[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100641099":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":25,"locations":31,"responsibleParty":45,"collaborators":20,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":49,"sex":55,"minAge":56,"maxAge":20,"enrollmentInfo":57,"targetDuration":20,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":68,"overallStatus":33,"whyStopped":20,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"University of Minnesota","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"PA-ChatS Intervention","EXPERIMENTAL","Participants will receive 6, 20-30 minute intervention sessions delivered over the telephone or using Zoom by an occupational therapist over 6 weeks (1 session\u002Fweek). They will also complete self-monitoring of step counts using a pedometer.",[13],"Behavioral: Physical Activity Chats after Stroke (PA-ChatS)",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","Physical Activity Chats after Stroke (PA-ChatS)","PA-ChatS consists of (1) self-monitoring step count using a pedometer, and (2) behavioral activation for stepping activity delivered via the telephone or Zoom and guided by the PA-ChatS workbook.\n\nParticipants will receive education regarding physical activity after stroke, American Heart Association guidelines for post-stroke physical activity levels, and an overview of the intervention activities. They will then use a pedometer to monitor average daily step counts, set new step count goals (increasing by 5 to 10% of the daily average step count from the prior week), and create a specific plan for achieving the new step count goal. The interventionist will collaboratively problem solve with the participant to identify strategies to overcome barriers to stepping activity and maintain safety.",[9],null,[22],{"name":23,"affiliation":5,"role":24},"Emily Kringle, PhD, OTR\u002FL","PRINCIPAL_INVESTIGATOR",[26],{"name":27,"role":28,"phone":29,"phoneExt":20,"email":30},"Karli Jahnke","CONTACT","612-626-4046","dwell@umn.edu",[32],{"facility":5,"status":33,"city":34,"state":35,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":20},"RECRUITING","Minneapolis","Minnesota","55455","United States","US",{"type":40,"coordinates":41},"Point",[42,43],-93.26384,44.97997,{"lat":43,"lon":42},{"type":46,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100641099","feasibility-of-a-remotely-delivered-step-count-intervention-in-chronic-stroke-100641099",false,"NCT07649135","Feasibility of a Remotely Delivered Step Count Intervention in Chronic Stroke","Feasibility of Engaging Stroke Survivors in a Brief Step Count Intervention During Chronic Stroke","PA-ChatS","Inclusion Criteria:\n\n* Stroke diagnosis confirmed by imaging\n* Stroke occurred 6 or more months before study enrollment\n* Meet criteria for \"inactive\" on the International Physical Activity Questionnaire-Short Form\n* Able to identify a support person that they interact with in-person at least once per week\n* Able and willing to participate fully in the study and provide informed consent or proxy consent with participant assent\n\nExclusion Criteria:\n\n* Currently receiving care in a transitional care unit, skilled nursing facility, or other institutional care setting\n* Currently receiving outpatient neurorehabilitation services (e.g., physical therapy, occupational therapy, speech therapy)\n* Severe cognitive or communication impairments (inability to respond accurately to complete study screening questions or to provide informed consent or assent)\n* Currently pregnant or expecting to become pregnant in the next 8 weeks Comorbid neurological disorder (Parkinson's disease, multiple sclerosis, amyotrophic lateral sclerosis, myasthenia gravis, dementia, Alzheimer's disease, Huntington's disease, glioblastoma, spinal cord injury, cerebral palsy)\n* Comorbid cancer, currently undergoing chemotherapy or radiation treatment\n* Received inpatient treatment or was hospitalized for a psychiatric condition and\u002For alcohol or substance abuse within the past 12 months\n* Current diagnosis of a terminal illness and\u002For currently receiving hospice care\n* History of allergic reaction to adhesives that precludes the use of an adhesive necessary for adherence to activPAL measurement\n* Uses wheelchair as primary mobility aid outside of home setting\n* Inability to speak, read, or understand English\n* Concurrent participation in another rehabilitation intervention research study\n* Resides more than 50 miles outside of the Twin Cities, Minnesota metropolitan area\n* Investigator discretion for safety or adherence reasons","ALL","18 Years",{"count":58,"type":59},24,"ESTIMATED","INTERVENTIONAL",[62],"NA","The goal of this study is to explore the feasibility of a new approach to rehabilitation that focuses on step count. Participants will complete 6 telephone or Zoom-based sessions with an occupational therapist over 6 weeks and use a step count tracker during that time. They will also complete questionnaires, assessments, surveys, and physical activity measurements during study weeks 0 (baseline), 3 (mid-point), 7 (post-intervention) and 12 (follow-up).",[65,66,67],"Stroke","Ischemic Stroke","Hemorrhagic Stroke",[69,70,71],"physical activity","behavior change","rehabilitation","2026-07-08",{"date":74,"type":75},"2026-07-10","ACTUAL",{"date":72,"type":75},{"date":78,"type":59},"2027-01",{"name":5,"class":6},1]