[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100648217":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":29,"locations":35,"responsibleParty":51,"collaborators":25,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":25,"eligibilityCriteria":59,"healthyVolunteers":56,"sex":60,"minAge":61,"maxAge":25,"enrollmentInfo":62,"targetDuration":25,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":25,"overallStatus":37,"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},"Morning Activation Program","EXPERIMENTAL","Participants will receive a six-week individualized behavioral program delivered in weekly sessions of approximately 60 minutes. The program is designed to support engagement in daily activities after waking, establish consistent daily routines, and improve mood and functioning after stroke.",[13],"Behavioral: Morning Activation Program",{"label":15,"type":16,"description":17,"interventionNames":18},"Health Education Program","ACTIVE_COMPARATOR","Participants will receive a six-week health education program delivered in weekly sessions of approximately 60 minutes. The program will provide general information relevant to health and recovery after stroke and will be matched to the experimental program in session frequency and duration. It will not include the individualized behavioral strategies provided in the experimental arm.",[19],"Behavioral: Health Education Program",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","A six-week individualized behavioral program delivered in weekly sessions of approximately 60 minutes. The program is designed to support engagement in daily activities after waking, establish consistent daily routines, and improve mood and functioning after stroke. Sessions will be tailored to participants' needs and abilities.",[9],null,{"type":22,"name":15,"description":27,"armGroupLabels":28,"otherNames":25},"A six-week health education program delivered in weekly sessions of approximately 60 minutes. The program will provide general information relevant to health and recovery after stroke and will be matched to the experimental program in session frequency and duration. It will not include the individualized behavioral strategies provided in the experimental arm.",[15],[30],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},"Stephen Lau","CONTACT","+852 2766 4283","chun-lun-stephen.lau@polyu.edu.hk",[36],{"facility":5,"status":37,"city":38,"state":25,"zip":25,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"RECRUITING","Hong Kong","HK",{"type":41,"coordinates":42},"Point",[43,44],114.17469,22.27832,{"lat":44,"lon":43},[47,48],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},{"name":49,"role":50,"phone":25,"phoneExt":25,"email":25},"Stephen Lau, PhD","PRINCIPAL_INVESTIGATOR",{"type":50,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"Prof. LAU Chun Lun Stephen","Assistant Professor","100648217","morning-activation-to-improve-mood-after-stroke-100648217",false,"NCT07719517","Morning Activation to Improve Mood After Stroke","Inclusion Criteria:\n\n* Age 18 years or older.\n* History of stroke at least 6 months before enrollment.\n* Patient Health Questionnaire-9 score of 10 or higher.\n* Difficulty getting started or engaging in activities in the morning.\n* Able to provide informed consent.\n\nExclusion Criteria:\n\n* Conditions that would interfere with study participation.\n* Neurological condition other than stroke.\n* Currently receiving psychological therapy for depression.\n* Significant cognitive impairment or dementia.\n* Current or past diagnosis of psychosis, bipolar disorder, or mania.\n* Hospitalization that would interfere with study participation.\n* Acute or significant suicidal ideation\n* Alcohol or substance use problems within the past month.\n* Use of antidepressant or anti-anxiety medication unless the dosage has been stable for at least 4 weeks and no changes are planned during the study.","ALL","18 Years",{"count":63,"type":64},30,"ESTIMATED","INTERVENTIONAL",[67],"NA","This pilot randomized controlled trial will evaluate the feasibility and preliminary effects of a six-week behavioral intervention designed to improve mood and daily functioning in adults who have experienced a stroke and report depressive symptoms and difficulty becoming engaged in activities after waking.\n\nParticipants will be randomly assigned to either the behavioral intervention or a health education program. Assessments will be completed before and immediately after the six-week program and will include questionnaires and seven-day monitoring of sleep, activity, and mood. The study will also examine feasibility indices such as participant retention, intervention attendance, acceptability, and preliminary changes in mood.",[70,71],"Stroke","Depressive Symptoms","2026-07-17",{"date":74,"type":75},"2026-07-22","ACTUAL",{"date":77,"type":75},"2026-05-15",{"date":79,"type":64},"2026-12",{"name":5,"class":6},1]