[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100580540":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":37,"responsibleParty":55,"collaborators":26,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":26,"eligibilityCriteria":64,"healthyVolunteers":60,"sex":65,"minAge":66,"maxAge":67,"enrollmentInfo":68,"targetDuration":26,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":78,"overallStatus":83,"whyStopped":26,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"University of Castilla-La Mancha","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Redcord exercises","EXPERIMENTAL","The participant in this group will attend physiotherapy twice a week, every other day to avoid the onset of fatigue, for 6 weeks.\n\nIn each physiotherapy session they will perform exercises in different plank positions using RedCord®, which is a tool with which exercises are performed in suspension and on an unstable base.",[13],"Device: Redcord",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard exercises","ACTIVE_COMPARATOR","The participant in this group will attend physiotherapy twice a week, every other day to avoid the onset of fatigue, for 6 weeks. In each physiotherapy session they will perform the same exercises as the intervention group, but on a stable basis.",[19],"Other: Control (Standard treatment)",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Redcord","Perticipants will perform exercises in different plank positions using RedCord® while applying local vibration in:\n\n* Supine plank position\n* Prone plank position\n* Lateral prone plank position",[9],null,{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Control (Standard treatment)","Participants will perform exercises in different plank positions:\n\nSupine plank position Prone plank position Lateral prone plank position",[15],[32],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},"Cristina Lirio-Romero, PhD","CONTACT","600320518","cristina.lirio@uclm.es",[38],{"facility":39,"status":26,"city":40,"state":40,"zip":41,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"University of Castilla La Macha","Toledo","45001","Spain","ES",{"type":45,"coordinates":46},"Point",[47,48],-4.02263,39.8581,{"lat":48,"lon":47},[51,52],{"name":26,"role":34,"phone":35,"phoneExt":26,"email":36},{"name":53,"role":54,"phone":26,"phoneExt":26,"email":26},"Alicia Martinez, MsC","PRINCIPAL_INVESTIGATOR",{"type":54,"investigatorFullName":56,"investigatorTitle":57,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Cristina Lirio","PhD","100580540","redcord-in-neurogenic-bowel-dysfunction-in-multiple-sclerosis-100580540",false,"NCT06838624","RedCord in Neurogenic Bowel Dysfunction in Multiple Sclerosis","Effectiveness of Treatment With RedCord in Neurogenic Bowel Dysfunction in People With Multiple Sclerosis","Inclusion Criteria:\n\n* People diagnosed with Multiple Sclerosis according to McDonald's criteria.\n* EDSS less than 6 points.\n* Willingness to participate.\n\nExclusion Criteria:\n\n* People with cognitive impairment, which makes it difficult to understand the questionnaires properly.\n* Pregnant women.\n* Severe psychological or psychiatric pathology diagnosed.","ALL","30 Years","60 Years",{"count":69,"type":70},76,"ESTIMATED","INTERVENTIONAL",[73],"NA","The study aims to evaluate the effectiveness of Redcord treatment for neurogenic bowel dysfunction in patients with multiple sclerosis. The main objectives are:\n\n* Assess the impact of Redcord on bowel function and quality of life in multiple sclerosis patients.\n* Compare the outcomes of Redcord treatment with standard care practices.\n\nParticipants will undergo Redcord therapy sessions and their bowel function will be monitored and compared to a control group receiving standard care. The study will measure improvements in bowel control, frequency, and overall patient satisfaction.",[76,77],"Multiple Sclerosis","Pelvic Floor Disorder",[76,79,80,81,82],"Constipation","Faecal Incontinence","Pelvic Floor","Abdominal Muscles","NOT_YET_RECRUITING","2025-02-20",{"date":86,"type":87},"2025-02-24","ACTUAL",{"date":89,"type":70},"2025-09-01",{"date":91,"type":70},"2026-12-15",{"name":5,"class":6},1]