[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100428192":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":37,"responsibleParty":52,"collaborators":54,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":18,"eligibilityCriteria":63,"healthyVolunteers":59,"sex":64,"minAge":65,"maxAge":18,"enrollmentInfo":66,"targetDuration":18,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":76,"overallStatus":40,"whyStopped":18,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"Umeå University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention group","EXPERIMENTAL","Intensive training with oral neuromuscular device (intervention group) and traditional compensatory swallowing training under 8 weeks with start 4 (±1) weeks post-operation.",[13],"Device: Oral neuromuscular training",{"label":15,"type":16,"description":17,"interventionNames":18},"Control group","NO_INTERVENTION","Traditional compensatory swallowing training under 8 weeks with start 4 (±1) weeks post-operation.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"DEVICE","Oral neuromuscular training","The oral device is used for 30 seconds, three times a day, before meals and implies new possibilities for training of the orofacial and pharyngeal muscles.",[9],[26],{"name":27,"affiliation":5,"role":28},"Patricia Hägglund, PhD\u002FSLP","PRINCIPAL_INVESTIGATOR",[30,34],{"name":27,"role":31,"phone":32,"phoneExt":18,"email":33},"CONTACT","+46907850000","patricia.hagglund@umu.se",{"name":35,"role":31,"phone":32,"phoneExt":18,"email":36},"Thorbjörn Holmlund, PhD\u002FMD","thorbjorn.holmlund@umu.se",[38],{"facility":39,"status":40,"city":41,"state":18,"zip":18,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"University Hospital of Umeå","RECRUITING","Umeå","Sweden","SE",{"type":45,"coordinates":46},"Point",[47,48],20.25972,63.82842,{"lat":48,"lon":47},[51],{"name":27,"role":31,"phone":18,"phoneExt":18,"email":33},{"type":53,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR",[55],{"name":56,"class":6},"University Hospital, Umeå","100428192","dysphagia-after-anterior-cervical-spine-surgery-100428192",false,"NCT04855838","Dysphagia After Anterior Cervical Spine Surgery","Impaired Swallowing Function After Anterior Cervical Spine Surgery- Incidence, Long-term Effect on Nutrition and Effect of Oral Neuromuscular Training","Inclusion Criteria:\n\n* All patients enrolled at the University Hospital of Umeå who have undergone ACSS between C2 and Th1 level due to trauma are eligible participants in the first part of the study.\n* Eligibility criteria to participate in part 2 is swallowing dysfunction on FEES at 4±1-week post-operation\n\nExclusion Criteria:\n\n* Patients \\\u003C18 years of age\n* known dysphagia prior to the trauma\u002Finjury\n* affected brainstem that is shown on a CT or MRI\n* severe brain damage.","ALL","18 Years",{"count":67,"type":68},60,"ESTIMATED","INTERVENTIONAL",[71],"NA","The purpose of this research project is to investigate the incidence of impaired swallowing (dysphagia) after anterior cervical spine surgery (ACSS) and to study the long-term effect of dysphagia on nutritional status 12 ± 3 months later. Furthermore, to investigate the effect of a new rehabilitation method for dysphagia among individuals with swallowing dysfunction after ACSS.",[74,75],"Dysphagia","Cervical Spinal Cord Injury",[77,78,79,80,81],"Swallowing disorder","Anterior cervical spine surgery","Intervention","Incidens","Nutritional status","2024-12-05",{"date":84,"type":85},"2024-12-11","ACTUAL",{"date":87,"type":85},"2020-12-17",{"date":89,"type":68},"2024-12-31",{"name":5,"class":6},1]