[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100606600":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":28,"locations":35,"responsibleParty":45,"collaborators":18,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":18,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":18,"studyType":63,"phases":64,"briefSummary":66,"conditions":67,"keywords":70,"overallStatus":77,"whyStopped":18,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},{"fullName":5,"class":6},"Ataturk University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Nurse Navigation Program Group","EXPERIMENTAL","The study includes women meeting inclusion criteria and consenting to participate. For the randomized intervention group, the process will last about eight months.The first meeting at 28-32 weeks gestation will be at the Family Health Center. The Personal Information Form, Prenatal Breastfeeding Self-Efficacy Scale, and researcher-developed Prenatal Breastfeeding Motivation Checklist will be applied as pretests.Each participant will attend at least four face-to-face sessions-two prenatal and two postpartum-with two additional sessions conducted in person or online per preference.Session 1: 28-32 weeks.\n\nS2: After 36 weeks, breastfeeding education and brochure; scales repeated.S3: Within one week postpartum; education reinforced; scales applied.S4: 6th postpartum week; training repeated; scales applied S5: 4th postpartum month, face-to-face or online; breastfeeding continuation assessed.S6: 6th postpartum month, face-to-face or online; exclusive breing or complementary feeding assessed.",[13],"Other: Breastfeeding Consultation Provided through the Nurse Navigation Program",{"label":15,"type":16,"description":17,"interventionNames":18},"Routine Care Group","NO_INTERVENTION","Data will be collected from the control group at parallel times with the intervention group, which will only receive routine applications without any intervention. In the data collection process, the Personal Information Form, the Prenatal Breastfeeding Self-Efficacy Scale, and the Prenatal Breastfeeding Motivation Table and Breastfeeding Motivation scales developed by the researcher to assess Breastfeeding Motivation will be used in parallel with the intervention group.",null,[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":18},"Breastfeeding Consultation Provided through the Nurse Navigation Program","The navigator nurse will meet with the pregnant woman\u002Fmother starting at 28-32 weeks of gestation and continuing until the sixth month postpartum. During these meetings, planned breastfeeding education will be provided, women's questions about breastfeeding will be answered, and counseling will be provided to address any concerns.",[9],[25],{"name":26,"affiliation":5,"role":27},"Ayşe AYDIN","STUDY_DIRECTOR",[29,33],{"name":26,"role":30,"phone":31,"phoneExt":18,"email":32},"CONTACT","+905434668220","aysea@atauni.edu.tr",{"name":26,"role":30,"phone":31,"phoneExt":18,"email":34},"aysea@ataun.edu.tr",[36],{"facility":5,"status":18,"city":37,"state":18,"zip":18,"country":38,"countryCode":18,"cosmosGeoPoint":39,"geoPoint":44,"contacts":18},"Erzurum","Turkey (Türkiye)",{"type":40,"coordinates":41},"Point",[42,43],41.27694,39.90861,{"lat":43,"lon":42},{"type":46,"investigatorFullName":47,"investigatorTitle":48,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Ayse Aydin","Principal Investigator","100606600","effect-of-a-nurse-navigation-program-on-breastfeeding-self-efficacy-and-motivation-in-primiparous-women-100606600",false,"NCT07177664","Effect of a Nurse Navigation Program on Breastfeeding Self-Efficacy and Motivation in Primiparous Women","The Effect of a Nurse Navigation Program on Breastfeeding Self-Efficacy Perception and Breastfeeding Motivation in Primiparous Women: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Being primiparous,\n* Not having a health problem that would prevent breastfeeding,\n* Being in the 28th-32nd weeks of pregnancy,\n* Being between the ages of 18 and 35,\n* Having at least a primary school degree,\n* Residing in the city center of Erzurum,\n* Not having a hearing or vision problem,\n* Not having been diagnosed with a psychiatric illness,\n* Being fluent in Turkish,\n* Being able to use a telephone,\n* Women who voluntarily agreed to participate in the study will be included in the sample.\n\nExclusion Criteria:\n\n* Having given birth before 37 weeks of gestation,\n* Having a health problem requiring the newborn to be in intensive care,\n* Having a health problem\u002Fbirth complication that would prevent breastfeeding during the study period,\n* Withdrawal from the study at the woman's request,",true,"FEMALE","18 Years","35 Years",{"count":61,"type":62},100,"ESTIMATED","INTERVENTIONAL",[65],"NA","Objective: To evaluate the effects of a nurse navigation program on breastfeeding self-efficacy and breastfeeding motivation in primiparous women. The research will be conducted as a randomized controlled trial with a pretest-posttest control group.",[68,69],"Breastfeeding","Breastfeeding Education",[71,72,73,74,75,76],"breastfeeding","Breastfeeding Self-Efficacy","Breastfeeding Motivation","Primiparous Women","Nurse Navigation Program","Breastfeeding Counseling","NOT_YET_RECRUITING","2026-01-20",{"date":80,"type":81},"2026-01-21","ACTUAL",{"date":83,"type":62},"2026-01-01",{"date":85,"type":62},"2027-10-01",{"name":5,"class":6},1]