[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chronic-obstructive-airway-disease\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chronic-obstructive-airway-disease":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,83],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100609419","digital-inhaler-use-in-obstructive-lung-disease-care-100609419",false,"NCT07214337","Digital Inhaler Use in Obstructive Lung Disease Care","Feasibility, Adoption and Efficacy of Digital Inhaler in the Management of Obstructive Lung Disease","Inclusion Criteria:\n\n* Any sex\n* Over the age of 18 years.\n* Physician-diagnosed obstructive lung disease\n* Speak, read, and understand English.\n* The current study is a feasibility pilot. Based on the results of the study, future studies will include non-English speakers as well.\n* Able to understand study requirements and comply with study procedures.\n* Ability to operate a smartphone or tablet (for questionnaire and symptoms input).\n* Patients who use either a DPI or an MDI device as controller medications. Medications will not be changed by the study team.\n\nExclusion Criteria:\n\n* Physically disabled such that they are incapable of using digital devices or metered dose inhalers.\n* Suffer from any visual, hearing or cognitive impairment that cannot be corrected enough to operate the devices properly. Mild\u002Fmoderate vision loss and mild hearing loss may be included with appropriate corrective measures that do not affect the device usage.\n* Suffering from serious uncontrolled medical conditions that may interfere with study conduct.\n* Inability or unwillingness of the participant to give written informed consent.\n* Pregnant women (due to complicated physiology)\n* The current study is a feasibility pilot. Based on the results of the study, future studies will likely include pregnant patients as well.\n* Prisoners","ALL","18 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","This is a pilot study to evaluate the role digital inhaler technology on patients with obstructive lung disease in preventing admissions and exacerbation, as well as improving symptom control. The primary objective is to evaluate feasibility of study protocol, patient recruitment, and patient retention with goal recruitment of 20 participants, 60% recruitment success, and 60% retention rate for 6 months duration. The secondary objectives are the evaluation of patient admission rate, exacerbation rates, and symptoms control with use of digital inhaler technology The subject population will be patients with physician diagnosed obstructive lung disease.",[26,27],"Chronic Obstructive Airways Disease Exacerbated","Chronic Obstructive Airway Disease",[29,30,31,32,33,34,35],"Chronic Obstructive Airways Disease","COPD","COPD Exacerbation","Severe COPD","Moderate COPD","Severe Chronic Obstructive Airways Disease","Moderate Chronic Obstructive Airways Disease","NOT_YET_RECRUITING","2025-10-07",{"date":39,"type":40},"2025-10-09","ACTUAL",{"date":42,"type":20},"2025-11-01",{"date":44,"type":20},"2027-06",{"name":46,"class":47},"Cedars-Sinai Medical Center","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":21,"phases":59,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":82},"100564476","make-every-step-count-personalised-music-feedback-to-walking-for-people-living-with-copd-100564476","NCT06629675","Make Every Step Count: Personalised Music Feedback to Walking for People Living With COPD","Personalised Music Feedback to Optimise Adherence to the Walking Exercise Prescription During Pulmonary Rehabilitation for Individuals Living With Chronic Obstructive Pulmonary Disease","MuSiC","Inclusion Criteria:\n\n* Willing and able to provide informed consent for participation in the study.\n* The patient is referred for PR at the UHL.\n* The patient has a confirmed diagnosis of COPD using spirometry (based on GOLD criteria)\n* Male or female, aged 18+ years.\n* Able to communicate in written and spoken English.\n\nExclusion Criteria:\n\n* Unable to provide valid informed consent.\n* Lack of motivation to participate in PR programme.\n* Any-contra-indications absolute or relative to exercise training.\n* Has had a cardiac event within last 6 weeks\n* Severe psychiatric disorders\n* Patients with a history of MRSA +ve screens (patients can be assessed and given an exercise programme but cannot attend the classes. Patients need to have 3 consecutive -ve MRSA swabs before they can attend).\n* Unable to understand written or spoken English.",{"count":58,"type":20},30,[23],"Pulmonary Rehabilitation (PR) is an evidence-based intervention to effectively manage the physiological and psychological effects of Chronic Obstructive Pulmonary Disease (COPD). The aims of PR are to improve symptoms of COPD, increase exercise capacity, increase independency, improve overall behaviour related to health (like exercising more), and enhance quality of life. The cornerstone of PR programmes is aerobic exercise prescription. Typically, walking exercise is used, and the prescription is individualised for each patient based on their maximal walking exercise capacity. However, adherence to walking exercise is challenging for service users, particularly when unsupervised at home. The use of music during exercise shows promise as a tool to decrease the perception of fatigue and increase motivation, but the integration of music via smartphone applications to support walking exercise adherence during PR has not been explored. This project aims to assess if a new mobile application BeatClearWalker (BCW) intervention is practical, acceptable, and effectively used by people living with COPD. The app is designed to help people living with COPD attending PR adhere to their prescribed walking pace during exercise. The BCW app provides real-time, personalised music feedback through music degradation to optimise the dose of walking exercise.",[62,63,27],"Chronic Obstructive Pulmonary Disease (COPD)","Chronic Obstructive Lung Disease",[65,66,67,68,69,70,71],"Auditory feedback","Chronic Obstructive Pulmonary Diseases","Digital Health Technology","Exercise","Exercise adherence","Pulmonary rehabilitation","Mobile applications","RECRUITING","2025-04-11",{"date":75,"type":40},"2025-04-16",{"date":77,"type":20},"2025-04-20",{"date":79,"type":20},"2025-09-26",{"name":81,"class":47},"University of Leicester",2,{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":4,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":16,"minAge":90,"maxAge":91,"enrollmentInfo":92,"targetDuration":94,"studyType":95,"phases":4,"briefSummary":96,"conditions":97,"keywords":102,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":5},"100249574","seoul-national-university-airway-registry-100249574","NCT02527486","Seoul National University Airway Registry","Airway Registry for Chronic Airway Diseases","COPD\n\nInclusion Criteria:\n\n* Postbronchodilator FEV1\u002FFVC \\\u003C 0.7 AND chronic respiratory symptom\n\nExclusion Criteria:\n\n\\-\n\nAsthma\n\nInclusion Criteria:\n\n* Never smoker or \\\u003C5PY of smoking history AND Recurrent episodes of asthma symptoms (wheezing, dyspnea, chest tightness, cough) AND (either Positive BDR OR positive metacholine\u002Fmannitol\u002Fexercise provocation test)\n\nExclusion Criteria:\n\n\\-\n\nACOS\n\nInclusion Criteria:\n\n* COPD AND Asthma (regardless of smoking status)\n\nExclusion Criteria:\n\n\\-","20 Years","90 Years",{"count":93,"type":20},800,"10 Years","OBSERVATIONAL","This is a multicenter, prospective observational cohort study, in which patients with chronic airway diseases including chronic obstructive pulmonary disease(COPD), asthma, asthma-COPD overlap syndrome (ACOS) will be recruited.",[62,98,99,100,101,27],"Asthma","Asthma With Chronic Obstructive Pulmonary Disease","Bronchiectasis","Inactive Tuberculosis of Lung",[30,98,103,100],"ACOS","2015-08-17",{"date":106,"type":20},"2015-08-19",{"date":108,"type":4},"2011-09",{"date":110,"type":20},"2031-12",{"name":112,"class":47},"Seoul National University Hospital"]