[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"insufficient-sleep\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:insufficient-sleep":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,45,70,93,128],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100493299","optimizing-a-mobile-health-platform-for-sleep-promotion-and-obesity-prevention-in-children-100493299",false,"NCT05703347","Optimizing a Mobile Health Platform for Sleep Promotion and Obesity Prevention in Children","Inclusion Criteria:\n\n1. Aged 8-12 years olds.\n2. Insufficient sleep duration (\\\u003C8.5 hours per night).\n3. Body mass index (BMI) between the 50th and 95th percentile for age and sex.\n4. One child per family.\n\nExclusion Criteria:\n\n1. Diagnosed with a chronic disease.\n2. Diagnosed with a behavioral health problem.\n3. Diagnosed with a condition that can impact sleep or growth.\n4. Diagnosed with a condition affecting physical growth and maturation or dietary intake.\n5. Children with a history of cancer, kidney, GI, musculoskeletal, or sleep disorders.\n6. Children who will transition to high-school during the study.\n7. Children using steroids\u002Fhormones.\n8. Children regularly taking medications related to exclusionary medical conditions or that impact sleep.\n9. Children with a history of significant behavioral health concerns.\n10. Parent reported PROMIS Parent Proxy Sleep Disturbance - Short Form 8a raw score of ≥28.",true,"ALL","8 Years","12 Years",{"count":20,"type":21},5000,"ESTIMATED","INTERVENTIONAL",[24],"NA","The overall objective of this application is to develop a mobile health platform for the pediatric care setting to promote longer sleep duration for childhood obesity prevention.",[27,28],"Insufficient Sleep","Obesity",[30,31],"insufficient sleep","obesity","RECRUITING","2026-05-22",{"date":35,"type":36},"2026-05-27","ACTUAL",{"date":38,"type":36},"2023-09-21",{"date":40,"type":21},"2027-06",{"name":42,"class":43},"Children's Hospital of Philadelphia","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":44},"100534553","sleep-promotion-program-primary-care-100534553","NCT06240325","Sleep Promotion Program Primary Care","A Sleep Promotion Program for Depressed Adolescents in Pediatric Primary Care","SPP PC","Inclusion Criteria:\n\nYouth:\n\n* Able and willing to provide informed assent (with consent from parent\u002Fguardian)\n* Ages 12-18\n* Currently a patient at Kids Plus Pediatrics\n* Currently depressed\n* Report short sleep duration (\\\u003C7 hours on school nights) and\u002For weekday-weekend sleep timing difference of \\>=2 hours\n\nParents:\n\nParents must be age 18 or older and the parent\u002Fguardian of an enrolled youth participant and must have at least 10 hours face-to-face interaction with the youth participant per week.\n\nExclusion Criteria:\n\nYouth:\n\n* Significant or unstable medical conditions\n* Diagnosis of sleep apnea, narcolepsy, restless leg syndrome, nightmare disorder, or periodic limb movement disorder\n* Diagnosis of PTSD, bipolar disorder, a psychotic disorder, or substance use disorder\n* Currently engaged in cognitive and\u002For behavioral therapy that aims to improve sleep\n* Changes in medications in the month prior to screening\n* Active suicidality requiring immediate treatment\n* Unable or unwilling to comply with study procedures\n* Have any physical or mental condition that would preclude study participation.\n\nParents will be excluded if they:\n\n* Express active suicidality that requires immediate treatment;\n* Have any physical or mental condition that would preclude study participation; OR\n* Are unable or unwilling to comply with study procedures.","18 Years",{"count":55,"type":21},100,[24],"Investigators developed a brief, scalable, behavioral Sleep Promotion Program (SPP) for adolescents with short sleep duration and sleep-wake irregularity, which relies on two individual sessions and smart phone technology to deliver evidence-based strategies. This R34 will test the feasibility and initial effectiveness of the SPP program and provider training via pilot randomized controlled trial (RCT, n=50) comparing SPP to Sleep Psychoeducation, a brief session on healthy sleep habits. Participants will be adolescents (12-18 years) with short sleep duration, sleep-wake irregularity, and depression.",[59,60,27],"Sleep","Sleep Disturbance","2026-03-02",{"date":63,"type":36},"2026-03-04",{"date":65,"type":36},"2024-12-13",{"date":67,"type":21},"2026-08",{"name":69,"class":43},"University of Pittsburgh",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":77,"maxAge":53,"enrollmentInfo":78,"targetDuration":4,"studyType":22,"phases":80,"briefSummary":81,"conditions":82,"keywords":84,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":44},"100565443","sleep-promotion-and-pediatric-hypertension-100565443","NCT06642246","Sleep Promotion and Pediatric Hypertension","Sleep Promotion Among Children Newly Diagnosed With Essential Hypertension","Inclusion Criteria:\n\n* Speak, read and write in English.\n* Parental\u002Fguardian permission (informed consent) and child assent.\n* Have a computer or a tablet computer with access to the Internet or own a smartphone with a data and text plan.\n* Parent reported sleep duration on school nights less than or equal to 7.5 hours.\n* Recently diagnosed with essential hypertension by Ambulatory Blood Pressure Monitoring (ABPM).\n* If taking over the counter sleep aides, willing to stop them over the course of the study.\n\nExclusion Criteria:\n\n* Any clinically diagnosed sleep disorder (e.g. sleep apnea) in the electronic health record and or regular use of prescribed sleep aide.\n* Underlying chronic medical conditions, defined as a medical condition with a duration or expected duration longer than 3 months that involved taking regular medication, taking medications that could affect blood pressure (e.g., anti-hypertensive medications, glucocorticoids, or stimulants), and patients with underlying diagnoses known to be associated with elevated blood pressure (e.g., cardiac disease, kidney disease or diabetes).\n\nInclusion Criteria for Parents\u002FLegal Guardians:\n\n* Be the parent\u002Fguardian of an eligible child enrolled in the main study.\n* Speak, read, and write in English.\n\nExclusion Criteria for Parents\u002FLegal Guardians:\n\n\\- Limited English proficiency","13 Years",{"count":79,"type":21},10,[24],"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.",[27,83],"Hypertension",[27,83],"2026-02-17",{"date":87,"type":36},"2026-02-18",{"date":89,"type":36},"2026-02-16",{"date":91,"type":21},"2026-06",{"name":42,"class":43},{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":99,"eligibilityCriteria":100,"healthyVolunteers":15,"sex":16,"minAge":53,"maxAge":101,"enrollmentInfo":102,"targetDuration":4,"studyType":22,"phases":104,"briefSummary":105,"conditions":106,"keywords":116,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":44},"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.","35 Years",{"count":103,"type":21},120,[24],"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.",[59,107,108,109,110,111,112,27,113,114,115],"Metabolism Changes","Circadian Rhythm","Lifestyle Factors","Sleep Hygiene","Sleep Hygiene, Inadequate","Sleep Deprivation","Circadian Misalignment","Circadian Dysregulation","Light Exposure",[59,115,117,108,118,109,110],"Metabolism","Food Intake","2026-01-20",{"date":121,"type":36},"2026-01-22",{"date":123,"type":36},"2025-12-19",{"date":125,"type":21},"2031-05-31",{"name":127,"class":43},"University of Utah",{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":132,"acronym":4,"eligibilityCriteria":133,"healthyVolunteers":11,"sex":16,"minAge":134,"maxAge":135,"enrollmentInfo":136,"targetDuration":4,"studyType":22,"phases":138,"briefSummary":141,"conditions":142,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":44},"100533458","phase-1-project-shine-sleep-health-initiative-for-equity-culturally-informing-a-sleep-extension-intervention-for-african-american-adults-100533458","NCT06226077","Project SHINE (Sleep Health INitiative for Equity): Culturally Informing a Sleep Extension Intervention for African American Adults","Inclusion Criteria:\n\nPhase 1:\n\n* Not meeting Physical Activity Guidelines\n* age range: 21 to 75 years\n* body mass index: ≥25.0 kg\u002Fm2\n* average self-reported habitual sleep duration of ≤6 hours\n* self-identify as Black or African American\n\nPhase 2:\n\n* Not meeting Physical Activity Guidelines\n* age range: 21 to 75 years\n* body mass index: ≥25.0 kg\u002Fm2\n* average self-reported habitual sleep duration of ≤6 hours\n* self-identify as Black or African American\n\nExclusion Criteria:\n\nPhase 1:\n\n* Self-reported organ-related disorder (COPD, cardiac arrhythmia, gastro-esophageal disorder)\n* pregnant or less than 4 months postpartum\n* infant living in household less than 1 year old\n\nPhase 2:\n\n* Self-reported organ-related disorder (COPD, cardiac arrhythmia, gastro-esophageal disorder)\n* pregnant or less than 4 months postpartum\n* infant living in household less than 1 year old","21 Years","75 Years",{"count":137,"type":21},90,[139,140],"PHASE1","PHASE2","The proposed research aims to reduce obesity-related health disparities by promoting healthy lifestyle behaviors among African Americans (AAs), given the high disease burdens associated with low physical activity, insufficient sleep, and obesity. There will be two phases to the proposed research. Phase 1 (Aim 1) will encompass formative research and community engagement activities, and Phase 2 (Aim 2a and 2b) will be a randomized clinical trial.\n\nThe primary goal of Aim 1 is to conduct in-depth qualitative interviews in order to: (1) better understand sleep-related social contextual factors, knowledge, behaviors, and beliefs, and (2) discuss and receive feedback on an existing sleep intervention design and materials. The primary goal of Aim 2 is to explore the feasibility, satisfaction, and preliminary efficacy of a sleep intervention to increase sleep and physical activity (PA) among sedentary and short sleeping (≤6 hrs\u002Fnight) African American adults with overweight\u002Fobesity, compared to a contact control group. (Aim 2a) An additional exploratory (Aim 2b) examines changes in cancer-relevant biomarkers between those who received the intervention vs the control condition (n = 20). Data will be collected from a sample of 20 participants (10 per condition) who volunteer to have their blood drawn pre- and post-intervention.\n\nThere are two phases of the study, and information gained during Phase 1 (Aim 1) will be used to inform Phase 2 (Aim 2). Thus, additional modifications to the protocol will be submitted prior to engagement in Phase 2.",[28,27],"2025-12-09",{"date":145,"type":36},"2025-12-17",{"date":147,"type":36},"2023-10-01",{"date":149,"type":21},"2026-11-01",{"name":151,"class":43},"University of Minnesota"]