[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"upper-limb-amputation-at-the-wrist\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:upper-limb-amputation-at-the-wrist":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":32,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100514681","level-up-adaptive-gaming-for-children-with-upper-limb-differences-100514681",false,"NCT05981664","Level Up! Adaptive Gaming for Children With Upper Limb Differences","Inclusion Criteria:\n\n* between the age of 7 and 17 years\n* has a unilateral limb difference\n* limb difference may be from any cause (congenital difference, traumatic loss, etc.)\n* limb difference may be of any level (partial hand, wrist disarticulation, transradial, elbow disarticulation, transhumeral, shoulder disarticulation)\n* ability to communicate in English\n* cognitive ability to follow instructions\n* eligible participants will be included regardless of history of prosthesis use\n* lives locally (Winnipeg) or willing and able to travel to Rehabilitation Centre for Children for 2 appointments\n\nExclusion Criteria:\n\n* less than 7 or greater than 17 years of age\n* bilateral or no limb upper limb difference\n* inability to communicate in English\n* cognitive inability to follow instructions\n* unable or unwilling to attend 2 appointments at Rehabilitation Centre for Children","ALL","7 Years","17 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to test a new one-handed video game controller adapter to determine if it helps improve how video games are played and enjoyed in children with an upper limb difference on one side. The main questions it aims to answer are:\n\n* Is performance improved while playing video games with the adapter?\n* Is user satisfaction or enjoyment improved while playing video games with the adapter?\n\nParticipants will:\n\n* Answer questions about their limb difference and other demographics\n* Be interviewed about their current and past video game playing experiences\n* Learn how to use the adapter and have their performance with it evaluated\n* Take the adapter home to use for 1 week, and be asked to record their experiences\n* Have their performance with the adapter re-evaluated after a week of practice\n* Be interviewed about their experience with the adapter",[26,27,28,29,30,31],"Upper Limb Amputation at the Wrist","Pediatric","Upper Limb Amputation","Upper Limb Amputation at the Hand","Amniotic Band Syndrome","Upper Limb Amputation Below Elbow (Injury)",[33,34,35],"pediatric","upper limb difference","one handed gaming","RECRUITING","2026-04-28",{"date":39,"type":40},"2026-05-05","ACTUAL",{"date":42,"type":40},"2024-01-01",{"date":44,"type":20},"2027-06",{"name":46,"class":47},"University of Manitoba","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":15,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":48},"100428144","evaluating-the-experience-of-upper-limb-prosthesis-use-100428144","NCT04855214","Evaluating the Experience of Upper Limb Prosthesis Use","Patient-specific Requirements and Experiences of Upper Limb Prosthetic Technology","Inclusion Criteria:\n\n* 18 years or older\n* Ability to give verbal informed consent\n* Ability to speak and understand English\n* Unilateral acquired trans-radial or trans-humeral amputee\n* At least six months from time of limb loss\n* Current user of an upper limb prosthesis\n* Use of the device they will be describing for at least six months (with the exception of sensory augmentation)\n\nExclusion Criteria:\n\n* Significant hearing impairment which would prevent telephone communication.\n* Unwillingness or inability to discuss experiences with prostheses\n* Emotional disturbance related to discussion the prosthesis or limb loss","18 Years",{"count":58,"type":20},178,"OBSERVATIONAL","The goal is to understand the critical factors associated with outcome acceptance following upper limb loss. The investigators aim to develop a unified theoretical model that describes the psychosocial experience of upper limb prosthesis use and predicts outcome acceptance following upper limb loss. The investigators will also examine experiences with prosthesis education, selection, and training as well as how psychological and social issues impact prosthesis use. In addition, the investigators will use the findings to develop a prototype decision tool to assist with matching persons to prostheses. Study findings will help providers, technology developers, and researchers better understand the complex experience of upper limb prosthesis use.\n\nThis conceptual framework will enable clinicians and researchers to evaluate and predict patient outcomes following limb loss, and to design interventions that improve outcomes. The proposed study is a mixed methods (qualitative and quantitative) study using an observational design. The qualitative component of the study will involve data collection through telephone interviews with 42 participants and analyses using a grounded theory approach with constant comparison methods. The quantitative component involves administration of standardized measures quantifying constructs of the theoretical model in 120 participants and analyses to produce a structural equation model of outcome acceptance. Participants will include persons with unilateral acquired upper limb loss at the trans radial or trans humeral level who use currently available prosthetic devices. Up to 16 individuals will participate in a series of focus groups that will be conducted to provide feedback on the model generated from previous data.",[62,63,26,64,31],"Prosthesis User","Amputation","Upper Limb Amputation Above Elbow (Injury)",[66,67,68,69,70,71,72,73,74,75,76,77,78],"Upper Limb Prosthesis User","Survey","Interview","User Experience","Body-powered","Myoelectric","Multiple degree of freedom","Sensory Feedback","Prosthetic device features","Upper Limb Loss","Amputee","Outcome Acceptance","Qualitative Research","2025-04-01",{"date":81,"type":40},"2025-04-04",{"date":83,"type":40},"2020-12-16",{"date":85,"type":20},"2026-09-30",{"name":87,"class":88},"Louis Stokes VA Medical Center","FED"]