[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100658281":3},{"organization":4,"outcomesModule":7,"designInfo":82,"detailedDescription":81,"studyPopulation":81,"armGroups":88,"interventions":95,"overallOfficials":101,"centralContacts":105,"locations":111,"responsibleParty":128,"collaborators":130,"id":134,"slug":135,"hasResults":136,"nctId":137,"briefTitle":138,"officialTitle":139,"acronym":81,"eligibilityCriteria":140,"healthyVolunteers":136,"sex":141,"minAge":142,"maxAge":143,"enrollmentInfo":144,"targetDuration":81,"studyType":147,"phases":148,"briefSummary":149,"conditions":150,"keywords":81,"overallStatus":153,"whyStopped":81,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":163},{"fullName":5,"class":6},"New York University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":81},[9],{"measure":10,"description":11,"timeFrame":12},"Intervention retention","Percentage of participants who complete the 2-week sleep intervention","From enrollment to 2-week post-intervention",[14,18,22,26,28,32,36,38,40,43,47,50,53,56,59,62,65,68,72,75,78],{"measure":15,"description":16,"timeFrame":17},"Feasibility of recruitment","Percentage of adults who meet the study criteria","From screening to baseline",{"measure":19,"description":20,"timeFrame":21},"Feasibility of study enrollment","Percentage of eligible participants who provide consent","From screening to enrollment",{"measure":23,"description":24,"timeFrame":25},"Feasibility of completing the study assessment","Percentage of enrolled participants who complete the baseline assessment","From enrollment to baseline",{"measure":23,"description":27,"timeFrame":12},"Percentage of enrolled participants who complete the post-intervention assessment",{"measure":29,"description":30,"timeFrame":31},"Intervention acceptability","Satisfaction with the intervention will be measured by the Client Satisfaction Questionnaire-8. The total score ranges from 8 to 32, with higher scores indicating greater satisfaction with the intervention.","2-week post-intervention",{"measure":33,"description":34,"timeFrame":35},"Intervention engagement","Total days of engaging with the chatbot","2-week post-intervention, 2-month follow-up, and 4-month follow-up",{"measure":33,"description":37,"timeFrame":35},"Total duration of engaging with the chatbot",{"measure":33,"description":39,"timeFrame":35},"Message exchanges per chat session",{"measure":41,"description":42,"timeFrame":31},"Intervention usability","Usability of the intervention will be measured by the Chatbot Usability Questionnaire. The total score ranges from 0 to 100. Higher scores indicate greater perceived chatbot usability.",{"measure":44,"description":45,"timeFrame":46},"Fitbit-measured sleep duration","Sleep duration will be measured objectively using Fitbit and defined as the total amount of time spent asleep during the primary sleep period, expressed in minutes.","Baseline, 2-week post-intervention",{"measure":48,"description":49,"timeFrame":46},"Fitbit-measured sleep onset","Sleep onset will be measured objectively using Fitbit and defined as the time from attempting to fall asleep to sleep onset, expressed in minutes.",{"measure":51,"description":52,"timeFrame":46},"Fitbit-measured sleep efficiency","Sleep efficiency will be measured objectively using Fitbit and defined as the percentage of time spent asleep while in bed, expressed as a percentage (%).",{"measure":54,"description":55,"timeFrame":46},"Fitbit-measured wake after sleep onset","Wake after sleep onset will be measured objectively using Fitbit and defined as the total amount of time participants are awake after initially falling asleep until the final awakening, expressed in minutes.",{"measure":57,"description":58,"timeFrame":46},"Fitbit-measured number of awakenings","Wake after sleep onset will be measured objectively using Fitbit and defined as the total count of times a person fully wakes up or regains consciousness after initially falling asleep during a sleep period",{"measure":60,"description":61,"timeFrame":46},"Fitbit-measured light sleep duration","Light sleep duration will be measured objectively using Fitbit and defined as the total time spent in the light sleep stage during the primary sleep period, expressed in minutes.",{"measure":63,"description":64,"timeFrame":46},"Fitbit-measured deep sleep duration","Deep sleep duration will be measured objectively using Fitbit and defined as the total time spent in the deep sleep stage during the primary sleep period, expressed in minutes.",{"measure":66,"description":67,"timeFrame":46},"Fitbit-measured rapid eye movement sleep duration","Rapid eye movement sleep duration will be measured objectively using Fitbit and defined as the total time spent in the rapid eye movement sleep stage during the primary sleep period, expressed in minutes.",{"measure":69,"description":70,"timeFrame":71},"Perceived sleep quality","Perceived sleep quality will be measured by the Pittsburgh Sleep Quality Index. The total score ranges from 0 to 21, with higher scores indicating worse sleep quality.","Baseline, 2-week post-intervention, 2-month follow-up, 4-month follow-up",{"measure":73,"description":74,"timeFrame":46},"Daytime sleepiness","Daytime sleepiness will be measured using the Epworth Sleepiness Scale. The total score ranges from 0 to 24, with higher scores indicating greater daytime sleepiness.",{"measure":76,"description":77,"timeFrame":46},"Dysfunctional beliefs and attitudes about sleep","Dysfunctional beliefs and attitudes about sleep will be measured using the Dysfunctional Beliefs and Attitudes about Sleep Scale (DBAS-16). The total score ranges from 0 to 10, with a higher score indicating more dysfunctional beliefs and attitudes about sleep.",{"measure":79,"description":80,"timeFrame":46},"Sleep hygiene","Sleep hygiene will be measured using the Sleep Hygiene Index. The total score ranges from 13 to 65, with a higher score indicating poorer sleep hygiene (a worse outcome)",null,{"allocation":83,"interventionModel":84,"interventionModelDescription":81,"primaryPurpose":85,"observationalModel":81,"timePerspective":81,"maskingInfo":86},"NA","SINGLE_GROUP","PREVENTION",{"masking":87,"maskingDescription":81,"whoMasked":81},"NONE",[89],{"label":90,"type":91,"description":92,"interventionNames":93},"Intervention","EXPERIMENTAL","Participants will receive access to an AI-based chatbot and engage with it via text messaging for 2 weeks.",[94],"Behavioral: Intervention Group",[96],{"type":97,"name":98,"description":99,"armGroupLabels":100,"otherNames":81},"BEHAVIORAL","Intervention Group","Participants engage with an AI chatbot for two weeks to learn personalized education and skills regarding sleep promotion",[90],[102],{"name":103,"affiliation":5,"role":104},"Xiaoyue Liu","PRINCIPAL_INVESTIGATOR",[106],{"name":107,"role":108,"phone":109,"phoneExt":81,"email":110},"Xiaoyue Liu, PhD","CONTACT","2129925994","xl5272@nyu.edu",[112],{"facility":5,"status":81,"city":113,"state":113,"zip":114,"country":115,"countryCode":116,"cosmosGeoPoint":117,"geoPoint":122,"contacts":123},"New York","10010","United States","US",{"type":118,"coordinates":119},"Point",[120,121],-74.00597,40.71427,{"lat":121,"lon":120},[124],{"name":125,"role":108,"phone":126,"phoneExt":81,"email":127},"Asian American Sleep Health Study","3479170118","aa-sleephealth@nyu.edu",{"type":104,"investigatorFullName":103,"investigatorTitle":129,"investigatorAffiliation":5,"oldNameTitle":81,"oldOrganization":81},"Assistant Professor",[131],{"name":132,"class":133},"National Institute on Minority Health and Health Disparities (NIMHD)","NIH","100658281","improving-sleep-health-for-asian-americans-100658281",false,"NCT07850687","Improving Sleep Health for Asian Americans","Pilot Testing a Sleep Intervention Among Filipino American Adults","Inclusion Criteria:\n\n* Age 30 to 70 years\n* Self-identify as having a Filipino background and reside in the United States\n* Poor sleep quality, defined as a Pittsburgh Sleep Quality Index (PSQI) score ≥ 5\n* Short sleep duration, defined as an average Fitbit-measured total sleep time \\\u003C 7 hours\u002Fnight over 7 days\n* Able to speak and read English\n* Willing to engage with the chatbot via text messaging\n\nExclusion Criteria:\n\n* Severe mental disorders, including major depressive symptoms\n* Medical conditions, including cognitive impairment, that may interfere with the ability to follow study procedures\n* Current participation in another lifestyle intervention\n* Night-shift or rotating-shift worker\n* Alcohol or substance abuse\n* Use of sleep medications more than 3 times per week","ALL","30 Years","70 Years",{"count":145,"type":146},40,"ESTIMATED","INTERVENTIONAL",[83],"Filipino Americans are at high risk of poor sleep and its adverse health consequences. The goal of this study is to test a generative AI-powered chatbot that delivers personalized, evidence-based sleep education and guidance to Filipino Americans who experience poor sleep.",[151,152],"Poor Sleep Quality","Short Sleep","NOT_YET_RECRUITING","2026-09-29",{"date":156,"type":157},"2026-10-02","ACTUAL",{"date":159,"type":146},"2026-10-01",{"date":161,"type":146},"2028-02-29",{"name":5,"class":6},1]