[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Roessingh Research and Development\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":89},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,43,64],{"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":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100053535","influence-of-hawthorne-effect-and-dual-tasks-on-gait-in-cp-100053535",false,"NCT05417399","Influence of Hawthorne Effect and Dual-tasks on Gait in CP","Ecological Validity of Clinical Gait Analysis in Children With Cerebral Palsy: Influence of the Hawthorne Effect and Dual-tasks. A Pilot Study","Inclusion Criteria:\n\n* Cerebral palsy, bilateral spastic, GMFCS classification I-III\n* Age \\\u003C16 years\n* Use of bilateral AFO's (rigid or ground reaction AFO's) to improve knee extension in stance\n\nExclusion Criteria:\n\n* Behavioural issues or poor instructability which might affect participation in the protocol\n* Significant visual disorders\n* Other diagnoses influencing gait\n* Not willing to sign informed consent before inclusion","ALL","4 Years","16 Years",{"count":20,"type":21},15,"ESTIMATED","OBSERVATIONAL","It is the clinical experience of the authors that some children with cerebral palsy who walk in crouch gait show sufficient knee extension during the clinical gait analysis, but walk in considerable knee flexion when they leave the gait laboratory. Possible differences between walking in a gait lab and walking in daily life may be caused by the effect of observational awareness in the lab (also known as the Hawthorne effect), and the lack of dual-tasks (DT) during the analysis (which are common during daily life walking). Since so far there is no technique to reliably measure gait kinematics in children with CP outside of the laboratory, the researchers aim to objectify the influence of both the Hawthorne effect and dual-tasks by introducing different conditions during a standard clinical 3D gait analysis.",[25,26,27,28,29],"Cerebral Palsy","Gait Disorders, Neurologic","Hawthorne Effect","Dual-tasks","Kinematics","RECRUITING","2026-07-10",{"date":33,"type":34},"2026-07-13","ACTUAL",{"date":36,"type":34},"2022-09-01",{"date":38,"type":21},"2028-12-01",{"name":40,"class":41},"Roessingh Research and Development","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":42},"100496989","technical-evaluation-of-commercial-imus-within-clinical-gait-analysis-100496989","NCT05751408","Technical Evaluation of Commercial IMUs Within Clinical Gait Analysis","Technical Evaluation of Commercial IMUs Within Clinical Gait Analysis in Adult Patients With Neurological Disorders","Subjects referred for clinical gait analysis at Roessingh Centre for Rehabilition in Enschede, the Netherlands:\n\nInclusion Criteria:\n\n* Disorders affecting walking, including amongst others stroke, traumatic brain injury, MS, incomplete spinal cord injury, CP, Spina Bifida, neuromuscular diseases\n* age minimum 18 years\n* Viosca score minimum 2; meaning minimal independent walking ability indoors\n* increased fall risk or increased effort of walking because of: 1) decreased stability during stance; and\u002For 2) decreased foot clearance during swing; and\u002For 3) not able to walk on bare feet because of equinovarus; and\u002For 4) fatigue during walking because of compansatory strategies.\n\nExclusion Criteria:\n\n* subjects referred for clinical gait analysis because of problems other than stiff knee gait or foot surgery\n* severe deficits in communication, memory and understanding at such a level that it would affect instructions during the measurements","18 Years",{"count":52,"type":21},40,"A standard clinical gait analysis consists of observing walking with video (2D) or advanced equipment (VICON 3D). This 3D method provides detailed information about the gait pattern, but is time-consuming in implementation and data analysis. There are commercial 3D systems on the market that are used in healthy individuals and in sports. These so-called Inertial Measurement Units (IMUs) may also be suitable for use in the clinic. In this research protocol, the aim is to test the usability of commercial sensors and technically compare them with standard clinical 3D gait analysis in adult patients with a neurological disorder.",[55],"Gait Analysis","2026-05-12",{"date":58,"type":34},"2026-05-13",{"date":60,"type":34},"2023-01-25",{"date":62,"type":21},"2028-12",{"name":40,"class":41},{"id":65,"slug":66,"hasResults":11,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":4,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":71,"enrollmentInfo":72,"targetDuration":4,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":42},"100518629","arm-use-with-soft-robotic-glove-100518629","NCT06033027","Arm Use With Soft-robotic Glove","Influence of Assistive Soft-robotic Glove Use on Actual Arm Use in Daily Life","Inclusion Criteria:\n\n* Age between 18 and 90 years\n* Experience difficulties in performing ADL due to hand function limitations as a result of trauma-related injury or neurologic disorder\n* Being in a chronic\u002Fstable phase of disease as judged by their physician\n* Able to activate the soft-robotic glove by generating pressure on finger\u002Fpalm sensors when grasping an object\n* Ability to relax an active grip\n* Sufficient cognitive status to understand two-step instructions\n* Having (corrected to) normal vision\n* Able to provide written informed consent\n* Living independently\n\nExclusion Criteria:\n\n* Severe sensory problems of the most-affected hand\n* Severe acute pain of the most-affected hand\n* Wounds on the hands that can provide a problem when using the glove\n* Severe contractures limiting passive range of motion to the extent that the glove can't be donned\u002Factivated comfortably\n* Co-morbidities limiting functional use\u002Fperformance of the arms and\u002For hands\n* Severe spasticity of the hand (≥2 points on Ashworth Scale)\n* Severe proximal weakness (MRC shoulder elevation\\\u003C4)\n* Used the Carbonhand system in the past 3 months\n* Participation in other studies that can affect functional performance of the arm\u002Fhand\n* Receiving arm-\u002Fhand function therapy during the course of the study\n* Insufficient digital literacy to conduct video calls\n* Insufficient knowledge of the Dutch or English language to understand the purpose or methods of the study","90 Years",{"count":73,"type":21},5,"INTERVENTIONAL",[76],"NA","This study, aimed at investigating the impact of using a supportive soft-robotic glove on actual arm and hand use in daily life, is designed as a single-case experimental design study. 3-5 patients with limitations in hand function due to trauma-related or neurological conditions are asked to participate. Participants will be asked to use a soft-robotic glove at home for six weeks during daily activities relevant to them, while that glove supports the grip of their most affected hand. For several weeks before, during and after the use of the soft-robotic glove, participants will be asked to do some short tests (wearing an activity meter on both wrists during the day, performing a hand squeeze test under the supervision of the researcher via video call) and to answer some questions related to perceived hand function and well-being (a total of at least 15 times during 12-14 weeks). The present study is a follow-up to previous studies that investigated the effect of (previous versions of) the same robotic glove (Carbonhand; Bioservo Technolo-gies AB, Kista, Sweden) on hand function, in order to better understand and explain the observed therapeutic effect.",[79,80],"Trauma Injury of Hand Multiple","Neurologic Disorder","2026-05-01",{"date":83,"type":34},"2026-05-07",{"date":85,"type":34},"2024-06-03",{"date":87,"type":21},"2027-12",{"name":40,"class":41},""]