[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"vital-signs\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:vital-signs":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,53,86,110,135,176,201,227,250],{"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":33,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100617754","the-effect-of-massage-on-sleep-quality-stress-comfort-and-vital-signs-in-preterm-infants-100617754",false,"NCT07322731","The Effect of Massage on Sleep Quality, Stress, Comfort, and Vital Signs in Preterm Infants","The Effect of Massage on Sleep Quality, Stress, Comfort, and Vital Signs in Preterm Infants: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Preterm infants born between 35-37 weeks gestational age.\n* Admitted to the neonatal intensive care unit (NICU).\n* Medically stable and cleared for massage therapy by neonatologist.\n* Parental\u002Fguardian consent obtained.\n\nExclusion Criteria:\n\n* Infants with congenital anomalies or major medical complications.\n* Infants requiring mechanical ventilation or intensive respiratory support.\n* Infants with known neurological disorders.\n* Parental\u002Fguardian refusal or inability to participate.","ALL","35 Months","37 Months",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled trial investigates the effects of massage therapy on sleep quality, stress, comfort, and vital signs in preterm infants (gestational age 35-37 weeks) admitted to the Neonatal Intensive Care Unit (NICU) at Van YYU Training and Research Hospital. Infants in the intervention group will receive a 15-minute massage three times a day for three consecutive days, while the control group will receive standard care. Data will be collected using the Premature Infant Comfort Scale, Neonatal Stress Scale, actigraphy for sleep monitoring, and vital sign measurements. The study aims to determine whether massage therapy can improve the overall well-being and development of preterm infants in NICU settings.",[27,28,29,30,31,32],"Premature Infants","Sleep Quality","İnfant Stress","İnfant Comfort","Vital Signs","NICU",[34,35,32,36,37,38,39],"Preterm infants","neonatal massage","sleep quality","stress reduction","comfort","vital signs","RECRUITING","2025-12-22",{"date":43,"type":44},"2026-01-07","ACTUAL",{"date":46,"type":44},"2025-08-15",{"date":48,"type":21},"2026-06-15",{"name":50,"class":51},"Yuzuncu Yil University","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":16,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":4,"studyType":22,"phases":65,"briefSummary":66,"conditions":67,"keywords":68,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":52},"100410688","validation-of-continuous-monitoring-of-vital-signs-in-children-with-a-connected-patch-100410688","NCT04627766","Validation of Continuous Monitoring of Vital Signs in Children With a Connected Patch","Validation of Continuous Monitoring of Vital Signs in Children With VTPatch Connected Device in the Pediatric Intensive Care Unit","VITALPICU","Inclusion Criteria:\n\n* Children (0 to 18 years old) admitted in St. Justine's Hospital's PICU.\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 is considered inappropriate by the physician or the nurse in charge because of the child's medical condition","0 Years","18 Years",{"count":64,"type":21},48,[24],"Small connected devices monitoring vital signs do not exist in children although they could be very useful to monitor patients once they have left the pediatric intensive care unit (PICU) in order to early identify patients at risk of PICU readmission.\n\nThe main objective of this study is to assess the accuracy of a connected thoracic patch (VT-Patch) for the continuous monitoring of vital signs in PICU patients.\n\nThis monitoring device will be used to monitor children in PICU for 8 hours and results will be compared to the standard of care in the unit which is the Philips monitoring system.\n\nThe investigators will assess the device's accuracy for the monitoring of 4 vital signs (SpO2, heart rate, respiratory rate and temperature) and perform exploratory assessment of three additional parameters (EKG, blood pressure and movement capture). The skin colour of each participant will be categorized based on Fitzpatrick scale and non-invasive spectroscopic method.",[31],[69,70,71,72,73,74,75,76],"Pediatrics","All-in-One","Wireless","Pateint remote monitoring","SpO2","Pulse oximeter","Skin Colour","VT-Patch","2025-12-11",{"date":79,"type":44},"2025-12-18",{"date":81,"type":44},"2025-02-02",{"date":83,"type":21},"2026-12-31",{"name":85,"class":51},"St. Justine's Hospital",{"id":87,"slug":88,"hasResults":11,"nctId":89,"briefTitle":90,"officialTitle":91,"acronym":4,"eligibilityCriteria":92,"healthyVolunteers":93,"sex":16,"minAge":94,"maxAge":95,"enrollmentInfo":96,"targetDuration":4,"studyType":98,"phases":4,"briefSummary":99,"conditions":100,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":52},"100548943","vital-signs-collection-via-comestai-app-100548943","NCT06427564","Vital Signs Collection Via \"Comestai\" App","Vital Signs Data Collection Using \"Comestai\" Application","Inclusion Criteria:\n\nPrior to enrollment in this study, subjects must meet all the following inclusion criteria:\n\n1. Subject must have the ability to understand and provide written informed consent.\n2. Male or Female subject ≥16 and ≤65 of age.\n3. Subject must be willing and able to comply with study procedures.\n\nExclusion Criteria:\n\nSubjects will be excluded from the study if any of the following conditions are present:\n\n1. Subject with compromised circulation, injury, or physical malformation of fingers, hands, ears or forehead\u002Fskull or other sensor Region of Interest (ROI) which would limit the ability to test ROI needed for the study.\n2. Subject has a tattoo in the optical path which would limit the ability to test ROI needed for the study.\n3. Subjects with severe contact allergies to standard adhesives, latex or other materials found in pulse oximetry sensors, respiration monitor electrodes or other medical sensors used for measuring vital signs.\n4. Subject with a medical condition which in the opinion of the investigator, does not allow performing the study assessments.\n5. Subject unfit to participate in the study to the judgment of the investigator.\n\nIn addition to the Inclusion\u002FExclusion criteria, the 70% of target population should include adult subjects with at least one of the following:\n\n* Pre-diabetes or diabetes HbA1C 5.7-13%\n* \\>30% of subjects with HbA1C 5.7-6.4%\n* \\>30% of subjects with HbA1C \\>6.4%\n* Hypertension with systolic measurements above 130 mmHg\n* \\>40% of subjects with systolic BP \\>130 mmHg\n* \\>20% of subjects with systolic BP \\>160 mmHg\n* Total cholesterol: \\>40% of subjects with \\>200 mg\u002Fdl and\u002For LDL above 130 mg\u002Fdl\n* Atrial fibrillation 1%\n* Smokers \\~ 20-30% of all subjects in the study\n\nNote: the same subject can have more than one of the above medical conditions. It is preferred that subjects will be treatment- naive for the medical condition they suffer from or are not under treatment at the time of participation (e.g. a subject who suffers from hypertension has not started his treatment to lower his blood pressure).",true,"16 Years","65 Years",{"count":97,"type":21},3000,"OBSERVATIONAL","The purpose of the study is to verify and validate the parameters collected from mobile devices via the app named \"Comestai\" and from reference devices. The assessments considered to define comorbidities are included.. Specifically, collection of vital parameters (Blood Pressure, Heart Rate, Respiratory Rate, Oxygen Saturation) through the \"Comestai\" Application via mobile phones (using photoplethysmographic method) and reference devices such as Withings-Blood Pressure Monitor Connect® (for Blood Pressure), Polar Verity Sense® (for Heart Rate), Masimo-finger sensor® (for Oxygen Saturation, Respiratory Rate), comparing and confirming them. Consent will be sought for the viewing and collection of blood test results that are normally included in evaluations for subjects with overweight and\u002For obesity and\u002For diabetes.\n\nEstimated time required for each measurement recording: 10-15 minutes per subject\n\nTotal number of subjects: 3000",[31],"2025-11-18",{"date":103,"type":44},"2025-11-21",{"date":105,"type":44},"2024-06-01",{"date":107,"type":21},"2026-01-01",{"name":109,"class":51},"Buzzi Children's Hospital",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":116,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":16,"minAge":62,"maxAge":4,"enrollmentInfo":118,"targetDuration":4,"studyType":98,"phases":4,"briefSummary":120,"conditions":121,"keywords":124,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":52},"100561219","remote-assessment-of-signs-and-symptoms-in-palliative-care-100561219","NCT06587321","Remote Assessment of Signs and Symptoms in Palliative Care","The ReASSure-PC Study: A Feasibility Study of Remote Assessment of Signs and Symptoms in Palliative Care","ReASSure-PC","Inclusion Criteria:\n\n* Primary diagnosis of advanced cancer or another life-limiting condition\n* Estimated prognosis greater than 3 months\n* Referred for community-based specialist palliative care\n* Living in own home (or home of family carer)\n* Living with a family carer\n\nExclusion Criteria:\n\n* Estimated prognosis less than 3 months or more than 12 months\n* Cognitive impairment - unable to provide consent \u002F complete assessments\n* Non-English speaker\n* Living in care home \u002F nursing home \u002F hospice \u002F community hospital\n* Not living with a family carer",{"count":119,"type":21},30,"Digital health interventions, including remote monitoring of patients, have been identified as a possible way to address current problems within the health service, including insufficient numbers of staff, and an increasing number of patients requiring services.\n\nThe aim of this study is to assess the feasibility of using remote monitoring for patients who are receiving palliative care and to see whether remote monitoring can improve care and outcomes for patients and their families.\n\nParticipants in this study will complete regular (daily, weekly, monthly) questionnaires online about how they are feeling. They will also be given equipment to measure their vital signs every day. The clinical team will have access to the results and be able to respond to any new problems as they arise. Patients and their carers will then complete a questionnaire at one month to assess satisfaction with the use of remote monitoring.",[122,31,123],"Palliative Care","Remote Monitoring",[125],"Remote monitoring","2025-06-23",{"date":128,"type":44},"2025-06-27",{"date":130,"type":44},"2024-04-01",{"date":132,"type":21},"2025-08-31",{"name":134,"class":51},"Our Lady's Hospice and Care Services",{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":141,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":16,"minAge":143,"maxAge":62,"enrollmentInfo":144,"targetDuration":4,"studyType":98,"phases":4,"briefSummary":145,"conditions":146,"keywords":152,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":52},"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":64,"type":21},": 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.",[31,147,148,149,150,151],"Oxygen Saturation","Children","Intensive Care Unit","Heart Rate","Respiratory Rate",[153,154,155,156,157,158,159,160,161,148,162,163,164,165],"Vital signs","SPO2","ECG","Continuous","Skin temperature","Heart rate","VitalTracer","Wearable","All-in-one","PICU","Different Skin Color","Dark skin color","Monk Scale","2025-03-05",{"date":168,"type":44},"2025-03-10",{"date":170,"type":44},"2025-02-03",{"date":172,"type":21},"2025-12-31",{"name":174,"class":175},"VitalTracer Ltd.","INDUSTRY",{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":182,"eligibilityCriteria":183,"healthyVolunteers":11,"sex":16,"minAge":62,"maxAge":4,"enrollmentInfo":184,"targetDuration":4,"studyType":98,"phases":4,"briefSummary":186,"conditions":187,"keywords":189,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":197,"leadSponsor":198,"locationsCount":200},"100557325","contactless-assessment-of-patient-vital-signs-for-triage-using-remote-photoplethysmography-in-the-emergency-department-100557325","NCT06536647","Contactless Assessment of Patient Vital Signs for Triage Using Remote Photoplethysmography in the Emergency Department","Contactless Assessment of Patient Vital Signs for Triage Using Remote Photoplethysmography in the Emergency Department - 1 Observational Study (CAPTURE-1 Study)","CAPTURE-1","Inclusion Criteria:\n\n* age \\>\u002F= 18 years\n* a valid written consent\n\nExclusion Criteria:\n\n* age \\\u003C 18 years\n* refusal of consent\u002Fpre-existing mental illness rending consent impossible",{"count":185,"type":21},1200,"Remote photoplethysmography (rPPG) is a camera-based method that enables contactless measurement of variation in light absorbance by haemoglobin as reflected by the changes in skin colour\u002Fpixel intensity unperceivable by human eyes. Beat-to-beat variation of light-absorbance can be used to estimate the change in the arterial blood volume underneath the skin and different vital signs including the blood pressure, heart rate, respiratory rate and oxygen saturation (SpO2) of the patient.\n\nThe investigators propose an observational prospective study to independently evaluate the accuracy of contactless vital sign measurements using a cell phone-based remote photoplethysmography (rPPG) technology. This study will recruit adult patients presenting to the Accident and Emergency Department (A\\&E) of Queen Mary Hospital (QMH) between 1 August 2024 and 30 October 2024. The study will be divided into 2 stages. In the initial run-in period, the investigators will collect facial video data from 200 patients to calibrate the VitalsTM system in the A\\&E environment. Then, the investigators will evaluate the accuracy of the VitalsTM in estimating vital signs of 1,000 ambulatory patients in the A\\&E setting.\n\nA trained research nurse and research assistant will be deployed from 09:00 to 17:00 on weekdays to screen for eligible patients in the A\\&E waiting hall and to recruit patient participants throughout the study period. In this study, the investigators will only recruit triage category 3 (semi-urgent) to 5 (non-urgent) patients who are clinically stable and evaluate the performance of the VitalsTM in a designated room in A\\&E. Written informed consent will be obtained from all patient participants after an explanation of the details of the study, including the rationale, benefits and risks of participation.\n\nAfter informed consent, contactless and manual measurement of patient blood pressure, heart rate, respiratory rate, body temperature and SpO2 will be carried out simultaneously in a designated room in A\\&E. A mounted light emitting diode (LED) will be used as the light source. Facial video of the patient participant will be captured using an iPhone, an iPad and a thermal camera placed at around 50 cm from the patient. A reference object for thermal and visual imaging will be placed at the background. Also, ambient temperature and light intensity will be measured.\n\nThe patient will be asked to sit down and remain still during video-recording. Manual measurement will be performed simultaneously by a trained research nurse or research assistant using standard hospital device or other medical-grade devices. A software program will be used to log vital sign measurements and recordings simultaneously so that data can be synchronised to reduce variations.\n\nThe primary outcome is the accuracy of the VitalsTM platform in estimating patient heart rate measured in intraclass correlation coefficient (ICC). The investigators will also measure of accuracy of the VitalsTM platform in estimating other vital signs, including blood pressure, respiratory rate, SpO2 and body temperature. The investigators will also evaluate patient satisfaction and comfort with the contactless and manual measurement techniques.\n\nThe accuracy of contactless measurement will be determined by calculating the ICC from the manual measurement readings as the ground truths. The investigators will also calculate the root mean square error (RMSE) and Pearson correlation between the contactless and manual measurement readings for individual vital signs. Altman Bland plot will be used to evaluate the bias and limits of agreement between two vital sign measurement methods.",[188,31],"Photoplethysmography",[188,31,190,191],"Emergency department","Triage","2025-01-14",{"date":194,"type":44},"2025-01-16",{"date":196,"type":44},"2024-09-23",{"date":172,"type":21},{"name":199,"class":51},"The University of Hong Kong",2,{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":4,"eligibilityCriteria":207,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":208,"targetDuration":4,"studyType":22,"phases":210,"briefSummary":211,"conditions":212,"keywords":217,"overallStatus":218,"whyStopped":4,"lastUpdateSubmitDate":219,"lastUpdatePostDateStruct":220,"startDateStruct":222,"completionDateStruct":223,"leadSponsor":225,"locationsCount":52},"100573778","pechakucha-as-a-reinforcement-tool-for-teaching-vital-signs-skills-in-nursing-students-100573778","NCT06750705","PechaKucha as a Reinforcement Tool for Teaching Vital Signs Skills in Nursing Students","The Effectiveness of PechaKucha as a Reinforcement Tool in Teaching Vital Signs Skills to Nursing Students: A Randomized Controlled Trial","Inclusion Criteria:\n\n* First-year nursing students currently enrolled in the nursing program.\n* Students who provide informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Foreign nationals.\n* Students repeating the course (taking the course as a retake).\n* Students who have graduated from a high school or associate degree program related to healthcare.\n* Students who are unable to attend the scheduled intervention sessions.\n* Students with physical or cognitive impairments that would affect their ability to participate in the skills assessment or intervention.",{"count":209,"type":21},100,[24],"This study aims to evaluate the effectiveness of the PechaKucha presentation method as a reinforcement tool in teaching vital signs skills to first-year nursing students. A total of 100 nursing students will participate and be divided into two groups of 50 students each. Before the intervention, all participants will complete a pre-test to assess their baseline knowledge related to vital signs. Based on the pre-test results, students will be randomized into either the experimental group or the control group.\n\nThe experimental group will receive reinforcement training using the innovative PechaKucha presentation method, while the control group will receive reinforcement through a traditional PowerPoint presentation. After the reinforcement sessions, both groups will be evaluated on their vital signs skills through a practical application exam.\n\nAdditionally, participants will complete a post-test to assess their knowledge after the intervention. Feedback and satisfaction with the training methods will also be gathered to understand their perspectives on the learning experience",[31,213,214,215,216],"Nursing Students","Teaching Method","PechaKucha Method","Skill Performance",[215,213,39],"NOT_YET_RECRUITING","2024-12-25",{"date":221,"type":44},"2024-12-30",{"date":221,"type":21},{"date":224,"type":21},"2025-01-10",{"name":226,"class":51},"Siirt University",{"id":228,"slug":229,"hasResults":11,"nctId":230,"briefTitle":231,"officialTitle":231,"acronym":4,"eligibilityCriteria":232,"healthyVolunteers":93,"sex":16,"minAge":62,"maxAge":4,"enrollmentInfo":233,"targetDuration":4,"studyType":22,"phases":235,"briefSummary":236,"conditions":237,"keywords":239,"overallStatus":218,"whyStopped":4,"lastUpdateSubmitDate":241,"lastUpdatePostDateStruct":242,"startDateStruct":244,"completionDateStruct":246,"leadSponsor":248,"locationsCount":4},"100565032","the-effect-of-acupressure-applied-before-suturing-procedure-in-the-emergency-department-on-anxiety-and-vital-signs-100565032","NCT06636903","The Effect of Acupressure Applied Before Suturing Procedure in the Emergency Department on Anxiety and Vital Signs","Inclusion Criteria:\n\n* Suturing is done with local anesthesia,\n* Those who are 18 years or older,\n* Conscious, oriented and cooperative,\n* Able to read and understand Turkish,\n* Agreeing to participate in the study,\n* Anxiety not diagnosed,\n* Not using medication for anxiety,\n* No acupressure experience,\n* No physical problems that would prevent acupressure application to Ht7 and Li4 points,\n* Not pregnant,\n* Patients who sign the \\"Voluntary Informed Consent Form\\" will be included.\n\nExclusion Criteria:\n\n* Those who are under 18 years of age,\n* Unconscious, unoriented and uncooperative,\n* Cannot read and understand Turkish,\n* Those who do not agree to participate in the study,\n* -Diagnosed with anxiety,\n* -Using medication for anxiety (anxiolytic, antidepressant, antipsychotic, etc.),\n* Having previous acupressure experience,\n* Having a physical problem that prevents the application of acupressure to Ht7 and Li4 points,\n* Pregnant,\n* Patients who do not sign the \\"Voluntary Informed Consent Form\\" will not be included.",{"count":234,"type":21},146,[24],"This study suggests that the anxiety experienced by patients during suturing in the emergency department can be reduced with acupressure and offers a research proposal on vital signs.\n\nProblem: During suturing in the emergency department, patients experience high levels of anxiety due to the pain they experience and fear of the procedure. This situation complicates the treatment process, negatively affects the health of patients and creates a difficult situation for healthcare professionals.\n\nSolution Suggestion: Acupressure can be used as a non-invasive, safe and effective method to reduce patients\\' anxiety. Acupressure reduces pain, provides relaxation and reduces anxiety by increasing the secretion of endorphins in the body.\n\nPurpose of the Study: The purpose of this study is to evaluate the effects of applying acupressure to patients before suturing in the emergency department on their anxiety levels and vital signs (such as blood pressure, heart rate).\n\nIn summary, this research has a significant potential that emergency room nurses can improve patients\\' quality of life and make treatment processes more effective by using acupressure in patient care.\n\nKey Words: Acupressure, Suturing, Anxiety, Vital Signs, Emergency Department",[238,31],"Anxiety",[240],"Acupressure, Suturing, Anxiety, Vital Signs, Emergency Department","2024-10-10",{"date":243,"type":44},"2024-10-15",{"date":245,"type":21},"2024-10-01",{"date":247,"type":21},"2025-04-30",{"name":249,"class":51},"Ezgi BOLAT",{"id":251,"slug":252,"hasResults":11,"nctId":253,"briefTitle":254,"officialTitle":254,"acronym":4,"eligibilityCriteria":255,"healthyVolunteers":11,"sex":16,"minAge":62,"maxAge":4,"enrollmentInfo":256,"targetDuration":4,"studyType":22,"phases":258,"briefSummary":259,"conditions":260,"keywords":4,"overallStatus":218,"whyStopped":4,"lastUpdateSubmitDate":263,"lastUpdatePostDateStruct":264,"startDateStruct":266,"completionDateStruct":268,"leadSponsor":270,"locationsCount":4},"100551883","the-effect-of-book-reading-on-comfort-hope-anxiety-and-vital-signs-of-intensive-care-unit-patients-100551883","NCT06465875","The Effect of Book Reading on Comfort, Hope, Anxiety and Vital Signs of Intensive Care Unit Patients","Inclusion Criteria:\n\n1. Over 18 years of age,\n2. Stable clinical condition after intensive care unit admission,\n3. Have no physical or mental impairment in answering the questions,\n4. No verbal communication disability (hearing and speech),\n5. No diagnosed psychiatric disorder,\n6. With a Glasgow Coma Scale score of 15,\n7. Not receiving sedation for at least 12 hours,\n8. Will be hospitalized for at least 3 days from the time of enrollment in the study,\n9. Individuals who agree to participate in the study will be included in the study.\n\nExclusion Criteria:\n\n1. People with hearing or vision problems,\n2. Intubated,\n3. Any diagnosed neurological or psychological disorder,\n4. Transferred to another unit or exitus before the specified period,\n5. Individuals who do not agree to participate in the study will not be included in the study.",{"count":257,"type":21},70,[24],"This study was planned to investigate the effect of reading aloud books on comfort, hope, anxiety and vital signs in patients hospitalized in intensive care unit. This study was designed as a randomized controlled clinical trial. Data will be collected by using the Descriptive Characteristics Questionnaire, General Comfort Scale, Dispositional Hope Scale, State-Trait Anxiety Inventory, and the Vital Signs Monitoring Form.",[261,262,238,31],"Hope","Comfort","2024-06-13",{"date":265,"type":44},"2024-06-20",{"date":267,"type":21},"2024-07-01",{"date":269,"type":21},"2024-12-31",{"name":271,"class":51},"TC Erciyes University"]