[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100652799":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":28,"locations":11,"responsibleParty":38,"collaborators":11,"id":40,"slug":41,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":42,"sex":48,"minAge":49,"maxAge":11,"enrollmentInfo":50,"targetDuration":11,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":65,"whyStopped":11,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":11},{"fullName":5,"class":6},"University Hospitals, Leicester","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"I-IMPACT","EXPERIMENTAL",null,[13],"Device: I-IMPACT",{"label":15,"type":16,"description":11,"interventionNames":17},"Usual Care","ACTIVE_COMPARATOR",[18],"Other: Pulmonary Rehabilitation",[20,24],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":11},"DEVICE","I-IMPACT (Individualised self-Management ProgrAmme for long-term CondiTions) is a digital self-management rehabilitation programme developed by the UHL NHS Trust. The programme is designed for individuals recovering from acute illness and those living with chronic respiratory and cardiac conditions. For this study, the programme will be set so that each participant's primary diagnosis is ILD. I-IMPACT delivers physical and psychological support through a comprehensive set of features.\n\nParticipants allocated to the I-IMPACT programme will be able to:\n\n* Access educational material, both general and diagnosis-specific.\n* Record cardiovascular and strength exercise sessions.\n* Update their symptoms using the health trackers.\n* Create and review personalised goals.\n* Contact their rehabilitation team via the \"Ask a Healthcare Professional\" feature.\n* Contact technical support for any IT or navigation challenges.",[9],{"type":6,"name":25,"description":26,"armGroupLabels":27,"otherNames":11},"Pulmonary Rehabilitation","An outpatient pulmonary rehabilitation programme delivered at the UHL NHS Trust. This is an 8-week, twice-weekly supervised programme at Glenfield Hospital.",[15],[29,34],{"name":30,"role":31,"phone":32,"phoneExt":11,"email":33},"Enya Daynes, PhD","CONTACT","0116 250 2759","e.daynes@nhs.net",{"name":35,"role":31,"phone":36,"phoneExt":11,"email":37},"Duha Azwai, BSc Biomedical Science","0116 250 2758","da356@leicester.ac.uk",{"type":39,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100652799","feasibility-acceptability-and-implementability-of-i-impact-for-ild-100652799",false,"NCT07780201","Feasibility, Acceptability, and Implementability of I-IMPACT for ILD","Feasibility, Acceptability, and Implementability of an Asynchronous Digital Pulmonary Rehabilitation Programme (I-IMPACT) Compared With Centre-Based Pulmonary Rehabilitation in Adults With Interstitial Lung Disease.","I-IMPACT ILD","Inclusion Criteria:\n\nPatient participants:\n\n* Age: ≥ 18 years\n* Consent: willing and able to provide informed consent to participate in the study\n* Diagnosis: physician-confirmed diagnosis of ILD of any subtype\n* Clinically stable: no ILD exacerbation or respiratory-related hospitalisation in the preceding four weeks.\n* Digital access: able to access and use the internet and an internet-enabled device to engage with I-IMPACT.\n* Language: able to read and write in English to complete the programme and study assessments.\n* Randomisation: willing to be randomised to either arm\n\nStaff participants:\n\n* Consent: willing and able to provide informed consent to participate in the study\n* Professional role: a qualified healthcare professional involved in delivering ILD care and\u002For pulmonary rehabilitation (PR) at the UHL NHS Trust or another healthcare organisation.\n* Employment duration (UHL staff only): must have been employed by the UHL NHS Trust for at least two years.\n* Language: able to read and write in English to complete the acceptability questionnaire and optional interview.\n\nExclusion Criteria:\n\nPatient participants:\n\n* Recent or concurrent PR: concurrent enrollment or recent completion of a PR programme within the 12-months preceding enrollment.\n* Contraindications to exercise: presenting with exercise-related contraindications (unstable cardiovascular disease; hypertension, etc., a full list is described by the American College of Sports Medicine and is routinely deployed).","ALL","18 Years",{"count":51,"type":52},50,"ESTIMATED","INTERVENTIONAL",[55],"NA","This is a single-centre, two-arm randomised controlled feasibility trial comparing I-IMPACT, an asynchronous digital rehabilitation programme, with conventional centre-based pulmonary rehabilitation (usual care) in adults with Interstitial Lung Disease (ILD). The study will be conducted at the University Hospitals of Leicester NHS Trust, and Glenfield Hospital is the central site for participant recruitment, baseline and longitudinal assessments, and delivery of the in-person usual care arm.\n\nThis is a feasibility study; therefore, the primary outcome is feasibility (recruitment, attrition, adherence, and acceptability), and the secondary outcomes comprise preliminary clinical and safety parameters. Outcomes will be assessed through a mixed-methods approach, involving both ILD patients and staff (healthcare professionals) participants.",[58],"Interstitial Lung Disease (ILD)",[60,9,61,62,63,64],"Interstitial lung disease (ILD)","feasibility","digital pulmonary rehabilitation","Randomised controlled trial","Implementation","NOT_YET_RECRUITING","2026-08-19",{"date":68,"type":69},"2026-08-21","ACTUAL",{"date":71,"type":52},"2026-11",{"date":73,"type":52},"2028-07",{"name":5,"class":6}]