[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100649109":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":28,"locations":34,"responsibleParty":46,"collaborators":25,"id":50,"slug":51,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":25,"eligibilityCriteria":56,"healthyVolunteers":52,"sex":57,"minAge":58,"maxAge":25,"enrollmentInfo":59,"targetDuration":25,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":69,"overallStatus":71,"whyStopped":25,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"The Hong Kong Polytechnic University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"ISleepFAST","EXPERIMENTAL","Participants will receive ISleepFAST, a six-week individualized behavioral sleep intervention delivered in six weekly, face-to-face sessions of approximately 60 minutes each.",[13],"Behavioral: ISleepFAST",{"label":15,"type":16,"description":17,"interventionNames":18},"Stroke and Sleep Health Education","ACTIVE_COMPARATOR","A six-week education program providing general information about stroke, sleep, and health.",[19],"Behavioral: Stroke and Sleep Health Education",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","A six-week, individual, face-to-face behavioral program designed to address sleep and sleep-wake difficulties following stroke. Participants attend one approximately 60-minute session per week. The program provides education and individualized behavioral strategies based on each participant's sleep-related needs.",[9],null,{"type":22,"name":15,"description":17,"armGroupLabels":27,"otherNames":25},[15],[29],{"name":30,"role":31,"phone":32,"phoneExt":25,"email":33},"Stephen Lau","CONTACT","+852 2766 4283","chun-lun-stephen.lau@polyu.edu.hk",[35],{"facility":5,"status":25,"city":36,"state":25,"zip":25,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Hong Kong","HK",{"type":39,"coordinates":40},"Point",[41,42],114.17469,22.27832,{"lat":42,"lon":41},[45],{"name":30,"role":31,"phone":32,"phoneExt":25,"email":33},{"type":47,"investigatorFullName":48,"investigatorTitle":49,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"PRINCIPAL_INVESTIGATOR","Prof. LAU Chun Lun Stephen","Assistant Professor","100649109","personalised-sleep-and-circadian-intervention-after-stroke-100649109",false,"NCT07731516","Personalised Sleep and Circadian Intervention After Stroke","Feasibility, Efficacy, and Patient Experience of a Personalised Transdiagnostic Intervention for Sleep and Circadian Dysfunction Following Stroke: a Mixed-method Randomised Controlled Feasibility Trial","Inclusion Criteria:\n\n1. \\>6 months from last stroke\n2. aged ≥18 years\n3. Cantonese language fluency\n4. ≥1 self-reported sleep or circadian problem(s) for 3 months: ≥30 min to get to sleep on ≥3 nights per week, waking in the middle of night ≥30 min on ≥3 nights per week, \\\u003C6-hr sleep per night or ≥9-hr sleep per 24 hour period on ≥3 nights per week, ≥1.09 hours of variability in sleep-wake schedule across one week, and\u002For bedtime after 2:00 a.m. on ≥3 nights per week\n5. adequate opportunities for sleep.\n\nExclusion Criteria:\n\n1. presence of an active and progressive physical or neurocognitive illness or substance abuse making participation infeasible\n2. past or current involvement in psychological treatment for sleep issues\n3. night shift work\n4. pregnancy or breastfeeding.","ALL","18 Years",{"count":60,"type":61},40,"ESTIMATED","INTERVENTIONAL",[64],"NA","This is a two-arm, parallel-group randomized controlled feasibility trial involving 40 community-dwelling adults with chronic stroke and ongoing sleep or circadian difficulties. Participants will be randomly assigned in a 1:1 ratio to either an individualized behavioral sleep intervention or an attention-matched health education program.\n\nBefore randomization, participants will complete questionnaires assessing sleep and related health outcomes, maintain a sleep diary, and wear a wrist-worn activity monitor for seven days. Participants will then attend six weekly, individual, face-to-face sessions lasting approximately one hour each.\n\nThe behavioral sleep intervention will provide individualized education and behavioral strategies to support sleep and daily sleep-wake functioning following stroke. The comparison program will provide education about stroke, sleep, and general health. The two programs will be matched in session frequency and duration.\n\nFollowing the six-week program, participants will repeat the questionnaires, sleep diary, and seven-day wrist-monitoring assessment. Participants will also provide feedback about their experiences with the study and program.\n\nThe trial will evaluate recruitment, retention, attendance, intervention delivery, acceptability, fidelity, and safety. Preliminary changes in sleep and sleep-wake outcomes will also be examined.",[67,68],"Stroke","Sleep",[67,68,70],"Circadian Rhythm","NOT_YET_RECRUITING","2026-07-22",{"date":74,"type":75},"2026-07-28","ACTUAL",{"date":77,"type":61},"2026-08",{"date":79,"type":61},"2028-07",{"name":5,"class":6},1]