[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Erzincan Binali Yildirim Universitesi\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":185},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,46,75,107,132,156],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":32,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":4},"100636831","mentor-supported-digital-literacy-training-100636831",false,"NCT07570797","Mentor-Supported Digital Literacy Training","Effects of Digital Literacy Mentoring Delivered by Young Migrants on eHealth and Digital Literacy Among Older Migrants: A Randomized Controlled Trial","MEDOYE","Inclusion Criteria:Young Participants (Migrants)\n\n* Aged between 18-64 years\n* Being a migrant\n* Literate (able to read and write)\n* Able to speak and write in Turkish\n* Able to communicate verbally\n* Having access to internet at home or workplace\n* Having access to a smartphone or a phone that belongs to a family member and can be used by the participant\n* Able to use the internet\n* Willing to participate in the study\n* Willing to act as a mentor\n\nOlder Participants (Migrants)\n\n* Aged between 65-74 years\n* Literate in Turkish\n* Having internet access at home\n* Using a smartphone\n\nExclusion Criteria:\n\nYoung Participants (Migrants)\n\n* Presence of visual or hearing impairments that would prevent participation in the study\n* Having a physical or mental health condition that may interfere with participation\n* Inability to attend training sessions regularly during the intervention period\n\nOlder Participants (Migrants)\n\n* Presence of visual or hearing impairments that would prevent participation in the study\n* Inability to attend training sessions regularly during the intervention period",true,"ALL","18 Years","74 Years",{"count":22,"type":23},80,"ESTIMATED","INTERVENTIONAL",[26],"NA","Purpose This study is a randomized controlled experimental trial aiming to evaluate the effects of mentoring-based digital literacy training delivered by young migrants on older migrants' eHealth literacy and their ability to seek and verify health information in digital environments. The study will be conducted among young and older Ahiska Turkish migrants living in the Üzümlü district of Erzincan province.\n\nMethod The study will be conducted in two phases. In the first phase, young migrants will receive digital literacy training that includes mentoring skills. In the second phase, these individuals will provide training to older migrants.\n\nThe sample size has been determined based on a power analysis and will consist of a total of 80 participants. Data will be collected using the eHealth Literacy Scale and the Digital Health Information Seeking and Verification Scale. Data will be analyzed using SPSS software, and appropriate parametric and\u002For non-parametric tests will be applied.\n\nTraining sessions will be conducted in controlled environments, in small groups, and tailored to participants' needs. Participant follow-up will be maintained throughout the process to support the sustainability of the intervention.\n\nResearch Hypotheses Primary Hypothesis\n\n* H0: Mentoring-based digital literacy training delivered by young migrants has no effect on older migrants' levels of eHealth literacy and digital literacy.\n* H1: Mentoring-based digital literacy training delivered by young migrants has a significant effect on older migrants' levels of eHealth literacy and digital literacy.\n\nSecondary Hypothesis\n\n* H0: Mentoring-based digital literacy training delivered by young migrants has no effect on older migrants' eHealth literacy levels.\n* H2: Mentoring-based digital literacy training delivered by young migrants has a significant effect on older migrants' eHealth literacy levels.\n\nThird Hypothesis\n\n* H0: Mentoring-based digital literacy training delivered by young migrants has no effect on older migrants' digital literacy levels.\n* H3: Mentoring-based digital literacy training delivered by young migrants has a significant effect on older migrants' digital literacy levels.",[29,30,31],"eHealth Literacy","Digital Literacy","Migrants",[33],"Digital literacy, E-health literacy, Migrants, Mentorship, Older adults","NOT_YET_RECRUITING","2026-04-30",{"date":37,"type":38},"2026-05-06","ACTUAL",{"date":40,"type":23},"2026-07-01",{"date":42,"type":23},"2027-02-25",{"name":44,"class":45},"Erzincan Binali Yildirim Universitesi","OTHER",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":24,"phases":56,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},"100632442","peng-vs-deep-iliacus-plane-block-in-intertrochanteric-femur-fractures-100632442","NCT07513740","PENG vs Deep Iliacus Plane Block in Intertrochanteric Femur Fractures","Comparison of the Analgesic Efficacy of the PENG Block and the Deep Iliacus Plane Block During Positioning for Spinal Anesthesia and in the Postoperative Period in Intertrochanteric Femur Fractures: A Prospective, Randomized Controlled Study","Inclusion Criteria:\n\n* Patients scheduled for elective surgery for intertrochanteric femur fractures\n* Patients with ASA physical status I, II, or III\n* Patients aged between 30 and 85 years\n\nExclusion Criteria:\n\n* Patients with ASA physical status IV or higher\n* Patients undergoing emergency surgery\n* Patients who refuse to participate or withdraw consent during the study\n* Patients with cognitive dysfunction such as Alzheimer's disease, dementia, or delirium\n* Patients with a history of local anesthetic toxicity\n* Patients with infection at the planned block site\n* Patients with bleeding diathesis\n* Patients undergoing additional surgical procedures or additional anesthesia (e.g., general anesthesia)\n* Patients with a history of chronic opioid use or receiving treatment for neuropathic pain","75 Years",{"count":55,"type":23},75,[26],"Intertrochanteric femur fractures are common in elderly patients and are associated with significant pain. Providing effective analgesia is clinically important both during positioning for spinal anesthesia and in the postoperative period in this patient population.\n\nThe Pericapsular Nerve Group (PENG) block is a regional anesthesia technique that targets the articular branches of the hip capsule and may provide effective analgesia with motor-sparing potential. The Deep Iliacus Plane Block (DIPB) is a newer approach that may spread to both the articular branches and the lateral femoral cutaneous nerve.\n\nAlthough both blocks are used in patients with intertrochanteric fractures, there is a lack of sufficient randomized controlled data comparing their effectiveness for pain during positioning for spinal anesthesia and for postoperative analgesia. Therefore, it is important to determine which technique provides greater clinical benefit.\n\nThe aim of this study is to compare the analgesic efficacy of the PENG block and the Deep Iliacus Plane Block during positioning for spinal anesthesia and in the postoperative period in patients undergoing surgery for intertrochanteric femur fractures.",[59,60],"Postoperative Analgesia","Hip Surgery",[62,60,63,64],"Deep İliacus Plane Block","PENG","Meta-PENG","RECRUITING","2026-03-31",{"date":68,"type":38},"2026-04-07",{"date":70,"type":38},"2026-03-01",{"date":72,"type":23},"2027-03-01",{"name":44,"class":45},1,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":83,"enrollmentInfo":84,"targetDuration":4,"studyType":24,"phases":86,"briefSummary":87,"conditions":88,"keywords":92,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":74},"100610908","im-njection-pain-cold-spray-and-stress-ball-100610908","NCT07233694","IM İnjection-PAIN-Cold Spray and Stress Ball","The Effects of Cold Spray and Stress Ball Methods on Perceived Pain, Comfort, and Satisfaction During Intramuscular Injection: A Randomized Controlled Trial","CSB-PAIN","Inclusion Criteria:\n\nAdults aged 18-65 years\n\nReceiving intramuscular injection\n\nVoluntarily agreed to participate in the study\n\nExclusion Criteria:\n\nSkin disease at the injection site\n\nAllergy to cold spray\n\nCognitive impairment preventing cooperation","65 Years",{"count":85,"type":23},66,[26],"Brief Summary:\n\nIntramuscular (IM) injection is a widely used method for drug administration, with over 12 billion applications globally each year. Despite its therapeutic advantages, IM injection often causes pain, which can negatively impact patient comfort and lead to injection fear, non-compliance, and avoidance of healthcare services. Effective pain management during IM injection is an ethical and professional responsibility for nurses. This randomized controlled study aims to compare the effectiveness of cold spray and stress ball squeezing methods against standard practice in reducing IM injection-related pain. The study will be conducted in the emergency department of a university hospital in Turkey between March and June 2025, involving 66 patients prescribed IM diclofenac sodium. Participants will be randomly assigned to one of three groups: cold spray, stress ball, or control. Pain will be assessed using the Visual Analog Scale (VAS) within the first minute after injection.",[89,90,91],"Pain, Procedural","Acute Pain","Injection Site",[93,94,95,96,97,98],"muscle intramuscular injection","Nursing","Nursing practice","Pain","stress ball","cold spray","2025-11-16",{"date":101,"type":38},"2025-11-18",{"date":103,"type":23},"2025-11-25",{"date":105,"type":23},"2025-12-10",{"name":44,"class":45},{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":11,"sex":18,"minAge":113,"maxAge":114,"enrollmentInfo":115,"targetDuration":4,"studyType":24,"phases":117,"briefSummary":118,"conditions":119,"keywords":121,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":4},"100578258","the-effect-of-bathtub-bath-on-stress-and-comfort-in-infants-receiving-phototherapy-100578258","NCT06808958","The Effect of Bathtub Bath on Stress and Comfort in Infants Receiving Phototherapy","Inclusion Criteria:\n\n* Newborns with a gestational age of 37 weeks and above\n* Birth weight of 2500 grams and above\n* Having completed 24 hours after birth\n* The newborn is hospitalized with a diagnosis of physiological hyperbilirubinemia and is receiving phototherapy\n* No accompanying disease\n* No accompanying treatment\n* Stable physiological parameters (no tachycardia and bradycardia)\n* No respiratory failure or distress (respiratory rate between 30-60, not being monitored on a ventilator, oxygen saturation of 90% and above, no need for continuous high concentration oxygen with methods such as Hood, CPAP, etc.)\n* The baby is hospitalized during data collection\n* The parents are willing for the newborn to participate in the study Exclusion Criteria\n* Preterms with a gestational age of 22-37 weeks,\n* The newborn has another concomitant disease diagnosis\n* Has been wiped or bathed in a tub within the last 12 hours\n* Has been hospitalized with a diagnosis of pathological hyperbilirubinemia\n* Has been given sedatives and\u002For muscle relaxants\n* The parent does not want the newborn to participate in the study or wants\u002Fwants to withdraw from the study while the study is ongoing","1 Day","28 Days",{"count":116,"type":23},62,[26],"After intrauterine life, intensive care is a stressful environment for newborns who have to start their lives in the NICU. Many care practices in the NICU, including environmental factors (such as light, sound), heel prick blood collection, routine care, invasive interventions and bathing, are sources of stress for newborns. At the same time, the physical structure of the NICU, that is, factors such as sound, light, odor, and the physiological and anatomical immaturity of newborn babies, routine care and invasive procedures can reduce the comfort of the baby. Controlling the factors that may cause stress in the infant in the NICU and reducing stress and increasing comfort at the same time may affect the baby's healing process and discharge process.\n\nRecently, nursing care practices that reduce stress and increase comfort are at the forefront and have become an important concept today. In the literature, massage, kangaroo care, swaddling, listening to the mother's voice, listening to music, positioning, mother-scented hand simulation, breastfeeding, wrapping, bathing . Neonatal bathing is among the practices frequently performed by neonatal intensive care nurses to reduce the stress of the newborn and increase comfort Bathing is a basic skin care process for newborns. Bathing is known to have beneficial effects for infants. It is reported that bathing causes relaxation in muscles, is calming and relaxing, is effective in regulating body temperature and reducing pain, regulating blood circulation and respiratory system, and supporting parent-infant bonding (interaction).\n\nBathing is a basic skin care process for newborns. Bathing is known to have beneficial effects for infants. It is reported that bathing causes relaxation in muscles, is calming and relaxing, is effective in regulating body temperature and reducing pain, regulating blood circulation and respiratory system, and supporting parent-infant bonding (interaction). Bowles (2013) found that neonatal bathing exfoliates dead skin cells, re-moisturizes the skin surface, reduces infant stress and agitation to provide comfort, encourages flexion and containment, and eventually provides developmentally supportive care. In the literature, there are many studies showing that bathing is also effective in reducing bilirubin levels in infants hospitalized with hyperbilirubinemia in neonatal intensive care units.\n\nStimuli such as lighting, noise and pain from repeated medical interventions in the NICU can cause stress in infants. Excessive lighting can cause negative effects such as weight gain disorder, sleep disturbance and stress in infants. Since phototherapy light is not only a source of stress for the baby receiving phototherapy but also one of the important factors affecting the comfort level, the comfort of babies receiving phototherapy should be monitored frequently. The physical conditions of NICUs, physiologic and anatomic conditions of the infants receiving treatment, invasive interventions and care lead to a decrease in the comfort level of newborns. This situation negatively affects the discharge time and recovery of newborns. Therefore, this study will be conducted to examine the effect of bathtub bathing on stress level and comfort in infants receiving phototherapy in neonatal intensive care.",[120],"Bathtub Bath",[120,122,123],"Infants","Phototherapy","2025-02-04",{"date":126,"type":38},"2025-02-05",{"date":128,"type":23},"2025-02-15",{"date":130,"type":23},"2025-06-30",{"name":44,"class":45},{"id":133,"slug":134,"hasResults":11,"nctId":135,"briefTitle":136,"officialTitle":137,"acronym":4,"eligibilityCriteria":138,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":139,"targetDuration":4,"studyType":24,"phases":140,"briefSummary":141,"conditions":142,"keywords":146,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":74},"100568052","progressive-relaxation-exercises-on-anxiety-levels-100568052","NCT06676202","Progressive Relaxation Exercises on Anxiety Levels","The Effect of Progressive Relaxation Exercises on Anxiety Levels in Patients Undergoing Total Knee Replacement Surgery: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Being 18 years old and above\n* Speaking and understanding Turkish\n* Having total knee replacement surgery\n* Staying in the ward for approximately 96 hours after surgery\n* Volunteering to participate in the study\n* Not having a psychiatric diagnosis\n\nExclusion Criteria:\n\n* Being under 18 years old\n* Having speech and comprehension problems\n* Not having total knee replacement surgery\n* Early discharge after surgery\n* Having complications after surgery\n* Not volunteering to participate in the study\n* Having a psychiatric diagnosis",{"count":85,"type":23},[26],"The research will be conducted to determine the effect of progressive relaxation exercises on the anxiety level of patients who have had total knee replacement surgery.",[143,144,145],"Anxiety","Exercises Therapy","Total Knee Replacement Surgery",[143,147,145],"Exercises","2024-11-04",{"date":150,"type":38},"2024-11-06",{"date":152,"type":23},"2024-11-30",{"date":154,"type":23},"2025-05-30",{"name":44,"class":45},{"id":157,"slug":158,"hasResults":11,"nctId":159,"briefTitle":160,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":17,"sex":18,"minAge":163,"maxAge":164,"enrollmentInfo":165,"targetDuration":4,"studyType":24,"phases":167,"briefSummary":168,"conditions":169,"keywords":171,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":74},"100560361","kaleidoscope-virtual-reality-glasses-pain-and-anxiety-levels-in-venous-blood-collection-children-100560361","NCT06576141","Kaleidoscope Virtual Reality Glasses Pain and Anxiety Levels in Venous Blood Collection Children","The Effect of Kaleidoscope and Virtual Reality Glasses on Pain and Anxiety Levels in Venous Blood Collection in Children Aged 9-12","Inclusion Criteria:\n\nThe child must be between the ages of 9-12, The child and parents must agree to participate in the research, The child must be able to communicate and be open to communication, The child must not have any hearing, speech or vision disorders\n\nExclusion Criteria:\n\nThe child is not within the age range specified above The child and parents do not agree to participate in the research. The child has a communication problem The child has a hearing, speech or vision disorder.","9 Years","12 Years",{"count":166,"type":23},105,[26],"The aim of our research is to investigate the effects of distracting children's attention with a kaleidoscope and virtual reality glasses during venous blood collection on perceived pain and anxiety levels.",[170],"Child, Only",[172,173,174,143,175,176],"PAİN","Kaleidoscope","Venous Blood Collection","Virtual Reality Glasses","Children","2024-08-26",{"date":179,"type":38},"2024-08-28",{"date":181,"type":23},"2024-09-01",{"date":183,"type":23},"2025-12-01",{"name":44,"class":45},""]