[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100630947":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":30,"centralContacts":34,"locations":26,"responsibleParty":43,"collaborators":46,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":51,"sex":57,"minAge":58,"maxAge":26,"enrollmentInfo":59,"targetDuration":26,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":68,"overallStatus":72,"whyStopped":26,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":26},{"fullName":5,"class":6},"Hong Kong Metropolitan University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Control group","ACTIVE_COMPARATOR","Participants will receive a 4-month general hygiene information.",[13],"Behavioral: Control group",{"label":15,"type":16,"description":17,"interventionNames":18},"Intervention group","EXPERIMENTAL","Subjects in this arm will receive a 4-month digital Personalized and Adaptive Sleep Support program (PASS).",[19],"Behavioral: 4-month Personalized and Adaptive Sleep Support program (PASS)",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","4-month Personalized and Adaptive Sleep Support program (PASS)","The 4-month Personalized and Adaptive Sleep Support (PASS) program incorporate 3 components: i) 20-minute brief motivational interviewing Session motivating participants, ii) digital platformThe digital platform enabling participants to access tailored health content, track PAP therapy adherence, log physical data such as activity and diet, and utilize integrated tools for self-monitoring and goal setting, iii) continuous personalized support offering chat-based messaging to promote program engagement and adherence.",[15],null,{"type":22,"name":9,"description":28,"armGroupLabels":29,"otherNames":26},"Participants will receive a 4-month general hygiene program, including (i) A 20-minute session, (ii) messaging, and (iii) phone call support. The content focuses on hand hygiene and food hygiene",[9],[31],{"name":32,"affiliation":5,"role":33},"Yuen Kwan Agnes Lai, PhD","PRINCIPAL_INVESTIGATOR",[35,39],{"name":32,"role":36,"phone":37,"phoneExt":26,"email":38},"CONTACT","(852)3970-2917","ayklai@hkmu.edu.hk",{"name":40,"role":36,"phone":41,"phoneExt":26,"email":42},"On Chu George Cheung, MPhil","(852)3970-2933","occheung@hkmu.edu.hk",{"type":33,"investigatorFullName":44,"investigatorTitle":45,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Dr Agnes LAI Yuen Kwan","Associate Professor",[47],{"name":48,"class":6},"Queen Mary Hospital, Hong Kong","100630947","personalised-active-self-management-of-sleep-apnea-program-100630947",false,"NCT07494292","Personalised Active Self-management of Sleep Apnea Program","A Personalised Active Self-management of Sleep Apnea Program (PASS) to Improve Positive Airway Pressure Treatment Uptake and Adherence: A Pilot Randomized Controlled Trial","PASS","Inclusion Criteria:\n\n* Aged 18 years and above\n* Newly diagnosed with OSA (diagnosis made within the past year)\n* Newly started or not yet started Positive Airway Pressure (PAP) treatment, with a treatment duration of less than 6 months\n* Physically inactive (self-reported moderate physical activity per week of \\\u003C150 minutes)\n* Overweight (BMI≥23 kg\u002Fm2)\n* Mentally, cognitively, and physically fit to join the trial as determined by the doctor in charge and responsible clinical investigators\n* Able to speak, read, and write Chinese\n* Willing to complete the questionnaires and assessments\n* Has a smartphone\n\nExclusion Criteria:\n\n* Clinically significant psychiatric disorder\n* Use of prescription drugs or clinically significant drugs affecting sleep.","ALL","18 Years",{"count":60,"type":61},60,"ESTIMATED","INTERVENTIONAL",[64],"NA","This study is to assess the feasibility and acceptability of the PASS in patients with OSA. Second, the study examines its effectiveness in improving PAP uptake and adherence, self-efficacy in self-care, changes in health-related habits, and health outcomes. We also assess the facilitators and barriers to implementing the PASS.\n\nThis is a two-group pilot randomized controlled trial (n=60) with a 4-month follow-up. Subjects assigned to the intervention group will receive a 4-month Personalized and Adaptive Sleep Support (PASS) program, a digital platform-based intervention. The 4-month program incorporates: i) a 20-minute brief motivational interviewing session; ii) a digital platform where users can view personalized OSA health-related videos and information, track their adherence to prescribed treatments, log their daily activities and dietary intake, and set personal health goals; and iii) continuous personalized chat-based messaging and phone call support. Participants in the control group will receive a 4-month general hygiene program, including (i) a 20-minute session, (ii) messaging, and (iii) phone call support.\n\nThe feasibility and acceptability of the PASS will be evaluated via semi-structured interviews at the 4-month follow-up. Self-administered questionnaires will be used at baseline, 2 months, and 4 months, and objective assessment tools (such as sleep tests) will be used at baseline and at the 2- and 4-month follow-ups. PAP adherence data will be downloaded from PAP machines (if available) for all subjects in both groups at baseline and at month 4.",[67],"Obstructive Sleep Apnea (OSA)",[69,70,71],"self-management","OSA","digital health","NOT_YET_RECRUITING","2026-03-20",{"date":75,"type":76},"2026-03-27","ACTUAL",{"date":78,"type":61},"2026-04-01",{"date":80,"type":61},"2027-03-31",{"name":5,"class":6}]