[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100654384":3},{"organization":4,"outcomesModule":7,"designInfo":28,"detailedDescription":27,"studyPopulation":27,"armGroups":34,"interventions":41,"overallOfficials":47,"centralContacts":51,"locations":60,"responsibleParty":77,"collaborators":27,"id":80,"slug":81,"hasResults":82,"nctId":83,"briefTitle":84,"officialTitle":84,"acronym":27,"eligibilityCriteria":85,"healthyVolunteers":82,"sex":86,"minAge":87,"maxAge":27,"enrollmentInfo":88,"targetDuration":27,"studyType":91,"phases":92,"briefSummary":93,"conditions":94,"keywords":27,"overallStatus":97,"whyStopped":27,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":107},{"fullName":5,"class":6},"University of Miami","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":27,"otherOutcomes":27},[9,13,17,21,24],{"measure":10,"description":11,"timeFrame":12},"Recruitment Rate","Percentage of eligible participants approached for participation who provide informed consent and enroll in the study. Recruitment feasibility will be considered achieved if at least 70% of eligible participants approached enroll in the study.","During the recruitment period",{"measure":14,"description":15,"timeFrame":16},"Retention Rate","Percentage of enrolled participants who complete the 3-month follow-up assessment. Retention feasibility will be considered achieved if at least 75% of enrolled participants complete the 3-month follow-up assessment.","3-month follow-up",{"measure":18,"description":19,"timeFrame":20},"Intervention Completion","Percentage of enrolled participants who complete all core intervention modules. Intervention feasibility will be considered achieved if at least 70% of enrolled participants complete the core intervention modules.","Over the 3-month intervention period",{"measure":22,"description":23,"timeFrame":16},"System Usability Scale (SUS) Score","Participant-reported usability of the intervention as assessed using the System Usability Scale (SUS), a 10-item questionnaire with total scores ranging from 0 to 100. Higher scores indicate greater perceived usability. Acceptability will be considered satisfactory if the mean SUS score is at least 70.",{"measure":25,"description":26,"timeFrame":16},"Participants Rating the Intervention as Helpful or Very Helpful","Percentage of participants who rate the intervention as \"helpful\" or \"very helpful\" on a participant satisfaction assessment. Acceptability will be considered satisfactory if at least 80% of participants rate the intervention as helpful or very helpful.",null,{"allocation":29,"interventionModel":30,"interventionModelDescription":27,"primaryPurpose":31,"observationalModel":27,"timePerspective":27,"maskingInfo":32},"NA","SINGLE_GROUP","PREVENTION",{"masking":33,"maskingDescription":27,"whoMasked":27},"NONE",[35],{"label":36,"type":37,"description":38,"interventionNames":39},"Single-Cohort Feasibility Trial","EXPERIMENTAL","Participants will undergo a routine standard-of-care breast cancer screening visit and receive the Sobriety digital behavioral intervention. Participants will maintain access to the digital intervention platform for 4 weeks following the screening visit.",[40],"Behavioral: Sobriety Digital Intervention",[42],{"type":43,"name":44,"description":45,"armGroupLabels":46,"otherNames":27},"BEHAVIORAL","Sobriety Digital Intervention","Participants will receive a digital behavioral intervention that includes alcohol use screening, personalized feedback, education on alcohol-related breast cancer risk, brief motivational content, and goal-setting exercises. Participants will retain access to the intervention platform for 4 weeks following the initial intervention.",[36],[48],{"name":49,"affiliation":5,"role":50},"Taghrid Asfar, MD,MSPH","PRINCIPAL_INVESTIGATOR",[52,56],{"name":49,"role":53,"phone":54,"phoneExt":27,"email":55},"CONTACT","305-243-3826","tasfar@med.miami.edu",{"name":57,"role":53,"phone":58,"phoneExt":27,"email":59},"Maria Fernanda Garcia, BS","561-569-7987","mfg136@miami.edu",[61],{"facility":62,"status":27,"city":63,"state":64,"zip":65,"country":66,"countryCode":67,"cosmosGeoPoint":68,"geoPoint":73,"contacts":74},"Don Soffer clinical research center","Miami","Florida","33136","United States","US",{"type":69,"coordinates":70},"Point",[71,72],-80.19366,25.77427,{"lat":72,"lon":71},[75,76],{"name":57,"role":53,"phone":58,"phoneExt":27,"email":59},{"name":49,"role":50,"phone":27,"phoneExt":27,"email":27},{"type":50,"investigatorFullName":78,"investigatorTitle":79,"investigatorAffiliation":5,"oldNameTitle":27,"oldOrganization":27},"Taghrid Asfar","Professor","100654384","implementing-a-digital-alcohol-intervention-to-raise-womens-awareness-of-alcohol-related-breast-cancer-risk-during-routine-screening-visits-100654384",false,"NCT07799467","Implementing a Digital Alcohol Intervention to Raise Women's Awareness of Alcohol-related Breast Cancer Risk During Routine Screening Visits","Inclusion Criteria:\n\n* Women attending their screening visit\n* Regular alcohol users\n* Aged 40+ years\n* Fluent in English\n* With or without cancer\n* Not currently receiving cancer treatment\n* Own a smartphone, iPad, or computer\n* Able to provide consent\n* Must not have participated in Stage 1 or Stage 2.\n\nExclusion Criteria:\n\n* Younger than 40 years\n* Non-English speaking\n* Unable to provide informed consent\n* Does not own a smartphone, iPad, or computer\n* Currently receiving cancer treatment\n* Prior participation in Stage 1 or Stage 2.","FEMALE","40 Years",{"count":89,"type":90},36,"ESTIMATED","INTERVENTIONAL",[29],"This study is a single-arm feasibility trial evaluating a digital behavioral intervention designed to increase women's awareness of the relationship between alcohol use and breast cancer risk during routine breast cancer screening visits. The study will enroll 36 women aged 40 years or older. Participants will complete baseline measures and receive the Sobriety digital intervention during the clinic visit, followed by 4 weeks of continued access to the platform. Assessments will be completed immediately after the intervention and at 3 months to evaluate feasibility, acceptability, engagement, and changes in alcohol-related knowledge and behavior.",[95,96],"Breast Cancer","Alcohol Drinking","NOT_YET_RECRUITING","2026-09-01",{"date":100,"type":101},"2026-09-02","ACTUAL",{"date":103,"type":90},"2026-10-15",{"date":105,"type":90},"2027-03",{"name":5,"class":6},1]