[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100581188":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":25,"centralContacts":31,"locations":37,"responsibleParty":70,"collaborators":73,"id":77,"slug":78,"hasResults":79,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":24,"eligibilityCriteria":83,"healthyVolunteers":79,"sex":84,"minAge":85,"maxAge":24,"enrollmentInfo":86,"targetDuration":24,"studyType":89,"phases":90,"briefSummary":92,"conditions":93,"keywords":24,"overallStatus":40,"whyStopped":24,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"Mayo Clinic","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Treatment Group","EXPERIMENTAL","Subjects randomized to the treatment arm will begin the home-based pulmonary rehabilitation intervention immediately.",[13],"Behavioral: Pulmonary rehabilitation program",{"label":15,"type":10,"description":16,"interventionNames":17},"Waitlist Control","Subjects randomized to the waitlist control (usual care) arm will be offered the home-based pulmonary rehabilitation intervention after completing the 12-week control period.",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"BEHAVIORAL","Pulmonary rehabilitation program","Participants are expected to engage in the home-based pulmonary rehabilitation routine at least 24 minutes a day, five to six days a week for the entire 12-week study period.\n\nThe pulmonary rehabilitation routine begins with slow upper body and timed breathing exercises, followed by two slow balance walks for 6 minutes each. The total exercise time again is 24 minutes, followed by a 4-minute mindful breathing meditation\u002Fcool down",[9,15],null,[26,29],{"name":27,"affiliation":5,"role":28},"Roberto Benzo, M.D.","PRINCIPAL_INVESTIGATOR",{"name":30,"affiliation":5,"role":28},"Teng Moua, M.D.",[32],{"name":33,"role":34,"phone":35,"phoneExt":24,"email":36},"Johanna Hoult, M.A.","CONTACT","507-293-1989","Hoult.Johanna@mayo.edu",[38,57],{"facility":39,"status":40,"city":41,"state":42,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"Mayo Clinic in Arizona","RECRUITING","Scottsdale","Arizona","85259","United States","US",{"type":47,"coordinates":48},"Point",[49,50],-111.89903,33.50921,{"lat":50,"lon":49},[53,55],{"name":54,"role":34,"phone":24,"phoneExt":24,"email":24},"Roberto P Benzo, M.D.",{"name":56,"role":28,"phone":24,"phoneExt":24,"email":24},"Roberto P Benzo",{"facility":58,"status":40,"city":59,"state":60,"zip":61,"country":44,"countryCode":45,"cosmosGeoPoint":62,"geoPoint":66,"contacts":67},"Mayo Clinic in Rochester","Rochester","Minnesota","55905",{"type":47,"coordinates":63},[64,65],-92.4699,44.02163,{"lat":65,"lon":64},[68,69],{"name":30,"role":34,"phone":24,"phoneExt":24,"email":24},{"name":30,"role":28,"phone":24,"phoneExt":24,"email":24},{"type":28,"investigatorFullName":71,"investigatorTitle":72,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"Roberto P. Benzo","Principal Investigator",[74],{"name":75,"class":76},"National Institute of Nursing Research (NINR)","NIH","100581188","pulmonary-rehabilitation-for-rural-patients-with-copd-100581188",false,"NCT06847061","Pulmonary Rehabilitation for Rural Patients With COPD","Decreasing Disparity in Lung Disease: Pulmonary Rehabilitation for Rural Patients With COPD","Inclusion Criteria\n\n* 40 years of age or older\n* Physician-diagnosed COPD\n* Living in a rural area defined by Rural-Urban Commuting Area Codes 4-10\n* mMRC score\\>=1\n* English Speaking\n\nExclusion Criteria\n\n* Inability to walk (orthopedic\u002Fneurologic\u002Fcardiac limitation causing immobility)\n* Cognitive impairment or inability to understand and follow instructions.\n* Patients with no COPD symptom burden, no breathlessness (mMRC score 0), as based on our previous studies they usually perceive no benefit from PR and do not have compliance with PR.\n* Traditional center-based PR was completed within 3 months of initial study recruitment.\n* Transition to hospice or end-of-life care at the time of screening.\n* Acute exacerbation at the time of screening.","ALL","40 Years",{"count":87,"type":88},306,"ESTIMATED","INTERVENTIONAL",[91],"NA","The purpose of this study is to test the uptake, effectiveness, and patient-caregiver-provider experience of a crucial treatment not provided in rural areas: pulmonary rehabilitation.",[94],"Chronic Obstructive Pulmonary Disease (COPD","2026-05-05",{"date":97,"type":98},"2026-05-07","ACTUAL",{"date":100,"type":98},"2025-04-01",{"date":102,"type":88},"2029-08-31",{"name":5,"class":6},2]