[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pressure-injury-prevention\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pressure-injury-prevention":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,48,74,100,130],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100648815","effect-of-a-risk-based-perioperative-pressure-injury-prevention-bundle-in-elective-surgery-patients-100648815",false,"NCT07725068","Effect of a Risk-Based Perioperative Pressure Injury Prevention Bundle in Elective Surgery Patients","Effect of a Risk-Based Perioperative Pressure Injury Prevention Bundle on Pressure Injury Development in Patients Undergoing Elective Surgery: A Randomized Controlled Trial","RiPPB","Inclusion Criteria:\n\n* Scheduled to undergo elective orthopedic, general, neurosurgical, or urological surgery\n* Anticipated surgical duration greater than 3 hours\n* No pressure injury present preoperatively\n* Willing and able to provide informed consent to participate\n\nExclusion Criteria:\n\n* Existing pressure injury at enrollment\n* Undergoing emergency surgery\n* Known allergy to dressing\u002Fadhesive materials used in the prevention bundle\n* Severe dermatological condition affecting skin integrity\n* Unplanned postoperative intensive care unit admission",true,"ALL","18 Years",{"count":21,"type":22},138,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study evaluates whether a risk-based perioperative pressure injury prevention bundle reduces the development of pressure injuries in patients undergoing elective surgery lasting 3 hours or longer.\n\nPressure injuries that develop during and after surgery are a common patient safety problem, especially in older adults and in longer procedures. In this randomized controlled trial, patients will be assigned by chance to either an intervention group or a control group. In the intervention group, each patient's pressure injury risk will be assessed before surgery using the Braden Scale together with additional perioperative risk factors, and patients will then receive one of three prevention bundles matched to their risk level (low, moderate, or high). The high-risk bundle includes prophylactic silicone foam dressings on the sacrum and heels, targeted positioning, and pressure-redistributing support surfaces. The control group will receive standard perioperative care without risk-based bundling, although Braden Scale assessment will still be performed.\n\nSkin assessments will be conducted at four time points: before surgery, in the post-anesthesia care unit, at 2-4 hours after surgery, and at 24 hours after surgery. The main outcome is whether patients develop early signs of pressure injury, including non-blanchable erythema, within the first 24 postoperative hours. The study hypothesizes that patients receiving the risk-based prevention bundle will have a lower incidence of postoperative pressure injury and non-blanchable erythema compared with patients receiving standard care.",[28,29,30,31],"Pressure Ulcer (PU)","Pressure Injury Prevention","Perioperative Care","Braden Scale",[33,34],"Surgical Wound","risk assessment","NOT_YET_RECRUITING","2026-07-21",{"date":38,"type":39},"2026-07-24","ACTUAL",{"date":41,"type":22},"2026-08-01",{"date":43,"type":22},"2026-12-30",{"name":45,"class":46},"Acibadem University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":23,"phases":57,"briefSummary":58,"conditions":59,"keywords":60,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":4},"100640354","the-effect-of-silicone-foam-dressing-and-repositioning-on-the-prevention-of-endotracheal-tube-related-pressure-injuries-100640354","NCT07608484","The Effect of Silicone Foam Dressing and Repositioning on the Prevention of Endotracheal Tube-related Pressure Injuries","The Effect of Silicone Foam Dressing and Repositioning on the Prevention of Endotracheal Tube-related Pressure Injuries: A Randomized Comparative Study","Inclusion Criteria:\n\n* Aged 18 years or older\n* Patients admitted to the General Intensive Care Unit and receiving mechanical ventilation support\n* Absence of pressure injuries, other lesions, or anomalies on the inner and outer surfaces of the lips and at the oral commissures prior to intubation\n* Absence of congenital anomalies that could interfere with the assessment of pressure injuries on the inner and outer surfaces of the lips and at the oral commissures\n\nExclusion Criteria:\n\n* Receiving mechanical ventilation support initiated prior to admission to the intensive care unit\n* Undergoing nasotracheal intubation\n* History of any intraoral surgical procedure\n* Presence of a contraindication to repositioning of the endotracheal tube\n* More than one hour having elapsed since intubation (for Group 1)",{"count":56,"type":22},75,[25],"The endotracheal tube is one of the medical devices most associated with pressure injuries related to medical devices. This study aims to evaluate the effectiveness of applying a silicone foam dressing over the endotracheal tube and repositioning the endotracheal tube in preventing endotracheal tube-related pressure injuries in patients receiving mechanical ventilation support.",[29],[61,62,63,64],"Pressure injury","Intensive care unit","Endotracheal tube","Prevention","2026-05-30",{"date":67,"type":39},"2026-06-02",{"date":69,"type":22},"2026-06-01",{"date":71,"type":22},"2027-08-30",{"name":73,"class":46},"Hacettepe University",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":23,"phases":84,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":4},"100609373","a-trial-to-investigate-the-new-caulis-pro-low-air-loss-lal-system-100609373","NCT07213739","A Trial to Investigate the New Caulis Pro® Low Air Loss (LAL) System","A Laboratory Trial to Investigate the Biomechanical and Physiological Responses to Prolonged Lying Postures During CLP When Combined With Pulsation Therapy on Caylis Pro® Low Air Loss (LAL) System","Inclusion Criteria:\n\n* Age 18-85\n* Healthy male or female\n\nExclusion Criteria:\n\n* Systemic skin disease\n* History of pressure ulcers in the sacrum or heels\n* Diabetes\n* Long term steroid use\n* Inability to maintain lying posture for prolonged periods","85 Years",{"count":83,"type":22},20,[25],"Investigation of biomechanical and physiological functions of laying on a new mattress in healthy volunteers.",[87,29],"Health Adult Subjects",[89],"caylis, Arjo","2025-10-02",{"date":92,"type":39},"2025-10-09",{"date":94,"type":22},"2025-09-30",{"date":96,"type":22},"2026-04-30",{"name":98,"class":99},"Arjo AB","INDUSTRY",{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":104,"acronym":4,"eligibilityCriteria":105,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":106,"enrollmentInfo":107,"targetDuration":4,"studyType":23,"phases":109,"briefSummary":110,"conditions":111,"keywords":116,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":47},"100591273","the-effect-of-artificial-intelligence-assisted-visual-case-analysis-on-nursing-students-knowledge-and-attitudes-towards-pressure-injury-prevention-a-single-blind-randomized-controlled-trial-100591273","NCT06978283","The Effect of Artificial Intelligence-assisted Visual Case Analysis on Nursing Students' Knowledge and Attitudes Towards Pressure Injury Prevention: A Single-blind Randomized Controlled Trial","Inclusion Criteria:\n\n* Taking the Fundamentals of Nursing II course for the first time\n* Not working as a nurse in a health institution.\n* Volunteering to participate in the study.\n\nExclusion Criteria:\n\n* Having previously received patient pressure injury prevention training;\n* Having repeated the Fundamentals of Nursing II course;\n* Having difficulty speaking and understanding Turkish;\n* Exceeding the course attendance time\n* Not attending pressure injury prevention training and evaluation\n* Filling in incomplete data\n* Graduating from a health-related high school or university.","24 Years",{"count":108,"type":22},84,[25],"The goal of this clinical trial is to examine the effect of artificial intelligence-assisted visual case analysis on nursing students' knowledge and attitudes towards pressure injury prevention. The main hypotheses it aims to answer are:\n\n* AI-assisted visual case analysis affects nursing students' knowledge about pressure injury prevention.\n* AI-assisted visual case analysis affects nursing students' attitudes toward pressure injury prevention.\n\nResearchers will compare AI-assisted case analysis to conventional case analysis to see if it affected nursing students' knowledge and attitudes about pressure injury prevention.\n\nParticipants,\n\n* The case group will shown an AI-supported presentation explaining the pressure injury prevention case. The control group will given a classic case analysis.\n* At the end of the case, the PUPKAI and APuP scales will administered to the students in written form in the classroom.",[112,113,114,29,115],"Artificial Intelligence (AI)","Visual Case Analysis","Nursing Students","A Single-blind Randomized Controlled Trial",[117,118,114,112,119,120],"AI-assisted","visual case analysis","pressure injury prevention","randomized controlled trial","2025-05-10",{"date":123,"type":39},"2025-05-18",{"date":125,"type":22},"2025-05-09",{"date":127,"type":22},"2025-07-10",{"name":129,"class":46},"Çankırı Karatekin University",{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":136,"enrollmentInfo":137,"targetDuration":4,"studyType":23,"phases":139,"briefSummary":140,"conditions":141,"keywords":142,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":4},"100580057","the-effect-of-web-based-training-and-counseling-given-to-caregivers-on-the-pressure-injury-risk-level-of-dependence-independence-and-caregivers-burden-of-care-in-bedridden-patients-100580057","NCT06832345","The Effect of Web-Based Training and Counseling Given to Caregivers on the Pressure Injury Risk, Level of Dependence-Independence, and Caregivers' Burden of Care in Bedridden Patients","Inclusion Criteria:\n\nThe patient;\n\n* Being over 18 years of age\n* Being open to communication (Mini Mental Test Score \\>25 points),\n* Medium or high risk according to the Braden pressure injury assessment scale (score ≤14 according to the Braden pressure injury risk assessment scale)\n* Being at least a moderately dependent patient according to the Barthel Index (score ≤90 according to the Barthel Index) The caregiver;\n* Being primarily responsible for patient care,\n* Being over 18 years of age\n* Having a family bond with the patient,\n* No monthly fee for providing care, (except for those receiving a monthly care pension from the state)\n* Lack of healthcare workers (physician, midwife, nurse),\n* Ability to read and write,\n* Having a smartphone and internet access,\n* Accepting a home visit,\n* There is no physical or psychiatric obstacle that prevents communication,\n\nExclusion Criteria:\n\nThe patient;\n\n* Having cancer,\n* Having an active skin disease,\n* Blood glucose and blood pressure are not under control,\n* Use of medication that may be associated with pressure injury (corticosteroid, immunosuppressive, sedative medication, antineoplastic medication, norepinephrine) is an exclusion criterion from the study.\n\nCriteria for Exclusion from the Study The patient;\n\n* The patient is hospitalized,\n* The patient\\'s exitus is a criterion for exclusion from the study.","100 Years",{"count":138,"type":22},31,[25],"Education and counseling of patients and caregivers, either face-to-face or using various communication technologies, are reported to have significant effects. Nurses are in a key position in the education and counseling of patients and their relatives for the prevention of pressure injury. Although the share of health technologies in the management of pressure injury is important, it is also important for nurses to use these technologies. Web-based education, which is a part of health technologies, is defined as an education and training program created by using the features of internet and computer technologies.",[29],[119],"2025-02-14",{"date":145,"type":39},"2025-02-18",{"date":147,"type":22},"2025-03-01",{"date":149,"type":22},"2025-06-01",{"name":151,"class":46},"Istanbul University - Cerrahpasa"]