[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"physiological-parameter\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:physiological-parameter":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,42,68,101,129],{"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":4,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":4},"100608197","predicting-success-of-decannulation-using-wearable-derived-physiology-100608197",false,"NCT07198425","Predicting Success of Decannulation Using Wearable-derived Physiology","Predicting Success of Decannulation Using Wearable-derived Physiology : A Prospective Cohort Study","Inclusion Criteria:\n\n* 18 years ≤ Age ≤ 90 years, non-mechanically ventilated patients.\n* Tracheotomy completed, ≥48 hours since cannula placement (postoperative early edema has stabilized).\n* Patient or legal representative has provided informed consent.\n\nExclusion Criteria:\n\n* Recent (≤48 hours) major neck\u002Fupper airway surgery requiring avoidance of upper airway airflow impact.\n* Severe consciousness disorder\u002Fdelirium (RASS ≤ -3 or ≥ +2), extreme anxiety\u002Finability to cooperate.\n* Total laryngectomy or laryngo-tracheal separation.\n* Oral endotracheal intubation.\n* Age \\\u003C18 years, Age \\> 90years.\n* Malignant tumor with an expected survival time ≤ 6 months.\n* Patients or legal representatives unable to obtain informed consent.\n* Known contraindications for tracheotomy decannulation.\n* Unable to comply with the use of wearable devices","ALL","18 Years","90 Years",{"count":20,"type":21},120,"ESTIMATED","OBSERVATIONAL","The population included in this study consists of tracheostomy patients admitted to the pulmonary department of Beijing Rehabilitation Hospital, undergoing decannulation rehabilitation treatment. Once patient conditions stabilized, they were all transitioned to the decannulation process established by our department in 2018, which utilizes a speaking valve instead of capping. Each enrolled patient received physiological monitoring upon admission and the day prior to the initial use of the speaking valve, with continuous monitoring for 24 hours through wearable devices.The monitored physiological parameters were compared between the successful decannulation group and the failed decannulation group, and a predictive decannulation model was established in advance based on clinical parameters.\n\nDecannulation criteria: If the patient can tolerate wearing the speaking valve continuously for 4 hours (gradually increasing the duration: 30 minutes, 1 hour, 2 hours, 4 hours), and if PEF \\> 100 liters\u002Fmin, planned removal of the tracheostomy tube can be considered.\n\nBased on decannulation outcomes, patients were categorized into the successful decannulation group and the failed decannulation group.\n\nSuccessful decannulation group: Patients who successfully completed the decannulation process and had their tubes removed, with no reinsertion of the tracheostomy tube or endotracheal intubation within 48 hours after decannulation.\n\nFailed decannulation group: Patients who did not pass the decannulation process, and the multidisciplinary team advised against removal of the tracheostomy tube; or patients who passed the decannulation process and had the tracheostomy tube removed but required reinsertion of the tracheostomy tube or endotracheal intubation within 48 hours due to medical conditions.",[25,26],"Tracheostomy Decannulation","Physiological Parameter",[28,26,29],"speaking valve","tracheostomy decannulation","NOT_YET_RECRUITING","2026-05-23",{"date":33,"type":34},"2026-05-28","ACTUAL",{"date":36,"type":21},"2026-06-02",{"date":38,"type":21},"2026-12-31",{"name":40,"class":41},"Bin Zhang","OTHER",{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":49,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":57,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":66,"locationsCount":67},"100639533","predicting-the-clinical-advantages-of-speaking-valves-through-wearable-devices-100639533","NCT07587762","Predicting the Clinical Advantages of Speaking Valves Through Wearable Devices","Predicting the Clinical Advantages of Speaking Valves Through Wearable Devices:A Prospective Cohort Study","Inclusion Criteria:\n\n* 90 years≥Age≥18 years;\n* Tracheotomy post-operation\\>48 hours；\n* Weaned off mechanical ventilation;\n* Clinically stable condition;\n* Tolerable for cuff deflation;\n* Able to tolerate wearing a speaking valve continuously for 30 minutes;\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Patients with abnormal skin conditions preventing continuous wearing of monitoring devices;\n* Inability to tolerate wearing a speaking valve continuously for 30 minutes;\n* Interruption of physiological monitoring data;\n* Poor quality of physiological monitoring data;\n* Recently underwent neck\u002Fupper airway surgery (≤48 hours, to avoid airflow impact on the upper airway);\n* Severe consciousness disturbance\u002Fdelirium (RASS score≤-3 or ≥ +2), extreme anxiety\u002Funcooperativeness;\n* Total laryngectomy or laryngotracheal separation;\n* Age \\\u003C18 years or \\>90 years;\n* Malignant tumor with an expected survival time ≤6 months;\n* The patient or legal representative is unable to sign the informed consent form.",{"count":20,"type":21},"INTERVENTIONAL",[52],"NA","The population included in this study consists of tracheostomy patients admitted to the pulmonary department of Beijing Rehabilitation Hospital, undergoing decannulation rehabilitation treatment. Once patient conditions stabilized, they were all transitioned to the decannulation process established by our department in 2018, which utilizes a speaking valve instead of capping.The initial duration for the patient to wear the speaking valve is 30 minutes.The monitoring period for wearable devices is from 1 hour before the initial use of the speaking valve to 1 hour after its removal.Monitored for a total of 2 hours and 30 minutes.Explore the clinical benefits of the speaking valve by comparing the changes in patients' physiological parameters and clinical index metrics before and after using the speaking valve.\n\nCriteria for the successful use of the speaking valve for 30 minutes:\n\n1. Breathing is steady at rest: no apparent dyspnea, chest tightness, or orthopnea, etc.\n2. Heart rate, blood pressure, and SpO₂ are all stable overall.SpO₂ reduction from baseline \\\u003C 5%.\n3. No frequent need for emergency sputum suction or indications of sputum blockage while wearing it.",[26,55,56],"Wearable Devices","Tracheostomy",[28,55,58,26],"tracheostomy","RECRUITING","2026-05-11",{"date":62,"type":34},"2026-05-14",{"date":64,"type":34},"2026-04-16",{"date":38,"type":21},{"name":40,"class":41},1,{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":16,"minAge":75,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":50,"phases":79,"briefSummary":80,"conditions":81,"keywords":87,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":67},"100571898","progressive-relaxation-exercises-before-mobilizationeffects-on-pain-anxiety-and-physiologic-parameters-cabg-patients-100571898","NCT06726239","Progressive Relaxation Exercises Before Mobilization:Effects on Pain, Anxiety and Physiologic Parameters CABG Patients","The Effect of Progressive Relaxation Exercises Applied Before Mobilization on Pain, Anxiety and Physiological Parameters in Patients With Coronary Artery Bypass Graft Surgery","Inclusion Criteria:\n\n* Ability to read and write in Turkish,\n* Analgesics given ≥4h before assessment,\n* Conscious and communicative,\n* Elective coronary artery bypass graft surgery planned,\n* Patients undergoing coronary artery bypass graft surgery for the first time were included in the study.\n\nExclusion Criteria:\n\n* Diagnosed with a psychiatric or neurological disorder,\n* Diagnosis of a musculoskeletal condition that could affect mobilization,\n* Patients with hearing and vision loss,\n* Patients participating in another clinical trial during the same period,\n* Patients who developed any complications during the postoperative period were excluded.","35 Years","65 Years",{"count":78,"type":21},68,[52],"This study is planned as a randomized controlled experimental study to determine the effect of progressive relaxation exercises applied before mobilization on pain, anxiety and physiological parameters in patients undergoing coronary artery bypass graft surgery.",[82,83,26,84,85,86],"Pain","Anxiety","Mobilization","Coronary Artery Bypass Graft Surgery (CABG)","PROGRESSIVE MUSCLE RELAXATION EXERCISES",[88,89,83,90,91],"coronary artery bypass graft surgery","pain","progressive relaxation exercise","physiological parameter","2025-06-26",{"date":94,"type":34},"2025-07-01",{"date":96,"type":34},"2024-05-31",{"date":98,"type":21},"2025-06-30",{"name":100,"class":41},"Istanbul University - Cerrahpasa",{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":107,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":76,"enrollmentInfo":109,"targetDuration":4,"studyType":50,"phases":111,"briefSummary":112,"conditions":113,"keywords":117,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":67},"100596004","the-effect-of-virtual-reality-and-eye-mask-during-dressing-after-cabg-surgery-100596004","NCT07039812","The Effect of Virtual Reality and Eye Mask During Dressing After CABG Surgery","The Effect of Virtual Reality and Eye Mask Application During Dressing After Coronary Artery Bypass Graft Surgery on Sternotomy Pain, Anxiety, and Physiological Parameters","CABG","Inclusion Criteria:\n\n* Adults aged 18-65 years\n* First-time coronary artery bypass graft (CABG) surgery for coronary artery disease\n* ASA physical status I, II, or III\n* Conscious, oriented, and cooperative\n* Able to communicate verbally\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Presence of sternal wound infection or inflammation\n* Intubated at the time of assessment\n* Undergoing revision surgery\n* Receiving anesthesia or sedation in the ICU\n* Experiencing intraoperative or postoperative complications\n* Inability to speak Turkish\n* Hearing or visual impairment\n* Diagnosed psychiatric or cognitive disorder\n* Diagnosis of epilepsy\n* Body mass index (BMI) ≥ 30\n* Participation in another clinical trial during the same period",{"count":110,"type":21},90,[52],"This study aims to evaluate the effects of virtual reality (VR) and eye mask (EM) applications on pain, anxiety, and physiological parameters during dressing after Coronary Artery Bypass Graft (CABG) surgery.\n\nPostoperative dressing procedures, especially after sternotomy, often cause significant pain and anxiety in patients. These issues can negatively impact recovery and increase the need for medication. Non-pharmacological interventions such as VR and EM may help reduce these symptoms.\n\nIn this randomized controlled trial, 90 patients are divided into three groups: VR group, EM group, and a control group receiving standard care. Pain and anxiety levels are monitored baseline, immediately after, and 15 minutes after both the first and second dressing procedures. Physiological parameters are measured baseline, during, immediately after, and 15 minutes after both dressing procedures. Additionally, analgesic use is followed baseline and immediately after each dressing procedure. The study is conducted in a cardiovascular intensive care unit in Istanbul, Türkiye. It is expected that the findings will support the integration of VR and EM as effective, low-cost, and non-invasive options for postoperative care, improving patient comfort and healthcare quality.",[107,26,114,115,116],"Postoperative Pain","Postoperative Anxiety","Coronary Artery Disease",[118,119,120,121,83,26],"Coronary Artery Bypass Graft","Virtual Reality","Eye Mask","Pain Management","2025-06-25",{"date":92,"type":34},{"date":125,"type":34},"2025-02-24",{"date":127,"type":21},"2025-08-30",{"name":100,"class":41},{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":135,"eligibilityCriteria":136,"healthyVolunteers":137,"sex":16,"minAge":138,"maxAge":139,"enrollmentInfo":140,"targetDuration":4,"studyType":50,"phases":142,"briefSummary":143,"conditions":144,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":146,"lastUpdatePostDateStruct":147,"startDateStruct":149,"completionDateStruct":151,"leadSponsor":153,"locationsCount":4},"100552446","this-study-assess-some-physiological-parameters-blood-picture-and-hemodynamic-parameters-blood-pressure-respiratory-assess-by-spo2-during-different-periods-in-laparoscopic-surgery-100552446","NCT06473194","This Study Assess Some Physiological Parameters, Blood Picture, and Hemodynamic Parameters, Blood Pressure, Respiratory Assess by SPO2, During Different Periods in Laparoscopic Surgery","Physiological and Biochemical Effects of Laparoscopic Anesthesia and Surgery","laparoscopy","Inclusion Criteria:\n\n1. elective abdominal surgery\n2. a healthy, fit person\n3. use of general anesthetics\n4. use of pneumoperitoneum and CO2 insufflation\n\nExclusion Criteria:\n\n1. emergency condition\n2. patient with cardiovascular disease",true,"20 Years","60 Years",{"count":141,"type":21},60,[52],"Laparoscopic surgery is widely used now. These benefits included many items, e.g. reducing post-operative pain, cosmetic the result was improved, and the patient also had more satisfaction for the patient and reduced hospital stay. This surgery involved insufflation of gas into the peritoneal cavity, producing pneumoperitoneum, and causing an increase in intra-abdominal pressure. The raised intraabdominal pressure of the pneumoperitoneum, the patient's position alteration, and the absorption of carbon dioxide into the abdomen have a direct effect on causing a change in physiology, especially in the cardiovascular and respiratory systems. These effects, as well as a direct effect of gas insufflation, may have significant effects on the patient especially if the patient has a comorbidity or is elderly.",[145,26],"Anesthesia Complication","2024-06-21",{"date":148,"type":34},"2024-06-25",{"date":150,"type":21},"2024-10-01",{"date":152,"type":21},"2026-11-01",{"name":154,"class":41},"Mohammed Abdulhameed"]