment | 1000 |
| Study Type | INTERVENTIONAL |
| Conditions | Depression / 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
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Fenerbahce University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Burn 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
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Fenerbahce University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Burn 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
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 57 |
| Study Type | INTERVENTIONAL |
| Conditions | Jet 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
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 198 |
| Study Type | OBSERVATIONAL |
| Conditions | Alcoholism |
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
| Status | Completed |
| Phase | Early Phase 1 |
| Sponsor | National Institute on Alcohol Abuse and Alcoholism (NIAAA) |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Normal 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 115 |
| Study Type | INTERVENTIONAL |
| Conditions | Delayed 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Institute of Rheumatology, Serbia |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Fibromyalgia 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Rutgers, The State University of New Jersey |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Sleep 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Utah State University |
| Enrollment | 79 |
| Study Type | INTERVENTIONAL |
| Conditions | Insomnia |
| 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
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Peking University First Hospital |
| Enrollment | 154 |
| Study Type | INTERVENTIONAL |
| Conditions | Old 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Michigan |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Inflammatory 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Universidad Católica de Cuenca |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Pediatric 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)
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Duke University |
| Enrollment | 469 |
| Study Type | INTERVENTIONAL |
| Conditions | Long 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…
NCT07680608 — Neurophysiological and Sleep-Related Effects of a Cosmetic Shampoo and Conditioner in Adults With Scalp Discomfort
| Status | Completed |
| Phase | N/A |
| Sponsor | Zentrela Inc. |
| Enrollment | 21 |
| Study Type | OBSERVATIONAL |
| Conditions | Dandruff |
| 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:
- 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)
| Status | Completed |
| Phase | N/A |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 94 |
| Study Type | OBSERVATIONAL |
| Conditions | Depressive 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Pardis Specialized Wellness Institute |
| Enrollment | 56 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Fenerbahce University |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Child 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Medipol University |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Brain 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Applied Science & Performance Institute |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Cognitive; 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.