[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"European University of Madrid\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":127},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,80,102],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100631384","influence-of-abdominal-muscle-function-on-knee-stability-for-injury-prevention-100631384",false,"NCT07499973","Influence of Abdominal Muscle Function on Knee Stability for Injury Prevention","Investigation of Core Neuromuscular Performance as a Determinant of Knee Stability and Injury Prevention in Young Female Athletes Using Vicon 3D Motion Capture and Functional Performance Tests","Inclusion Criteria:\n\n* Female participants\n* Age between 18 and 35 years\n* Performing regular physical activity ≥ 6 hours per week.\n* Able to complete all assessment procedures (Prone Bridge Test, Lateral Squat Down, Y-Balance Test, Drop Vertical Jump).\n* Willing to comply with the 8-week study procedures (training program or control condition)\n\nExclusion Criteria:\n\n* Current musculoskeletal injury affecting the lower limbs, trunk, or spine\n* History of surgery in the lower limbs or spine in the past 12 months\n* Known neurological, cardiovascular, or systemic conditions that may interfere with physical testing\n* Pregnancy\n* Participation in any structured core-strengthening program during the study period\n* Inability to abstain from core training if assigned to the control group",true,"FEMALE","18 Years","35 Years",{"count":21,"type":22},35,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn whether an 8-week core stabilization training program can improve abdominal strength and knee stability in physically active women aged 18 to 35. The main questions it aims to answer are:\n\nDoes core stabilization training improve abdominal endurance as measured by the Prone Bridge Test? Does this training enhance knee stability as measured by the Lateral Squat Down, Y-Balance Test, and Drop Vertical Jump?\n\nResearchers will compare participants' results before and after the intervention to see whether the training program leads to measurable improvements in strength and stability.\n\nParticipants will:\n\nComplete baseline testing of abdominal strength and knee stability using standardized assessments (Prone Bridge Test, Lateral Squat Down, Y-Balance Test, Drop Vertical Jump) recorded with a Vicon motion-capture system.\n\nPerform an 8-week supervised core stabilization program that includes front plank, side plank, and Nordic hamstring exercises following a structured progression.\n\nComplete the same performance tests again after the intervention.",[28,29],"Core Strength","Knee Stability",[31,29,32,33],"Core Stability","Injury Prevention","Biomechanics","RECRUITING","2026-03-25",{"date":37,"type":38},"2026-03-30","ACTUAL",{"date":40,"type":38},"2026-03-06",{"date":42,"type":22},"2026-09",{"name":44,"class":45},"European University of Madrid","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":54,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":46},"100625486","evaluation-of-a-digital-neurorehabilitation-program-using-exergames-for-adults-with-mild-cognitive-impairment-100625486","NCT07423260","Evaluation of a Digital Neurorehabilitation Program Using Exergames for Adults With Mild Cognitive Impairment","Digital Exergame Neurorehabilitation to Enhance Quality of Life and Functional Autonomy in Institutionalized Older Adults With Mild Cognitive Impairment: Randomized Controlled Trial","Inclusion Criteria:\n\n* Age 70 years or older.\n* Diagnosis of mild cognitive impairment, defined by Montreal Cognitive Assessment (MoCA) score between 18 and 25.\n* Ability to maintain standing and\u002For ambulate with or without assistive devices.\n* Institutional residence for at least 3 months.\n* Informed consent provided by participant or legal representative.\n\nExclusion Criteria:\n\n* Acute illness, musculoskeletal condition, or pain that limits safe participation in training.\n* Uncompensated sensory deficits (vision or hearing) that interfere with task performance.\n* Disruptive behavior or neuropsychiatric symptoms that impede participation.\n* Active epilepsy or medical contraindications for physical exercise.","ALL","70 Years",{"count":57,"type":22},38,[25],"The goal of this clinical trial is to learn whether a semi-autonomous digital telerehabilitation program using therapeutic video games (\"exergames\") can help improve quality of life and functional independence in older adults living in long-term care centers who have mild cognitive impairment (MCI).\n\nThe main questions we want to answer are:\n\nDoes this exergame-based program help participants move better, walk more safely, and perform daily activities with more independence? Does it improve confidence while moving and lower the fear of falling? Is this program cost-effective compared with a standard one-to-one physiotherapy program?\n\nResearchers will compare two groups:\n\nIntervention group: participants will use a CE-marked digital rehabilitation platform that provides lower-limb and balance training through interactive exergames.\n\nControl group: participants will receive an individual physiotherapy program of similar duration and intensity.\n\nParticipants will:\n\nTake part in a 6-week training program (using exergames or standard physiotherapy, depending on their group).\n\nComplete tests that measure mobility, balance, walking while doing a cognitive task (called \"dual task\"), confidence in avoiding falls, and daily functioning.\n\nAnswer short questionnaires about well-being and quality of life.\n\nThis pilot study will help determine whether the exergame-based program is safe, useful, and feasible for older adults with MCI living in long-term care settings.",[61],"Mild Cognitive Impairment",[63,64,65,66,67,68,69,70],"mild cognitive impairment","older adults","digital neurorehabilitation","Telerehabilitation","Therapeutic video games","Exergames","Gait and dual-task performance","Balance training","NOT_YET_RECRUITING","2026-02-17",{"date":74,"type":38},"2026-02-20",{"date":76,"type":22},"2026-03",{"date":78,"type":22},"2026-10",{"name":44,"class":45},{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":16,"sex":54,"minAge":18,"maxAge":87,"enrollmentInfo":88,"targetDuration":4,"studyType":23,"phases":90,"briefSummary":91,"conditions":92,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":101,"locationsCount":4},"100592471","acute-effect-of-forearm-neuromuscular-taping-on-pain-biological-and-functional-variables-post-exercise-100592471","NCT06993857","Acute Effect of Forearm Neuromuscular Taping on Pain, Biological and Functional Variables Post-exercise.","Acute Effect of Forearm Neuromuscular Taping on Maximal Grip Strength, Pressure Pain Threshold, and Muscle Oxygenation in Healthy Collegiate Athletes Post-exercise: A Randomized Controlled Trial.","Inclusion Criteria:\n\n* Age between 18 and 30 years.\n* Both genders.\n* Body mass index between 18.50 and 23.99 kg\u002Fm².\n* No musculoskeletal disorders in the last 3 months and intact skin on the forearm.\n* No neurological or circulatory disease.\n* No additional exercise or treatment during the study.\n* No induced fatigue before the experiment.\n* Physically active individual (defined as performing at least 150-300 minutes of moderate activity or 75-150 minutes of vigorous activity per week for at least 6 months).\n\nExclusion Criteria:\n\n* Acute soft tissue injury to the upper extremity in the past month.\n* Allergy to NMT or similar drugs.\n* History of surgical procedures on the upper extremities.\n* Functional impairment of vision or vestibular sensation.\n* Frequent use of neuromuscular taping on the upper extremities.\n* Analgesic intervention for musculoskeletal pain in the past 3 weeks.\n* Participation in a physical therapy rehabilitation program in the past 3 months.\n* Serious physical injuries that limit the ability to perform these procedures.","30 Years",{"count":89,"type":22},40,[25],"This study aims to evaluate the acute effect of neuromuscular taping applied to the forearm on maximal grip strength, pressure pain threshold, and muscle oxygenation in healthy university athletes after exercise. Using a randomized controlled trial design, the study aims to provide rigorous evidence that will help clarify the potential benefits of Neuromuscular Taping (NMT) in a sports context. The relevance of this research lies in providing useful information for health and sports professionals, facilitating informed decision-making regarding the use of this technique in daily practice. A randomized controlled trial will be conducted, with participants divided into four groups: two experimental groups, one placebo group, and one control group. One experimental group will receive NMT with proximal-to-distal tension, while the other will receive distal-to-proximal tension. The placebo group will receive NMT without tension, and the control group no NMT application.",[93,94],"KINESIOTAPING","NEUROMUSCULAR TAPING","2025-05-27",{"date":97,"type":38},"2025-05-29",{"date":99,"type":22},"2025-06",{"date":99,"type":22},{"name":44,"class":45},{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":54,"minAge":18,"maxAge":55,"enrollmentInfo":109,"targetDuration":4,"studyType":23,"phases":111,"briefSummary":112,"conditions":113,"keywords":115,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":126},"100572575","impact-of-virtual-reality-physiotherapy-on-multiple-sclerosis-patients-100572575","NCT06735053","Impact of Virtual Reality Physiotherapy on Multiple Sclerosis Patients","Experimental Study on the Impact of a Virtual Reality-Based Physiotherapy Program as a Complement to a Conventional Physiotherapy Program in Patients With Moderate to Severe Multiple Sclerosis","Inclusion Criteria:\n\n* Confirmed diagnosis of Multiple Sclerosis based on McDonald criteria, with an evolution time of more than two years.\n* All patients with Multiple Sclerosis are included according to the Kurtzke Multiple Sclerosis Disability Status Scale (EDSS) (ANNEX II) with a score greater than or equal to 6.5 (Need of two types of support to walk -two canes, walker...- about 20 meters without resting).\n* Stable medical treatment for at least six months prior to intervention.\n* Absence of cognitive impairment, with ability to understand instructions and to obtain a score equal to or greater than 24 on the Minimental Test.\n\nExclusion Criteria:\n\n* Diagnosis of another neurological disease or musculoskeletal disorder other than MS.\n* Diagnosis of any cardiovascular, respiratory or metabolic disease, or other conditions that may interfere with this study.\n* To have suffered an exacerbation or hospitalization in the last 3 months before starting the assessment protocol, nor during the therapeutic intervention process.\n* To have received a course of steroids, intravenously or orally, 6 months prior to the start of the assessment protocol and within the intervention period of the study duration.\n* Visual disturbances not corrected by ocular devices.",{"count":110,"type":22},26,[25],"The goal of this clinical trial is to learn if virtual reality combined with conventional physiotherapy intervention works to treat moderate to severe multiple sclerosis persons. The main questions it aims to answer are:\n\n* Does the application of a virtual reality-based program along with conventional physiotherapy produces improvements compared to the application of conventional physiotherapy and placebo virtual reality in motor aspects of patients with multiple sclerosis?\n* Does the application of a virtual reality-based program along with conventional physiotherapy produces improvements compared to the application of conventional physiotherapy and placebo virtual reality in cognitive aspects of patients with multiple sclerosis\n\nResearchers will compare a virtual reality-based program along with conventional physiotherapy with a placebo virtual reality to see if virtual reality improve motor and cognitive aspects of multiple sclerosis.\n\nParticipants will:\n\n* Visit the clinic twice a week for 10 weeks to receive a 1-hour session of virtual reality and conventional physiotherapy.\n* Be assessed using various scales and questionnaires at three different times: at the start of the study, at the end of the treatment, and 4 weeks after the study ends.",[114],"Multiple Sclerosis",[116,117],"multiple sclerosis","virtual reality","2025-02-20",{"date":120,"type":38},"2025-02-21",{"date":122,"type":22},"2025-02",{"date":124,"type":22},"2025-07",{"name":44,"class":45},2,""]