[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Palacky University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":188},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,43,72,95,122,154],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100617658","reflex-therapy-of-temporomandibular-dysfunctions-100617658",false,"NCT07321483","Reflex Therapy of Temporomandibular Dysfunctions","Evaluation of the Therapeutic Efficacy of Reflex Therapy Using Dry Needling in Patients With Functional Temporomandibular Pain Syndrome: A Prospective, Randomized, Controlled Pilot Study.","Inclusion Criteria:\n\n* Diagnosed with functional temporomandibular pain syndrome without structural temporomandibular joint damage.\n* Aged ≥18 years.\n* Stable health condition suitable for outpatient rehabilitation.\n* Willingness to participate and ability to follow the therapeutic protocol.\n\nExclusion Criteria:\n\n* Presence of degenerative, post-traumatic, or inflammatory changes in the temporomandibular joint.\n* Cognitive or psychiatric disorders limiting cooperation.\n* Lack of informed consent or non-compliance during treatment","ALL","18 Years",{"count":19,"type":20},100,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study aims to evaluate the effectiveness of dry needling in patients with functional temporomandibular pain syndrome by comparing standard rehabilitation therapy alone with therapy combined with dry needling to reduce pain, improve jaw function and enhance quality of life.",[26],"Temporomandibular Joint Dysfunction; Myofascial Pain Syndrome; Orofacial Pain; Musculoskeletal Disorders",[28,29],"headache; temporomandibular disorders; dry needling; rehabilitation therapy; pain; quality of life","temporomandibular disorders; dry needling; rehabilitation therapy; pain; quality of life","RECRUITING","2026-08-09",{"date":33,"type":34},"2026-08-11","ACTUAL",{"date":36,"type":34},"2025-12-20",{"date":38,"type":20},"2027-08-02",{"name":40,"class":41},"Palacky University","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":51,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":71,"locationsCount":42},"100647773","effect-of-hydrogen-rich-water-during-tapering-on-recovery-after-functional-overreaching-in-basketball-players-100647773","NCT07714057","Effect of Hydrogen-rich Water During Tapering on Recovery After Functional Overreaching in Basketball Players","Effect of Hydrogen-rich Water Supplementation During Tapering on Recovery After Functional Overreaching in Competitive Male Basketball Players: A Randomized, Double-blind, Placebo-controlled Paralel-group Trial","Inclusion Criteria:\n\n* Competitive male basketball players.\n* Signed informed consent.\n* Completion of entry medical and laboratory screening.\n\nExclusion Criteria:\n\n* Acute injury or infection.\n* History or presence of relevant cardiovascular, respiratory, metabolic, or other disease that may affect the study results.\n* Use of medication affecting recovery markers or study results.",true,"MALE","35 Years",{"count":54,"type":20},30,[23],"The goal of this clinical trial is to evaluate whether hydrogen-rich water supplementation during tapering improves recovery after functional overreaching in competitive male basketball players aged 18-35 years. The main questions it aims to answer are:\n\n* Does hydrogen-rich water improve autonomic recovery after functional overreaching?\n* Does hydrogen-rich water improve recovery in biochemical, performance, and subjective feeling outcomes during tapering?\n\nResearchers will compare hydrogen-rich water to placebo (water containing no molecular hydrogen) to determine whether molecular hydrogen improves recovery after accumulated fatigue has been induced by functional overreaching. Participants will:\n\n* Complete a training cycle including normal training, functional overreaching, and tapering.\n* Consume hydrogen-rich or placebo water daily during the one-week tapering period.\n* Undergo repeated testing of autonomic nervous system, blood biochemical markers, performance, and subjective soreness.",[58],"Healthy Active Athletes",[60,61,62,63,64],"molecular hydrogen","functional overreaching","tapering","heart rate variability","basketball","2026-07-27",{"date":67,"type":34},"2026-07-28",{"date":65,"type":34},{"date":70,"type":20},"2026-12",{"name":40,"class":41},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":50,"sex":79,"minAge":17,"maxAge":80,"enrollmentInfo":81,"targetDuration":4,"studyType":21,"phases":83,"briefSummary":84,"conditions":85,"keywords":87,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":93,"leadSponsor":94,"locationsCount":42},"100642210","effect-of-pre-exercise-inhalation-of-molecular-hydrogen-on-metabolic-response-during-graded-exercise-in-healthy-women-100642210","NCT07644000","Effect of Pre-exercise Inhalation of Molecular Hydrogen on Metabolic Response During Graded Exercise in Healthy Women","Effect of Repeated Pre-exercise Inhalation of Molecular Hydrogen on Metabolic Response During Graded Exercise in Healthy Women: A Randomized, Double-blind, Placebo-controlled Crossover Trial","Inclusion Criteria:\n\n* Healthy female participants.\n* Regular menstrual cycle with exercise testing scheduled outside the menstrual phase.\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Pregnancy or breastfeeding.\n* History or presence of cardiovascular disease.\n* History or presence of respiratory disease.\n* Regular use of medications affecting metabolism.\n* Use of dietary supplements affecting metabolism within 14 days prior to intervention.\n* Strenuous physical activity within 24 hours prior to exercise testing.\n* Any contraindication to exercise testing or study participation determined by a physician.","FEMALE","30 Years",{"count":82,"type":20},22,[23],"The goal of this clinical trial is to evaluate if molecular hydrogen can reduce the metabolic response during graded exercise in healthy women aged 18-30 years. The main questions it aims to answer are:\n\n* Does molecular hydrogen reduce the respiratory exchange ratio?\n* Does molecular hydrogen reduce oxygen uptake?\n\nResearchers will compare molecular hydrogen to a placebo (ambient air containing no molecular hydrogen) to see if molecular hydrogen reduces the metabolic response.\n\nParticipants will:\n\n* Inhale molecular hydrogen for 60 minutes each day for 7 days.\n* Undergo an exercise testing twice after a two-week washout period.",[86],"Healthy Adult Females",[60,88],"metabolic response","2026-06-22",{"date":91,"type":34},"2026-06-25",{"date":89,"type":34},{"date":70,"type":20},{"name":40,"class":41},{"id":96,"slug":97,"hasResults":11,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":11,"sex":16,"minAge":102,"maxAge":103,"enrollmentInfo":104,"targetDuration":4,"studyType":21,"phases":106,"briefSummary":107,"conditions":108,"keywords":110,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":42},"100632115","comparing-game-based-reward-systems-to-support-childrens-engagement-100632115","NCT07509489","Comparing Game-Based Reward Systems to Support Children's Engagement:","Effect of Gamification-Based Incentive Schemes on Behavioral Adherence in Children","Inclusion Criteria:\n\nChildren aged 9-12 years Regular smartphone use (at least 4 days per week) Has access to a smartphone throughout most of the day Brings a smartphone to school Owns a personal smartphone with a touchscreen Owns a smartphone with Android operating system (version 9 or higher) Has access to mobile internet on their device Is allowed to use a smartphone at school during breaks (e.g., lunch or longer breaks) for questionnaire completion and to wear a smartwatch Native Czech speaker\n\nExclusion Criteria:\n\nDoes not meet one or more of the inclusion criteria Has a sibling already enrolled in the study","9 Years","12 Years",{"count":105,"type":20},160,[23],"This Randomized Control Trial evaluates the impact of different gamification-based incentive schemes (levels, streaks and their combination) on adherence to target behaviors in children. Participants are randomized into four groups with different types of motivational frameworks.",[109],"Children",[111,112,113],"incentive","financial","behaviour","2026-05-05",{"date":116,"type":34},"2026-05-08",{"date":118,"type":34},"2026-03-28",{"date":120,"type":20},"2027-12-01",{"name":40,"class":41},{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":127,"acronym":4,"eligibilityCriteria":128,"healthyVolunteers":50,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":129,"targetDuration":4,"studyType":131,"phases":4,"briefSummary":132,"conditions":133,"keywords":138,"overallStatus":145,"whyStopped":4,"lastUpdateSubmitDate":146,"lastUpdatePostDateStruct":147,"startDateStruct":149,"completionDateStruct":151,"leadSponsor":153,"locationsCount":42},"100627659","implementation-of-machine-learning-into-optical-pedography-100627659","NCT07451509","Implementation of Machine Learning Into Optical Pedography","Implementing Machine Learning Into Optical Pedography: Development and Validation of a Novel Instrument: a Validation Study","Inclusion Criteria:\n\n* A healthy individual with no absence of lower extremity\n* Aged ≥18 years\n* Willingness to participate and ability to follow the assessors instructions.\n\nExclusion Criteria:\n\n* Presence of foot diseases alternating foot contact area\n* Cognitive or psychiatric disorders limiting cooperation\n* Lack of informed consent or non-compliance during imaging",{"count":130,"type":20},150,"OBSERVATIONAL","This study aims to evaluate the validity and reliability of a proposed plantar pressure assessment intrument based on an implementation of machine learning into optical pedography.",[134,135,136,137],"Healthy","Foot","Pressure Area","Pressure Distribution",[139,140,141,142,143,144],"pedography","machine learning","AI","plantar pressure","validity","reliability","NOT_YET_RECRUITING","2026-02-28",{"date":148,"type":34},"2026-03-05",{"date":150,"type":20},"2026-03",{"date":152,"type":20},"2027-12",{"name":40,"class":41},{"id":155,"slug":156,"hasResults":11,"nctId":157,"briefTitle":158,"officialTitle":159,"acronym":4,"eligibilityCriteria":160,"healthyVolunteers":50,"sex":16,"minAge":161,"maxAge":80,"enrollmentInfo":162,"targetDuration":4,"studyType":21,"phases":164,"briefSummary":165,"conditions":166,"keywords":173,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":180,"lastUpdatePostDateStruct":181,"startDateStruct":183,"completionDateStruct":185,"leadSponsor":187,"locationsCount":42},"100603393","effects-of-single-sodium-bicarbonate-supplementation-on-national-level-finswimming-performance-100603393","NCT07135934","Effects of Single Sodium Bicarbonate Supplementation on National-Level Finswimming Performance","Evaluation of the Effects of Single Sodium Bicarbonate Supplementation on Finswimming Performance of National Level Finswimmers: A Randomized, Double-Blind, Placebo-Controlled Crossover Study","Inclusion Criteria:\n\n1. Member of a wider national selection in finswimming (junior or senior level)\n2. Regular participation in competitive finswimming training (≥4 sessions per week)\n3. Age between 15 and 30 years\n4. Absence of chronic illness or injury\n5. No use of medications or dietary supplements during the study period\n6. Signed informed consent (for minors, also signed by a legal guardian)\n\nExclusion Criteria:\n\n1. History of gastrointestinal disorders affecting supplement tolerance\n2. Presence of cardiovascular, metabolic, or musculoskeletal disorders\n3. Current illness or acute infection\n4. Regular use of substances that may interfere with acid-base balance\n5. Refusal to comply with pre-test restrictions (e.g., 48 hours without training)","15 Years",{"count":163,"type":20},20,[23],"This randomized, double-blind, placebo-controlled crossover trial will investigate the acute effects of sodium bicarbonate supplementation on performance, stroke biomechanics, and selected physiological and perceptual responses during a simulated 200-meter Bi-Fins race in elite finswimmers.",[167,168,169,170,171,172],"Sport Performance","Acid Base Imbalance","Ergogenic Support","Sodium Bicarbonate","Water Sports","Biomechanics",[170,174,175,176,177,172,178,179],"Stroke Rate","Finswimming","Stroke Length","Athletes","Gastrointestinal Discomfort","Rate of Perceived Exertion","2025-08-20",{"date":182,"type":34},"2025-08-22",{"date":184,"type":34},"2025-07-01",{"date":186,"type":20},"2026-12-20",{"name":40,"class":41},""]