[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100521318":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":30,"centralContacts":34,"locations":39,"responsibleParty":56,"collaborators":59,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":25,"eligibilityCriteria":76,"healthyVolunteers":72,"sex":77,"minAge":78,"maxAge":25,"enrollmentInfo":79,"targetDuration":25,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":42,"whyStopped":25,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":102},{"fullName":5,"class":6},"Federal University of Minas Gerais","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental group","EXPERIMENTAL","Telehealth intervention involving the HEARTS technical package and the use of Smartwatch Mi Band 7® activity monitor. The HEARTS technical package presents the 5As brief intervention (Ask, Advise, Assess, Assist, Arrange) to promote physical activity participation. Participants will receive a physical activity monitor (as instructed in the HEARTS technical package) and will be monitored by telephone call, once a week, in order to reinforce successes and identify solutions to difficulties (as instructed in the HEARTS technical package) to practice physical activity. These individuals will undertake a 12-week intervention program. In the first week, individuals will perform the first four steps of the 5As brief intervention in person, where they will be instructed on how to use the physical activity monitor, they will receive a diary of regular physical activity practice, will be guided on how to fill it out, and will schedule the best times to receive the weekly telephone call.",[13],"Behavioral: Telehealth intervention: HEARTS technical package + activity monitor (Smartwatch Mi Band 7®)",{"label":15,"type":16,"description":17,"interventionNames":18},"Control group","ACTIVE_COMPARATOR","Participants will undergo the same intervention as the experimental group, but will not receive the physical activity monitor (Smartwatch Mi Band 7®).",[19],"Behavioral: Telehealth intervention: HEARTS technical package",[21,26],{"type":22,"name":23,"description":11,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Telehealth intervention: HEARTS technical package + activity monitor (Smartwatch Mi Band 7®)",[9],null,{"type":22,"name":27,"description":28,"armGroupLabels":29,"otherNames":25},"Telehealth intervention: HEARTS technical package","The same intervention as the experimental group, but without the additional use of the physical activity monitor (Smartwatch Mi Band 7®).",[15],[31],{"name":32,"affiliation":5,"role":33},"Christina Faria, PhD","PRINCIPAL_INVESTIGATOR",[35],{"name":32,"role":36,"phone":37,"phoneExt":25,"email":38},"CONTACT","+55 (31) 34097448","cdcmf@ufmg.br",[40],{"facility":41,"status":42,"city":43,"state":44,"zip":45,"country":46,"countryCode":47,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"Universidade Federal de Minas Gerais","RECRUITING","Belo Horizonte","Minas Gerais","31270-901","Brazil","BR",{"type":49,"coordinates":50},"Point",[51,52],-43.93778,-19.92083,{"lat":52,"lon":51},[55],{"name":32,"role":36,"phone":37,"phoneExt":25,"email":38},{"type":33,"investigatorFullName":57,"investigatorTitle":58,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"Christina Danielli Coelho de Morais Faria","Doctor",[60,62,65,67],{"name":61,"class":6},"Fundação de Amparo à Pesquisa do estado de Minas Gerais",{"name":63,"class":64},"Conselho Nacional de Desenvolvimento Científico e Tecnológico","OTHER_GOV",{"name":66,"class":64},"Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.",{"name":68,"class":69},"Worldwide Universities Network","UNKNOWN","100521318","telehealth-intervention-involving-hearts-technical-package-and-activity-monitor-to-promote-physical-activity-post-stroke-100521318",false,"NCT06068036","Telehealth Intervention Involving HEARTS Technical Package and Activity Monitor to Promote Physical Activity Post-stroke","Telehealth Intervention Involving the HEARTS Technical Package and the Use of an Activity Monitor to Increase Physical Activity Level Post-stroke: a Feasibility Randomized Controlled Trial","Inclusion Criteria:\n\n* Diagnosis of stroke for more than six months;\n* ≥18 years of age;\n* Be rated as \"Inactive\" according to Human Activity Profile (HAP);\n* Provide medical approval to practice physical activity.\n\nExclusion Criteria:\n\n* Positive screening test for possible cognitive alterations;\n* Pain or other adverse health condition that compromises the performance of the proposed intervention program, such as vestibular disorders, severe arthritis or any other diagnosis of disease of the nervous system.","ALL","18 Years",{"count":80,"type":81},24,"ESTIMATED","INTERVENTIONAL",[84],"NA","Objectives: The aim of this feasibility randomized controlled trial (RCT) study is to investigate whether the theoretically informed telehealth intervention involving the HEARTS Technical Package and the use of an activity monitor to increase physical activity level post-stroke is feasible and to estimate the parameters for conducting a fully powered RCT.\n\nDesign: A Phase 1 feasibility RCT study with blinded assessment will assign eligible participants to experimental or control group. Participants in both groups will undergo a theoretically informed telehealth intervention based on the HEARTS technical package (a face-to-face session and telephone call follow-up). The experimental group will have additional use of the Mi Band 7® Smartwatch activity monitor. For both groups, the intervention will last for 12 weeks. The feasibility outcomes will be identified considering the different phases of conducting the study. A trained researcher, blinded to the group allocation, will collect the sociodemographic, anthropometric, and clinical outcomes, in a university laboratory setting.\n\nStudy Outcomes: Feasibility of recruitment, intervention, and measurement, and clinical outcomes.\n\nConclusions: Results from this feasibility RCT study will inform on the design and sample required for a fully powered RCT with a similar aim.",[87],"Stroke",[87,89,90,91,92],"Physical activity","Telehealth","Feasibility Study","Randomized controlled trial","2025-02-25",{"date":95,"type":96},"2025-02-27","ACTUAL",{"date":98,"type":96},"2023-09-27",{"date":100,"type":81},"2025-07",{"name":5,"class":6},1]