[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100575718":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":30,"locations":40,"responsibleParty":58,"collaborators":25,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":62,"sex":68,"minAge":69,"maxAge":25,"enrollmentInfo":70,"targetDuration":25,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":79,"overallStatus":43,"whyStopped":25,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Swiss Paraplegic Research, Nottwil","NETWORK",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"RT-OT","EXPERIMENTAL","A stratified randomisation procedure will be used to allocate the sequence with either RT followed by OT or vice versa. The participants will performe unilateral robot-asssited therapy for 3 x 30 minutes per week for 6 weeks first, and then the unilateral conventional occupational therapy also for 3 x 30 minutes per week for 6 weeks.",[13,14],"Other: Unilateral robot-assisted therapy (RT)","Other: Unilateral conventional occupational therapy (OT)",{"label":16,"type":10,"description":17,"interventionNames":18},"OT-RT","A stratified randomisation procedure will be used to allocate the sequence with either OT followed by RT or vice versa. The participants will perform unilateral conventional occupational therapy for 3 x 30 minutes per week for 6 weeks first, and then unilateral robot-assisted therapy also for 3 x 30 minutes per week for 6 weeks.",[13,14],[20,26],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"OTHER","Unilateral robot-assisted therapy (RT)","RT will be performed as an add-on therapy to the clinical routine therapy scheme for 3 x 30 minutes per week for 6 weeks. RT is applied using the ArmeoSpring, an exoskeleton that provides adjustable antigravity weight support for the arm through a system of springs (no actuators).",[16,9],null,{"type":21,"name":27,"description":28,"armGroupLabels":29,"otherNames":25},"Unilateral conventional occupational therapy (OT)","The OT is applied as add-on therapy for 3 x 30 minutes per week for 6 weeks. OT comprises strengthening exercises (concentric and eccentric) with and without resistance, grasping exercises, fine motor training, peg games, and activity-based tasks which are unilaterally doable.",[16,9],[31,36],{"name":32,"role":33,"phone":34,"phoneExt":25,"email":35},"Mario Widmer, Dr. sc. ETH","CONTACT","0041 41 939 51 97","mario.widmer@paraplegie.ch",{"name":37,"role":33,"phone":38,"phoneExt":25,"email":39},"Chantal Wunderlin","0041 41 939 66 15","chantal.wunderlin@paraplegie.ch",[41],{"facility":42,"status":43,"city":44,"state":45,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":55},"Swiss Paraplegic Centre","RECRUITING","Nottwil","Canton of Lucerne","6207","Switzerland","CH",{"type":50,"coordinates":51},"Point",[52,53],8.13774,47.13469,{"lat":53,"lon":52},[56],{"name":32,"role":33,"phone":57,"phoneExt":25,"email":35},"0041419395197",{"type":59,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR","100575718","robot-assisted-vs-conventional-occupational-therapy-of-the-upper-limb-in-individuals-with-cervical-spinal-cord-injury-100575718",false,"NCT06775925","Robot-assisted Vs. Conventional Occupational Therapy of the Upper Limb in Individuals with Cervical Spinal Cord Injury","Robot-assisted Vs. Conventional Occupational Therapy of the Upper Limb in Individuals with Cervical Spinal Cord Injury: the Armeo X-over Trial","Armeo X-over","Inclusion Criteria:\n\n* Informed Consent signed by the subject\n* Intermediate (\\>16 days and ≤81 days post-injury) traumatic or non-traumatic cSCI during primary rehabilitation at the Swiss Paraplegic Centre (SPC)\n* Neurological level of injury: C1-T1\n* American Spinal Injury Association Impairment Scale (AIS): A-D\n* Impairment of upper limb function (GRASSP-QtG score unilateral \\\u003C 25 at baseline t0)\n* Ability to sit for 60 minutes and perform training with ArmeoSpring\n* Stratification parameters available\n\nExclusion Criteria:\n\n* Inability to follow the procedures of the investigation\n* Severe concomitant neurological disease\n* Concomitant neurodegenerative or progressive diseases\n* Impairment of upper limb function due to peripheral nerve lesions\n* Severe concurrent medical disease or any other issue that in the opinion of the investigator would confound the results\n* Orthopedic limitations of the upper limb\n* Device specific contraindications\n* Participation in other interventional trials","ALL","18 Years",{"count":71,"type":72},40,"ESTIMATED","INTERVENTIONAL",[75],"NA","The goal of this clinical trial is to learn the effects of robot-assisted therapy using the ArmeoSpring on upper limb function compared to conventional occupational therpay in individuals with cervical spinal cord injury (cSCI). The main questions it aims to answer are:\n\n\\- Which of the two forms of therapy, robot-assisted therapy or conventional occupational therapy, is more effective in terms of improving arm and hand function?\n\nThe study is designed as a cross-over trial, which means that each participant will receive both therapy forms consecutively, whereas the order is assigned randomly (either robot-assisted therapy first and then occupational therapy, or vice versa).\n\nIn addition to their clinical routine therapy , participants will:\n\n* complete a baseline assessment\n* practice one therapy form (either robot-assisted or occupational therapy) with one arm for 6 weeks (3 x 30 min per week)\n* complete a intermediate assessment\n* practice the other therapy form (either occupational or robot-assisted therapy) with one arm for 6 weeks (3 x 30 min per week)\n* complete a post assessment\n* complete a follow-up assessment (if the post assessment was completed prior to 150 days post-injury)",[78],"Cervical Spinal Cord Injury",[80,81,82],"upper limb function","robot-assisted therapy","occupational therapy","2025-03-05",{"date":85,"type":86},"2025-03-10","ACTUAL",{"date":88,"type":86},"2025-02-01",{"date":90,"type":72},"2027-12",{"name":5,"class":6},1]