[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"muscular-strength\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:muscular-strength":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,51],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100640667","effectiveness-of-dance-therapy-in-stroke-patients-100640667",false,"NCT07578493","Effectiveness of Dance Therapy in Stroke Patients.","Effectiveness of Proprioceptive Neuromuscular Facilitation-based Dance Therapy for Patients With Chronic Stroke.","Inclusion Criteria:\n\n* Chronic hemiparesis (≥ 6 months post-stroke).\n* Ability to maintain independent standing or with minimal assistance.\n* Clinical stability to perform moderate physical exercise.\n* Sufficient understanding to follow simple instructions.\n\nExclusion Criteria:\n\n* Severe aphasia or other cognitive disorders that limit comprehension.\n* Behavioral disorders that hinder group participation.\n* Severe musculoskeletal disorders or concomitant neurological conditions.","ALL","18 Years","80 Years",{"count":20,"type":21},16,"ESTIMATED","INTERVENTIONAL",[24],"NA","Hemiparesis following a stroke is associated with persistent deficits in postural control, balance, and social participation, especially in the chronic phase. Dance therapy, as a multisensory intervention based on movement, music, and body expression, could promote sensorimotor integration and improve postural stability, complementing conventional physiotherapy. The primary objective of this pilot study is to evaluate the effect of a therapeutic dance program on postural control in individuals with chronic hemiparesis. A secondary objective is to analyze changes in functional balance and gait, as well as subjective satisfaction with the therapy. A controlled study with two parallel groups will be conducted. Sixteen participants with chronic hemiparesis will be recruited (n=8 experimental group; n=8 control group). Both groups will receive standard physiotherapy, but the experimental group will also receive an 8-week therapeutic dance program, with one 30-minute session per week to complement their usual therapy. Pre- and post-intervention assessments will be performed. ThThe experimental group is expected to show a significantly greater improvement in posturographic and clinical parameters compared to the control group. The results could support the implementation of dance therapy as a complementary intervention in community neurorehabilitation programs.",[27,28,29,30,31],"Balance","Gait Analysis","Thermography","Range of Motion, Articular","Muscular Strength",[33,34,35,36,37],"Dance Therapy","Stroke","Postural balance","Gait","Physical Therapy Modalities","NOT_YET_RECRUITING","2026-05-05",{"date":41,"type":42},"2026-05-11","ACTUAL",{"date":44,"type":21},"2026-05-15",{"date":46,"type":21},"2026-11-30",{"name":48,"class":49},"University of Salamanca","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":58,"sex":16,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":22,"phases":63,"briefSummary":64,"conditions":65,"keywords":67,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":4},"100620639","determining-the-effect-of-shoulder-flexion-angle-on-latissimus-dorsi-and-forearm-flexor-hypertrophy-100620639","NCT07360236","Determining the Effect of Shoulder Flexion Angle on Latissimus Dorsi and Forearm Flexor Hypertrophy","LPDLR","Inclusion Criteria:\n\n1. Any sex\n2. Able to understand and communicate in English\n3. 19-30 years of age\n4. All \"No\" answers on the CSEP Get Active questionnaire or doctors' approval to participate\n5. Trained participants: Structured resistance training over at least the past 12-months (i.e., ≥ 2 hours per week of structured\u002Fperiodized training)\n\nExclusion Criteria:\n\nParticipants will be excluded from this study if they meet any of the following criteria:\n\n1. BMI lower than 18 or greater than 30\n2. Difficulty to understand and communicate in English\n3. Current use of cigarettes or other nicotine devices\n4. Any major uncontrolled cardiovascular, muscular, metabolic, and\u002For neurological disorders\n5. Any medical condition impacting the ability to participate in maximal exercise\n6. Type one or type two diabetes\n7. Diagnosis of cancer or undergoing cancer treatment in the past 12 months\n8. Drug therapy with any drugs that alter skeletal muscle metabolism (i.e., Metformin, Benzodiazepines)\n9. Implants containing ferrous metal\n10. Surgery or tattoos (including tattooed eyeliner) in the last 6 weeks\n11. Pregnancy\n\nMagnetic Resonance Imaging (MRI) Exclusion Criteria\n\nCANNOT participate if you have any of the following:\n\n1. Retained wires from an electronic implant that has been removed (i.e., pacemaker wires not attached to a pacemaker)\n2. Cardiac pacemaker or defibrillator\n3. Metal in eye or orbit\n4. Ferromagnetic aneurysm clip\n5. Makeup tattoos that are not designed to fade over time\n6. Stainless steel intrauterine device (IUD)\n\nDepending on the individual situation, you may not be able to participate if you have\u002Fhad any of the following:\n\n1. Artificial heart valve\n2. Ear or eye implant\n3. Brain aneurysm clip\n4. Implanted electronic device (i.e., drug infusion pump, electrical stimulator)\n5. Orthopedic hardware (artificial joint, plate, screw, rod)\n6. Shrapnel, bullets, or other metal fragments\n7. Surgery, medical procedure, or tattoos (including tattooed eyeliner) in the last six weeks\n8. Other metallic prostheses",true,"19 Years","30 Years",{"count":62,"type":21},20,[24],"The goal of this clinical trial is to learn the effect of training a muscle at a longer or shorter muscle length during resistance exercise in young and healthy adults. Participants will undergo two types of resistance training conditions that are randomly assigned to the left and right arm. The LATPULLDOWN (LPD) condition refers to performing an exercise that places the latissimus dorsi muscle at a long muscle length when the shoulder is elevated to 180° of shoulder flexion. The LATROW (LR) condition refers to performing an exercise that places the latissimus dorsi muscle at a shorter muscle length when the shoulder is elevated to 90° of shoulder flexion.\n\nThe main questions the trial aims to answer are:\n\n1. Does resistance training the latissimus dorsi muscle at a long muscle length result in greater muscle growth than training at a shorter muscle length?\n2. Does resistance training the latissmus dorsi muscle at long or short muscle lengths result in regional muscle growth differences of the latissimus dorsi?\n\nWe hypothesize that:\n\n1. LAT PULLDOWN will induce greater hypertrophy compared to LAT ROW condition\n2. LAT PULLDOWN will result in greater increases in 1RM compared to LATROW condition\n3. LAT PULLDOWN and LAT ROW will result in angle specific differences in Isokinetic strength\n4. LAT PULLDOWN will result in greater inferior Latissimus Dorsi hypertrophy\n5. LAT ROW will result in greater superior Latissimus Dorsi hypertrophy\n\nThe investigators will compare the change in muscle volume and muscular strength between the LAT PULLDOWN and LAT ROW training conditions, which each participant will have the left and right arm randomly assigned to either exclusively LAT PULLDOWN or LAT ROW conditions.\n\nParticipants will:\n\n* Resistance train the left and right arm with two separate conditions; LAT PULLDOWN and LAT ROW for 12 weeks, with the first and last weeks dedicated to only strength testing (Isotonic and Isokinetic) and measuring muscle volume via magnetic resonance imaging (MRI)\n* Visit the gym for resistance training 2 times per week\n* Visit the UBC MRI Research Facility in weeks 1 and 12 for MRI of muscle volume",[66,31],"Muscle Hypertrophy",[68,69,70,71,72,73,74,75,76,77,78,79],"Muscle hypertrophy","Long muscle length","Short muscle length","Range of motion","Muscular strength","1RM","Length-tension Relationship","Resistance Training","Neuromechanical Matching","Latissimus dorsi","Lat Pulldown","Lat Row","2026-01-14",{"date":82,"type":42},"2026-01-22",{"date":84,"type":21},"2026-01-15",{"date":86,"type":21},"2026-07-01",{"name":88,"class":49},"University of British Columbia"]