[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"disease-prevention\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:disease-prevention":45},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":5},"100567764",false,"NCT06672432","Preventing Perinatal Depression with an App-Based CBT Program","Preventing Perinatal Depression Using an App-based Cognitive Behavioral Therapy Program","Inclusion Criteria:\n\n* aged 18-45 years\n* at 20-24 weeks of gestation\n* at risk of depression but not experiencing severe depressive symptoms at recruitment, as indicated by an Edinburgh Postnatal Depression Scale (EPDS) score of between 5 and 12\n* own a smartphone\n* are able to independently engage with the program\n\nExclusion Criteria:\n\n* have serious medical conditions or pregnancy complications that may affect their psychological condition, as determined by their medical doctor\n* have a prior diagnosis of any mental disorders\n* are currently or were recently (within the past six months) receiving any kinds of psychological services or treatments\n* have a history of self-harm or suicide\n* have any suicidal thoughts in the past 12 months\n* experienced fetal deaths in the past 18 months",true,"FEMALE","18 Years","45 Years",{"count":20,"type":21},290,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn if CareMom, a mobile app-based cognitive behavioral therapy program works to prevent perinatal depression among Chinese mothers. The main questions the trial aims to answer are:\n\n1. Does CareMom lower depression scores after an 8-week intervention?\n2. Does CareMom lower depression scores at 6 weeks after childbirth?\n3. How satisfied are participants with CareMom?\n4. What unfavorable events, if any, are associated with the use of CareMom?\n\nResearchers will compare CareMom to a matched attention control (a mobile app-based program that offers participants a similar level of interaction and daily activities) to see if CareMom works to prevent perinatal depression.\n\nParticipants will:\n\n1. Engage in the CareMom program or a relaxation training program every day for 8 weeks\n2. Complete a series of online questionnaire tests before and after the 8-week intervention.\n3. Report any discomfort experienced throughout the study period.",[27,28],"Perinatal Depression","Disease Prevention",[30,31,32],"Perinatal depression","cognitive behavioral therapy","iCBT","NOT_YET_RECRUITING","2024-10-31",{"date":36,"type":37},"2024-11-04","ACTUAL",{"date":39,"type":21},"2024-11",{"date":41,"type":21},"2025-11",{"name":43,"class":44},"Jintang County Maternal and Child Health Hospital","OTHER",""]