[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Karamanoğlu Mehmetbey University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":312},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,44,78,107,137,158,176,201,227,253,285],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":4},"100638063","climate-awareness-among-healthcare-students-an-educational-study-on-carbon-footprint-and-climate-change-awareness-100638063",false,"NCT07582224","Climate Awareness Among Healthcare Students: an Educational Study on Carbon Footprint and Climate Change Awareness","Inclusion Criteria:\n\n* Being over 18 years old, being a volunteer, being a healthcare student\n\nExclusion Criteria:\n\n* Not being a volunteer",true,"ALL","18 Years",{"count":19,"type":20},130,"ESTIMATED","INTERVENTIONAL",[23],"NA","This research was planned to investigate whether the education provided in universities causes a change in carbon footprints and climate change.",[26],"Climate Change Awareness",[28,29,30,31],"climate change","awareness","carbon footprint","healthcare student","NOT_YET_RECRUITING","2026-05-16",{"date":35,"type":36},"2026-05-20","ACTUAL",{"date":38,"type":20},"2026-05-15",{"date":40,"type":20},"2026-12-30",{"name":42,"class":43},"Karamanoğlu Mehmetbey University","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":62,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":4},"100631332","the-effects-of-circadian-rhythm-based-progressive-relaxation-exercises-in-hemodialysis-patients-100631332","NCT07499297","THE EFFECTS OF CIRCADIAN RHYTHM-BASED PROGRESSIVE RELAXATION EXERCISES IN HEMODIALYSIS PATIENTS","THE EFFECTS OF CIRCADIAN RHYTHM-BASED PROGRESSIVE RELAXATION EXERCISES ON SYMPTOM MANAGEMENT, SLEEP QUALITY, COMFORT, AND MENTAL WELL-BEING IN HEMODIALYSIS PATIENTS","Inclusion Criteria:\n\n* 18 and 65 years of age,\n* have no mental or physical disabilities that would prevent them from answering the questions,\n* have no problems related to touch, temperature perception, hearing, or vision,\n* are relatively independent in performing daily activities,\n* do not use any pharmacological or non-pharmacological methods to facilitate sleep,\n* have been receiving hemodialysis (HD) treatment for at least 3 months,\n* are able to communicate and cooperate.\n\nExclusion Criteria:\n\n* are bedridden,\n* have physical limitations preventing them from performing relaxation exercises,\n* have been practicing relaxation exercises (such as breathing exercises, meditation, yoga, etc.) within the last 6 months,\n* are classified as intermediate type (neither type) according to the Morningness-Eveningness Questionnaire,\n* engage in regular exercise,\n* have been diagnosed with psychiatric disorders such as depression or schizophrenia,\n* do not consent to participate in the study.","65 Years",{"count":53,"type":20},75,[23],"The aim of this study is to determine the effect of Progressive Relaxation Exercise (PGE) applied according to the circadian rhythms of hemodialysis (HD) patients on symptom management, sleep quality, comfort and mental well-being levels and to examine the experiences of HD patients regarding PGE application. A sequential mixed method research design will be used in the study. The quantitative part of the study was planned as a randomized controlled double-blind experimental study. The qualitative part will be conducted as a qualitative research to be carried out with individual in-depth interview method in order to examine the opinions of the individuals in the intervention group regarding the 8-week PGE applied according to the circadian rhythm. In the collection of research data, the Introductory Information Form, Morningness-Eveningness Questionnaire (MEQ), Dialysis Symptom Index, Hemodialysis Comfort Scale - Version II, Pittsburg Sleep Quality Index (PSQI), Warwick-Edinburgh Mental Well-Being Scale (WEMIOÖ), Individual Follow-up Form, Progressive Relaxation Exercise Application Guideline (PGEUY) and In-Depth Interview Form with Individuals in the Intervention Group will be used.",[57,58,59,60,61],"Nursing","Hemodialysis Patient","Circadian Rhythm","Relaxation Exercise","Symptom Management",[57,63,64,65,66,67,68,69],"hemodialysis","circadian rhythm","relaxation exercise","symptom management","sleep quality","comfort","mental well-being","2026-04-02",{"date":72,"type":36},"2026-04-08",{"date":74,"type":20},"2026-04-01",{"date":76,"type":20},"2026-09-22",{"name":42,"class":43},{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":85,"minAge":17,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":21,"phases":89,"briefSummary":90,"conditions":91,"keywords":93,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":103,"leadSponsor":105,"locationsCount":106},"100624205","the-effect-of-presence-of-father-in-the-operating-room-on-quality-of-recovery-of-the-parturient-100624205","NCT07406607","The Effect of Presence of Father in the Operating Room on Quality of Recovery of the Parturient","The Effect of Presence of Father During Elective Cesarean Section Under Spinal Anesthesia on Parturient's Quality of Recovery","Inclusion Criteria:\n\n* Patients scheduled for an elective cesarean section.\n* Patients and their partners must be literate in Turkish (able to read and write) to accurately complete the study questionnaires\n* Patients and their partners must be willing and able to provide written informed consent\n* Healthy pregnant women with no additional chronic or systemic diseases (comorbidities)\n* The operating surgeon must have at least 5 years of professional experience and no chronic health conditions.\n\nExclusion Criteria:\n\n* Patients undergoing emergency cesarean sections.\n* Patients with any known chronic or systemic additional diseases\n* Surgeons with any known chronic or systemic diseases.\n* Individuals unable to read or understand the Turkish questionnaires (implied by the literacy requirement).\n* Patients with American Society of Anesthesiologists (ASA) classification of 3 or more\n* Patients with history of chronic pain, chronic use of analgesic drugs, or history of opioid or intravenous drug abuse\n* Patients who have refused spinal anesthesia, or those in whom it is contraindicated.\n* Pregnancy with preeclampsia or eclampsia\n* Pregnancy with gestational diabetes mellitus or diabetes mellitus","FEMALE","45 Years",{"count":88,"type":20},110,[23],"The presence of a partner to support the mother during cesarean and vaginal deliveries is a well-established practice in most countries worldwide. It is evident that allowing the partner into the operating room during a cesarean section provides psychosocial benefits for both the mother and the partner. This study aims to investigate the effect of the presence of partner in the operating room on quality of recovery of parturients at the postoperative period.",[92],"Caesarean Section",[94,95,96,97],"spinal anesthesia","obstetric quality of recovery","Caesarean section","surgeon comfort","RECRUITING","2026-02-19",{"date":101,"type":36},"2026-02-20",{"date":99,"type":36},{"date":104,"type":20},"2026-06-08",{"name":42,"class":43},1,{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":114,"targetDuration":4,"studyType":21,"phases":116,"briefSummary":117,"conditions":118,"keywords":120,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":106},"100616182","the-effectiveness-of-pain-neuroscience-education-for-patients-with-carpal-tunnel-syndrome-100616182","NCT07302282","The Effectiveness of Pain Neuroscience Education for Patients With Carpal Tunnel Syndrome","The Effectiveness of Pain Neuroscience Education for Patients With Mild to Moderate Carpal Tunnel Syndrome","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Having a diagnosis of mild or moderate CTS confirmed by ENMG\n* Having complaints of pain and numbness in the first three fingers of the hand for at least 3 months\n\nExclusion Criteria:\n\n* Presence of severe CTS findings on electrophysiological examination\n* Presence of metabolic diseases such as uncontrolled diabetes and hypothyroidism\n* Presence of inflammatory rheumatic disease (e.g., rheumatoid arthritis)\n* Presence of other neuromuscular diseases affecting the hand and wrist (Polyneuropathy, Cervical radiculopathy, peripheral nerve damage, Brachial plexus damage, other entrapment neuropathies, etc.)\n* History of hand and wrist trauma\n* History of neck and wrist surgery\n* History of steroid injection into the carpal tunnel within the last 3 months\n* History of physical therapy application to wrist within the last 3 months\n* Deformity preventing the use of a splint on the wrist\n* Previous participation in a program for the psychological management of chronic pain\n* Cognitive dysfunction preventing cooperation with tests",{"count":115,"type":20},48,[23],"The goal of this clinical trial is to investigate the effects of Pain Neuroscience Education applied in the treatment of mild and moderate carpal tunnel syndrome (CTS).\n\nThe main question it aims to answer is: Does PNE have a therapeutic effect on carpal tunnel syndrome in clinical and ultrasonographic terms? Researchers will compare whether PNE creates a synergistic effect alongside home based exercise programs and splint application in mild to moderate CTS, and will objectively demonstrate potential benefits such as relief from pain and numbness.",[119],"Carpal Tunnel Syndrome (CTS)",[121,122,123,124,125,126,127,128],"Median Neuropathy","Mononeuropathies","Nerve Compression Syndromes","Education","Exercise","Pain neuroscience education","Carpal tunnel syndrome","Median nerve gliding exercise","2026-01-02",{"date":131,"type":36},"2026-01-06",{"date":133,"type":36},"2025-12-29",{"date":135,"type":20},"2026-08-17",{"name":42,"class":43},{"id":138,"slug":139,"hasResults":11,"nctId":140,"briefTitle":141,"officialTitle":142,"acronym":4,"eligibilityCriteria":143,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":51,"enrollmentInfo":144,"targetDuration":4,"studyType":21,"phases":146,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":106},"100527945","action-observation-and-motor-imagery-therapy-in-parkinsons-disease-100527945","NCT06154356","Action Observation and Motor Imagery Therapy in Parkinson's Disease","Effect of Action Observation and Motor Imagery Therapy on Balance, Functional Status and Quality of Life in Parkinson's Disease, Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients with a diagnosis of Parkinson's Disease\n* Hoehn and Yahr Stage 1-3\n\nExclusion Criteria:\n\n* Patients with cognitive dysfunction (those who cannot follow simple verbal instructions)\n* Patients with severe hearing problems\n* Patients with severe vision problems\n* Patients with additional musculoskeletal system pathology that will affect physical performance (such as amputation, severe joint mobility limitation, peripheral nerve damage)\n* Patients with uncontrolled hypertension and diabetes mellitus\n* Patients with a history of symptomatic lung disease (such as asthma, chronic obstructive pulmonary disease, emphysema)\n* Patients with a history of symptomatic cardiac disease (such as coronary artery disease, arrhythmia, heart failure)",{"count":145,"type":20},54,[23],"In recent years, motor imagery (MI) and action observation (AO) therapy strategies have been used in rehabilitation programs to increase motor learning in Parkinson's disease (PD). Visuomotor training strategies such as AO and MI therapy rely on the activity of the mirror neuron system to facilitate motor re-learning. Mirror neurons are activated during the performance of goal-directed actions, also when observing the same action and visualizing the action in the mind.\n\nThe aim of this clinical trial is to test whether the application of AO and MI treatment in PD in addition to conventional rehabilitation programs has an additional effect on Balance, Functional Status and Quality of Life.",[149],"Parkinson's Disease","2025-12-04",{"date":152,"type":36},"2025-12-11",{"date":154,"type":36},"2023-12-14",{"date":156,"type":20},"2026-06",{"name":42,"class":43},{"id":159,"slug":160,"hasResults":11,"nctId":161,"briefTitle":162,"officialTitle":163,"acronym":4,"eligibilityCriteria":164,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":51,"enrollmentInfo":165,"targetDuration":4,"studyType":21,"phases":167,"briefSummary":168,"conditions":169,"keywords":4,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":171,"startDateStruct":172,"completionDateStruct":174,"leadSponsor":175,"locationsCount":106},"100528906","action-observation-and-motor-imagery-therapy-in-stroke-100528906","NCT06166862","Action Observation and Motor Imagery Therapy in Stroke","Effect of Action Observation and Motor Imagery Therapy on Balance, Functional Status and Quality of Life in Stroke, Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients who had a stroke in the last year\n* Functional Ambulation Classification score 2-5\n\nExclusion Criteria:\n\n* Patients who have had repeated strokes\n* Patients with neglect\n* Patients with cognitive dysfunction (those who cannot follow simple verbal instructions)\n* Patients with severe hearing problems\n* Patients with severe vision problems\n* Patients with additional musculoskeletal system pathology that will affect physical performance (such as amputation, severe joint mobility limitation, peripheral nerve damage)\n* Patients with uncontrolled hypertension and diabetes mellitus\n* Patients with a history of symptomatic lung disease (such as asthma, chronic obstructive pulmonary disease, emphysema)\n* Patients with a history of symptomatic cardiac disease (such as coronary artery disease, arrhythmia, heart failure)\n* Patients with peripheral artery disease",{"count":166,"type":20},56,[23],"In recent years, motor imagery (MI) and action observation (AO) therapy strategies have been used in rehabilitation programs to increase motor learning in stroke. Visuomotor training strategies such as AO and MI therapy rely on the activity of the mirror neuron system to facilitate motor re-learning. Mirror neurons are activated during the performance of goal-directed actions, also when observing the same action and visualizing the action in the mind.\n\nThis clinical trial aims to test whether the application of AO and MI treatment in stroke in addition to conventional rehabilitation programs has an additional effect on motor recovery, activities of daily living, and quality of life.",[170],"Stroke",{"date":152,"type":36},{"date":173,"type":36},"2023-12-12",{"date":156,"type":20},{"name":42,"class":43},{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":4,"eligibilityCriteria":182,"healthyVolunteers":11,"sex":16,"minAge":183,"maxAge":4,"enrollmentInfo":184,"targetDuration":4,"studyType":186,"phases":4,"briefSummary":187,"conditions":188,"keywords":191,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":195,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":200,"locationsCount":106},"100527862","does-edema-affect-the-adjustment-of-tens-amplitude-100527862","NCT06153277","Does Edema Affect the Adjustment of TENS Amplitude","Does Edema After Knee Arthroplasty Affect the Adjustment of TENS Amplitude","Inclusion Criteria:\n\n* Age ≥ 40 years\n* Patients undergoing unilateral total knee arthroplasty\n\nExclusion Criteria:\n\n* Patients with scars in any of both knee areas\n* Patients who have previously had surgery on the control leg\n* Patients undergoing surgery due to trauma or cancer\n* Patients with sensory impairments\n* Patients with excessive effusion and edema in the knee joints before the surgery (eg. Inflammatory arthropathy, gonarthrosis exacerbation, etc.)\n* Mental impairment, or poor general health status that would interfere with assessments during TENS application.\n* Any contraindication for TENS (allergy to the TENS electrodes, skin conditions or skin sensation impairment in the areas where the electrodes will be placed, pacemaker or other implanted electrical device, epilepsy, pregnancy)","40 Years",{"count":185,"type":20},125,"OBSERVATIONAL","The goal of this pre-post clinical trial is to compare the amplitude settings of three different frequency TENS modes (Conventional TENS, LF TENS, HF TENS) in patients who had undergone total knee arthroplasty, both with the preoperative state and with the contralateral knee. The main question it aims to answer is: Can the electrical resistance of edematous tissue be affected and change the TENS amplitude setting? Participants will be evaluated before and after surgery. For each TENS modulation the amplitude at which tingling is felt, the current is clearly felt, and is maximum tolerated and\u002For muscle contraction occurred, will be documented. TENS amplitudes for all three TENS modes will be compared, both with the preoperative state and with the contralateral knee.",[189,190],"Edema Leg","Pain",[192,193,194],"Transcutaneous electrical nerve stimulation","Amplitude adjustment","Arthroplasty",{"date":152,"type":36},{"date":197,"type":36},"2023-12-07",{"date":199,"type":20},"2026-04",{"name":42,"class":43},{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":15,"sex":85,"minAge":207,"maxAge":4,"enrollmentInfo":208,"targetDuration":4,"studyType":21,"phases":210,"briefSummary":211,"conditions":212,"keywords":215,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":219,"lastUpdatePostDateStruct":220,"startDateStruct":222,"completionDateStruct":224,"leadSponsor":226,"locationsCount":4},"100603489","the-effect-of-physical-activity-on-cardiovascular-disease-risk-awareness-and-self-worth-in-young-women-100603489","NCT07137182","The Effect of Physical Activity on Cardiovascular Disease Risk Awareness and Self-Worth in Young Women","Inclusion Criteria:\n\n* Being over 18 years of age\n* Voluntarily participating in the study\n* Being female\n\nExclusion Criteria:\n\n* Having any physical disability,\n* Having had an injury or accident,\n* Being pregnant or having recently given birth,\n* Having a cognitive impairment that would prevent completing the survey and maintaining communication,","18 Weeks",{"count":209,"type":20},60,[23],"The main purpose of this study was to reveal the self-worth perceptions of women who regularly participate in physical activity and to investigate the effect of physical activity on self-worth perception and cardiovascular risk awareness.",[213,214],"Cardiovascular (CV) Risk","Physical Activities",[216,217,218],"cardiovascular risk","physical activities","self worth","2025-08-22",{"date":221,"type":36},"2025-08-29",{"date":223,"type":20},"2025-09-15",{"date":225,"type":20},"2026-02-01",{"name":42,"class":43},{"id":228,"slug":229,"hasResults":11,"nctId":230,"briefTitle":231,"officialTitle":232,"acronym":4,"eligibilityCriteria":233,"healthyVolunteers":11,"sex":16,"minAge":234,"maxAge":235,"enrollmentInfo":236,"targetDuration":4,"studyType":21,"phases":238,"briefSummary":239,"conditions":240,"keywords":4,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":251,"locationsCount":252},"100459490","the-effect-of-two-different-cognitive-behavioral-combined-programs-in-blood-collection-100459490","NCT05263297","The Effect of Two Different Cognitive-Behavioral Combined Programs in Blood Collection","The Effect of Two Different Cognitive-Behavioral Combined Programs in Blood Collection on Children's Pain, Fear and Anxiety and Parents' Satisfaction Level: A Randomized Controlled Study","Inclusion Criteria:\n\n* Parents and children are willing to participate in the research,\n* Written and verbal consent of parents, verbal consent of children,\n* The child is in the 8-10 age group,\n* The child has come to the center to have blood drawn,\n* The child does not have a hearing or auditory problem,\n* Absence of pain,\n* The child and parent speak and understand Turkish comfortably,\n* The child's mental development level to be able to answer the questions asked,\n* Not using drugs that will create an analgesic effect in the last 6 hours before the application,\n* Children's cognitive level and motor development are suitable for playing video games or using a kaleidoscope,\n* Having a video game played by the child on the parent's phone,\n* Vascular access is made in one go,\n* Vascular access is performed by the same nurse\n\nExclusion Criteria:\n\n* The child is not in the 8-10 age group,\n* The child has a hearing or auditory problem,\n* Having pain,\n* The child's and parent's inability to speak and understand Turkish comfortably,\n* The child is not at the level of mental development to be able to answer the questions asked,\n* Parents and children are not willing to participate in the research,\n* Parents do not give written and verbal consent, children do not give verbal consent,\n* To have used drugs that will create an analgesic effect in the last 6 hours before the application,\n* Children's cognitive level and motor development are not suitable for playing video games or using a kaleidoscope,\n* Not having a video game played by the child on the parent's phone,\n* Vascular access cannot be performed in one go,\n* Vascular access is not performed by the same nurse.","8 Years","10 Years",{"count":237,"type":20},96,[23],"The aim of this study is to investigate the effect of two different cognitive-behavioral combined programs, including video games or kaleidoscope, on the pain, fear and anxiety experienced by children who apply for therapeutic or diagnostic venous blood collection, and their parents' satisfaction levels. In addition, this research aims to create a holistic approach to child health due to the evaluation of both children and parents.\n\nThe population of the research will be children aged 8-10 who come to the Children's Blood Collection Unit of Karaman Training and Research Hospital between February 2022 and March 2022. The sample of the study will consist of 96 children and their parents who applied to the Blood Collection Unit on the specified dates, met the inclusion criteria and agreed to participate in the study. The pediatric blood collection unit provides service between 08:00 and 16:00 on weekdays. In order to determine the number of samples, power analysis was performed using the G\\*Power (v3.1.9) program. It was planned to carry out the research with a total of 96 children and their parents, 32 in each group, considering possible case losses during the research period.\n\nEvaluation of the data will be done in the computer environment with the SPSS (Statistical Package for Social Sciences) 22.0 package program. Percentage distributions, mean, standard deviation, chi-square test, analysis of variance will be used in the analysis of the data. In addition, the variance of the groups will be examined with the Levene test in order to make further analysis. In cases where the variance is equal, Bonferroni analysis will be used in post hoc advanced analyses, and Dunnett T3 analysis will be used in cases where the variance is not equal. The research findings will be evaluated at the 95% confidence interval, at the p\\\u003C0.05 significance level.",[241,242,243],"Child Behavior","Pain, Acute","Fear","2025-02-10",{"date":246,"type":36},"2025-02-12",{"date":248,"type":36},"2022-04-01",{"date":250,"type":20},"2025-09-30",{"name":42,"class":43},2,{"id":254,"slug":255,"hasResults":11,"nctId":256,"briefTitle":257,"officialTitle":258,"acronym":4,"eligibilityCriteria":259,"healthyVolunteers":11,"sex":16,"minAge":260,"maxAge":17,"enrollmentInfo":261,"targetDuration":4,"studyType":21,"phases":263,"briefSummary":264,"conditions":265,"keywords":267,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":277,"lastUpdatePostDateStruct":278,"startDateStruct":280,"completionDateStruct":282,"leadSponsor":284,"locationsCount":106},"100577166","effects-of-core-stabilization-exercises-in-children-with-acute-lymphoblastic-leukemia-100577166","NCT06794762","Effects of Core Stabilization Exercises in Children with Acute Lymphoblastic Leukemia","Examination of the Effects of Core Stabilization Exercises on Physical Function, Functional Muscle Strength, Functional Exercise Capacity, Postural Control and Fatigue in Children with Acute Lymphoblastic Leukemia Receiving Maintenance Treatment","Inclusion Criteria:\n\n* Children aged 7-18\n* Diagnosed with ALL\n* In the maintenance phase of chemotherapy\n* Children without acute thrombosis, active ischemia, hemodynamic instability\n* Children without uncontrolled pain\n* Children who can follow verbal instructions.\n\nExclusion Criteria:\n\n* Children who have received or are receiving cranial radiotherapy\n* Children with any cardiovascular disease, acute or chronic respiratory disease\n* Children with acute or chronic bone, joint, muscle problems\n* Children diagnosed with neuromotor deficits or genetic disorders\n* Children with vision problems other than refractive errors","6 Years",{"count":262,"type":20},34,[23],"The goal of this clinical trial is to investigate the effects of core stabilization exercises applied in addition to the conventional exercise program on physical function, functional muscle strength, functional exercise capacity, postural control and fatigue in children with acute lymphoblastic leukemia receiving maintenance treatment.\n\nParticipants will be divided into two groups; the first group will be given a conventional exercise program, while the second group will be given core stabilization exercises in addition to the conventional exercise program.",[266],"Acute Lymphoblastic Leukemia",[266,268,269,125,270,271,272,273,274,275,276],"Maintenance Chemotherapy","Rehabilitation","Core Stabilization Exercises","Cancer","Physical Function","Functional Muscle Strength","Functional Exercise Capacity","Postural Control","Fatigue","2025-01-29",{"date":279,"type":36},"2025-01-31",{"date":281,"type":36},"2025-01-14",{"date":283,"type":20},"2026-02",{"name":42,"class":43},{"id":286,"slug":287,"hasResults":11,"nctId":288,"briefTitle":289,"officialTitle":290,"acronym":4,"eligibilityCriteria":291,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":51,"enrollmentInfo":292,"targetDuration":4,"studyType":21,"phases":294,"briefSummary":295,"conditions":296,"keywords":299,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":304,"lastUpdatePostDateStruct":305,"startDateStruct":307,"completionDateStruct":309,"leadSponsor":311,"locationsCount":4},"100568021","the-effect-of-catheter-protector-on-catheter-dwell-time-and-complications-100568021","NCT06675786","The Effect of Catheter Protector on Catheter Dwell Time and Complications","The Effect of Catheter Protector on Catheter Dwell Time and Complications in Patients with Peripheral Venous Catheter in the Oncology Clinic","Inclusion Criteria:\n\n* Inclusion Criteria\n* Hospitalized in the oncology clinic\n* The one with the PVK attached,\n* Volunteered to participate in the research,\n* Treated in the same clinic during the study period,\n* No verbal, perceptual and visual communication problems,\n* 22-24 G (Blue) size catheter used,\n* Between the ages of 18 and 65,\n* Literate,\n* Patients without scar tissue, infection, hematoma, edema at the sites to be used for PVK placement were included in the study.\n\nExclusion Criteria:\n\n* \\- With a clotting disorder,\n* Patients with problems with skin integrity or limb movement such as scar tissue, infection, hematoma, edema at the PVK site,\n* Blood or blood products given through a catheter,\n* Patients who wanted to leave, were referred to a different clinic or discharged during the study were excluded from the study.",{"count":293,"type":20},70,[23],"Objective: This study aimed to determine the effect of applying the IV House Ultradressing catheter protector on the frequency of peripheral venous catheter (PVC) replacements and complications in patients with peripheral venous catheterization in an oncology clinic.\n\nMaterials and Methods: The research was planned as a randomized controlled experimental study. The population of the study consisted of patients hospitalized in the oncology clinic. The sample of the study was calculated based on the data from the study by Büyükyılmaz et al. (2019), which found a significant difference in the average duration of catheter-related phlebitis in the intervention group (2.10 ± 1.55 days) compared to the control group (1.27 ± 0.45 days), with an effect size of d=0.72. As a result of the sample size calculation, 32 patients were predicted for each group. Considering that 10% of patients might drop out during the study, a total of 70 patients, with 35 in each group, were decided to be included. After the catheter is inserted, patients in the intervention group will have their catheter area protected with IV House Ultradressing, while no protective measures will be applied to the control group. Both groups will be evaluated in terms of catheter duration and PVC complications. It is planned to use t-tests and chi-square tests for data analysis.",[297,298],"Peripheral Catheterization","Complications",[300,301,302,303],"Peripheral Venous Catheterization","IV House","Complication","Phlebitis","2024-11-04",{"date":306,"type":36},"2024-11-05",{"date":308,"type":20},"2024-11-01",{"date":310,"type":20},"2025-05-30",{"name":42,"class":43},""]