[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100547766":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":24,"locations":30,"responsibleParty":44,"collaborators":19,"id":46,"slug":47,"hasResults":48,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":19,"eligibilityCriteria":52,"healthyVolunteers":48,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":19,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":32,"whyStopped":19,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":77},{"fullName":5,"class":6},"Tan Tock Seng Hospital","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"RELab tenoexo","EXPERIMENTAL","3 weeks in clinic training (9 training sessions, two clinical assessment and 2 usability evaluations) followed by 2 weeks home training (1-hour daily training and to the extent participants desire). Lastly 1-month follow up clinical assessment and IMU data collection.",[13],"Device: RELab tenoexo",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"DEVICE","The RELab tenoexo is a fully wearable and portable RHO developed at the Rehabilitation Engineering Laboratory (RELab) at ETH Zurich.",[9],null,[21],{"name":22,"affiliation":5,"role":23},"Tegan Plunkett","PRINCIPAL_INVESTIGATOR",[25],{"name":26,"role":27,"phone":28,"phoneExt":19,"email":29},"Megan Lau","CONTACT","68894580","megan_se_lau@ttsh.com.sg",[31],{"facility":5,"status":32,"city":33,"state":33,"zip":19,"country":33,"countryCode":34,"cosmosGeoPoint":35,"geoPoint":40,"contacts":41},"RECRUITING","Singapore","SG",{"type":36,"coordinates":37},"Point",[38,39],103.85007,1.28967,{"lat":39,"lon":38},[42],{"name":26,"role":27,"phone":19,"phoneExt":19,"email":43},"Megan_SE_Lau@ttsh.com.sg",{"type":45,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100547766","an-exploratory-study-of-a-wearable-robotic-hand-orthosis-100547766",false,"NCT06412237","An Exploratory Study of a Wearable Robotic Hand Orthosis","An Exploratory Study of a Wearable Robotic Hand Orthosis in the Chronic Stroke Population in Singapore: A Clinic to Home Feasibility Trial","Inclusion Criteria:\n\n* Patient with first ever clinical stroke (ischaemic or haemorrhagic) with hemiplegic motor deficit(s) due to stroke as diagnosed by CT or MRI.\n* Post stroke of at least 6 months with stable neurological status.\n* Age 21 to 80 years of age.\n* Hemiplegic pattern and shoulder abduction MRC motor power \\> 2\u002F5 and elbow extension \\>2\u002F5\n* Has a stable home abode and a carer\u002FNOK to assist with donning of device and supervise home based exercise\n* MOCA \\> or equal to 22\u002F30\n* Able to give and sign informed consent at research site.\n* Able to speak English\n\nExclusion Criteria:\n\n* Non-stroke related causes of arm motor impairment.\n* Has unstable or terminal medical conditions which may affect participation (e.g.: unresolved sepsis, postural hypotension, end stage renal failure, cancer, retroviral disease, on immunosuppressive therapy) or anticipated life expectancy of \\\u003C1 year due to malignancy or neurodegenerative disorder.\n* Local factors which may be worsened by intensive arm therapy: spasticity of Modified Ashworth Scale grades 3-4, skin wounds, shoulder pain Pain Scale \\>5\u002F10, active\u002Fnon-united fractures or arthritis or fixed joint\u002Ftissue flexion contractures of shoulder, elbow, wrist or fingers incompatible with tenoexo interface.\n* Patient with severe cognitive, perceptual (include hemi-neglect), and\u002For emotional-behavioural issues that preclude participation.\n* Experiencing moderate to severe levels of pain (Numerical Vertical Pain Scale \\> 5).\n* Is pregnant or breast feeding. Neither the tenoexo nor the IMUs have been tested to evaluate the usage with pregnant and\u002For breast feeding mothers. Further, due to the length of the study, pregnancy may make it difficult to follow the study schedule.\n* Have a pacemaker. Magnets are used throughout the system.","ALL","21 Years","80 Years",{"count":57,"type":58},20,"ESTIMATED","INTERVENTIONAL",[61],"NA","Upper limb deficits usually remain in 75% of the stroke survivors despite completing full rehabilitation. This is due to lack of effectiveness of rehabilitation and the degree of support and resources available.\n\nIn this study, the investigators plan to study the use of assistive technologies in chronic stroke survivors.",[64],"Stroke",[66,67],"Hand exoskeleton robot","Robotic hand orthosis","2025-04-10",{"date":70,"type":71},"2025-04-15","ACTUAL",{"date":73,"type":71},"2024-06-01",{"date":75,"type":58},"2026-01",{"name":5,"class":6},1]