[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"heart-rate\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:heart-rate":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,13,0,[8,49,80,123,151,198,218,251,282,322,344,370,391],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100638110","effects-of-breathing-retraining-exercises-in-pregnant-females-with-postural-orthostatic-tachycardia-syndrome-100638110",false,"NCT07579026","Effects of Breathing Retraining Exercises in Pregnant Females With Postural Orthostatic Tachycardia Syndrome.","Effects of Breathing Retraining Exercises on Heartrate, Blood Pressure and Orthostatic Intolerance in Pregnant Females With Postural Orthostatic Tachycardia Syndrome.","Inclusion Criteria:\n\n* • Pregnant female between the age of 19 to 35 years.\n\n  * Active standing results in a sustained increase in heart rate (HR) of at least 30 bpm or ≥120 bpm.\n  * POTS patients with a subacute onset of lightheadedness, dizziness, and presyncope provoked by standing.\n  * palpitations with chest discomfort, breathing difficulties, or feeling faint\n\nExclusion Criteria:\n\n* • Uncontrolled hypertension\u002Fpre-eclampsia\n\n  * cardiovascular disorder\n  * Patients with uncontrolled diabetes\n  * Patient with Anemia, severe heart failure and neurodegenerative diseases.\n  * Females with the history of deep venous thrombosis.","FEMALE","19 Years","35 Years",{"count":20,"type":21},44,"ESTIMATED","INTERVENTIONAL",[24],"NA","Postural orthostatic tachycardia POTS is characterized by excessive increase in heart rate when moving from lying to standing position, often accompanied by symptoms such as dizziness, fatigue, brain fog, lightheadedness, rapid heartbeat and palpitation.it most commonly effects the females of reproductive age and can be triggered by events like viral infections, trauma and hormonal changes. During pregnancy females may experience worsening of symptoms in first trimester due to hormonal changes and decreased blood volume later on in second and third trimester the blood volume begins to increase. However, breathing exercises helps to regulate the nervous system, improves parasympathetic activity and reduce sympathetic activity.\n\nThe study will be randomized clinical trial and will be conducted at Bashir hospital Sialkot and Fatima hospital Sialkot. The study will be completed in 10 months of duration after the approval of synopsis. Non probability convenience sampling will be used and 44 participants will be included in the study after randomization. The subjects will be divided into two groups. Group A (experimental group) will receive diaphragmatic breathing exercises whereas Group B (control group) will receive educational retraining whereas both groups will receive baseline treatments which includes progressive muscle relaxation techniques. The tools used for the study will be Vanderbilt orthostatic symptom score VOSS to evaluate orthostatic intolerance, blood pressure will be measured using non-invasive blood pressure measurement and pulse oximetry will be used to access the heart rate. After data completion data will be analyzed by using SPSS version 21.",[27,28,29],"Orthostatic Hypotension","Heart Rate","Blood Pressure",[31,32,33,34,35],"pregnancy","blood pressure","vital signs","orthostatic intolerance","postural orthostatic tachycardia syndrome","RECRUITING","2026-05-05",{"date":39,"type":40},"2026-05-11","ACTUAL",{"date":42,"type":40},"2025-08-31",{"date":44,"type":21},"2026-09",{"name":46,"class":47},"Riphah International University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":62,"conditions":63,"keywords":66,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":4},"100629603","anxiety-and-physiological-responses-in-ambulatory-surgery-100629603","NCT07476820","Anxiety and Physiological Responses in Ambulatory Surgery","Subjective Anxiety and Physiological Parameters in First-Time Ambulatory Surgery Patients","Inclusion Criteria:\n\n1. Be at least 18 years old.\n2. Undergo outpatient surgery for the first time.\n3. Be mentally clear and able to communicate in Chinese and complete the questionnaire.\n4. Agree to wear physiological monitoring devices and sign the consent form.\n\nExclusion Criteria:\n\n1. Hearing impairment or the need to use a hearing aid.\n2. Currently using sleeping pills\u002Fsedatives or having a mental illness.\n3. Severe cardiovascular disease or having an implanted pacemaker.\n4. Diseases that affect autonomic nervous system function.",true,"ALL","18 Years",{"count":60,"type":21},90,[24],"This study aims to investigate the effects of music intervention on subjective anxiety and physiological indicators, including heart rate, blood pressure, and heart rate variability, in first-time ambulatory surgery patients, and to compare the differential effects between self-selected and standardized music interventions.",[64,65,28,29],"Anxiety","Heart Rate Variability (HRV)",[67,64,68,69],"Music","Ambulatory Surgery","Physiological Indicators","NOT_YET_RECRUITING","2026-03-12",{"date":73,"type":40},"2026-03-17",{"date":75,"type":21},"2026-02-23",{"date":77,"type":21},"2026-12-30",{"name":79,"class":47},"Da-Yeh University",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":102,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":48},"100579954","assessing-the-effect-of-cool-roofs-on-health-using-smartwatches-in-colima-mexico-100579954","NCT06831006","Assessing the Effect of Cool Roofs on Health Using Smartwatches in Colima, Mexico","A Randomized Controlled Trial (RCT) Evaluating the Effects of Cool Roofs on Health Outcomes Using Smartwatches in Colima, Mexico","REFLECT","Inclusion Criteria:\n\n* Permanent household resident\n\nExclusion Criteria:\n\n* Roof damage, inaccessible or instability of roof adversely affecting cool roof coating application.\n* Participant unable to provide written\u002Fverbal informed consent. Participants will be excluded if they are not willing or able to wear a smartwatch.\n* Participants will be excluded if they do not have a smartphone with an internet connection that can connect to the smartwatch.\n* Only one participant per household.",{"count":89,"type":21},800,[24],"Ambient air temperatures in Mexico have broken record highs in 2024. Solutions are needed to build heat resilience in communities and adapt to increasing heat from climate change. Sunlight-reflecting cool roof coatings may passively reduce indoor temperatures and energy use to protect home occupants from extreme heat. Occupants living in poor housing conditions in the northern zone of Mexico are susceptible to increased heat exposure.\n\nHeat exposure can instigate and worsen numerous physical, mental and social health conditions. The worst adverse health effects are experienced in communities that are least able to adapt to heat exposure. By reducing indoor temperatures, cool roof use may promote heart health, sleep and physical activity in household occupants.\n\nThe long-term research goal of the investigators is to identify viable passive housing adaptation technologies with proven health benefits to reduce the burden of heat stress in communities affected by heat in Mexico. To meet this goal, the investigators will conduct a randomized controlled trial to establish the effects of cool roof use on heart rate, sleep and physical activity in Colima, Mexico.",[28,93,94,95,96,97,98,99,100,101],"All-day Steps","Distance Walked","Active Minutes","Moderate-intensity Activity Minutes","Vigorous-intensity Activity Duration","Sleep Quantity","Time in Sleep Stages","Awake Duration","Sleep Score",[103,104,105,106,107,108,109,110,111,112,113],"Hot Temperature","Humidity","Housing","Wearable","Smartwatch","Heart rate","Cardiovascular","Physical activity","Sleep","Cool roof","Heat stress","2026-03-09",{"date":116,"type":40},"2026-03-11",{"date":118,"type":21},"2026-04-01",{"date":120,"type":21},"2027-09-01",{"name":122,"class":47},"University of Auckland, New Zealand",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":128,"acronym":4,"eligibilityCriteria":129,"healthyVolunteers":11,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":130,"targetDuration":4,"studyType":22,"phases":132,"briefSummary":133,"conditions":134,"keywords":138,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":48},"100619458","effects-of-music-on-procedural-pain-in-distal-radius-fracture-reduction-100619458","NCT07344883","Effects of Music on Procedural Pain in Distal Radius Fracture Reduction","Effects of Music on Pain in Orthopedic Patients With Distal Radius Fractures Undergoing Non-surgical Reduction: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients of both sexes, 18 years of age or older\n* Patients with distal radius fracture requiring non-surgical (closed) reduction\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Patients with severe hearing impairment\n* Patients diagnosed with cognitive or psychiatric disorders\n* Patients requiring emergency\u002Furgent intervention\n* Open fractures (exposed fractures)",{"count":131,"type":21},192,[24],"This randomized controlled trial (RCT) evaluates the effectiveness of music as a complementary intervention for pain control during non-surgical reduction of distal radius fractures in orthopedic patients. Distal radius fractures are among the most common traumatic injuries presenting to emergency departments and are frequently associated with intense procedural pain and significant physiological stress responses. Despite standard pharmacological analgesia, optimal pain management during fracture reduction remains a clinical challenge, and evidence regarding non-pharmacological adjuncts in the emergency orthopedic setting is still limited The study will enroll 192 adult patients admitted to the orthopedic emergency departments of AUSL Piacenza and AOU Parma with distal radius fractures requiring closed reduction. Participants will be randomly assigned (1:1:1) to one of three groups: a 20-minute session of patient-preferred music, a 20-minute session of standardized music selected by a music therapist, or standard care without music. Pain intensity will be assessed using the Numerical Rating Scale (NRS), while physiological stress will be evaluated through heart rate and blood pressure measurements, collected at baseline (T0) and 20 minutes later (T1), immediately after the reduction procedure The trial is designed as a prospective, randomized, controlled study with blinded data analysis, and all data will be collected and managed in compliance with current privacy and data protection regulations. By generating robust evidence on a low-cost, safe, and easily implementable intervention, the PolSound trial aims to improve procedural pain management and patient experience in emergency orthopedic care, potentially supporting the integration of music-based interventions into standard analgesic protocols.",[135,29,28,136,137],"Pain","Music Therapy","Nursing",[139,140,141],"nursing","musictherapy","pain","2026-01-08",{"date":144,"type":40},"2026-01-15",{"date":146,"type":21},"2026-02",{"date":148,"type":21},"2027-02",{"name":150,"class":47},"Azienda Unita Sanitaria Locale di Piacenza",{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":156,"acronym":4,"eligibilityCriteria":157,"healthyVolunteers":56,"sex":16,"minAge":158,"maxAge":159,"enrollmentInfo":160,"targetDuration":4,"studyType":22,"phases":162,"briefSummary":163,"conditions":164,"keywords":179,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":48},"100617476","evaluation-of-the-impact-of-a-nutritional-formulation-on-cognitive-performance-following-stress-exposure-100617476","NCT07319117","Evaluation of the Impact of a Nutritional Formulation on Cognitive Performance Following Stress Exposure.","A Double-blind, Placebo-controlled, Randomised, Acute, Repeated Measures Cross-over Study to Evaluate the Impact of Skoshify 'Think Tank' Nutritional Formulation on Cognitive Performance Following Stress Exposure.","Inclusion Criteria:\n\n1. Willing and able to provide written informed consent (in English)\n2. Aged 40-60\n3. Female\n4. Daily caffeine drinkers\n5. Healthy and free from significant physical and psychiatric disorders\n\nExclusion Criteria:\n\n1. Current cigarette smokers\u002Fvapers.\n2. Known food allergy or intolerance to the investigational products or control products.\n3. Not willing to consume coffee.\n4. Individuals diagnosed with psychiatric\u002Fmental health conditions.\n5. Individuals engaging in recreational drug use.\n6. Individuals with diagnosed cardiovascular conditions (e.g. heart disease, high blood pressure)\n7. Individuals taking prescribed medication except contraceptives\u002Fhormone replacement therapy\n8. Individuals suffering from Raynaud's or circulatory issues\n9. Individuals who have suffered an injury or infection in their hand\u002Farm in the last month\n10. Individuals who have suffered from chronic pain conditions or experience extreme numbness or pain in response to cold temperatures.\n11. Previous brain injury\u002Fbrain surgery\n12. Individuals who work night shifts.\n13. Currently pregnant or breastfeeding.\n14. Previous participants in a laboratory stress protocol.","40 Years","60 Years",{"count":161,"type":21},40,[24],"The proposed project will evaluate the synergistic effects of a nutritional formulation, 'Think Tank' on cognitive performance following exposure to a psychological and physical stressor. Adopting a double-blind repeated measures cross-over design, middle-aged females (40-60 years) will be recruited to take part in a two-stage research study that will examine whether the formulation enhances cognitive performance and subjective well-being following the challenge of a stressor, compared to placebo. Cognitive assessments will examine the impact of the nutritional formulation on working memory, sustained attention, cognitive flexibility and inhibitory control. The study will also assess physiological (heart rate, blood pressure and cortisol) and subjective (well-being, anxiety, positive and negative mood, stress) markers of stress reactivity. The study will also explore levels sleep quality, mental and physical fatigue, effort, productivity, and perceived impact of the intervention.",[165,166,167,168,169,170,171,172,64,173,174,29,28,175,176,177,178],"Cognitive Assessment","Working Memory","Executive Function (Cognition)","Sustained Attention","Inhibitory Control","Cognitive Flexibility","Cortisol","Stress","Depression","Sleep Quality","Mental Fatigue","Physical Fatigue","Productivity","Effort",[180,181,182,183,184,185,186,187,188],"Cognitive Performance","Stress Response","Creatine","Magnesium","L-Tyrosine","L-Theanine","Rhodiola","Phosphatidylserine","Citicoline","2025-12-19",{"date":191,"type":40},"2026-01-06",{"date":193,"type":21},"2025-12-15",{"date":195,"type":21},"2026-08-31",{"name":197,"class":47},"Leeds Beckett University",{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":204,"enrollmentInfo":205,"targetDuration":4,"studyType":22,"phases":206,"briefSummary":207,"conditions":208,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":193,"lastUpdatePostDateStruct":211,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":48},"100553584","asleep-fiberoptic-vs-direct-laryngoscopy-effect-on-hemodynamic-stability-using-opioid-free-anesthesia-induction-100553584","NCT06487988","Asleep Fiberoptic vs Direct Laryngoscopy Effect on Hemodynamic Stability Using Opioid Free Anesthesia Induction","Inclusion Criteria:\n\n* ASA (American Society of Anesthesiologists) physical status I and II\n* Range age of 18-55 years' old\n* Scheduled for elective surgery under general anesthesia.\n\nExclusion Criteria:\n\n* History of cardiovascular diseases.\n* History of lung disease.\n* Hypertensive patient (BP\\> 140\u002F90)\n* Patient taking medications that affect blood pressure and heart rate\n* Morbid obesity (BMI \\>30)\n* Severe GERD\n* Predicted difficult airway (Short TMD \\\u003C6 cm, Upper li bite test grade III, Mallampati score\n\n  \\>III)\n* Neck instability\n* Patient planned to receive rapid sequence intubation\n* Patient refusal to participate\n* History of difficult intubation\u002F ventilation","55 Years",{"count":60,"type":21},[24],"The goal of this clinical trial is to compare blood pressure and heart rate between the fiberoptic and direct oral intubation using opioid free anesthesia induction. Secondary objectives include comparing the time needed for intubation and the incidence of postoperative sore throat, hoarseness, and upper airway trauma in adults aging between 18 to 55 years, scheduled for elective surgery under general anesthesia.\n\nThe main question it aims to answer is:\n\nDoes fiberoptic intubation cause less hemodynamic instability than direct oral intubation using opioid free anesthesia induction?",[209,210,28,29],"Analgesics, Opioid","Anesthesia, General",{"date":189,"type":40},{"date":213,"type":40},"2024-09-11",{"date":215,"type":21},"2026-01-01",{"name":217,"class":47},"American University of Beirut Medical Center",{"id":219,"slug":220,"hasResults":11,"nctId":221,"briefTitle":222,"officialTitle":223,"acronym":224,"eligibilityCriteria":225,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":226,"enrollmentInfo":227,"targetDuration":4,"studyType":22,"phases":229,"briefSummary":230,"conditions":231,"keywords":236,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":243,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":249,"locationsCount":48},"100614033","frequency-dependent-effects-of-auricular-vagus-nerve-stimulation-on-autonomic-and-cardiovascular-parameters-100614033","NCT07274332","Frequency-Dependent Effects of Auricular Vagus Nerve Stimulation on Autonomic and Cardiovascular Parameters","Acute Effects of Different Frequencies of Auricular Vagus Nerve Stimulation on HRV, Blood Pressure, and Respiratory Rate: A Sham-Controlled, Randomized, Crossover Dose-Response Study","AVNS-DRC","Inclusion Criteria:\n\n* 18-30 years\n* Healthy (self-reported)\n* No cardiovascular, neurological, metabolic or psychiatric disorders\n* No regular medication affecting autonomic function\n* Non-smoker\n* BMI 18-29.9\n\nExclusion Criteria:\n\n* Pregnancy\n* Cardiac arrhythmia\n* Hypertension or hypotension\n* Chronic respiratory disorders\n* Active infection\n* Metal implants in cervical area\n* Epilepsy\n* Syncope history\n* Prior vagus stimulation experience","30 Years",{"count":228,"type":21},36,[24],"This randomized, sham-controlled, crossover study investigates the acute autonomic effects of transcutaneous cervical vagus nerve stimulation (tcVNS) applied at five different frequencies (0 Hz\u002Fsham, 10 Hz, 25 Hz, 50 Hz, 100 Hz) in healthy adults. The primary objective is to determine how stimulation frequency modulates heart rate variability (HRV), blood pressure, and respiratory rate. The study aims to establish a frequency-specific dose-response model using validated physiological measurements.",[232,233,28,29,234,235],"Vagus Nerve Stimulation","Autonomic Nervous System","Respiration","Healthy Volunteers",[237,238,239,240,241],"Transcutaneous Cervical Vagus Nerve Stimulation","Neuromodulation","Non-invasive Vagus Stimulation","Parasympathetic Activation","Heart Rate Variability","2025-11-27",{"date":244,"type":40},"2025-12-10",{"date":246,"type":21},"2025-12-22",{"date":248,"type":21},"2026-03-15",{"name":250,"class":47},"SEFA HAKTAN HATIK",{"id":252,"slug":253,"hasResults":11,"nctId":254,"briefTitle":255,"officialTitle":256,"acronym":4,"eligibilityCriteria":257,"healthyVolunteers":56,"sex":57,"minAge":258,"maxAge":259,"enrollmentInfo":260,"targetDuration":4,"studyType":22,"phases":262,"briefSummary":263,"conditions":264,"keywords":268,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":273,"lastUpdatePostDateStruct":274,"startDateStruct":276,"completionDateStruct":278,"leadSponsor":280,"locationsCount":48},"100381894","effect-of-kangaroo-care-on-test-weighing-100381894","NCT04252547","Effect of Kangaroo Care on Test Weighing","The Effect Of Kangaroo Mother Care On Test Weighing In Preterm Infants","Inclusion Criteria:\n\n\\- Agreeing to participate in the study for parents.\n\nThe inclusion criteria for infants were as follows;\n\n* Attaining to oral feeding by the physician in the neonatal intensive care unit\n* Being born at 26-36+6 gestational week which is determined according to the mother's last period cycle\n* Being at 32-39+6 postmenstrual week during the time they are included in the study\n* Having body weight of 1500 grams and above\n* Being breastfed at least once\n* Having no health problems other than being preterm\n\nExclusion Criteria:\n\nThe exclusion criteria for infants were as follows;\n\n* Suffering from gastrointestinal, neurological or genetic diseases (such as necrotizing enterocolitis, intracranial bleeding, hydrocephalia, omphalocele, down syndrome, gastroschisis) and other diseases\n* Having a condition obstructing oral feeding (such as cleft palate, cleft lip, facial muscle paralysis, craniofacial abnormalities etc.)\n* Receiving oxygen support","32 Weeks","40 Weeks",{"count":261,"type":21},46,[24],"The study will be conducted with the Crossover Randomized Controlled Method. The infants who have attained oral feeding in the neonatal intensive care unit will be divided into two groups via randomization in the computer environment. After the randomization, kangaroo care will be applied to the infants in Group 1 during the first feeding hour when they are included in the study and they will be breastfed by their mothers without any other application during the next feeding. On the other hand, no application will be performed on the infants in Group 2 during the first feeding hour when they are included in the study and kangaroo care will be applied to them during the second feeding hour. The infants in both groups will be breastfed by their mothers during the feeding hours.",[265,266,267,28],"Kangaroo Care","Weight Gain","Oxygen Saturation",[269,270,108,271,272],"kangaroo care","test weighing","oxygen saturation","preterm infants","2025-04-29",{"date":275,"type":40},"2025-05-02",{"date":277,"type":40},"2024-06-09",{"date":279,"type":21},"2026-01-09",{"name":281,"class":47},"Istanbul University - Cerrahpasa",{"id":283,"slug":284,"hasResults":11,"nctId":285,"briefTitle":286,"officialTitle":287,"acronym":288,"eligibilityCriteria":289,"healthyVolunteers":11,"sex":57,"minAge":290,"maxAge":58,"enrollmentInfo":291,"targetDuration":4,"studyType":293,"phases":4,"briefSummary":294,"conditions":295,"keywords":300,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":312,"lastUpdatePostDateStruct":313,"startDateStruct":315,"completionDateStruct":317,"leadSponsor":319,"locationsCount":48},"100473975","validation-of-vital-signs-recording-with-vt-patch-connected-devices-in-children-100473975","NCT05451875","Validation of Vital Signs Recording With VT-Patch Connected Devices in Children","Validation of Vital Signs Recording With VT-Patch® Connected Devices in Children","VT","Inclusion Criteria:\n\n* PICU monitoring for the next 24 hours\n\nExclusion Criteria:\n\n* Recent cardiac or thoracic surgery\n* Thoracic skin lesion that contraindicates the VT patch\n* No parental consent\n* Intermittent presence of one study observer in the patient room considered inappropriate by the physician or the nurse in charge because of the child's medical condition","1 Day",{"count":292,"type":21},48,"OBSERVATIONAL",": Patient readmission to PICU is a major point of concern for physicians because, although being a rare event, it has been strongly associated with more morbidity and death. Patient monitoring once they have left the PICU is drastically modified, and small connected devices could be an option to early identify patients at risk of PICU readmission. Such devices have been manufactured for the recording of vital signs in adults, but they do not exist for children.\n\nBesides, studies have recently shown that devices that use optical sensors may be less accurate in individuals with dark skin pigmentation since dark skin tones impose a limitation on optical biometric sensing. The wearable and medical device industry has not sufficiently addressed this issue yet. This is one of the main challenges that need to be addressed in this area to make sure the connected devices using this technology will work with all different skin colours including very dark skin.",[296,267,297,298,28,299],"Vital Signs","Children","Intensive Care Unit","Respiratory Rate",[301,302,303,304,305,108,306,106,307,297,308,309,310,311],"Vital signs","SPO2","ECG","Continuous","Skin temperature","VitalTracer","All-in-one","PICU","Different Skin Color","Dark skin color","Monk Scale","2025-03-05",{"date":314,"type":40},"2025-03-10",{"date":316,"type":40},"2025-02-03",{"date":318,"type":21},"2025-12-31",{"name":320,"class":321},"VitalTracer Ltd.","INDUSTRY",{"id":323,"slug":324,"hasResults":11,"nctId":325,"briefTitle":326,"officialTitle":327,"acronym":86,"eligibilityCriteria":328,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":329,"targetDuration":4,"studyType":22,"phases":331,"briefSummary":332,"conditions":333,"keywords":334,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":335,"lastUpdatePostDateStruct":336,"startDateStruct":338,"completionDateStruct":340,"leadSponsor":342,"locationsCount":48},"100580848","assessing-the-effect-of-cool-roofs-on-health-using-smartwatches-in-ouagadougou-burkina-faso-100580848","NCT06842641","Assessing the Effect of Cool Roofs on Health Using Smartwatches in Ouagadougou, Burkina Faso","A Cluster Randomized Controlled Trial (cRCT) Evaluating the Effects of Cool Roofs on Health Outcomes Using Smartwatches in Ouagadougou, Burkina Faso","Inclusion Criteria:\n\n* • Permanent household resident\n\nExclusion Criteria:\n\n* • Roof damage, inaccessible or instability of roof adversely affecting cool roof coating application.\n\n  * Participant unable to provide written\u002Fverbal informed consent. Participants will be excluded if they are not willing or able to wear a smartwatch.\n  * One participant per household.",{"count":330,"type":21},200,[24],"Ambient air temperatures in Africa, have broken record highs in 2024. Solutions are needed to build heat resilience in communities and adapt to increasing heat from climate change. Sunlight-reflecting cool roof coatings may passively reduce indoor temperatures and energy use to protect home occupants from extreme heat. Occupants living in poor housing conditions- for example in informal settlements, slums, and low-socioeconomic households - are susceptible to increased heat exposure.\n\nHeat exposure can instigate and worsen numerous physical, mental and social health conditions. The worst adverse health effects are experienced in communities that are least able to adapt to heat exposure. By reducing indoor temperatures, cool roof application may improve heart health, sleep and physical activity in household occupants.\n\nThe long-term research goal is to identify viable passive housing adaptation technologies with proven health benefits to reduce the burden of heat stress in communities affected by heat. To meet this goal, the investigators will use smartwatches to measure the effects cool roof application on heart health, sleep and physical activity in Ouagadougou, Burkina Faso.",[28,93,94,95,96,98,99,100,101],[103,104,105,106,107,108,109,110,111,112],"2025-02-18",{"date":337,"type":40},"2025-02-24",{"date":339,"type":21},"2025-03-20",{"date":341,"type":21},"2026-03-20",{"name":343,"class":47},"Institut Supérieur des Sciences de la Population",{"id":345,"slug":346,"hasResults":11,"nctId":347,"briefTitle":348,"officialTitle":349,"acronym":4,"eligibilityCriteria":350,"healthyVolunteers":11,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":351,"targetDuration":4,"studyType":293,"phases":4,"briefSummary":353,"conditions":354,"keywords":357,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":361,"lastUpdatePostDateStruct":362,"startDateStruct":364,"completionDateStruct":366,"leadSponsor":368,"locationsCount":48},"100569025","the-study-is-about-the-inuence-of-the-combination-of-music-and-noise-cancelling-as-a-non-pharmacological-aid-in-reducing-anxiety-and-discomfort-during-wisdom-tooth-removal-the-level-of-fear-is-measured-by-a-questionnaire-which-the-patients-answer-twice-and-a-measurement-of-the-heartbeat-100569025","NCT06688877","The Study is About the influence of the Combination of Music and Noise Cancelling as a Non-pharmacological Aid in Reducing Anxiety and Discomfort During Wisdom Tooth Removal. The Level of Fear is Measured by a Questionnaire Which the Patients Answer Twice and a Measurement of the Heartbeat","Einfluss Der Kombination Von Musik Und Noise Cancelling Als nichtmedikamentöse Unterstützung Bei Angst Und Unwohlsein während Der Weisheitszahnentfernung","Inclusion Criteria:\n\n* willing to participate in the clinical trial, understood and signed the information sheet\n\nExclusion Criteria:\n\n* younger than 18 years old\n* hearing impairment",{"count":352,"type":21},156,"The goal of this clinical trial is to learn if the reduction of the noises (through head phones with music and noise cancelling) that occur during wisdom teeth removal, leads to a significant reduction in fear levels in patients compared to patients who do not have any noise reduction. The main questions it aims to answer are:\n\nDo music and noise cancelling help patients to have less fear during wisdom teeth removal surgery by reducing the sounds of the surgery? Is there a difference between just the noise cancelling function or is it better to combine noise cancelling and music together?\n\nParticipants will:\n\nJust come to their regular appointment (wisdom teeth removal) to our clinic, no follow ups needed. All participants will answer one questionnaire before and one after the surgery. All of them will have their rate of heartbeat measured for three times (before, during and after surgery, measured by a puls oximeter on the finger). They will be allocated to one of the three study groups (no headphones, headphones with noise cancelling or headphones with noise cancelling and music).",[355,356,28],"Fear Anxiety","Wisdom Tooth Removal",[358,359,360],"fear level","wisdom teeth removal","noise reduction by music and noise cancelling","2024-11-13",{"date":363,"type":40},"2024-11-14",{"date":365,"type":21},"2024-11-18",{"date":367,"type":21},"2025-06-29",{"name":369,"class":47},"Sigmund Freud PrivatUniversitat",{"id":371,"slug":372,"hasResults":11,"nctId":373,"briefTitle":374,"officialTitle":374,"acronym":4,"eligibilityCriteria":375,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":226,"enrollmentInfo":376,"targetDuration":4,"studyType":22,"phases":377,"briefSummary":378,"conditions":379,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":382,"lastUpdatePostDateStruct":383,"startDateStruct":385,"completionDateStruct":387,"leadSponsor":389,"locationsCount":48},"100565894","effects-of-sleep-body-temperature-on-body-composition-100565894","NCT06648109","Effects of Sleep Body Temperature on Body Composition","Inclusion Criteria:\n\n\\- Participants aged 18-30 years, inclusive of both male and female genders.\n\nExclusion Criteria:\n\n* Individuals suffering from serious diseases such as heart, liver, kidney, brain, hematopoietic, immune, thyroid, malignant tumors, etc.;\n* Those with familial hereditary hypertension (both parents are hypertensive) or those diagnosed with hypertension;\n* Individuals with cognitive or mental impairments that prevent the completion of the questionnaire;\n* Persons with physical disabilities that hinder normal walking;\n* Persons who have experienced a weight change of \\>3.0 kg within 1 month or \\>10 kg within 6 months prior to screening (as per the study in Nutrients. 2020 Oct 21;12(10):3221);\n* Individuals required to take antibiotics from one week before the trial starts until its conclusion;\n* Those with habitual diarrhea or who have experienced diarrhea from one week before the trial starts until its end;\n* Subjects who have participated in other ambient temperature-related trials within the last 6 months;\n* Individuals with extreme sleep schedules (i.e., not falling asleep between 21:00 and 2:00 a.m. the following morning, or waking up before 5:00 a.m.);\n* Those with sleep latency (the time it takes to fall asleep after going to bed) greater than one hour;\n* Pittsburgh Sleep Quality Index (PSQI) scores greater than 16;\n* Participants who do not sign the informed consent form or are deemed unsuitable by the investigator for any other reason.",{"count":161,"type":21},[24],"This will be a crossover controlled trial designed to recruit 40 participants, who will be divided into two groups of 20 subjects each. The participants will be randomly assigned to either Group A or Group B. Group A will receive the sleep electric blanket intervention for a period of 7 days, while Group B will serve as the control group without any additional intervention. After the intervention period, there will be a washout period of 7 days to ensure that any effects of the intervention have subsided before the crossover.\n\nFollowing the washout period, the groups will switch roles: Group B will then receive the sleep electric blanket intervention, and Group A will become the control group. This second phase will also last for 7 days, preceded and followed by the same assessment procedures as the initial phase. This design will allow for a comparison of the intervention's effects against a control period within the same group of participants, enhancing the study's internal validity.",[380,28,381],"Blood Pressure Check (Hypertension Screening)","Aldosterone Disorder","2024-10-17",{"date":384,"type":40},"2024-10-18",{"date":386,"type":21},"2024-10-20",{"date":388,"type":21},"2025-01-30",{"name":390,"class":47},"Jinan University Guangzhou",{"id":392,"slug":393,"hasResults":11,"nctId":394,"briefTitle":395,"officialTitle":396,"acronym":4,"eligibilityCriteria":397,"healthyVolunteers":56,"sex":57,"minAge":398,"maxAge":399,"enrollmentInfo":400,"targetDuration":4,"studyType":22,"phases":402,"briefSummary":403,"conditions":404,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":406,"lastUpdatePostDateStruct":407,"startDateStruct":409,"completionDateStruct":411,"leadSponsor":413,"locationsCount":48},"100457419","performance-of-the-aktiia-optical-blood-pressure-monitoring-device-against-double-auscultation-100457419","NCT05236348","Performance of the Aktiia Optical Blood Pressure Monitoring Device Against Double Auscultation","Single-center Prospective Clinical Trial to Validate the Performance of the Aktiia Optical Blood Pressure Monitoring (OBPM) Device at the Wrist Against Double Auscultation","Inclusion Criteria:\n\n* Adult subjects (aged between 21 and 85 years old)\n* Subjects can read and speak French\n* Subjects can perform simple physical exercises\n* Subjects agreeing to attend the totality of 9 visits\n* Subjects that have signed the informed consent form\n\nExclusion Criteria:\n\n* Clinical staff collaborating with study PI\n* Subjects with tachycardia (heart rate at rest \\> 120bpm)\n* Subjects with atrial fibrillation\n* Subjects with diabetes\n* Subjects with renal dysfunctions\n* Subjects with hyper-\u002Fhypothyroidism\n* Subjects with pheochromocytoma\n* Subjects with Raynaud's disease\n* Subjects with trembling and shivering\n* Subjects with interarm systolic difference \\> 15 mmHg\n* Subjects with interarm diastolic difference \\> 10 mmHg\n* Subjects with arm paralysis\n* Women in known pregnancy (for ARM 1 only)\n* Subjects with an arteriovenous fistula\n* Subjects with arm amputations\n* Subjects with the upper arm circumference \\\u003C 22cm or \\> 42 cm\n* Subjects with the wrist circumference \\> 21 cm\n* Subjects with the exfoliative skin diseases\n* Subjects with lymphoedema","21 Years","85 Years",{"count":401,"type":21},225,[24],"This study with N = 225 participants (1 cohort of a minimum of 85 and maximum of 140 participants, and an additional cohort with 85 participants) over 9 visits has been designed to assess the accuracy of Aktiia.product-us systolic and diastolic blood pressure measurements against double-auscultation reference measurements. In order to induce blood pressure changes and to simulate ambulatory scenarios, the study participants will be asked to perform a set of activities, involving body position changes and physical exercises. Additionally, this study will compare the heart rate measured by Aktiia.product-us against the reference readings provided by a finger pulse oximeter (as per ISO80601-2-61). The reliability of the auscultation readings will be controlled with simultaneous volume-clamp measurements.",[405,29,28],"Hypertension","2024-08-16",{"date":408,"type":40},"2024-08-19",{"date":410,"type":40},"2022-01-11",{"date":412,"type":21},"2025-03-31",{"name":414,"class":321},"Aktiia SA"]