[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"West Park Healthcare Centre\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":121},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,48,75,96],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100421383","a-non-pharmacological-cough-control-therapy-100421383",false,"NCT04767074","A Non-pharmacological Cough Control Therapy","A Non-pharmacological Cough Control Therapy as an Adjuvant of Pulmonary Rehabilitation in People With Interstitial Lung Diseases and Chronic Cough - A Feasibility Study","Inclusion Criteria:\n\n* Individuals will be included if having confirmed diagnosis of any ILD by a physician (as per Canadian Thoracic Society's guideline for evaluating patients with fibrotic interstitial lung disease) and a chronic cough lasting more than 8 weeks in duration\n\nExclusion Criteria:\n\n* self-reports of moderate or large sputum production\n* effective or suspected exacerbation of the respiratory condition in the past month\n* upper respiratory tract infection in the past month\n* use of angiotensin-converting enzyme inhibitor medication\n* changes in the prescribed medication in the previous month\n* evidence of traction bronchiectasis in the HRCT\n* evidence of other medical conditions that prevent performance of an exercise training program\n* unable to read or speak in English \u002F unable to provide informed consent.","ALL","18 Years","85 Years",{"count":20,"type":21},24,"ESTIMATED","INTERVENTIONAL",[24],"NA","Coughing affects almost all individuals with ILD leading to physical, psychological and social distress and prevents individuals from performing their activities of daily living, working or socialising in public places. Unfortunately, there are no licensed medications available to treat chronic cough and the few drugs that have been tried resulted in little efficacy and significant side effects. Drug-free cough control interventions have shown promise in reducing the severity and impact of coughing on patients' lives but have not been tested in individuals with ILD. This study aims to explore the feasibility and effectiveness of a non-pharmacological cough control therapy, as an adjuvant of pulmonary rehabilitation, in patients with ILD and chronic cough (\\>8 weeks in duration).",[27,28,29,30],"Cough","ILD","Pulmonary Disease","Pulmonary Fibrosis",[27,28,32,33,34],"Pulmonary rehabilitation","chronic cough","non-pharmacological cough therapy","RECRUITING","2025-03-28",{"date":38,"type":39},"2025-04-03","ACTUAL",{"date":41,"type":39},"2020-09-01",{"date":43,"type":21},"2025-12",{"name":45,"class":46},"West Park Healthcare Centre","OTHER",2,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},"100567403","promoting-physical-activity-following-dysvascular-amputation-100567403","NCT06667739","Promoting Physical Activity Following Dysvascular Amputation","A Behaviour Change Intervention Promoting Physical Activity Following Dysvascular Amputation: a Pilot Study","Inclusion Criteria:\n\n* Dysvascular LLA (LLA due to diabetes or vascular disease)\n* major LLA (at the ankle or above)\n* living in the community\n* adult at least 18 years of age\n* comfortable communicating in English and able to understand basic English\n* receptive to using a phone or tablet (e.g., to enable peer coaching, access to modules.\n\nExclusion Criteria:\n\n* actively receiving rehabilitation services related to physical activity\u002Fmobility\n* recommended medical supervision for physical activity by health care provider, or skin problems preventing usual activity\n* not able to provide informed consent.",{"count":56,"type":21},40,[24],"Loss of a lower limb due to diabetes can have a devastating impact on physical and mental health and quality of life. Individuals are at risk of other diseases such as cardiovascular disease, loss of the other limb and death. Physical activity can reduce risk of chronic disease and improve health outcomes; however, physical activity levels in people with limb loss are low, often due to reduced balance and walking ability. Rehabilitation services are not readily available and the cost of delivering such programs remains high. Working with individuals with lower limb amputation, we created a virtual, peer-led physical activity behaviour change intervention called IMproving Physical Activity through Coaching and Technology following Lower Limb Loss (IMPACT-L3). We will conduct a pilot study to assess feasibility and optimize design of a future trial of effectiveness.",[60,61],"Amputation","Lower Limb Amputation Knee",[63,64,65],"Physical activity","Behaviour change","Peer coaching","2025-02-20",{"date":68,"type":39},"2025-02-24",{"date":70,"type":39},"2025-01-23",{"date":72,"type":21},"2026-03",{"name":45,"class":46},1,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":84,"phases":4,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":74},"100502324","tele-rehabilitation-in-chronic-respiratory-disease-an-observational-cohort-study-100502324","NCT05820776","Tele-rehabilitation in Chronic Respiratory Disease: an Observational Cohort Study","Remote Exercise-based Pulmonary Rehabilitation Telemedicine in Chronic Respiratory Disease: an Observational Cohort Study","Inclusion Criteria:\n\n* stable chronic respiratory disease\n* qualified candidates for pulmonary rehabilitation,\n* current non-smoker;\n* primary diagnosis chronic respiratory disease limited by dyspnea (mMRC≥2);\n* free of exacerbation at the time of admission, and\n* stable co-existing conditions\n\nExclusion Criteria:\n\n* completed PR within the previous 12 months of the current admission and\n* being unable to communicate with the treating team.",{"count":83,"type":21},50,"OBSERVATIONAL","Pulmonary rehabilitation is a program that helps people with lung disease improve their function. It uses exercise, education, and self-management strategies to improve physical ability and quality of life. Because some people are unable to visit West Park Healthcare Centre, we established a remote supervised pulmonary rehabilitation program that patients can access via an electronic device (computer, tablet or smart phone). Regular quality assurance is necessary to ensure that the program is effective. We plan to collect and summarize the program's results. The benefit of doing so is that it allows us to make any changes or improvements that may help patients with chronic respiratory conditions.",[87],"Chronic Respiratory Disease","2024-07-25",{"date":90,"type":39},"2024-07-26",{"date":92,"type":39},"2023-04-06",{"date":94,"type":21},"2025-12-31",{"name":45,"class":46},{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":102,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":104,"targetDuration":4,"studyType":22,"phases":105,"briefSummary":106,"conditions":107,"keywords":109,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":74},"100552912","comparing-centre-based-remotely-supervised-and-self-administered-sts-tests-in-individuals-with-crd-100552912","NCT06479252","Comparing Centre-based, Remotely Supervised, and Self-administered STS Tests in Individuals With CRD","Comparing Centre-based, Remotely Supervised, and Self-administered Sit-to-stand Tests in Individuals With Chronic Respiratory Diseases","STS24","Inclusion Criteria:\n\n* Physician diagnosis of chronic respiratory disease (e.g., Chronic Obstructive Pulmonary Disease, Interstitial Lung Disease, Asthma).\n* Male and female patients ≥18 years of age.\n* Able to perform at least 5 repetitions in the 1-min sit-to-stand test without use of upper extremities.\n* Access to a portable pulse oximeter at home to measure heart rate and oxygen saturation.\n* Access to technology for remote supervision (e.g., mobile phone, laptop\u002Fcomputer, iPad)\n\nExclusion Criteria:\n\n* Lower limb surgery in the preceding 3 months.\n* Medically unstable to perform exercise tests (e.g., no exacerbation in the preceding two weeks).\n* Predominant neurological or musculoskeletal limitations to completing sit-to-stand.\n* At risk of falling during sit-to-stand due to impaired balance, as indicated in their clinical record, and\u002For PR assessment.",{"count":83,"type":21},[24],"Despite evidence on the psychometric properties of sit-to-stand (STS) tests in chronic respiratory disease (CRD) populations, most studies have been conducted face-to-face. Given the recent emphasis on virtual pulmonary rehabilitation (VPR), there is a need to identify reliable and valid exercise tests that can be delivered in home-based settings, either supervised remotely or self-administered by patients. A repeated-measures crossover design will be used to test the home-based administration of STS tests. The 30-second STS (30-s STS) and 1-minute STS (1-min STS) tests will be randomly administered across three test conditions (centre-based, remotely supervised, and self-administered). Data will summarize the feasibility of remotely supervised and self-administered STS tests and compare the performances of centre-based tests with remotely supervised and self-administered versions of STS tests in patients with CRD.",[108],"Chronic Lung Disease",[110,111,112],"Assessment","Pulmonary Rehabilitation","Remote","2024-07-03",{"date":115,"type":39},"2024-07-08",{"date":117,"type":39},"2024-06-22",{"date":119,"type":21},"2024-12-31",{"name":45,"class":46},""]