[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100596184":3},{"organization":4,"armGroups":7,"interventions":21,"overallOfficials":36,"centralContacts":40,"locations":49,"responsibleParty":67,"collaborators":26,"id":70,"slug":26,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":26,"eligibilityCriteria":75,"healthyVolunteers":71,"sex":76,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":26,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":52,"whyStopped":26,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":103},{"fullName":5,"class":6},"University of California, Irvine","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Movement Variability","EXPERIMENTAL","The movement variability group will have a smartwatch app that records movement variability. Their movement goal will be centered on increasing their total movement variability as measured by the watch.",[13,14],"Other: Smartwatch App for Movement Variability","Behavioral: Motivational Interviewing (Within Subjects)",{"label":16,"type":17,"description":18,"interventionNames":19},"Active Time (Control)","PLACEBO_COMPARATOR","This group will only receive active-time feedback (the number of minutes and hours moving the upper extremity). Their goal will focus on increasing their total movement time.",[20,14],"Other: Smartwatch App for Active Time",[22,27,31],{"type":6,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"Smartwatch App for Movement Variability","This app measures movement variability in the upper extremity as described in our previous study (doi:10.3390\u002Fs24165266).",[9],null,{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Smartwatch App for Active Time","The other software we are using measures total active time of the upper extremity.",[16],{"type":32,"name":33,"description":34,"armGroupLabels":35,"otherNames":26},"BEHAVIORAL","Motivational Interviewing (Within Subjects)","Motivational Interviewing is an established therapeutic technique designed to increase patient adherence to therapy by addressing ambivalence. The motivational Interviewing sessions will include a variety of techniques such as: Open ended questions, Active Listening, Affirmation, Summarization, Questions focused on change talk, and Providing Information.",[16,9],[37],{"name":38,"affiliation":5,"role":39},"David Reinkensmeyer, PhD","PRINCIPAL_INVESTIGATOR",[41,46],{"name":42,"role":43,"phone":44,"phoneExt":26,"email":45},"Vicky Chan, DPT","CONTACT","9498248423","vchan2@uci.edu",{"name":47,"role":43,"phone":26,"phoneExt":26,"email":48},"Natanya Gunn, Medical Student","natanyag@hs.uci.edu",[50],{"facility":51,"status":52,"city":53,"state":54,"zip":55,"country":56,"cosmosGeoPoint":57,"geoPoint":62,"contacts":63},"University of California Irvine","RECRUITING","Irvine","California","92697","United States",{"type":58,"coordinates":59},"Point",[60,61],-117.82311,33.66946,{"lat":61,"lon":60},[64,66],{"name":42,"role":43,"phone":65,"phoneExt":26,"email":45},"949-824-8423",{"name":38,"role":39,"phone":26,"phoneExt":26,"email":26},{"type":39,"investigatorFullName":68,"investigatorTitle":69,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"David Reinkensmeyer","Professor","100596184",false,"NCT07042152","Wearable Device and Behavioral Support for Enhancing Arm Use After Stroke","Sensor Enhanced Activity Motivation After Stroke","Inclusion Criteria:\n\n* 18 to 85 years of age\n* Experienced a single or multiple, ischemic or hemorrhagic stroke, with unilateral weakness, over six months previously\n* An ability to score at least 3 blocks on the Box and Block Test. BBT score of the affected arm is at least 5% worse than that present with the unaffected arm.\n* Absence of major depression, as defined by DSM V criteria or a score on the Geriatric Depression Scale \\\u003C 10.\n\nExclusion Criteria:\n\n* Any substantial decrease in alertness, language reception, or attention\n* Single or multiple, ischemic or hemorrhagic stroke less than 6 months ago\n* Severe muscle tone at the upper extremity (score ≥ 3 on the Modified Ashworth Spasticity scale)\n* Pregnant or lactating\n* Advanced liver, kidney, cardiac, or pulmonary disease\n* Coexistent major neurological disease\n* Coexistent major psychiatric disease\n* Plans to alter any current participation in other rehabilitation therapy in the time period of the study\n* A terminal medical diagnosis consistent with survival \\\u003C 1 year\n* A history of significant alcohol or drug abuse in the prior 3 years\n* Current enrollment in another study related to stroke or stroke recovery\n* Any other medical contraindication to participation in the study, as evaluated by our team physician.\n* Visual Analog of Pain Scale Score of 7 or greater","ALL","18 Years","84 Years",{"count":80,"type":81},32,"ESTIMATED","INTERVENTIONAL",[84],"NA","The goal of this study is to determine the effectiveness of behavioral support and feedback from a wearable device that senses arm movement in improving upper extremity function in a pilot, randomized controlled trial with chronic stroke patients",[87],"Chronic Stroke Patients",[89,90,91,92,93],"Sensor","SmartWatch","Stroke Recovery","Stroke Rehabilitation","Motivational Interviewing","2025-08-14",{"date":96,"type":97},"2025-08-19","ACTUAL",{"date":99,"type":81},"2025-08-20",{"date":101,"type":81},"2026-01-29",{"name":5,"class":6},1]