[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"The Jerzy Kukuczka Academy of Physical Education in Katowice\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":170},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,53,84,111,142],{"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":33,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100644813","dietary-macronutrients-and-gut-microbiota-inflammation-and-metabolic-markers-100644813",false,"NCT07672691","Dietary Macronutrients and Gut Microbiota, Inflammation, and Metabolic Markers","Effects of Diets Differing in Macronutrient Composition on Gut Microbiota Composition, Intestinal Inflammation Markers, Gene Expression Profiles, and Blood Biochemical Parameters in Diverse Populations.","DIETMICRO","Inclusion Criteria:\n\nIn addition to the physical activity requirements described above, the study will include men and women aged 18-60 years with:\n\nBMI not exceeding 40kg\u002Fm²\n\nHabitual mixed diet prior to study enrollment\n\nNormal blood pressure\n\n* Exclusion Criteria:\n\nPoprawiłem już \\*\\*Exclusion Criteria\\*\\* w poprzedniej odpowiedzi - wszystkie te kryteria już tam są wpisane. Oto pełna, ostateczna wersja z wszystkimi wskazanymi kryteriami wyłączenia:\n\n\\*\\*\\* \\*\\*Exclusion Criteria:\\*\\*\n\n* Use of medications regulating \\*\\*glucose levels\\*\\* (e.g., metformin) or \\*\\*blood lipids\\*\\* (e.g., \\*\\*statins\\*\\*)\n* \\*\\*Hypertension\\*\\* or pharmacological treatment for hypertension\n* Diagnosed \\*\\*gastrointestinal disorders\\*\\*, including:\n* Gastric and duodenal ulcers\n* \\*\\*Irritable bowel syndrome (IBS)\\*\\*\n* \\*\\*Ulcerative colitis\\*\\*\n* \\*\\*Celiac disease\\*\\*\n* Chronic use of medications such as:\n* \\*\\*Mesalazine\\*\\*\n* \\*\\*Corticosteroids\\*\\*\n* \\*\\*Statins\\*\\*\n* \\*\\*Proton pump inhibitors (PPI)\\*\\*\n* \\*\\*Non-steroidal anti-inflammatory drugs (NSAIDs)\\*\\*\n* \\*\\*Anticonceptional medications\\*\\*\n* \\*\\*Any supplements\\*\\*\n* \\*\\*Alcohol consumption\\*\\* \\> 2 times\u002Fweek with \\> 15 g alcohol per occasion (approximately 15 g alcohol = 330 mL beer, 150 mL dry red wine, or 50 mL vodka)\n* \\*\\*Smoking cigarettes\\*\\*\n* Following a \\*\\*ketogenic diet\\*\\* or \\*\\*vegetarian diet\\*\\* within \\*\\*1 month\\*\\* prior to study enrollment",true,"ALL","18 Years","60 Years",{"count":22,"type":23},200,"ESTIMATED","INTERVENTIONAL",[26],"NA","Poniżej znajduje się bardziej płynna i mniej powtarzalna wersja tekstu:\n\nThis 12-week randomized controlled trial will investigate the effects of dietary patterns with different macronutrient compositions on gut microbiota, intestinal inflammation, gene expression, and metabolic health in healthy adults.\n\nParticipants will be randomly assigned to one of three dietary interventions: a ketogenic diet (KD), a vegetarian diet (VD), or a control diet (CD) reflecting their habitual mixed dietary pattern. Adherence to the assigned diet will be monitored through dietary records and regular nutritional counseling.\n\nThe study will evaluate changes in gut microbiota composition, inflammatory biomarkers, transcriptomic profiles, and blood biochemical parameters associated with lipid and glucose metabolism. Blood and stool samples will be collected at predefined time points throughout the intervention, while participants in the KD group will additionally undergo ketone monitoring to assess dietary compliance.\n\nBy comparing the ketogenic and vegetarian diets with a standard mixed diet, this study aims to determine their effects on gut health, metabolic function, and systemic inflammation, thereby providing evidence to inform dietary recommendations.\n\nTa wersja eliminuje powtórzenia (\"diet\", \"study\", \"monitor\", \"effects\"), jest bardziej naturalna stylistycznie i odpowiada standardowi językowemu publikacji w czasopismach z zakresu żywienia i medycyny.",[29,30,31,32],"Nutrition","Ketogenic Diet","Gene Expression","Diet",[34,35,36,37,38,39],"ketogenic diet","gene expression","transcriptomics","biochemical parameters","stool microbiome","ketone bodies","RECRUITING","2026-07-01",{"date":43,"type":44},"2026-07-02","ACTUAL",{"date":46,"type":44},"2024-09-02",{"date":48,"type":23},"2028-12-30",{"name":50,"class":51},"The Jerzy Kukuczka Academy of Physical Education in Katowice","OTHER",2,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":17,"sex":18,"minAge":60,"maxAge":20,"enrollmentInfo":61,"targetDuration":4,"studyType":24,"phases":62,"briefSummary":63,"conditions":64,"keywords":67,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":83},"100643004","effects-of-high-dose-vitamin-d-on-hormones-neuromuscular-function-cognition-and-body-composition-in-athletes-100643004","NCT07641075","Effects of High-Dose Vitamin D on Hormones, Neuromuscular Function, Cognition, and Body Composition in Athletes","The Effect of High-dose Vitamin D Supplementation on Selected Hormone Concentrations, Neuromuscular Transmission, Athletic Performance, Cognitive Functions, and Body Composition in Athletes.","Inclusion Criteria:\n\n* a minimum of 8 years of training experience,\n* absence of injuries in the 6 months leading up to the assessments,\n* consistent engagement in training sessions a minimum of 5 times per week over the last 6 months.\n\nExclusion Criteria:\n\n* vitamin D supplementation within one month prior to the study,\n* use of multivitamin supplements,\n* intestinal disorders.","17 Years",{"count":22,"type":23},[26],"This study aims to evaluate the effects of high-dose vitamin D3 supplementation on selected physiological, neuromuscular, and cognitive parameters in athletes. At the baseline visit, participants will undergo a series of assessments at the Functional Research Laboratory at AWF Katowice, including a 10 mL venous blood sample collection, body composition analysis (via InBody and DEXA scans), neuromuscular function evaluation using tensiomyography (TMG), and computerized cognitive tests via the Vienna Test System.\n\nFollowing baseline testing, participants will be randomly assigned to either the vitamin D3 group or the placebo group. The active group will receive a daily dose of 4,000 IU of vitamin D3 (1 capsule with dinner), while the control group will receive an identical placebo. The intervention period will last for 4 or 8 weeks. Upon completion of the supplementation period, all baseline assessments will be repeated to evaluate the post-intervention changes.",[65,66],"Vitamin D 25-Hydroxylase Deficiency","Vitamin D Deficiency\u002FInsufficiency",[68,69,70,71,72,73,74],"vitamin D","athletes","coggnitive function","neuro-muscular function","hormones","speed","performance","2026-06-08",{"date":77,"type":44},"2026-06-11",{"date":79,"type":44},"2025-07-01",{"date":81,"type":23},"2028-12-31",{"name":50,"class":51},1,{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":92,"targetDuration":94,"studyType":95,"phases":4,"briefSummary":96,"conditions":97,"keywords":99,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":83},"100638516","prevalence-of-musculoskeletal-disorders-among-musicians-100638516","NCT07600437","Prevalence of Musculoskeletal Disorders Among Musicians","Assessment of the Prevalence of Playing-related Musculoskeletal Disorders Among Instrumental Musicians","nill","Inclusion Criteria:\n\n* consent to participate in the study,\n* over 18 years of age,\n* professionally active musician - instrumentalist or musician-hobbyist not working as a professionalist musician\n\nExclusion Criteria:\n\n* lack of consent to participate in the study, age under 18,\n* artist - singer,\n* pregnancy,\n* active cancer,\n* acute viral, bacterial or other infections,\n* current exacerbation of chronic diseases or other conditions that may affect playing the instrument (e.g. osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, fibromyalgia, etc.),\n* previous surgeries and serious injuries of the musculoskeletal system (e.g. road accidents) within the last 5 years.",{"count":93,"type":23},450,"1 Day","OBSERVATIONAL","Research conducted at the Faculty of Physiotherapy, Academy of Physical Education in Katowice, examines musculoskeletal disorders among instrumental musicians.\n\nThe study protocol was approved by the Ethics Committee of Polish Physiotherapy Associationon (Resolution No. 05\u002F06\u002F2025) on June 11, 2025.\n\nThe application form includes QuickDASH software enabling the functioning of the system and the MPIIQM-P system, which monitors the functioning of the musculoskeletal system and its impact on everyday musical performance.",[98],"Musckloskeletal US",[100,101,102],"Playing-related Musculoskeletal Disorders","PRMDs","musicians","2026-05-13",{"date":105,"type":44},"2026-05-20",{"date":107,"type":44},"2025-06-01",{"date":109,"type":23},"2026-06-30",{"name":50,"class":51},{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":17,"sex":18,"minAge":118,"maxAge":119,"enrollmentInfo":120,"targetDuration":4,"studyType":24,"phases":122,"briefSummary":123,"conditions":124,"keywords":126,"overallStatus":133,"whyStopped":4,"lastUpdateSubmitDate":134,"lastUpdatePostDateStruct":135,"startDateStruct":137,"completionDateStruct":139,"leadSponsor":141,"locationsCount":4},"100615795","temporomandibular-joints-mobility-and-head-posture-influence-of-manual-therapy-and-exercises-in-dental-patients-100615795","NCT07297251","Temporomandibular Joints Mobility and Head Posture: Influence of Manual Therapy and Exercises in Dental Patients.","Assessment of Temporomandibular Joint Mobility With Different Head Postures. Analysis of the Influence of Selected Manual Therapy Techniques on Temporomandibular Joint Mobility and Head Posture.","Inclusion Criteria:\n\n* Patients aged 11 to 13 years with a confirmed occlusion class (Class I, II, or III) with parental\u002Flegal guardian consent.\n* Patients aged 13 to 17 years with personal assent and parental\u002Flegal guardian consent.\n* Adult patients (up to 65 years of age) who have provided informed consent.\n\nExclusion Criteria:\n\n* Inability to perform required study tests or procedures.\n* Positive safety tests indicating contraindications to manual intervention.\n* History of surgeries or trauma to the maxillofacial region.\n* Genetic defects or neurological disorders.\n* Current orthodontic treatment with fixed appliances.\n* Current splint therapy.\n* Pregnancy.\n* Lack of consent from a parent or legal guardian (for minors).\n* Lack of cooperation from the participant (especially children).","11 Years","65 Years",{"count":121,"type":23},100,[26],"Goal: This clinical study aims to investigate how the range of motion of the temporomandibular joints (TMJ) changes in relation to the patient's head posture. Furthermore, we will assess the efficacy of a specific physiotherapy program in improving TMJ mobility and influencing head alignment in patients undergoing orthodontic treatment or prosthetic reconstruction.\n\nScope: The project will evaluate TMJ function and head alignment in orthodontic or prosthetic patients aged 11-65. The core focus is to analyze the correlation between head posture and TMJ mobility and to measure changes in these parameters before and after the manual physiotherapy intervention.",[125],"Temporomandibular Joint Disorders",[127,128,129,130,131,132],"temporomandibular joint","range of motion","cervical spine","kinematic","manual therapy","exercices","NOT_YET_RECRUITING","2025-12-19",{"date":136,"type":44},"2025-12-22",{"date":138,"type":23},"2026-01-20",{"date":140,"type":23},"2027-12-30",{"name":50,"class":51},{"id":143,"slug":144,"hasResults":11,"nctId":145,"briefTitle":146,"officialTitle":147,"acronym":4,"eligibilityCriteria":148,"healthyVolunteers":11,"sex":18,"minAge":149,"maxAge":150,"enrollmentInfo":151,"targetDuration":4,"studyType":24,"phases":153,"briefSummary":154,"conditions":155,"keywords":157,"overallStatus":133,"whyStopped":4,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":167,"leadSponsor":169,"locationsCount":52},"100589816","influence-of-sensory-stimulation-on-sensory-parameters-and-motor-function-in-children-with-developmental-coordination-disorder-100589816","NCT06959329","Influence of Sensory Stimulation on Sensory Parameters and Motor Function in Children With Developmental Coordination Disorder","The Influence of Intensified Sensory Stimulation on Upper Extremity Sensory Parameters and Motor Function in Children With Developmental Coordination Disorder","Inclusion Criteria:\n\n* between 12-16 years of age\n* diagnosed severe symptoms of the developmental coordination disorder based on The Movement Assessment Battery for Children 2nd Edition (M-ABC 2), with scores ranging from 40 to 50\n* typical intellectual development (i.e., children attending mainstream education)\n* voluntary participation and informed consent signed by parents or legal guardians\n\nExclusion Criteria:\n\n* current or previous diagnosis of serious orthopaedic or neurological conditions (e.g. fractures, congenital deformities, cerebral palsy, etc.)\n* history of any surgical procedures\n* history of significant musculoskeletal pain or dysfunction lasting more than two weeks and requiring medical or physiotherapeutic intervention, or any such symptoms occurring within one month prior to the study\n* any current musculoskeletal dysfunction and\u002For pain\n* body mass index exceeding 22 kg\u002Fm³","12 Years","16 Years",{"count":152,"type":23},80,[26],"The goal of this clinical trial is to evaluate whether intensive sensory stimulation therapy can improve upper limb motor skills and sensory function in children aged 12-16 years with severe symptoms of Developmental Coordination Disorder (DCD). The main questions it aims to answer are:\n\n1. Will children with DCD who undergo intensive sensory stimulation therapy show greater improvement in upper limb motor function compared to those receiving standard therapy?\n2. Will intensive sensory stimulation therapy lead to better sensory function outcomes, including joint position sense, resistance sense, pressure sense, temperature perception, and two-point discrimination? Researchers will compare children receiving intensive sensory stimulation therapy to those receiving standard therapy without intensive sensory stimulation to see if the targeted intervention results in superior improvements in motor and sensory function.",[156],"Developmental Coordination Disorder",[158,159,160,161,162],"developmental coordination disorder","sensory function","motor function","sensory stimulation","adolescents","2025-05-07",{"date":165,"type":44},"2025-05-13",{"date":107,"type":23},{"date":168,"type":23},"2026-04-30",{"name":50,"class":51},""]