[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"orthotic-device\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:orthotic-device":28},{"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":31,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":4},"100603448","custom-cadcam-insoles-for-plantar-pressure-improvement-in-foot-deformities-100603448",false,"NCT07136649","Custom CAD\u002FCAM Insoles for Plantar Pressure Improvement in Foot Deformities","Effects of Custom CAD\u002FCAM Insoles on Plantar Pressure Distribution in Individuals With Foot Deformities: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18-65 years\n* Clinically diagnosed with a foot deformity (e.g., pes planus, pes cavus, hallux valgus)\n* Able to use custom insoles for at least six months\n* Able to stand and walk for pedobarographic measurements\n* Willing to participate and provide informed consent\n\nExclusion Criteria:\n\n* Presence of neurological or systemic diseases affecting foot function (e.g., diabetic neuropathy)\n* History of lower extremity surgery in the last six months\n* Severe musculoskeletal conditions impairing sensorimotor function\n* Any condition preventing compliance with insole use\n* Contraindications for participating in gait or pressure measurements","ALL","18 Years","65 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled trial will investigate the effects of custom CAD\u002FCAM insoles on plantar pressure distribution and gait parameters in individuals with foot deformities, such as pes planus, pes cavus, and hallux valgus. A total of 30 participants will be randomly assigned to either the intervention group, receiving custom CAD\u002FCAM insoles, or the control group, receiving no insole intervention.\n\nPlantar pressure measurements will be performed using the As200 Gait Scan Pedobarography System at baseline and after eight weeks. Static and dynamic plantar pressure variables, contact area, and center of pressure displacement will be assessed, along with gait parameters including step length, step time, and walking speed.\n\nThe results of this study may contribute to the development of effective conservative treatment strategies to improve foot biomechanics and reduce pressure-related complications in individuals with foot deformities.",[27,28,29,30],"Foot Deformities","Orthotic Device","3D Printing","CAD",[32,33,34,35,36,37,29,38],"Custom CAD\u002FCAM Insoles","Pes Planus","Pes Planovalgus","Pes Cavus","Pedobarography","Plantar Pressure","Orthotics","NOT_YET_RECRUITING","2025-08-21",{"date":42,"type":43},"2025-08-22","ACTUAL",{"date":45,"type":21},"2025-09-01",{"date":47,"type":21},"2025-11-30",{"name":49,"class":50},"Fenerbahce University","OTHER",{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":73},"100594289","the-effects-of-a-proprioception-enhancing-assistive-orthosis-on-balance-and-joint-sense-in-geriatric-patients-100594289","NCT07017504","THE EFFECTS OF A PROPRIOCEPTION-ENHANCING ASSISTIVE ORTHOSIS ON BALANCE AND JOINT SENSE IN GERIATRIC PATIENTS","The Effects of a Proprioception-enhancing Assistive Orthosis on Balance and Joint Sense in Geriatric Patients","Inclusion Criteria:\n\n1. Patients with age-related diseases affecting balance and joint sense, who meet two or more of the following criteria for sarcopenia:\n\n   * Muscle strength: Handgrip strength \\\u003C 28 kg (men), \\\u003C 18 kg (women)\n   * Physical performance: Short Physical Performance Battery (SPPB) ≤ 8 points\n   * Muscle mass: Bioimpedance analysis showing \\\u003C 7.0 kg\u002Fm² (men), \\\u003C 5.7 kg\u002Fm² (women)\n2. Able to fully understand and follow instructions related to walking, sitting, and balance.\n\nExclusion Criteria:\n\n1. Unable or unwilling to provide informed consent\n2. High risk of falls due to severe visual impairment or dizziness\n3. Communication difficulties due to speech, language, or hearing problems\n4. Inability to walk independently without assistive devices\n5. History of diseases affecting gait, efficiency, or endurance, such as:\n\n   * Neurological disorders (e.g., stroke, Parkinson's disease)\n   * Musculoskeletal disorders affecting the lower limbs\n   * History of major orthopedic surgery on the lower limbs\n   * Severe back pain or musculoskeletal pain affecting gait\n   * Cardiovascular disease including heart failure or uncontrolled hypertension\n   * Pulmonary diseases requiring regular oxygen therapy\n   * Cancer requiring treatment within the past 3 years (except for non-melanoma skin cancer or early-stage breast\u002Fprostate cancer)\n   * Psychiatric disorders such as schizophrenia, other psychoses, or bipolar disorder\n   * Any other disease that significantly limits mobility",{"count":20,"type":21},[24],"This study investigates the effects of a proprioception-enhancing assistive orthosis on balance and joint sense in geriatric patients with age-related diseases. The study uses wearable devices that deliver vibration stimuli to improve proprioceptive feedback. A total of 20 participants will be enrolled in a 24-month, IRB-approved trial at Seoul National University Hospital. The study assesses functional balance and joint position sense before and after using the device.",[62,63,28],"Balance","Fall Prevention","2025-06-03",{"date":66,"type":43},"2025-06-12",{"date":68,"type":21},"2025-07-01",{"date":70,"type":21},"2027-07-01",{"name":72,"class":50},"Seoul National University Hospital",1]