[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100605609":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":34,"centralContacts":41,"locations":49,"responsibleParty":79,"collaborators":81,"id":85,"slug":23,"hasResults":86,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":86,"sex":92,"minAge":93,"maxAge":23,"enrollmentInfo":94,"targetDuration":23,"studyType":97,"phases":98,"briefSummary":100,"conditions":101,"keywords":105,"overallStatus":52,"whyStopped":23,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":119},{"fullName":5,"class":6},"Johns Hopkins University","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Short Arm Intervention","EXPERIMENTAL","8 weeks (short arm) of a pulmonary rehabilitation (PR) program",[13],"Behavioral: 8 week (short arm) Intervention - pulmonary rehabilitation",{"label":15,"type":10,"description":16,"interventionNames":17},"Long Arm Intervention","24 weeks (extended arm) of a pulmonary rehabilitation (PR) program",[18],"Behavioral: 24 week (long arm) Intervention - pulmonary rehabilitation",{"label":20,"type":21,"description":22,"interventionNames":23},"Standard of care","NO_INTERVENTION","Standard TB treatment without specific pulmonary rehabilitation",null,[25,30],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":23},"BEHAVIORAL","8 week (short arm) Intervention - pulmonary rehabilitation","8 weeks (short arm) of a pulmonary rehabilitation (PR) program, administered during TB treatment, comprising of exercise training, counselling and education, and airway clearance techniques.",[9],{"type":26,"name":31,"description":32,"armGroupLabels":33,"otherNames":23},"24 week (long arm) Intervention - pulmonary rehabilitation","24 weeks (extended arm) of a pulmonary rehabilitation (PR) program, administered during TB treatment, comprising of exercise training, counselling and education, and airway clearance techniques.",[15],[35,39],{"name":36,"affiliation":37,"role":38},"Akshay Gupte, PhD MBBS MSPH","Boston University","PRINCIPAL_INVESTIGATOR",{"name":40,"affiliation":5,"role":38},"Jonathan Golub, PhD MPH",[42,46],{"name":36,"role":43,"phone":44,"phoneExt":23,"email":45},"CONTACT","617-358-2454","agupte1@bu.edu",{"name":40,"role":43,"phone":47,"phoneExt":23,"email":48},"443-287-2969","jgolub@jhmi.edu",[50,66],{"facility":51,"status":52,"city":53,"state":23,"zip":23,"country":54,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"Yenepoya (Deemed to be University","RECRUITING","Mangalore","India",{"type":56,"coordinates":57},"Point",[58,59],74.85603,12.91723,{"lat":59,"lon":58},[62],{"name":63,"role":43,"phone":64,"phoneExt":23,"email":65},"Poonam R Naik, MD","+91-7259346643","drpoonamnaik@gmail.com",{"facility":67,"status":52,"city":68,"state":23,"zip":23,"country":54,"cosmosGeoPoint":69,"geoPoint":73,"contacts":74},"Symbiosis Medical College for Women & Symbiosis University Hospital and Research Center","Pune",{"type":56,"coordinates":70},[71,72],73.85535,18.51957,{"lat":72,"lon":71},[75],{"name":76,"role":43,"phone":77,"phoneExt":23,"email":78},"Meenaksh Bhakare, MD","+91-9096555775","meenakshi.bhakare@smcw.siu.edu.in",{"type":80,"investigatorFullName":23,"investigatorTitle":23,"investigatorAffiliation":23,"oldNameTitle":23,"oldOrganization":23},"SPONSOR",[82],{"name":83,"class":84},"National Institute of Allergy and Infectious Diseases (NIAID)","NIH","100605609",false,"NCT07164742","Parent Study Name: Pulmonary Rehabilitation to Reduce Post-Tuberculosis Morbidity (TB Pure)","Pulmonary Rehabilitation to Reduce Post-Tuberculosis Morbidity (TB PURE) A Randomized Multi-Centre Trial","TB Pure","Inclusion Criteria:\n\n* Age at least 18 years\n* Microbiologically confirmed (smear microscopy, GeneXpert or culture) pulmonary TB disease\\*\n* Not completed more than 2 weeks of TB treatment\n* Receiving TB care at the outpatient clinics at the TB PuRe study sites\n* Willingness to complete 48 weeks of study evaluations.\n* Access to a smartphone.\n\nExclusion Criteria:\n\n* Modified Medical Research Council score of 0 points (dyspnea only with strenuous exercise)\n* Multi or extensively drug-resistant TB disease\\*\n* Extrapulmonary TB disease at any clinical sites without pulmonary involvement\n* TB meningitis or TB of the spine\n* Symptomatic cardiovascular disease, including coronary artery disease, arrhythmias and congestive cardiac failure.\n* Karnofsky Score \\\u003C 40 points\n* Any medical condition that prevents pulmonary rehabilitation eg: fracture of lower\u002Fupper limbs\u002Fpregnancy\n* Bronchodilators and\u002For corticosteroids inhaled or otherwise.","ALL","18 Years",{"count":95,"type":96},690,"ESTIMATED","INTERVENTIONAL",[99],"NA","Individual-level, unblinded randomized controlled trial of an 8-week (short arm) or 24-week (extended arm) pulmonary rehabilitation program, relative to standard of care, to prevent post-tuberculosis respiratory morbidity. 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