[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100617549":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":19,"locations":25,"responsibleParty":42,"collaborators":10,"id":46,"slug":47,"hasResults":48,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":48,"sex":54,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":10,"studyType":60,"phases":10,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":27,"whyStopped":10,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},{"fullName":5,"class":6},"Istanbul Esenyurt University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Pulmonary Rehabilitation Group (PRGr)",null,"Pulmonary Rehabilitation Group (PRGr)\n\nParticipant selection for the study was conducted using a purposive sampling approach. All participants experienced inspiratory muscle training for a total of 3 days per week over 8 weeks, with 2 days per week via video conference and 1 day per week as part of a home program. All interviews will be conducted online via a video conference website and recorded using a digital voice recorder. The recorded data will be transcribed word for word in Turkish.",[13],"Other: other",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":10},"other","Other: Telephone concept elicitation interview\n\nAll interview questions are designed to be quite open-ended in order to determine participants' preferences in an unbiased manner (as much as possible). Additional questions will only be used when necessary to ensure that all relevant concepts are covered. Participants will be asked questions about the effects of inspirational muscle training they have previously experienced on their daily lives, coping strategies, and self-management processes.",[9],[20],{"name":21,"role":22,"phone":23,"phoneExt":10,"email":24},"Esra PEHLİVAN, PhD","CONTACT","+90 216 777 96 00","fztesrakambur@yahoo.com",[26],{"facility":5,"status":27,"city":28,"state":28,"zip":29,"country":30,"countryCode":10,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"RECRUITING","Istanbul","34890","Turkey (Türkiye)",{"type":32,"coordinates":33},"Point",[34,35],28.94966,41.01384,{"lat":35,"lon":34},[38],{"name":39,"role":22,"phone":40,"phoneExt":10,"email":41},"Cahidenur Koçak","05511812675","cahidekocak25@gmail.com",{"type":43,"investigatorFullName":39,"investigatorTitle":44,"investigatorAffiliation":45,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Principal investigator","Saglik Bilimleri Universitesi","100617549","imt-in-asthma-activity-coping-self-management-100617549",false,"NCT07320066","IMT in Asthma: Activity, Coping, Self-Management","Reflections of Inspiratory Muscle Training on Patient Experiences in Asthma Rehabilitation","IMT in Asthma","Inclusion Criteria:\n\n* Being between the ages of 18-65\n* Having been diagnosed with severe persistent, non-allergic asthma by a pulmonologist in accordance with the Global Initiative for Asthma (GINA) guideline criteria,\n* Patients with type 2 inflammation markers. According to accepted standards; peripheral eosinophils \\\u003C150\u002FµL and\u002For negative skin prick test and\u002For total IgE \\\u003C30 kU\u002FL\n* Bronchodilator response (\\>12% or 200 mL improvement in FEV1% predicted following inhalation of 400 mg salbutamol)\n* Diagnosis-follow-up period: Patients diagnosed at least 6 months prior, under follow-up and treatment, and\u002For with controlled asthma\n* Having completed the pulmonary rehabilitation program\n* Completion of 8 weeks of inspiratory muscle training (IMT)\n* Patients who have read, understood, and signed the informed consent form\n\nExclusion Criteria:\n\n* Having recently had a respiratory tract infection recently (within the last month),\n* Having a smoking history of more than 10 pack-years or having a history of smoking within 6 months after quitting smoking\n* Having received oral corticosteroid treatment in the last 4 weeks,\n* Having a Body Mass Index \\>35,\n* Eosinophilic Granulomatosis Polyangiitis (EGPA) and Allergic Bronchopulmonary Aspergillosis (ABPA),\n* Vasculitis,\n* History of malignancy,\n* Pregnancy,\n* Previous lung surgery, use of long-term oxygen therapy\n* Having accompanying restrictive lung diseases (advanced kyphoscoliosis, ankylosing spondylitis) and neuromuscular diseases (myastania gravis, muscular dystrophies, myopathies) that will prevent healthy respiratory function testing and rehabilitation.\n* Cognitive dysfunction, mental retardation, dementia, or other conditions that make it difficult to follow the protocol,\n* Unwillingness to continue participating in the study,\n* Communication difficulties or intellectual deficiencies","ALL","18 Years","65 Years",{"count":58,"type":59},15,"ESTIMATED","OBSERVATIONAL","The aim of this study is to investigate asthma patients' experiences with an 8 week IMT and the perceived effects of this intervention on physical activity, coping strategies, and asthma self-management. A qualitative methodological design will be applied to understand the experiences of patients participating in the IMT program, how the program affected their daily activities, how they coped with symptoms and difficulties, and how they managed their condition.",[63],"Qualitative Research",[65,66,67,68,69],"asthma","inspiratory muscle training","telerehabilitation","self-management","qualitative research","2026-01-07",{"date":72,"type":73},"2026-01-09","ACTUAL",{"date":75,"type":73},"2026-01-05",{"date":77,"type":59},"2027-12-19",{"name":5,"class":6},1]