[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"obstructive-sleep-apnea-osas\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:obstructive-sleep-apnea-osas":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,78,106],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100650125","obstructive-sleep-apnea-and-body-awareness-100650125",false,"NCT07743892","Obstructive Sleep Apnea and Body Awareness","The Relationship Between Body Awareness and Clinical Parameters in Patients With Obstructive Sleep Apnea","Inclusion Criteria:\n\n* Receiving a diagnosis of OSA after polysomnography,\n* Having an Apnea-Hypopnea Index ≥5 for OSA,\n* Volunteering to participate in the study.\n\nExclusion Criteria:\n\n* Having severe orthopedic, neurological, or cardiac diseases,\n* Having a diagnosed lung disease,\n* Having a previous or current history of psychiatric or neurological disorders,\n* Not voluntarily participating in the study.",true,"ALL","18 Years","65 Years",{"count":21,"type":22},47,"ESTIMATED","OBSERVATIONAL","Obstructive Sleep Apnea Syndrome (OSAS) is a chronic disease characterized by intermittent hypoxia and sleep fragmentation resulting from recurrent upper airway obstructions. The physiological and neurocognitive changes caused by the disease can affect how individuals perceive and interpret bodily sensations. Although body awareness plays a significant role in the perception and management of symptoms, its relationship with clinical parameters in individuals with OSAS has not been sufficiently investigated. Therefore, the aim of our study is to examine the relationship between body awareness and respiratory function, disease severity, fatigue, shortness of breath, and sleep quality in OSAS patients.",[26],"Obstructive Sleep Apnea (OSAS)","RECRUITING","2026-07-31",{"date":30,"type":31},"2026-08-04","ACTUAL",{"date":33,"type":31},"2026-05-21",{"date":35,"type":22},"2027-06-30",{"name":37,"class":38},"Karabuk University","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":47,"targetDuration":4,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":58,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":39},"100648411","identification-of-biomarkers-of-obstructive-sleep-apnea-100648411","NCT07723144","Identification of Biomarkers of Obstructive Sleep Apnea.","Identification of Biomarkers to Understand the Pathogenesis of Obstructive Sleep Apnea.","Inclusion Criteria:\n\n1. Participants with obstructive sleep apnea (OSA):\n\n   * Age 18 to 65 years.\n   * Moderate or severe obstructive sleep apnea confirmed by overnight polysomnography (apnea-hypopnea index \\[AHI\\] ≥15 events\u002Fhour).\n   * Willing and able to provide written informed consent.\n   * Willing to undergo repeated blood sampling and study assessments.\n   * Willing to use positive airway pressure (PAP) therapy and accept random assignment to immediate or delayed treatment.\n2. Control participants:\n\n   * Age 18 to 65 years.\n   * No obstructive sleep apnea (AHI \\\u003C5 events\u002Fhour on overnight polysomnography).\n   * Willing and able to provide written informed consent.\n   * Willing to undergo study assessments and blood sampling.\n\nExclusion Criteria:\n\n* Mild obstructive sleep apnea (AHI 5 to \\\u003C15 events\u002Fhour).\n* Central sleep apnea.\n* Previous treatment for obstructive sleep apnea within the previous 3 months.\n* Body mass index (BMI) ≥40 kg\u002Fm².\n* Severe cardiovascular disease.\n* Severe kidney disease or impaired renal function.\n* Significant liver disease.\n* Chronic inflammatory, autoimmune, or rheumatic disease.\n* Active cancer or other condition associated with systemic inflammation.\n* Chronic respiratory diseases, including asthma or chronic obstructive pulmonary disease.\n* Respiratory infection within 4 weeks before enrollment.\n* Major surgery or significant injury within the previous 3 months.\n* Chronic rhinosinusitis.\n* Current treatment with systemic corticosteroids, immunosuppressive drugs, cytotoxic drugs, chronic anti-inflammatory medications, or other medications that may influence inflammatory biomarkers.\n* Pregnancy or any condition that, in the opinion of the investigators, would make participation unsafe or interfere with interpretation of the study results.",{"count":48,"type":22},120,"INTERVENTIONAL",[51],"NA","Obstructive sleep apnea (OSA) is a common sleep disorder associated with intermittent hypoxia, systemic inflammation, oxidative stress, and an increased risk of cardiovascular and metabolic diseases. Current diagnostic methods are effective but have limited availability and do not adequately predict disease burden or treatment response.\n\nThe purpose of this study is to identify and validate blood biomarkers that may improve the screening, diagnosis, risk stratification, and monitoring of adults with OSA. A total of 120 participants will undergo clinical evaluation and overnight polysomnography. Participants with moderate-to-severe OSA will be randomly assigned to either immediate or delayed positive airway pressure (PAP) therapy, while participants without OSA will serve as controls. Blood samples will be collected at predefined time points and analyzed for inflammatory, metabolic, oxidative stress, and other candidate biomarkers.\n\nThe study aims to determine which biomarkers are associated with OSA severity and how they change in response to PAP therapy. The results may contribute to the development of more accessible and personalized diagnostic and monitoring strategies for patients with OSA.",[54,55,26,56,57],"Obstructive Sleep Apnea","Obstructive Sleep Apnea (OSA)","Obstructive Sleep Apnea (SAOS)","Obstructive Sleep Apnea (Moderate to Severe)",[59,60,61,62,63,64,65,66,67,68],"Obstructive sleep apnea","OSA","Positive airway pressure therapy","CPAP","Blood biomarkers","Polysomnography","Inflammation","Oxidative stress","Metabolomics","Precision medicine","2026-07-20",{"date":71,"type":31},"2026-07-23",{"date":73,"type":31},"2025-12-19",{"date":75,"type":22},"2029-06-19",{"name":77,"class":38},"Medical University of Bialystok",{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":49,"phases":88,"briefSummary":89,"conditions":90,"keywords":91,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":39},"100607297","home-based-under-mattress-monitor-for-osa-100607297","NCT07186725","Home-based Under Mattress Monitor for OSA","Home-Based Under-Mattress Monitoring Device to Estimate Mandibular Advancement in Oral Appliance Therapy for Obstructive Sleep Apnea","Inclusion Criteria:\n\n* Diagnosis of Obstructive Sleep Apnea demonstrated with a sleep study polysomnography or home sleep study (PSG or HSAT), manually scored by a sleep physician according to the 2017 American Academy of Sleep medicine scoring guidelines.\n* Willingness to commute to the OFP clinic every 2 weeks during MAD titration period.\n* Consent to partake in the study.\n\nExclusion Criteria:\n\n* Diagnosis of central or mixed sleep apnea.\n* Neurocognitive disease.\n* Concomitant therapy with PAP therapy.\n* Allergic to the appliance material (Polyamide 12).\n* Presence of active dental decay, ill-fitting dental restorations, or crown to root ratio unfavorable.\n* Inadequate English language comprehension.\n* Lack of coordination or dexterity to insert\u002Fremove the MAD intraorally.\n* Inability to tolerate digital dental impressions.\n* Patients with concomitant diagnosed sleep disorders, including narcolepsy, restless leg syndrome, rapid eye movement sleep behavior disorder).","80 Years",{"count":87,"type":22},70,[51],"The aim of the study is to evaluate the effectiveness of the under-mattress monitoring device to aid in the titration process of a mandibular advancement device (MAD) for the management of obstructive sleep apnea (OSA). A secondary aim is to evaluate changes in subjective OSA symptoms and patient's satisfaction with MAD. A third aim is to analyze if there are differences between the sleep parameters recorded by the under-mattress monitor between responders and non-responders to MAD therapy.",[26,56],[92,93,94,95,54,96],"Mandibular Advancement","Sleep Apnea","Oral Appliance","Home-based","Home-based device","2026-02-02",{"date":99,"type":31},"2026-02-03",{"date":101,"type":31},"2026-01-07",{"date":103,"type":22},"2027-03",{"name":105,"class":38},"Isabel Moreno Hay",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":49,"phases":114,"briefSummary":115,"conditions":116,"keywords":120,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":39},"100615802","a-prospective-randomnised-controlled-trial-comparing-overall-patient-compliance-in-a-bariatric-surgical-pathway-using-the-standard-versus-a-more-intensified-and-interactive-version-of-the-get-ready-smartphone-application-100615802","NCT07297342","A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance in a Bariatric Surgical Pathway Using the Standard Versus a More Intensified and Interactive Version of the \"Get Ready\" Smartphone Application.","Inclusion Criteria:\n\n* Patients undergoing bariatric surgery\n\nExclusion Criteria:\n\n* Previous bariatric surgery",{"count":113,"type":22},200,[51],"The aim of this study is to assess the impact of a newly intensified digital platform following bariatric surgery. This will be measured using several questionnaires. The following objectives will be evaluated: the exact amount of weight loss achieved preoperatively with the preparatory diet; the occurrence of dumping symptoms; the assessment of quality of life (QOL); and compliance with supplement intake.\n\nBy examining the impact of an enhanced digital platform, we aim to address critical questions regarding the effectiveness of improved patient support in the digital domain. Moreover, given the increasing prevalence of bariatric surgery as a therapeutic option for obesity, it is of utmost importance to identify strategies to optimize patient education and support through digital tools. This study not only contributes to the scientific understanding of digital support in bariatric care but also has important implications for the further development of the \"Get Ready\" application, ensuring that it remains at the forefront of providing comprehensive and patient-centered support in the evolving landscape of bariatric surgery.",[117,118,26,119],"Obesity &Amp; Overweight","Hypertension","Diabetes Mellitus ( Type 1 and Type 2)",[121,122,123,124],"Get Ready","application","bariatric","compliance","2025-12-16",{"date":127,"type":31},"2025-12-22",{"date":129,"type":31},"2025-04-02",{"date":131,"type":22},"2027-06",{"name":133,"class":134},"Sint Dimpna Ziekenhuis Geel","NETWORK"]