[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644213":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":21,"locations":27,"responsibleParty":40,"collaborators":44,"id":48,"slug":20,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":20,"eligibilityCriteria":53,"healthyVolunteers":49,"sex":54,"minAge":55,"maxAge":20,"enrollmentInfo":56,"targetDuration":20,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":66,"overallStatus":70,"whyStopped":20,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"University of Virginia","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Digital Intervention","EXPERIMENTAL","Participants are provided with a suite of digital micro-interventions over an 8 week period",[13],"Behavioral: Digital Micro-Interventions",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","Digital Micro-Interventions","Digital Micro-Interventions are brief interventions that target specific behavioral and cognitive mechanisms of mental health, designed for brief periods of engagement.",[9],null,[22],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},"Philip Chow, PhD","CONTACT","434-924-8082","pic2u@virginia.edu",[28],{"facility":5,"status":20,"city":29,"state":30,"zip":31,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":20},"Charlottesville","Virginia","22904","United States","US",{"type":35,"coordinates":36},"Point",[37,38],-78.47668,38.02931,{"lat":38,"lon":37},{"type":41,"investigatorFullName":42,"investigatorTitle":43,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"PRINCIPAL_INVESTIGATOR","Philip Chow, Ph.D.","Associate Professor",[45],{"name":46,"class":47},"National Cancer Institute (NCI)","NIH","100644213",false,"NCT07665346","A Pre-post Pilot of a Smartphone Intervention","A Pre-post Pilot of Behavioral Interventions Delivered Through Smartphones","Inclusion Criteria:\n\n* age = 18 years\n* 0-5 years post-diagnosis of Stage I, II, or III female breast cancer\n* elevated symptoms of depression and\u002For anxiety as measured by the PHQ-8 (score \\> 9) or GAD-7 (score \\> 7).\n\nExclusion Criteria:\n\n* receiving individual (1 on 1) treatment for depression and\u002For anxiety to avoid treatment interference (note, individuals will be permitted to enroll if they are taking antidepressant medication and have not had an appointment to adjust the dosage over the past 2 weeks)\n* active suicidal ideation during the enrollment\u002Fscreening call based on a trained staff member orally administering the suicidality item from the PHQ-9 to individuals on the phone (\"In the last 2 weeks, have you had thoughts that you would be better off dead, or thoughts of hurting yourself in some way?\"). If an individual responds in any way other than \"not at all\" based on the available response options (i.e., either \"several days\", \"more than half the days\", or \"nearly every day\"), or if they mention having suicidal ideation or thoughts of death during the enrollment\u002Fscreening call, the Pitt-Optimum risk assessment tool will be administered. Only participants deemed low risk may proceed in enrollment; all will be given additional resources\n* do not have an app-compatible phone\n* cannot read and speak English (intervention and measures only available in English).","FEMALE","18 Years",{"count":57,"type":58},44,"ESTIMATED","INTERVENTIONAL",[61],"NA","Digital mental and behavioral health interventions have potential to significantly improve accessibility for the large number of breast cancer survivors who need treatments. However, the landscape of digital interventions tested in this population remains limited, with the few that have been tested primarily focused on reducing symptoms of mental disorders. This is problematic given the range of psychosocial needs among breast cancer survivors, including those who may not have active mental health symptoms, yet could benefit from learning effective coping skills.\n\nDigital health interventions delivered through smartphones have strong potential to improve access to care for the large number of breast cancer survivors who need mental and behavioral health support. There is a need to evaluate a range of supportive interventions that target different aspects of mental health, including negative thinking, coping skills, and knowledge. Our research team has previously tested individual digital interventions in relatively small samples, and found that they were effective in reducing mood symptoms among women with breast cancer.\n\nThe ultimate goal of this project is to evaluate how integrating these interventions into a single 8-week long app program affects mood and overall mental health in breast cancer survivors. The digital micro-interventions to be tested in this study are brief interventions that target specific behavioral and cognitive mechanisms of mental health. These include skills such as reducing negative thinking patterns, increasing knowledge of mental health factors, fostering a grateful outlook, promoting the practice of relaxation breathing, savoring positive memories, and acceptance-based mindfulness approaches.",[64,65],"Mental Health Issue","Breast Cancer",[67,68,69],"depression","anxiety","well-being","NOT_YET_RECRUITING","2026-06-18",{"date":73,"type":74},"2026-06-24","ACTUAL",{"date":76,"type":58},"2026-07",{"date":78,"type":58},"2026-09",{"name":5,"class":6},1]