[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100651556":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":29,"centralContacts":33,"locations":39,"responsibleParty":55,"collaborators":57,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":62,"sex":68,"minAge":69,"maxAge":28,"enrollmentInfo":70,"targetDuration":28,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":80,"overallStatus":84,"whyStopped":28,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"University of Edinburgh","OTHER",[8,14,18],{"label":9,"type":10,"description":11,"interventionNames":12},"Baseline period 5 days","ACTIVE_COMPARATOR","Up to 3 participants will be randomly allocated to a baseline phase of 5 days prior to starting the intervention phase of music-listening.",[13],"Behavioral: Music intervention",{"label":15,"type":10,"description":16,"interventionNames":17},"Baseline period of 8 days","Up to 3 participants will be randomly allocated to a baseline phase of 8 days prior to starting the intervention phase of music-listening.",[13],{"label":19,"type":10,"description":20,"interventionNames":21},"Baseline period of 12 days.","Up to 3 participants will be randomly allocated to a baseline phase of 12 days prior to starting the intervention phase of music-listening.",[13],[23],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":28},"BEHAVIORAL","Music intervention","Two week personalised music listening intervention, with daily self-directed listening for a minimum of 30 minutes per day. Participants will meet with researcher after first week to review the listening material.",[9,19,15],null,[30],{"name":31,"affiliation":5,"role":32},"Satu Baylan, DClinPsy, PhD, BSc","STUDY_DIRECTOR",[34],{"name":35,"role":36,"phone":37,"phoneExt":28,"email":38},"Joanna Rickman, MSc, BSc","CONTACT","0131 651 3969","J.B.Rickman@sms.ed.ac.uk",[40],{"facility":41,"status":28,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"NHS Fife","Kirkcaldy","Fife","KY2 5AH","United Kingdom","UK",{"type":48,"coordinates":49},"Point",[50,51],-3.15999,56.11683,{"lat":51,"lon":50},[54],{"name":35,"role":36,"phone":37,"phoneExt":28,"email":38},{"type":56,"investigatorFullName":28,"investigatorTitle":28,"investigatorAffiliation":28,"oldNameTitle":28,"oldOrganization":28},"SPONSOR",[58],{"name":41,"class":59},"OTHER_GOV","100651556","measuring-the-effects-of-music-listening-on-distress-after-intensive-care-100651556",false,"NCT07762196","Measuring the Effects of Music-Listening On Distress After Intensive Care","Measuring the Effects of Music-Listening On Distress After Intensive Care (MELODIC): A Single Case Experimental Design Study.","MELODIC","Inclusion Criteria:\n\n* 18 years or older.\n* Experienced an admission to an ICU\u002FHDU of any length and not yet participated in InS:PIRE.\n* Access to an internet-enabled device and internet connection whilst at home.\n* Experiencing some distress relating to their ICU\u002FHDU admission - a cut-off score of 4 on the VAS 'Distress Thermometer' has been used previously (Hofhuis et al., 2025).\n\nExclusion Criteria:\n\n* Are unable to give informed consent e.g. have a significant cognitive impairment due to illness, injury or neurological condition, or are currently experiencing delirium or acute psychotic illness.\n* Have significant communication difficulties or limited English and cannot access validated outcome measures or translation services in the given language.\n* Are experiencing a mental health crisis or have recently attempted suicide, where ongoing significant risk of harm to themselves or others remains.\n* Have an uncorrected hearing impairment that would prevent them from hearing their music playlist.\n* Are participating in another study aimed at reducing distress.","ALL","18 Years",{"count":71,"type":72},9,"ESTIMATED","INTERVENTIONAL",[75],"NA","The primary goal of this single-case experimental design study is to investigate the effectiveness of personalised music listening on daily levels of distress after discharge from a critical care ward. The study will also aim to understand the effect of personalised music listening on symptoms of post-traumatic stress, anxiety, depression and health-related quality of life post-discharge.\n\nThe main questions the study aims to answer are included below.\n\nAfter discharge from critical care, does personalised music-listening:\n\n* Reduce psychological distress?\n* Reduce symptoms of anxiety and depression?\n* Improve health-related quality of life (HRQoL)?\n\nThe study will have 3 phases, allowing for participant data gathered during the baseline phase (treatment as usual) to be compared to data gathered during intervention (music-listening) and follow-up phases.\n\nParticipants will:\n\n* rate their distress on a visual analogue scale each day.\n* listen to a minimum of 30 minutes of self-selected music each day during the intervention phase.\n* complete measures of mood, anxiety, post-traumatic stress and health-related quality of life at baseline, intervention and follow-up phases.",[78,79],"Post-ICU Patients","PICS",[81,82,83],"music-listening","post-ICU","psychological distress","NOT_YET_RECRUITING","2026-08-07",{"date":87,"type":88},"2026-08-13","ACTUAL",{"date":90,"type":72},"2026-08",{"date":92,"type":72},"2027-05",{"name":5,"class":6},1]