[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sleep-hygiene\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sleep-hygiene":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,49,72,111,140,168,194,231,259,288,309,333],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100628161","the-impact-of-a-infant-sleep-hygiene-training-program-on-infant-sleep-habits-and-parental-self-efficacy-100628161",false,"NCT07458035","The Impact of a Infant Sleep Hygiene Training Program on Infant Sleep Habits and Parental Self-Efficacy","The Impact of a Comfort Theory-Based Infant Sleep Hygiene Training Program on Infant Sleep Habits and Parental Self-Efficacy","Inclusion Criteria:\n\n1. Being a primiparous pregnant woman (first pregnancy)\n2. Being between 24 and 32 weeks of pregnancy\n3. Having a risk-free pregnancy\n4. Not having a mental disorder\n5. Speaking and understanding Turkish as a native language\n6. Being literate\n7. Not having received training on infant sleep\n8. Agreeing to participate in the study\n\nExclusion Criteria:\n\n1. The baby being born outside of the 38th to 42nd week of pregnancy\n2. The baby having a birth weight of less than 2,500 grams or more than 4,000 grams\n3. The baby being admitted to the neonatal intensive care unit after birth\n4. The baby having a condition that affects sleep, such as colic or hernia\n5. The baby having a chronic illness\n6. The parent wanting to leave work",true,"FEMALE",{"count":19,"type":20},48,"ESTIMATED","INTERVENTIONAL",[23],"NA","This randomized controlled trial aims to evaluate the effectiveness of a structured, Infant Sleep Hygiene Education Program initiated during pregnancy on infant sleep habits and parental self-efficacy related to infant sleep in the postpartum period. The program is grounded in developmental science and attachment-sensitive principles and focuses on promoting healthy sleep habits through responsive caregiving, consistent bedtime routines, and evidence-based sleep hygiene practices.\n\nPregnant women will be randomly assigned to either an intervention group receiving a multi-session prenatal education program with postnatal follow-up support, or a control group receiving routine antenatal care. Primary outcomes include parental self-efficacy regarding infant sleep and infant sleep habits (e.g., night awakenings, sleep duration, sleep onset latency, and routine consistency), assessed at 1, 3, and 6 months postpartum.\n\nSecondary outcomes include adherence to recommended sleep-supportive parenting practices and infant sleep diary indicators. In addition, the mediating role of parental self-efficacy in the relationship between the intervention and infant sleep outcomes will be examined. Program evaluation outcomes will assess parental knowledge before and after the education, participation and adherence to the sessions, and parental satisfaction with the education program.\n\nThis study aims to provide evidence for an ethical, developmentally appropriate, and preventive infant sleep education model integrated into routine prenatal care.",[26,27,28,29],"Sleep Hygiene","Infant Sleeping Habits","Parent Education","Self Efficacy",[31,32,33,34,35],"infant sleep","sleep hygiene","parent education","educational program","comfort theory","NOT_YET_RECRUITING","2026-03-04",{"date":39,"type":40},"2026-03-09","ACTUAL",{"date":42,"type":20},"2026-06",{"date":44,"type":20},"2027-03",{"name":46,"class":47},"Karabuk University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":60,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":68,"leadSponsor":70,"locationsCount":48},"100626819","effectiveness-of-a-sleep-hygiene-education-in-female-para-athletes-100626819","NCT07440589","Effectiveness of a Sleep Hygiene Education in Female Para Athletes","Effectiveness of a Sleep Hygiene Education in Female Para Athletes: A Mixed-Methods Study Using PSQI, Sleep Behaviour, and Qualitative Experiences","Inclusion Criteria:\n\n* Being an elite athlete who is a member of the Turkey Women's National Sitting Volleyball Team.\n* Actively participating in regular training sessions and competitions.\n* Willingness to participate in the planned sleep hygiene education program throughout the study period.\n* Having sufficient cognitive capacity to complete the Pittsburgh Sleep Quality Index (PSQI) and the Athlete Sleep Behavior Questionnaire (ASBQ).\n* Agreeing to participate in focus group interviews.\n* Providing voluntary participation and signing an informed consent form.\n\nExclusion Criteria:\n\n* Inability to participate regularly in training sessions during the study period due to acute injury, illness, or surgical intervention.\n* Failure to attend the education program or assessment procedures regularly.\n* Incomplete completion of data collection instruments or non-participation in focus group interviews.",{"count":5,"type":20},[23],"It is imperative to recognise elite female sitting volleyball players as a high-risk group with regard to sleep deprivation. However, there is a paucity of research investigating the efficacy of sleep hygiene education for this demographic.\n\nThe objective of this study is to The present study aims to examine the effect of sleep hygiene education on sleep quality and behaviour in elite female sitting volleyball players using mixed methods.",[26],[61,62,63],"Sleep hygiene","Para-Athlete","Sleep Behaviour","2026-02-26",{"date":66,"type":40},"2026-02-27",{"date":66,"type":20},{"date":69,"type":20},"2026-03-30",{"name":71,"class":47},"Abant Izzet Baysal University",{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":16,"sex":80,"minAge":81,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":21,"phases":85,"briefSummary":86,"conditions":87,"keywords":98,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":48},"100618258","nighttime-synchrony-of-your-nutrition-and-circadian-health-100618258","NCT07329283","Nighttime Synchrony of Your Nutrition and Circadian Health","Nighttime Synchrony of Your Nutrition and Circadian Health: The N-Sync Study","N-Sync","Inclusion Criteria:\n\n1. Age: 18-35 years old; equal numbers of men and women\n2. Body Mass Index (BMI): 18.5-24.9 kg\u002Fm2\n3. Sleep Habits: habitual self-reported average total sleep time (TST) 7-9 hours per night for prior 6 months\n\nExclusion Criteria:\n\n1. Clinically diagnosed sleep disorder or apnea hypopnea index (AHI) ≥5\n2. Evidence of significant organ system dysfunction or disease (e.g., heart disease, diabetes)\n3. Fasting plasma glucose ≥100 mg\u002FdL\n4. Major psychiatric illness (e.g., major depressive disorder)\n5. Cancer that has been in remission less than 5 years\n6. History of shift-work in prior year\n7. Weight change \\>5% of body weight over prior six months\n8. Currently following a weight-loss program\n9. Menopause\n10. Pregnant\u002Fnursing\n11. Greater than 5-day variation in menstrual cycle length month-to-month\n12. Currently smoking\n13. Alcohol intake \\>14 drinks\u002Fweek or \\>3 drinks\u002Fday.\n14. Use of prescription medications (except oral contraceptives) within one month prior to or during in-lab visits.\n15. Consumption of illegal drugs or \\>500mg per day of caffeine.","ALL","18 Years","35 Years",{"count":84,"type":20},120,[23],"Sleep is an important factor for overall health. This study will see how different light exposure patterns and food intake impact a person's metabolism (how the body breaks down food) when sleeping is reduced.\n\nParticipants will attend 6 to 8 in-person visits to the study clinic, including three overnight stays. People will complete surveys and medical tests. The study will last about 4 to 6 months.",[88,89,90,91,26,92,93,94,95,96,97],"Sleep","Metabolism Changes","Circadian Rhythm","Lifestyle Factors","Sleep Hygiene, Inadequate","Sleep Deprivation","Insufficient Sleep","Circadian Misalignment","Circadian Dysregulation","Light Exposure",[88,97,99,90,100,91,26],"Metabolism","Food Intake","RECRUITING","2026-01-20",{"date":104,"type":40},"2026-01-22",{"date":106,"type":40},"2025-12-19",{"date":108,"type":20},"2031-05-31",{"name":110,"class":47},"University of Utah",{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":80,"minAge":118,"maxAge":119,"enrollmentInfo":120,"targetDuration":4,"studyType":21,"phases":122,"briefSummary":123,"conditions":124,"keywords":127,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":48},"100435373","sleepup-digital-cbti-based-platform-for-insomnia-100435373","NCT04949360","SleepUp Digital CBTi-based Platform for Insomnia","Evaluation of SleepUp Digital CBTi-based Platform in the Treatment of Insomnia","Inclusion Criteria:\n\n* Literate Brazilian portuguese speakers.\n* Insomnia symptoms (as measured by ISI).\n* An Android-based smartphone or tablet with access to the Internet.\n\nExclusion Criteria:\n\n* Previous experience with CBTi.\n* Use of sleeping pills or any other treatment for insomnia for two or more days a week in the last three months.","20 Years","60 Years",{"count":121,"type":20},280,[23],"Cognitive-Behavioral Therapy for insomnia (CBTi) is a well-established therapeutic intervention for insomnia. SleepUp provides a digital therapeutics platform based on CBTi and additional features. This clinical trial aims at analyzing the efficacy of the CBTi-based platform offered by SleepUp in reducing symptoms of insomnia and will be conducted in 2 phases.\n\nPhase 1\n\nThe sample will be composed of 160 individuals, both males and females, from 20 to 60 years old, with insomnia symptoms considered as at least mild. Those who accept to participate will be randomized and distributed in four groups:\n\n* Standard CBTi (CBTi-S): This treatment consists of an eight-week treatment composed by weekly and structure appointments with board-certified sleep psychologists. The appointments will be made remotely (video calls with psychologists).\n* Minimal intervention - Sleep hygiene (MI-SH): This group will receive an educational program on sleep hygiene through the SleepUp app. Its content covers topics that are also covered in the online CBTi sessions. This procedure is more adequate as a control than the commonly used no treatment or waiting list controls, due to the behavioral\n* Online CBTI (CBTI-O): This group will receive access to an eight-weeks CBTi-based treatment through the SleepUp app. The participants of this group will receive interventions equivalent to the standard in-person CBTi, but provided through a digital platform.\n* Online CBTi + additional features (CBTi-O+): This group will have access to the complete premium version of SleepUp platform. It includes those presented in the CBTi-O group and other therapeutic and complementary features (including meditation audios and videos, mindfulness therapy, relaxation soundtracks, sleep hygiene tips, virtual assistant, and telehealth.\n\nAll participants in all groups will be assessed periodically throughout the eight weeks of intervention with standard sleep questionnaires and sleep logs. Equivalent intervals will be applied to the MI-SH group.\n\nPhase 2\n\nThis phase will comprise 120 individuals, both males and females, from 20 to 60 years old, with insomnia symptoms considered as at least mild. Those who accept to participate will be randomized and distributed in three groups:\n\n* Minimal intervention - Sleep hygiene (MI-SH): This group will receive an educational program on sleep hygiene through the SleepUp app. Its content covers topics that are also covered in the online CBTi sessions. This procedure is more adequate as a control than the commonly used no treatment or waiting list controls, due to the behavioral\n* Online CBTI (CBTI-O): This group will receive access to an eight-weeks CBTi-based treatment through the SleepUp app. The participants of this group will receive interventions equivalent to the standard in-person CBTi, but provided through a digital platform.\n* Online CBTi + additional features (CBTi-O+): This group will have access to the complete premium version of SleepUp platform. It includes those presented in the CBTi-O group and other therapeutic and complementary features (including meditation audios and videos, mindfulness therapy, relaxation soundtracks, sleep hygiene tips, virtual assistant, and telehealth.\n\nAll participants in all groups will be assessed periodically throughout the eight weeks of intervention with standard sleep questionnaires and sleep logs. Equivalent intervals will be applied to the MI-SH group.",[125,126,26],"Insomnia","Sleep Disorder",[125,88,128,129],"Cognitive-behavioral therapy","CBTi","2025-12-20",{"date":132,"type":40},"2025-12-29",{"date":134,"type":40},"2025-05-19",{"date":136,"type":20},"2026-12-01",{"name":138,"class":139},"SleepUp Tecnologia em Saúde Ltda","INDUSTRY",{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":144,"acronym":145,"eligibilityCriteria":146,"healthyVolunteers":11,"sex":80,"minAge":147,"maxAge":148,"enrollmentInfo":149,"targetDuration":4,"studyType":21,"phases":151,"briefSummary":152,"conditions":153,"keywords":156,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":48},"100471583","impact-of-sleep-duration-on-immune-balance-in-urban-children-with-asthma-100471583","NCT05420766","Impact of Sleep Duration on Immune Balance in Urban Children With Asthma","AIMS","Inclusion:\n\n* Children 7-11 years old\n* Has physician-diagnosed asthma, per parent and pediatrician report\n* Meets criteria for current persistent asthma with a current prescription for an asthma controller medicine\n* Obtains 9.0-11.0 h of sleep per 24 h day in the past month\n* Has a positive allergy skin test performed at the clinic visit\n* Resides and attend school in one of the targeted urban areas (Rhode Island: East Providence, North Providence, Providence, Warwick, Cranston, Woonsocket, Central Falls, Pawtucket, Lincoln, Johnston. Massachusetts: Attleboro, North Attleboro, Fall River.\n* Has a primary caregiver who speaks English\n\nExclusion:\n\n* No asthma diagnosis\n* No use of asthma controller medication\n* Severe persistent asthma that is poorly controlled\n* Diagnosis of additional pulmonary disease or medical condition or immune deficiency disorders\n* Use of systemic steroids \\\u003C30 days of screening\n* Asthma-related emergency department visit and\u002For asthma-related hospitalization in past 90 days\n* Marked developmental delay, psychiatric conditions, academic\u002Fbehavioral problems, learning disabilities\n* Tanner stage 3-5 of pubertal development\n* Diagnosed ADHD; Use of stimulants to treat ADHD\n* An Apnea-Hypoxia Index \\>5 (indicator of sleep disordered breathing)","7 Years","11 Years",{"count":150,"type":20},204,[23],"Urban children with asthma are at high risk for short sleep, due to an environment that jeopardizes both sleep and asthma management. Further, urban children with asthma suffer from altered immune balance, a key biological process contributing to individual differences in asthma morbidity and sleep health. In the proposed research, the researchers will examine the effects of shortened and recovery sleep on immune balance and associated changes in lung function in urban children with allergic asthma through an experimental design.",[154,26,155],"Asthma in Children","Sleep, Inadequate",[26,157,158],"Children with asthma","Immune function in children","2025-09-19",{"date":161,"type":40},"2025-09-22",{"date":163,"type":40},"2022-05-15",{"date":165,"type":20},"2026-07-31",{"name":167,"class":47},"Rhode Island Hospital",{"id":169,"slug":170,"hasResults":11,"nctId":171,"briefTitle":172,"officialTitle":173,"acronym":4,"eligibilityCriteria":174,"healthyVolunteers":11,"sex":80,"minAge":81,"maxAge":175,"enrollmentInfo":176,"targetDuration":4,"studyType":21,"phases":178,"briefSummary":179,"conditions":180,"keywords":181,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":192,"locationsCount":4},"100607616","sleep-hygiene-in-undergraduate-students-studying-in-the-field-of-health-100607616","NCT07190872","Sleep Hygiene in Undergraduate Students Studying in the Field of Health","Sleep Hygiene Among Undergraduate Students Studying in the Health Field: A Study on Awareness and Behavioural Change","Inclusion Criteria:\n\n* Being an associate degree student at Bilecik Şeyh Edebali University School of Health Services.\n\nBeing a student who has started clinical practice and is actively doing an internship in the clinic.\n\nBeing between the ages of 18 and 25\n\nScoring ≥ 30 on the Sleep Hygiene Index (UHI) (poor sleep hygiene score)\n\nAgreeing to volunteer for the study and signing the informed consent form\n\nNot having received any sleep hygiene training in the last 3 months.\n\nBeing able to participate regularly in the research process (pre-test, training intervention, and post-tests).\n\nExclusion Criteria:\n\n* Having been diagnosed with a sleep disorder (e.g., insomnia, sleep apnea, narcolepsy, etc.).\n\nReceiving a diagnosis of a psychiatric illness that can affect mental health and\u002For taking psychiatric medication regularly.\n\nHaving a chronic illness and taking regular medication (e.g., diabetes, epilepsy, cardiovascular diseases).\n\nWorking nite shifts or having irregular sleep schedules (e.g., students on duty).\n\nDeclaring that they will be unable to regularly participate in the study process or failing to comply with interventions during the study.","25 Years",{"count":177,"type":20},100,[23],"This study looks at sleep hygiene-the daily habits and environment that help people sleep well-among 2nd-year students at the Health Services Vocational School of Bilecik Şeyh Edebali University (Türkiye). Many health sciences students have busy schedules, clinical practice, and exam stress, which may reduce sleep quality. Good sleep is important for learning, attention, mood, and overall health.\n\nPurpose:\n\nThe aim is to assess the current sleep hygiene and quality of students, and determine whether a brief, in-person education program can enhance their knowledge, habits, and sleep quality in the upcoming weeks.\n\nWho can take part:\n\nThe program is designed for daytime (normal education) 2nd-year students in programs such as Operating Room Services, Paramedic, Opticianry, Pharmacy Services, Medical Laboratory Techniques, Medical Documentation and Secretariat, and Child Development who volunteer and give written consent. Participation is voluntary, and you may leave the study at any time without any penalty.\n\nWhat will happen if you join:\n\nYou will complete short forms before the education session to measure sleep habits and sleep quality (for example, bedtime, caffeine use, and screen time).\n\nYou will attend four classroom sessions (each about 40 minutes). These sessions explain practical sleep tips (regular bed\u002Fwake times, reducing evening caffeine and screen time, preparing a quiet\u002Fdark room, simple relaxation after clinical shifts) and help you create a personal sleep plan.\n\nYou will fill out the same forms again 2 weeks and 4 weeks after the education to see changes over time.\n\nWhat we measure:\n\nSleep hygiene behaviors (how often helpful\u002Funhelpful habits are used)\n\nSleep quality refers to how restful sleep feels, the time it takes to fall asleep, the frequency of night awakenings, and overall daytime functioning.\n\nKnowledge about sleep hygiene (a short quiz) We will also look at factors like stress level, evening screen use, and caffeine intake.\n\nPossible benefits:\n\nYou may learn practical ways to improve sleep, which can help with attention, mood, and daily performance.\n\nPossible risks\u002Fdiscomforts:\n\nThis is an educational program. Risks are minimal (for example, brief discomfort when answering personal questions about sleep). You can skip any question you do not want to answer.\n\nPrivacy:\n\nAll information will be kept confidential and used only for research. Reports will not include names or identifying details.\n\nCosts and payment:\n\nThere is no cost to taking part, and there is no payment for participation.\n\nWithdrawal:\n\nParticipation is voluntary. You may stop at any time without affecting your courses or grades.",[26],[32,182,183,184],"sleep quality","behavior change","transtheoretical model","2025-09-17",{"date":187,"type":40},"2025-09-24",{"date":189,"type":20},"2025-10-30",{"date":191,"type":20},"2026-04-30",{"name":193,"class":47},"Bilecik Seyh Edebali Universitesi",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":200,"eligibilityCriteria":201,"healthyVolunteers":11,"sex":17,"minAge":81,"maxAge":202,"enrollmentInfo":203,"targetDuration":4,"studyType":21,"phases":205,"briefSummary":206,"conditions":207,"keywords":219,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":222,"startDateStruct":224,"completionDateStruct":226,"leadSponsor":228,"locationsCount":230},"100457248","better-lifestyle-counseling-for-african-american-women-during-pregnancy-100457248","NCT05234125","Better Lifestyle Counseling for African American Women During Pregnancy","A Randomized Control Trial to Improve Metabolic Outcomes in African American Pregnant Women","BETTER","Inclusion Criteria:\n\n* African American pregnant woman.\n* Women between 16 and 22 GWs.\n* Overweight or obese - pregravid Body Mass Index \\>25.0 kg\u002Fm2.\n* Singleton gestation.\n* Established prenatal care at The University of Illinois Hospital \\& Health Sciences.\n* System Obstetric (UIHHSS' OB) clinics. Able to understand, speak and write in English.\n\nExclusion Criteria:\n\n* Multiple gestations.\n* Night-shift work.\n* Diagnosed sleep disorders.\n* Known fetal chromosomal or anatomical abnormalities.\n* Diagnosed mood disorders.\n* Gestational diabetes in early pregnancy.\n* Glycated Hemoglobin (HbA1c) ≥ 6.5%.\n* Hypoglycemic medications.\n* Stimulant medication or taking a sleeping aid.\n* Active drug abuse\u002Fexcessive alcohol intake.","40 Years",{"count":204,"type":20},150,[23],"The purpose of this randomized controlled trial is to establish the effectiveness of a culturally targeted and individually tailored behavioral intervention to promote maternal glucose metabolism in African American women.",[208,209,210,26,211,212,213,214,215,216,217,218],"Overweight or Obesity","Pregnancy Related","Sleep Disturbances","Pregnancy Complications","Diversity","Stress, Psychological","Fitness Trackers","Exercise","African Americans","Disparities in Pregnancy Complications","Sleep Disparities",[220],"Sleep, Pregnancy, Intervention, glucose metabolism,","2025-04-01",{"date":223,"type":40},"2025-04-04",{"date":225,"type":40},"2022-08-16",{"date":227,"type":20},"2027-04-30",{"name":229,"class":47},"University of Illinois at Chicago",2,{"id":232,"slug":233,"hasResults":11,"nctId":234,"briefTitle":235,"officialTitle":235,"acronym":4,"eligibilityCriteria":236,"healthyVolunteers":16,"sex":80,"minAge":81,"maxAge":237,"enrollmentInfo":238,"targetDuration":4,"studyType":21,"phases":240,"briefSummary":241,"conditions":242,"keywords":245,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":251,"lastUpdatePostDateStruct":252,"startDateStruct":254,"completionDateStruct":256,"leadSponsor":258,"locationsCount":48},"100572729","the-dream-team-testing-implementation-of-a-sleep-intervention-for-perinatal-women-delivered-by-direct-care-workers-100572729","NCT06737055","The Dream Team: Testing Implementation of a Sleep Intervention for Perinatal Women Delivered by Direct Care Workers","Phase 1 Inclusion Criteria:\n\nTo qualify for Phase 1 enrollment, participants must be:\n\n* over 18 years of age;\n* working with expectant and new mothers in a community setting (i.e., outpatient clinic, social service agency, home visiting program, community center);\n* in a role where they would be expected to meet with the same client on at least 4 occasions during the perinatal period; in situations where a team-based approach is used to provide services and a client may not see the exact same person at each visit, team members will qualify if they all enroll in the study (e.g., two nurse midwives who provide coverage for each other may both enroll);\n* have access to a smart phone to view the training videos, complete the assessments, and access the free CBTi Coach app; speak and read English or Spanish;\n* express interest in providing their clients with additional tools to manage sleep disturbances in pregnancy and the postpartum period.\n\nPhase 1 Exclusion Criteria:\n\nThe investigators will exclude potential participants who:\n\n* already have certification or a specialty in perinatal sleep (e.g., therapists with formal training in CBTi, individuals with sleep coaching practices);\n* those who do not have longitudinal relationships with clients (e.g., intake workers).\n\nPhase 2 Inclusion Criteria:\n\nTo qualify, Phase 2 participants must be:\n\n* expectant parents OR new parents up to 1 year postpartum;\n* age 18 to 45 years old;\n* receiving community-based health, well-being, and or mental health services or treatment from individuals who participated in Phase 1;\n* speak and read English or Spanish;\n* have access to a smart phone to view the training videos and complete the assessments;\n* have clinically significant sleep difficulties defined as an Insomnia Severity Index score greater than 7.\n\nPhase 2 Exclusion Criteria:\n\nThe investigators will exclude potential participants whose infants will not be living in the home or who will have a nighttime caregiver.","99 Years",{"count":239,"type":20},55,[23],"Insufficient and disrupted sleep are rarely addressed in expectant and new mothers, despite evidence that disturbed sleep is a modifiable risk factor for negative health outcomes for mothers and their children. In this study the investigators will adapt, refine, and pilot test the implementation of a behavioral sleep intervention consisting of short videos designed to accompany a free behavioral sleep app. In Phase 1, the investigators will develop and refine the intervention with input from direct care workers who serve at-risk perinatal women. In Phase 2, direct care workers will deploy the training to expectant mothers with sleep concerns and the investigators will assess the reach, effectiveness, adoption, implementation, and maintenance of this scalable, efficient intervention to improve sleep.",[88,243,209,125,93,26,244],"Postpartum Depression","Sleep Disturbance",[246,247,248,249,250],"Home visitors","sleep diaries","education","implementation","RE-AIM","2024-12-23",{"date":253,"type":40},"2024-12-27",{"date":255,"type":40},"2023-08-08",{"date":257,"type":20},"2025-06-30",{"name":167,"class":47},{"id":260,"slug":261,"hasResults":11,"nctId":262,"briefTitle":263,"officialTitle":264,"acronym":4,"eligibilityCriteria":265,"healthyVolunteers":16,"sex":80,"minAge":81,"maxAge":266,"enrollmentInfo":267,"targetDuration":4,"studyType":21,"phases":269,"briefSummary":270,"conditions":271,"keywords":277,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":280,"lastUpdatePostDateStruct":281,"startDateStruct":283,"completionDateStruct":285,"leadSponsor":287,"locationsCount":48},"100529981","effect-of-sleep-extension-on-ceramides-in-people-with-overweight-and-obesity-100529981","NCT06180837","Effect of Sleep Extension on Ceramides in People with Overweight and Obesity","Biomarkers of Habitual Short Sleep and Related Cardiometabolic Risk","Inclusion Criteria:\n\n1. Age: 18-45 years old; equal numbers of men and women\n2. Body mass index (BMI): 27.5-34.9 kg\u002Fm2\n3. Sleep Habits: habitual self-reported average total sleep time (TST) \\\u003C6.5 hours per night for prior 6 months\n\nExclusion Criteria:\n\n1. Clinically diagnosed sleep disorder or major psychiatric illness\n2. Evidence of significant organ dysfunction or disease (e.g., heart disease, kidney disease)\n3. Clinically diagnosed diabetes or fasting plasma glucose ≥126 mg\u002FdL or HbA1c ≥6.5%\n4. Use of prescription drugs or substances known to influence sleep or glucose metabolism, or anticoagulant medications.\n5. Cancer that has been in remission less than 5 years\n6. Pregnant\u002Fnursing, experiencing menopause or post-menopausal\n7. Shift-work: current or history of within last year\n8. Weight change: \\>10% of body weight over prior six months\n9. Current enrollment in weight loss or physical activity program like the Diabetes Prevention Program\n10. Currently smoking\n11. Alcohol intake\\>14 drinks per week or \\>3 drinks per day","45 Years",{"count":268,"type":20},70,[23],"The overall goal is to determine how a sleep extension intervention (increasing time in bed) in individuals who maintain less than 6.5 hours sleep per night affects their plasma ceramides and insulin sensitivity. Participants will undergo a randomized controlled trial, with sleep extension (intervention) and healthy lifestyle (control) groups. The sleep extension is designed to increase participant's time in bed by 2 hours per night. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).",[91,272,273,274,26,275,88,93,276],"Overweight and Obesity","Insulin Sensitivity","Eating Habit","Type 2 Diabetes","Insufficient Sleep Syndrome",[278,279],"sleep","insulin sensitivity","2024-12-18",{"date":282,"type":40},"2024-12-20",{"date":284,"type":40},"2024-02-12",{"date":286,"type":20},"2028-01",{"name":110,"class":47},{"id":289,"slug":290,"hasResults":11,"nctId":291,"briefTitle":292,"officialTitle":293,"acronym":294,"eligibilityCriteria":295,"healthyVolunteers":16,"sex":80,"minAge":81,"maxAge":266,"enrollmentInfo":296,"targetDuration":4,"studyType":21,"phases":298,"briefSummary":299,"conditions":300,"keywords":4,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":280,"lastUpdatePostDateStruct":303,"startDateStruct":304,"completionDateStruct":306,"leadSponsor":308,"locationsCount":48},"100511760","circadian-intervention-to-improve-cardiometabolic-health-100511760","NCT05943626","Circadian Intervention to Improve Cardiometabolic Health","Timing of Circadian Synchronizers: the TOCS Study","TOCS","Inclusion Criteria:\n\n1. Age: 18-45 years old; equal numbers of men and women\n2. Body mass index (BMI): 25.0-34.9 kg\u002Fm2,\n3. Sleep Habits: habitual self-reported average total sleep time (TST) \\\u003C6.5 hours per night for prior 6 months\n\nExclusion Criteria:\n\n1. Clinically diagnosed sleep disorder or major psychiatric illness\n2. Evidence of significant organ dysfunction or disease (e.g., diagnosed diabetes, cardiovascular disease, or kidney disease)\n3. Use of prescription drugs or substances known to influence sleep or glucose metabolism\n4. Shift-work: current or history of within last year\n5. Weight change: \\>10% of body weight over prior six months\n6. Experiencing menopause or post-menopausal\n7. Current enrollment in weight loss or physical activity program like the Diabetes Prevention Program\n8. Currently pregnant or planning to become pregnant, or currently lactating.\n9. Currently smoking\n10. Alcohol intake \\>3 drinks per day or \\>14 drinks per week",{"count":297,"type":20},20,[23],"The overall goal is to examine the efficacy of a circadian intervention in people with overweight and obesity and habitual short sleep duration (HSSD). Participants will undergo a randomized controlled trial, with circadian intervention and control (healthy lifestyle) groups. The circadian intervention is designed to reduce nighttime light exposure and after-dinner snack food intake. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).",[301,275,88,302,91,272,273,274,26],"Cardiometabolic Syndrome","Time Restricted Feeding",{"date":282,"type":40},{"date":305,"type":40},"2023-06-13",{"date":307,"type":20},"2026-03",{"name":110,"class":47},{"id":310,"slug":311,"hasResults":11,"nctId":312,"briefTitle":313,"officialTitle":314,"acronym":4,"eligibilityCriteria":315,"healthyVolunteers":11,"sex":80,"minAge":316,"maxAge":4,"enrollmentInfo":317,"targetDuration":4,"studyType":21,"phases":319,"briefSummary":320,"conditions":321,"keywords":4,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":323,"lastUpdatePostDateStruct":324,"startDateStruct":326,"completionDateStruct":328,"leadSponsor":330,"locationsCount":332},"100572721","modifying-the-inpatient-environment-to-reduce-delirium-in-older-adults-100572721","NCT06736951","Modifying the Inpatient Environment to Reduce Delirium in Older Adults","Modifying the Inpatient Environment to Reduce the Incidence and Burden of Delirium Among Hospitalized Older Adults (≥70 Years).","Inclusion criteria:\n\n* Non-critically ill patients (≥70 years)\n* All sexes\n* All races and ethnicities\n* Admitted to the pre-specified clinical units which are part of the study\n\nExclusion criteria (applied during analysis):\n\n* Patients with active alcohol or substance withdrawal.\n* Patients with acute psychiatric illness\n* Patients with initial admission to intensive care unit including requirement for mechanical ventilation.\n* Patients present on a unit at the time of unit randomization","70 Years",{"count":318,"type":20},10890,[23],"The overall goal is to reduce the incidence and burden of delirium, as measured by the delirium burden index (DBI) among hospitalized older adults (≥70 years), by modifying the inpatient environment to decrease its sleep antagonism. The investigators propose to implement a multi-modal sleep hygiene (MMSH) bundle, an enhancement of a previously reported sleep-focused intervention which had 88 - 100% compliance for intervention components, and reduced ICU delirium by 50%.",[322,26],"Delirium","2024-12-11",{"date":325,"type":40},"2024-12-17",{"date":327,"type":40},"2024-06-01",{"date":329,"type":20},"2029-03-31",{"name":331,"class":47},"Farhaan S. Vahidy",5,{"id":334,"slug":335,"hasResults":11,"nctId":336,"briefTitle":337,"officialTitle":338,"acronym":4,"eligibilityCriteria":339,"healthyVolunteers":11,"sex":80,"minAge":118,"maxAge":4,"enrollmentInfo":340,"targetDuration":4,"studyType":341,"phases":4,"briefSummary":342,"conditions":343,"keywords":4,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":348,"lastUpdatePostDateStruct":349,"startDateStruct":351,"completionDateStruct":353,"leadSponsor":355,"locationsCount":48},"100454099","sleep-hygiene-sarcopenia-and-cognitive-function-in-respiratory-disease-100454099","NCT05193136","Sleep Hygiene, Sarcopenia, and Cognitive Function in Respiratory Disease","Examination of the Relationship Between Sleep Hygiene, Sarcopenia, and Cognitive Function in Patients With Chronic Obstructive Pulmonary Disease or Idiopathic Pulmonary Fibrosis","Inclusion Criteria:\n\n* Subjects with COPD or IPF.\n\nExclusion Criteria:\n\n* Subjects who have been hospitalized for exacerbation of respiratory failure within 1 month of study participation\n* Subjects who have already been diagnosed with sarcopenia or cognitive dysfunction\n* Subjects receiving long-term oxygen therapy (LTOT) or non-invasive ventilation therapy (NIV)\n* Subjects with obstructive sleep apnea who are indicated for continuous positive airway pressure (CPAP)\n* Subjects with severe complications such as cardiovascular disease, liver disease, renal disease, malignancy, and neurological disease.",{"count":84,"type":20},"OBSERVATIONAL","We aim to clarify the relationship between sleep hygiene and the onset of sarcopenia or cognitive dysfunction using sleep time, arousal, and sleep quality as indicators in COPD or IPF patients, and clarify the effects of sleep hygiene on disease progression and life prognosis.",[26,344,345,346,347],"Sarcopenia","Cognitive Function","COPD","IPF","2023-03-25",{"date":350,"type":40},"2023-03-28",{"date":352,"type":40},"2021-12-10",{"date":354,"type":20},"2027-12",{"name":356,"class":47},"National Hospital Organization Minami Kyoto Hospital"]