[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Delta University for Science and Technology\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":260},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,46,73,103,129,154,176,197,217,238],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":4},"100652526","mobile-game-simulation-for-nursing-students-decision-making-100652526",false,"NCT07774026","Mobile Game Simulation for Nursing Students' Decision-Making","An Interactive Mobile Game-Based Simulation Educational Program for Enhancing Decision-Making and Problem-Solving Among Nursing Students: A Quasi-Experimental Study","Inclusion Criteria:\n\n* First-year nursing students at the Faculty of Nursing, Delta University for Science and Technology.\n* Students who voluntarily consent to participate in the study.\n* Students who are willing and able to use the mobile application.\n\nExclusion Criteria:\n\n* Students who have previously participated in a similar mobile game-based or simulation-based educational program.\n* Students with any condition that prevents them from using a smartphone\u002Fmobile application.\n* Students who fail to complete the pre-test, the educational program, or the post-test.\n* Students who withdraw consent during the study.",true,"ALL",{"count":19,"type":20},258,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study will test whether an interactive mobile game-based simulation program helps first-year nursing students improve their decision-making and problem-solving skills. Students will complete knowledge, decision-making, and problem-solving assessments before and after taking part in a 4-week program (8 sessions) that uses mobile game scenarios to practice clinical decisions in a safe, simulated setting. The results will show whether this type of training is more effective than traditional teaching methods for building these skills.",[26],"Clinical Decision-Making and Problem-Solving Skills in Nursing Education",[28,29,30,31,32,33],"mobile game-based learning","simulation","nursing education","clinical decision-making","problem-solving","nursing students","NOT_YET_RECRUITING","2026-08-19",{"date":37,"type":38},"2026-08-20","ACTUAL",{"date":40,"type":20},"2026-09-01",{"date":42,"type":20},"2026-12-01",{"name":44,"class":45},"Delta University for Science and Technology","OTHER",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":56,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":71,"locationsCount":72},"100651688","correlation-between-forward-head-posture-cervical-muscles-endurance-and-proprioceptive-fuctions-in-cervicogenic-headache-among-late-adolescent-students-100651688","NCT07763886","CORRELATION BETWEEN FORWARD HEAD POSTURE, CERVICAL MUSCLES ENDURANCE, AND PROPRIOCEPTIVE FUCTIONS IN CERVICOGENIC HEADACHE AMONG LATE ADOLESCENT STUDENTS.","Inclusion Criteria:\n\nFifty-six junior students diagnosed with cervicogenic headache\n\n* Sudents from both sexes will participate in this study.\n* The students' ages will be ranged from 17 to 18 years.\n* All participants will be referred from neurologists\n* All participants will be free from any medical disease, visual or hearing problem.\n\nExclusion Criteria:\n\n* • Patients with a history of cervical spine surgery.\n\n  * Patients with Whiplash injury..\n  * Patients with any vestibular disorders.\n  * Patients with visual and hearing impairments.\n  * Patients with diabetes mellitus.","15 Years","18 Years",{"count":55,"type":20},100,"1 Month","OBSERVATIONAL","Forward Head Posture (FHP) is a common postural deviation characterized by anterior translation of the head relative to the trunk, which increases load on cervical muscles and joints. This postural change is associated with muscle fatigue, joint compression, and tension in cervical soft tissues, contributing to cervicogenic headache (Al-Mutairi et al., 20242; Koseoglu et al., 2023). The deep cervical flexor (DCF) muscles, especially the longus colli and longus capitis, are key stabilizers of the cervical spine, and weakness or fatigue of these muscles leads to overuse of superficial muscles such as the sternocleidomastoid and anterior scalene, creating an imbalance between deep and superficial systems. Diminished endurance of deep cervical flexors has been linked to forward head posture, impaired motor control, and persistent neck pain (Ismail et al., 2023). Cervical proprioception is crucial for accurate head position sense. Impaired cervical proprioception results in distorted information about head orientation, causing dizziness, incoordinated movement, and neck discomfort, and has been frequently observed in juniors with cervicogenic headache, increasing muscular strain and headache intensity. In the present study, therefore, we aim to investigate the correlation between FHP, cervical endurance, and proprioceptive function in junior students with cervicogenic headache",[60],"Cervicogenic Headache",[62,63,64],"Forward Head Posture","Headache","Cervicogenic headache","2026-08-09",{"date":67,"type":38},"2026-08-13",{"date":69,"type":20},"2026-08-10",{"date":40,"type":20},{"name":44,"class":45},1,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":17,"minAge":81,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":21,"phases":85,"briefSummary":86,"conditions":87,"keywords":89,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":72},"100645525","compare-the-effect-of-radiofrequency-tecar-and-ultrasound-on-sensation-hand-dexterity-and-quality-of-life-in-patients-with-carpal-tunnel-syndrome-100645525","NCT07700316","Compare the Effect of Radiofrequency (TECAR) and Ultrasound on Sensation, Hand Dexterity, and Quality of Life in Patients With Carpal Tunnel Syndrome.","Radiofrequency Versus Ultrasound on Sensation, Hand Dexterity and Quality of Life in Patients With Carpal Tunnel Syndrome","TECAR","Inclusion Criteria:\n\nThe patients will be selected according to the following criteria:\n\n* Adults aged 35 to 50 years.\n* Presence of typical CTS symptoms for at least one month.\n* Cutoff values of VAS are defined between 35 mm and 64 mm.\n* Patients were diagnosed with moderate carpal tunnel syndrome clinically by physical examination (positive Phalen's test and Tinel's sign) and confirmed by an electrodiagnostic study (EDX) with a fractionated sensory nerve conduction velocity for the median nerve across the wrist of 40 m\u002Fs or less and with sensory distal latency more than 3.6 ms and less than 4 ms and a normal CMAP amplitude in the APB muscle.\n* Body mass index from 18.5 to 24.9. and ability and willingness to provide informed consent and comply with the study protocol.\n\nExclusion Criteria:\n\n\\- Participants will be excluded if they meet any of the following criteria:\n\n* Severe carpal tunnel syndrome requires surgical intervention.\n* Presence of systemic diseases associated with CTS, such as diabetes mellitus, rheumatoid arthritis, hypothyroidism, or other inflammatory disorders.\n* Pregnancy.\n* History of fractures, trauma, or surgery in the wrist or hand region.\n* Corticosteroid injection in the carpal tunnel within the last three months.\n* Use of wrist splints or other CTS treatments in the past three months.\n* Presence of peripheral neuropathy or other neurological disorders affecting the upper limb.\n* Burns or skin lesions in the hand or forearm area.\n* Presence of pacemakers, metal implants, prostheses, or intrauterine devices (IUDs) that may interfere with electrotherapy modalities.\n* Peripheral vascular diseases affect the upper limb.","35 Years","50 Years",{"count":84,"type":20},42,[23],"The purpose of the current study is to:\n\nCompare the effect of radiofrequency (TECAR) therapy and ultrasound on sensation, manual dexterity, and quality of life in individuals diagnosed with carpal tunnel syndrome (CTS). The study also correlates sensation, hand dexterity, and quality of life in patients with carpal tunnel syndrome.",[88],"Carpal Tunnel Syndrome (CTS)",[88,79,90,91,92,93,94],"Radiofrequency","Ultrasound","Hand Dexterity","Sensation","Quality of Life","2026-07-27",{"date":97,"type":38},"2026-07-28",{"date":99,"type":20},"2026-08-01",{"date":101,"type":20},"2026-12-31",{"name":44,"class":45},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":111,"targetDuration":4,"studyType":21,"phases":113,"briefSummary":114,"conditions":115,"keywords":117,"overallStatus":120,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":72},"100648265","smart-normal-labor-healthcare-providers-experience-with-an-ai-based-mobile-app-100648265","NCT07720531","Smart Normal Labor: Healthcare Providers' Experience With an AI-Based Mobile App","Smart Normal Labor From Healthcare Providers' Perspective: Evaluating Clinical Decision-Making Speed, Diagnostic Accuracy, Satisfaction, and Experience Using an AI-Based Mobile Application","Smart labor","Inclusion Criteria\n\nParticipants must meet the following conditions to be included in the study:\n\n1. Healthcare providers (obstetricians and nurses) currently working in the Labor Kiosk, Obstetrics and Gynecology Department, or Outpatient Gynecology Clinics at Mansoura University Hospital.\n2. Direct involvement in the care and supervision of women in active labor.\n3. For the intervention group: previous exposure to and use of the AI-based smart normal labor application for a minimum defined period (e.g., 1 month).\n4. For the control group: no prior use of the AI-based application, following standard care practices.\n5. Willingness to participate and provide informed consent. Exclusion Criteria\n\nParticipants will be excluded if they:\n\n1. Are healthcare providers not directly involved in labor management (e.g., administrative staff or laboratory personnel).\n2. Have less than the minimum required clinical experience in labor management (e.g., \\\u003C6 months).\n3. Are on leave or unavailable during the study period.\n4. Decline to participate or do not provide informed consent.",{"count":112,"type":20},427,[23],"Pregnancy and childbirth are uniquely important events in women's lives because they are accompanied by major physical, emotional, and psychological changes. Maternal satisfaction, emotional well-being, and perceptions of childbirth are strongly influenced by the quality of labor management. A woman's childbirth experience is shaped by multiple factors, including communication, autonomy, and active participation in the decision-making process. These factors are widely recognized as important indicators of the quality of maternity care. \\[1\\]\n\nRecent demographic changes and global population growth have placed increasing demands on healthcare systems, particularly maternal health services. High birth rates in some regions, combined with shortages of trained healthcare professionals, have created a need for scalable, adaptable, and innovative models of care. In response to these challenges, digital health technologies have emerged as promising tools to enhance the quality of maternity care and support both healthcare providers and pregnant women. \\[2\\]",[116],"Normal Labor",[116,118,119],"Clinical Decision-Making in Labor","Artificial Intelligence","RECRUITING","2026-07-21",{"date":123,"type":38},"2026-07-22",{"date":125,"type":38},"2026-05-06",{"date":127,"type":20},"2026-07-30",{"name":44,"class":45},{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":17,"minAge":135,"maxAge":136,"enrollmentInfo":137,"targetDuration":4,"studyType":21,"phases":139,"briefSummary":140,"conditions":141,"keywords":143,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":151,"leadSponsor":153,"locationsCount":4},"100643972","effect-of-aquatic-therapy-program-on-balance-in-children-with-spastic-diplegic-cerebral-palsy-100643972","NCT07669350","Effect of Aquatic Therapy Program on Balance in Children With Spastic Diplegic Cerebral Palsy","Inclusion Criteria:\n\n1. Confirmed diagnosis of spastic diplegic cerebral palsy by a paediatric neurologist or developmental paediatrician\n2. Age between 5 and 12 years\n3. Classified at GMFCS levels I-III\n4. Bilateral lower limb spasticity with a Modified Ashworth Scale (MAS) score of ≥ 1\n\nExclusion Criteria:\n\n1. Athetoid, ataxic, or mixed-type cerebral palsy\n2. GMFCS levels IV or V (non-ambulatory children)\n3. Uncontrolled seizure disorder or epilepsy not managed by medication\n4. Open wounds, skin infections, or active dermatological conditions contraindicating water immersion\n5. Fear of water (aquaphobia) or inability to tolerate the aquatic environment","5 Years","12 Years",{"count":138,"type":20},50,[23],"1. Evaluate the effect of a structured aquatic therapy programme on static balance in children with spastic diplegic cerebral palsy.\n2. Assess the effect of the same programme on dynamic balance in this patient population.\n3. Compare balance outcomes between children receiving aquatic therapy and those receiving conventional land-based physiotherapy.",[142],"Cerebral Palsy (CP)",[144,145,146],"Aquatic therapy","Diaplegia","cerebral palsy","2026-06-20",{"date":149,"type":38},"2026-06-25",{"date":149,"type":20},{"date":152,"type":20},"2026-09-15",{"name":44,"class":45},{"id":155,"slug":156,"hasResults":11,"nctId":157,"briefTitle":158,"officialTitle":158,"acronym":159,"eligibilityCriteria":160,"healthyVolunteers":11,"sex":17,"minAge":161,"maxAge":162,"enrollmentInfo":163,"targetDuration":4,"studyType":21,"phases":165,"briefSummary":166,"conditions":167,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":172,"completionDateStruct":174,"leadSponsor":175,"locationsCount":72},"100638330","children-with-surgically-corrected-acyanotic-congenital-heart-disease-100638330","NCT07605832","Children With Surgically Corrected Acyanotic Congenital Heart Disease","Pediatrics","Inclusion Criteria:\n\n* For cyanotic postoperative congenital heart disease group:\n\n  1. Children diagnosed with acyanotic postoperative congenital heart disease.\n  2. Underwent surgical repair for CHD.\n  3. Has a history of only one surgical intervention.\n  4. Age between 48 and 72 months.\n  5. Mentally normal, with an IQ between 85 and 115.\n\n     For the healthy control group (HCG):\n* For healthy children aged 48 to 72 months. Full school attendance. Full participation in social and recreational activities. Parents\u002Fguardians provided written informed consent.\n\nExclusion Criteria:\n\nChildren were excluded if they had:\n\n1. Genetic disorders.\n2. Severe neurological disorders.\n3. Cyanotic congenital heart disease.\n4. Perinatal complications.","48 Months","72 Months",{"count":164,"type":20},80,[23],"The goal of this quasi-experimental pretest-posttest controlled study is to learn whether moderate-intensity treadmill exercise can improve gait kinematics, walking capacity, and motor performance in preschool children aged 48-72 months with surgically corrected acyanotic congenital heart disease.\n\nThe main questions it aims to answer are:\n\nDoes moderate-intensity treadmill training improve gait kinematics, including stride length, walking speed, and double-stance percentage? Does moderate-intensity treadmill training improve walking capacity and balance in children with surgically corrected acyanotic congenital heart disease?\n\nResearchers compared children with surgically corrected acyanotic congenital heart disease who received treadmill training with age-matched healthy children to see whether the exercise program could reduce gait, balance, and walking-capacity differences between the groups.\n\nParticipants with congenital heart disease completed:\n\nFour treadmill walking sessions per week for 10 weeks. Moderate-intensity walking at approximately 70% of maximal heart rate. Pre- and post-intervention assessments of gait kinematics using three-dimensional motion analysis.\n\nBalance assessment using the Pediatric Balance Scale. Walking capacity assessment using the six-minute walk test.",[168],"Acyanotic Congenital Heart Disease","2026-05-18",{"date":171,"type":38},"2026-05-26",{"date":173,"type":20},"2026-05-31",{"date":40,"type":20},{"name":44,"class":45},{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":4,"eligibilityCriteria":182,"healthyVolunteers":11,"sex":17,"minAge":183,"maxAge":184,"enrollmentInfo":185,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":186,"conditions":187,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":4},"100617630","correlation-between-cervical-deep-flexors-endurance-and-proprioception-function-in-cervical-radiculopathy-100617630","NCT07321119","Correlation Between Cervical Deep Flexors Endurance and Proprioception Function in Cervical Radiculopathy","Correlation Between Endurance and Proprioception Function in Cervical Radiculopathy","Inclusion Criteria:\n\n* Adults diagnosed with cervical radiculopathy based on clinical examination (± imaging confirmation).\n\nPresence of neck pain with radiating symptoms to the upper limb for at least 4 weeks.\n\nAge range 20-60 years.\n\nAbility to understand instructions and participate in cervical endurance and proprioception assessments.\n\nExclusion Criteria:\n\n* History of cervical spine surgery or acute cervical trauma.\n\nPresence of neurological disorders other than cervical radiculopathy (e.g., stroke, multiple sclerosis).\n\nVestibular disorders or conditions affecting balance and head position sense.\n\nInflammatory, rheumatologic, or severe musculoskeletal conditions involving the cervical spine.","30 Years","45 Years",{"count":164,"type":20},"In cervical radiculopathy, reduced endurance of the deep cervical flexor muscles is associated with impaired cervical proprioception. This relationship reflects altered sensorimotor control due to muscle dysfunction and neural compromise, emphasizing the need for deep flexor endurance training in rehabilitation.",[188],"Cervical Radiculopathy","2025-12-26",{"date":191,"type":38},"2026-01-06",{"date":193,"type":20},"2026-01-01",{"date":195,"type":20},"2026-03-01",{"name":44,"class":45},{"id":198,"slug":199,"hasResults":11,"nctId":200,"briefTitle":201,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":11,"sex":17,"minAge":183,"maxAge":184,"enrollmentInfo":204,"targetDuration":4,"studyType":21,"phases":205,"briefSummary":206,"conditions":207,"keywords":208,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":210,"lastUpdatePostDateStruct":211,"startDateStruct":213,"completionDateStruct":214,"leadSponsor":216,"locationsCount":72},"100615207","effect-of-tecar-on-cervical-radiculopathy-100615207","NCT07289607","Effect of TECAR on Cervical Radiculopathy","Effect of TECAR Therapy on Proprioception Function in Patients With Cervical Radiculopathy","Inclusion Criteria:\n\n* • Diagnosed cervical radiculopathy confirmed by clinical and radiological findings\n\n  * Age 30-40 years\n  * Pain duration \\> 4 weeks\n\nExclusion Criteria:\n\n* • Cervical fracture or surgery\n\n  * Vestibular disorders\n  * Rheumatologic or neurological diseases\n  * Cognitive impairment or pregnancy",{"count":164,"type":20},[23],"Cervical radiculopathy is characterized by pain, sensory disturbances, and impaired neuromuscular control due to nerve root compression. Proprioception dysfunction is often an overlooked component of this condition and can affect balance, posture, and motor control.\n\nTECAR (Transfer of Energy Capacitive and Resistive) therapy is a form of deep heat electrotherapy known to improve tissue perfusion and neuromuscular function. Although TECAR is widely used for pain relief and mobility, its role in improving proprioception remains under-investigated, especially in cervical conditions. This study aims to bridge this gap by assessing proprioceptive outcomes in patients with cervical radiculopathy receiving TECAR therapy.",[188],[209],"TECAR , radiculopathy , Proprioception","2025-12-17",{"date":212,"type":38},"2025-12-18",{"date":193,"type":20},{"date":215,"type":20},"2026-04-05",{"name":44,"class":45},{"id":218,"slug":219,"hasResults":11,"nctId":220,"briefTitle":221,"officialTitle":222,"acronym":4,"eligibilityCriteria":223,"healthyVolunteers":11,"sex":17,"minAge":224,"maxAge":82,"enrollmentInfo":225,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":227,"conditions":228,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":230,"lastUpdatePostDateStruct":231,"startDateStruct":233,"completionDateStruct":235,"leadSponsor":237,"locationsCount":4},"100610696","effects-of-neck-proprioception-impairment-on-balance-in-cervical-spondylosis-patients-100610696","NCT07230938","Effects of Neck Proprioception Impairment on Balance in Cervical Spondylosis Patients","The Influence of Cervical Proprioception Deficits on Postural Stability in Patients With Cervical Spondylosis","Inclusion Criteria:\n\n* Eighty-two patients with cervical spondylosis, the patient will be diagnosed and referred by physician.\n* Mild to moderate cervical disability according to neck disability index( MacDermid et al., 2009).\n* Age ranges from 25 to 45 years.\n* Body mass index from 18.5 - 24.9.\n\nExclusion Criteria:\n\n* The patients will be excluded if they have one of the following:\n* visual or vestibular sensory disorders or cerebellar disease.\n* Cervical myelopathy.\n* Patients with previous cervical surgery.\n* inflammatory diseases involving cervical spine such as rheumatoid arthritis or ankylosing spondylitis.\n* History of cervical trauma including whiplash associated disorders (WAD).\n* History of cervical tumors.\n* History of ankle instability.\n* No previous foot and ankle surgery.","25 Years",{"count":226,"type":20},82,"This observational cross-sectional study aims to investigate the impact of cervical proprioception deficits on postural stability in patients with cervical spondylosis. Using pedobarographic analysis, the study will assess static balance parameters in affected individuals. The main question it aims to answer is: Does Cervical proprioception deficits affect postural stability in patients with cervical spondylosis measured by pedobarographic parameters?",[229],"Postural Stability","2025-11-13",{"date":232,"type":38},"2025-11-17",{"date":234,"type":20},"2025-11-15",{"date":236,"type":20},"2025-12-30",{"name":44,"class":45},{"id":239,"slug":240,"hasResults":11,"nctId":241,"briefTitle":242,"officialTitle":242,"acronym":4,"eligibilityCriteria":243,"healthyVolunteers":11,"sex":17,"minAge":244,"maxAge":245,"enrollmentInfo":246,"targetDuration":4,"studyType":21,"phases":248,"briefSummary":249,"conditions":250,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":252,"lastUpdatePostDateStruct":253,"startDateStruct":255,"completionDateStruct":257,"leadSponsor":259,"locationsCount":72},"100557834","efficacy-of-cryotherapy-in-managing-chemotherapy-induced-peripheral-neuropathy-in-children-with-leukemia-100557834","NCT06543264","Efficacy of Cryotherapy in Managing Chemotherapy-Induced Peripheral Neuropathy in Children With Leukemia","Inclusion Criteria:\n\n1. Their age will ranging from eight to seventeen years.\n2. Children participated in this study will from both sexes.\n3. Children receiving chemotherapy as medical treatment protocol\n4. All children have polyneuropathy caused by chemotherapy.\n\nExclusion Criteria:\n\n1. Children with Epilepsy.\n2. Children with blood clotting disorder.\n3. Children have Open wounds \u002F broken skin\n4. Children with severe cardiac disease\n5. Uncooperative patients.","8 Years","17 Years",{"count":247,"type":20},60,[23],"This study aimed to assess the efficacy of cryotherapy in controlling Peripheral Neuropathy in cancer children",[251],"Cancer","2024-08-08",{"date":254,"type":38},"2024-08-12",{"date":256,"type":20},"2024-09-01",{"date":258,"type":20},"2025-01-01",{"name":44,"class":45},""]