[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"postpartum-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:postpartum-care":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,51,76,102,133,166,193,223,262],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100634695","kangaroo-care-breastfeeding-success-and-maternal-role-100634695",false,"NCT07543029","Kangaroo Care: Breastfeeding Success and Maternal Role","The Effect of Kangaroo Mother Care Applied in the Early Postpartum Period to Primiparous Mothers on Breastfeeding Success and Perception of the Maternal Role","Inclusion Criteria:\n\n* For mothers:\n\n  * It must be the mother's first birth,\n  * Birth must have been vaginal,\n  * The mother must be healthy,\n  * The mother must voluntarily participate in the study,\n  * The mother must not have any communication-impairing conditions (language, cognitive problems, etc.),\n\nFor babies:\n\n* Birth weight must be between 2500-4000 grams;\n* The newborn must be healthy,\n* Exclusively breastfed,\n* The newborn must be at term gestation (38-42 weeks),\n* The newborn's Apgar score at 1 and 5 minutes must be above 7,\n* The newborn must not have any health problems that could affect breastfeeding (cleft palate, cleft lip, esophageal atresia, etc.).\n\nExclusion Criteria:\n\n\\-",true,"FEMALE","18 Years","49 Years",{"count":21,"type":22},112,"ESTIMATED","INTERVENTIONAL",[25],"NA","Purpose: This is a randomized controlled trial designed to investigate the effects of Kangaroo Mother Care (KMC) applied in the early postpartum period to primiparous mothers on breastfeeding success and the perception of the maternal role.\n\nMethodology and Sample:\n\nSetting and Period: The study will be conducted at the Bucak State Hospital Delivery Unit between June 2025 and June 2026.\n\nSample Size: Based on G\\*Power analysis (alpha=0.05, power=80%, effect size d=0.566), a total of 112 mothers (56 intervention, 56 control) will be included, accounting for a 10% potential attrition rate. Participants will be assigned to groups using the sealed envelope method and randomization via www.random.org.\n\nIntervention:\n\nExperimental Group: Following routine care, the newborn will be placed in a \"chest-to-chest\" position on the mother's bare chest for Kangaroo Care. Intermittent KMC will be maintained for 24 hours, during which breastfeeding attempts will be supported.\n\nControl Group: Mothers and newborns will receive only the hospital's routine care (standard skin-to-skin contact and breastfeeding support).\n\nData Collection Tools:\n\nPersonal Information Form, Semantic Differential Scale-Myself as a Mother (to measure maternal role perception), LATCH Breastfeeding Assessment Tool (to evaluate breastfeeding success).",[28,29,30,31],"Breastfeeding","Maternal Role","Postpartum Care","Kangaroo Care",[33,34,35,36,37],"Primiparity","newborn","breastfeeding","maternal role","kangaroo care","RECRUITING","2026-06-11",{"date":41,"type":42},"2026-06-15","ACTUAL",{"date":44,"type":42},"2025-06-01",{"date":46,"type":22},"2026-12-30",{"name":48,"class":49},"Recep Tayyip Erdogan University","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":23,"phases":60,"briefSummary":61,"conditions":62,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100619277","early-intervention-for-postpartum-ptsd-comparing-written-exposure-and-capnometry-guided-breathing-therapy-100619277","NCT07342530","Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry-Guided Breathing Therapy","Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry Guided Breathing Therapy","Inclusion Criteria:\n\n* Age ≥18\n* Delivered a live infant within 5 days\n* Severe maternal morbidity or infant admitted to NICU\n* PCL-5 ≥28\n* English-speaking\n* Able to consent and participate\n\nExclusion Criteria:\n\n* Active psychosis or mania\n* Current suicidal crisis\n* Current suicidal intent or plan\n* Cognitive impairment preventing participation",{"count":59,"type":22},70,[25],"The purpose of this study is to examine two early interventions, Written Exposure Therapy and Capnometry Guided Breathing, to reduce post-traumatic stress disorder (PTSD) symptoms in women after childbirth as compared to usual care.",[63,64,65,30],"Written Exposure Therapy","Breathing Techniques","PTSD (Childbirth-Related)","2026-04-21",{"date":68,"type":42},"2026-04-24",{"date":70,"type":42},"2026-03-09",{"date":72,"type":22},"2027-12",{"name":74,"class":49},"Stanford University",2,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":23,"phases":85,"briefSummary":86,"conditions":87,"keywords":89,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":50},"100583498","healing-at-home-20---enhanced-chat-tool-for-lowering-postpartum-depression-100583498","NCT06877104","Healing at Home 2.0 - Enhanced Chat Tool for Lowering Postpartum Depression","HEALED","Inclusion Criteria:\n\n* Postpartum patients who have delivered a singleton baby at or after 37w0d at the Hospital of the University of Pennsylvania\n* Self-identify as a person of color (listed on chart as non-White race and confirmed with patient)\n* Able to speak, read and write English\n* Age ≥18\n* Prenatal care at outpatient practice affiliated with the Hospital of the University of Pennsylvania\n* Completion of clinically administered EPDS during inpatient stay\n* Routine discharge timing, day 2 or more after vaginal delivery, day 3 or more after cesarean delivery\n\nExclusion Criteria:\n\n* Unable to provide informed consent\n* Baby not discharged with mother at postpartum discharge\n* Does not have access to a mobile phone",{"count":84,"type":22},156,[25],"The purpose of the study is to determine if access to a text-message based holistic chatbot support program \"Healing at Home 2.0\" decreases depressive symptoms as measured by the Edinburgh Postnatal Depression Scale (EPDS) compared to usual postpartum care for patients of color.",[88,30],"Depression, Postpartum",[90,91,92,30],"Chat tool","Depression","Text message based program","2026-03-25",{"date":95,"type":42},"2026-03-27",{"date":97,"type":42},"2025-03-13",{"date":99,"type":22},"2026-11",{"name":101,"class":49},"University of Pennsylvania",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":23,"phases":112,"briefSummary":113,"conditions":114,"keywords":122,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":50},"100627359","the-effect-of-reiki-on-breastfeeding-pain-and-comfort-after-cesarean-section-100627359","NCT07447609","THE EFFECT OF REIKI ON BREASTFEEDING, PAIN AND COMFORT AFTER CESAREAN SECTION","THE EFFECT OF REIKI APPLIED DURING THE POSTPARTUM PERIOD ON BREASTFEEDING, PAIN, AND COMFORT IN WOMEN WHO DELIVERED BY CESAREAN SECTION","Inclusion Criteria:\n\n* Mothers aged 18 and over,\n* Literate in Turkish,\n* Non-smoker, non-drug user,\n* Gave birth by cesarean section at term,\n* Baby with them after birth,\n* Not using any breast milk-increasing medication, vitamins, or supplements,\n* Baby's birth weight between 2500-4000 grams,\n* Baby's Apgar score at least seven points at 1 and 5 minutes,\n* Having had a cesarean section under spinal anesthesia,\n* Those who agree to participate in the study.\n\nExclusion Criteria:\n\n* Preeclampsia\u002Feclampsia, active postpartum hemorrhage, sepsis\u002Ffever ≥38°C,\n* Need for intensive care,\n* Birth before 37 weeks,\n* Serious neonatal problems,\n* Baby arriving at the ward after mother (follow-up in neonatal intensive care unit without hospitalization after birth),\n* Excessive sedation due to analgesia,\n* Communication difficulties,\n* Markedly negative attitude towards Reiki.","45 Years",{"count":111,"type":22},99,[25],"EFFECT OF REİKİ APPLİED DURİNG THE POSTPARTUM PERİOD ON BREASTFEEDİNG, PAİN, AND COMFORT IN WOMEN WHO DELİVERED BY CESAREAN SECTİON\n\nThe aim of this randomized controlled trial is to determine the effect of Reiki applied to volunteer women after cesarean section on breastfeeding, pain, and comfort in the postpartum period. The main questions it aims to answer are:\n\nIs there a difference in postpartum breastfeeding, pain, and comfort between the group receiving Reiki and the group receiving standard care? Is there a difference in postpartum breastfeeding, pain, and comfort between the group receiving Reiki and the group receiving Sham Reiki? Participants will receive Reiki six times postpartum: three times one-on-one during their hospital stay, and remotely in the second, third, and fourth weeks. The control group will receive standard care. The Sham Reiki group will receive Reiki points applied by a person without Reiki knowledge.",[115,30,116,117,118,119,120,121],"Postpartum Comfort","Cesarean Section Pain","Breastfeeding Self-Efficacy","Perceived Insufficient Milk Supply","Reiki","Reiki Therapy","Postpartum Pain",[123],"Cesarean section, postpartum care, Reiki, breastfeeding, pain, comfort","2026-02-26",{"date":126,"type":42},"2026-03-03",{"date":128,"type":42},"2025-01-15",{"date":130,"type":22},"2026-05-20",{"name":132,"class":49},"Saglik Bilimleri Universitesi",{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":139,"eligibilityCriteria":140,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":141,"enrollmentInfo":142,"targetDuration":4,"studyType":23,"phases":144,"briefSummary":145,"conditions":146,"keywords":151,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":50},"100625756","comparison-of-outpatient-rehabilitation-versus-self-training-for-the-treatment-and-prevention-of-postpartum-pelvic-floor-dysfunction-100625756","NCT07426770","Comparison of Outpatient Rehabilitation Versus Self-training for the Treatment and Prevention of Postpartum Pelvic Floor Dysfunction","Prevention of Female Pelvic Floor Dysfunction Rehabilitation Postpartum.","DDDPREV","Inclusion Criteria:\n\n* 18 years or older\n* This pregnancy was singleton\n* No contraindications for physical activity\n* No connective tissue disorders (for example Ehlers-Danlos syndrome)\n* No neurological disorders to influence pelvic floor symptoms (for example clinically significant spinal disc herniation)\n\nExclusion Criteria:\n\n* Younger than 18 years\n* Twins or triplet pregnancy\n* Contraindications for physical activity\n* Connective tissue disorders\n* Neurological disorders","50 Years",{"count":143,"type":22},80,[25],"The main goal of this study to compare self-training postpartum and training with a specialist support (physiotherapist and physical medicine and rehabilitation doctor) effect on pelvic floor dysfunction prevention and treatment in postpartum period.\n\nHypothesis: The implementation of postpartum rehabilitation helps to alleviate existing symptoms of pelvic floor dysfunction and prevents pelvic floor dysfunction.\n\nStudy goals:\n\n* To objectively evaluate changes in pelvic organ position and pelvic floor muscle function in postpartum period, before and after specialised rehabilitation program\n* To objectively evaluate pelvic floor symptoms and their influence on woman life quality\n* To compare data (changes in pelvic floor muscle coordination and strength, pelvic organ position and changes in life quality according to validated questionnaires)\n\nStudy participants will:\n\n* Get an examination by obstetrician-gynaecologist, physical medicine and rehabilitation doctor and physiotherapist in 6 to 10 weeks postpartum period.\n* One group of participants will attend physiotherapy, biofeedback and electro stimulation procedures with a guidance of a specialist.\n* Other group of participants gets a recommendations and instructions of training and self-trains at home. To remind of training and help record training time \"squeezy\" app (an application designed for a mobile device) will be offered.\n* All groups of participants will be asked to fill life quality related questionnaires: (ICIQ-UI SF: International Consultation on Incontinence Questionnaire; P-QoL: Prolapse Quality-of-Life Questionnaire; PISQ-IR: Pelvic Organ Prolapse\u002F Urinary Incontinence Sexual Questionnaire IUGA revised; FSFI: female sexual function index; MOS-SF36 Medical Outcomes Study Short Form-36).",[147,30,115,148,149,150],"Pelvic Floor Dysfunction","Female Urinary Incontinence and Pelvic Organ Prolapse","Rectus Diastasis","Sexual Dysfunction Female",[152,153,154,155,156],"Pelvic floor dysfunction postpartum","Postpartum urinary incontinence","Postpartum sexual dysfunction","Diastasis postpartum","Rehabilitation postpartum","2026-02-16",{"date":159,"type":42},"2026-02-23",{"date":161,"type":42},"2024-01-30",{"date":163,"type":22},"2029-09-30",{"name":165,"class":49},"Vilnius University",{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":170,"acronym":171,"eligibilityCriteria":172,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":109,"enrollmentInfo":173,"targetDuration":4,"studyType":23,"phases":175,"briefSummary":177,"conditions":178,"keywords":181,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":191,"locationsCount":50},"100589008","phase-2-effectiveness-study-of-a-lifestyle-intervention-versus-metformin-in-mothers-with-recent-gestational-diabetes-100589008","NCT06948825","Effectiveness Study of a Lifestyle Intervention Versus Metformin in Mothers With Recent Gestational Diabetes","GooDMomS2","Inclusion Criteria:\n\n* Mothers between 8 weeks and 12 months postpartum from a pregnancy complicated by GDM will be recruited. The research team will begin recruiting women who are at least 8 weeks postpartum to provide time to describe the study and answer any questions. Mothers who want to participate will be enrolled in the study between 12 weeks and 12 months postpartum.\n* BMI of 25 kg\u002Fm2 to 45 kg\u002Fm2\n* Singleton delivery\n* Participants must also have a working cell phone, be willing to accept email or text messages attend Zoom calls, and be willing to be potentially randomized to drug therapy with Metformin.\n\nExclusion Criteria:\n\n* Pregnant or planned pregnancy within the next 6 months.\n* Participation in any other weight loss program or taking weight loss medication.\n* Normal or underweight BMI (BMI \\\u003C 24.9 kg\u002Fm2)\n* Multi-fetal (twins or triplets) gestation\n* Women with type 1 or type 2 diabetes, malignancy, other serious co-morbidities (advanced kidney disease, NYHA class 3-4 CHF, advanced COPD), schizophrenia or other major psychiatric disease, and substance abuse or AIDS.\n* Women whose infants have significant medical conditions, such as congenital heart disease, renal impairment, or hepatic impairment.",{"count":174,"type":22},60,[176],"PHASE2","The goal of this clinical trial is to evaluate the effectiveness of a 6-month lifestyle intervention compared to Metformin in postpartum women who have delivered a singleton, live born infant within the last 12 weeks to 1 year and had a pregnancy complicated by gestational diabetes. The main question this study aims to answer is:\n\nIs a Lifestyle Intervention or Metformin more effective for weight loss in postpartum women with recent gestational diabetes?\n\nResearchers will compare a 6-month Lifestyle Intervention and Metformin to see if either intervention is more effective in achieving weight loss and improving health outcomes.\n\nParticipants will:\n\n* Attend an in-person baseline visit to receive a Bluetooth-enabled scale and Fitbit, have blood drawn for testing, and have their height, weight, and blood pressure measured. Participants will also be asked to bring in their infant, and the study team will measure the infant's weight and length.\n* Track diet, physical activity, and weight using the Fitbit and Looseit! apps.\n* Attend weekly online group sessions for the first 4 weeks, then biweekly sessions.\n* If not meeting weight loss goals, be randomized to either Enhanced Lifestyle Intervention or Metformin arms of the study.\n* If randomized to Metformin, participants will attend one in-person meeting with the study provider, get blood drawn for testing, and undergo a urine pregnancy test before starting the medication.\n* Continue with biweekly group sessions or have regular check-in calls.\n* If randomized to the Enhanced Lifestyle Intervention, participants will get a free Instacart membership, a 1:1 session with the study health counselor focused on meal planning and free grocery delivery once a week for the remainder of the study.\n* Participants will meet every other week via Zoom with the health counselor and other participants in the enhanced lifestyle arm.\n* At the end of the 6 months, all participants will come for an in-person visit to get blood drawn for testing. Participants will also be asked to bring in their infant, and the study team will measure the infant's weight and length.",[179,180,30],"Weight Loss","Gestational Diabetes Mellitus in Pregnancy",[182,183,184],"diabetes prevention","gestational diabetes","lifestyle intervention","2026-01-12",{"date":187,"type":42},"2026-01-13",{"date":189,"type":42},"2025-10-27",{"date":99,"type":22},{"name":192,"class":49},"George Washington University",{"id":194,"slug":195,"hasResults":11,"nctId":196,"briefTitle":197,"officialTitle":198,"acronym":4,"eligibilityCriteria":199,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":200,"targetDuration":4,"studyType":23,"phases":202,"briefSummary":203,"conditions":204,"keywords":210,"overallStatus":213,"whyStopped":4,"lastUpdateSubmitDate":214,"lastUpdatePostDateStruct":215,"startDateStruct":217,"completionDateStruct":219,"leadSponsor":221,"locationsCount":50},"100614469","effect-of-a-respectful-maternity-care-based-action-plan-in-postpartum-care-on-maternal-and-neonatal-outcomes-100614469","NCT07280000","Effect of a Respectful Maternity Care-Based Action Plan in Postpartum Care on Maternal and Neonatal Outcomes","The Effect of the Action Plan Developed Within the Framework of Respectful Maternity Care in Postpartum Care on Maternal and Neonatal Outcomes","Inclusion Criteria:\n\n* Postpartum women aged 18 years and older\n* Gave birth at 37-42 gestational weeks (vaginal or cesarean)\n* Have a single, healthy newborn\n* No chronic medical conditions\n* No history of high-risk pregnancy or fetal complications\n* No communication barriers (e.g., visual or hearing impairment)\n* Able to speak and understand Turkish\n* Literate and able to read and write in Turkish\n\nExclusion Criteria:\n\n* Development of maternal or neonatal complications during the postpartum follow-up period\n* Inability to reach the mother at the 8-week postpartum follow-up",{"count":201,"type":22},500,[25],"This study will examine whether a Respectful Maternity Care-based action plan can improve the quality of postpartum care and maternal and newborn outcomes. Nurses and midwives will receive a three-day interactive training about respectful, evidence-based postpartum care. After training, a unit-level action plan will be implemented, including supportive visits, educational materials, and feedback meetings. Women receiving routine postpartum care before the intervention will be compared with women receiving care after implementation. Outcomes will include respectful maternity care experiences, maternal satisfaction, exclusive breastfeeding at 6-8 weeks, maternal mental health, mother-infant bonding, and postpartum complications. The goal of this study is to promote respectful, high-quality postpartum care and improve the health and well-being of mothers and newborns.",[30,205,206,207,28,208,209],"Maternal Health Care","Newborn Health","Postpartum Depression (PPD)","Quality of Care","Maternal Satisfaction",[211,30,212,206],"Respectful Maternity Care","Maternal Health","NOT_YET_RECRUITING","2025-12-01",{"date":216,"type":42},"2025-12-12",{"date":218,"type":22},"2025-12-10",{"date":220,"type":22},"2026-12-01",{"name":222,"class":49},"ilayda sel",{"id":224,"slug":225,"hasResults":11,"nctId":226,"briefTitle":227,"officialTitle":228,"acronym":4,"eligibilityCriteria":229,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":109,"enrollmentInfo":230,"targetDuration":4,"studyType":23,"phases":232,"briefSummary":233,"conditions":234,"keywords":237,"overallStatus":213,"whyStopped":4,"lastUpdateSubmitDate":252,"lastUpdatePostDateStruct":253,"startDateStruct":255,"completionDateStruct":257,"leadSponsor":259,"locationsCount":50},"100605859","informative-video-before-lmwh-postpartum---randomized-controlled-trial-100605859","NCT07168005","Informative Video Before LMWH Postpartum - Randomized Controlled Trial","Does an Informative Video Reduce Anxiety and Pain Before LMWH Treatment Postpartum? - A Randomized Controlled Trial","Inclusion Criteria:\n\nWomen 18-45 years, postpartum, indicated for LMWH, Hebrew-literate, gave consent\n\nExclusion Criteria:\n\nUse of LMWH pre-delivery, IUFD, pregnancy termination, language\u002Fcognitive barrier",{"count":231,"type":22},160,[25],"This single-center randomized controlled trial evaluates whether a short informative video can reduce anxiety and pain before the first postpartum administration of low molecular weight heparin (LMWH, Clexane). Eligible women will be randomized to receive either standard explanation alone or standard explanation plus a short educational video. The primary outcome is anxiety level assessed via the State-Trait Anxiety Inventory (STAI). Secondary outcomes include pain, satisfaction, and treatment adherence.",[235,30,236],"Venous Thromboembolism (VTE)","Anxiety",[238,239,240,241,242,243,236,244,245,246,247,248,30,249,250,251],"Postpartum","Venous Thromboembolism","VTE","LMWH","Low Molecular Weight Heparin","Clexane","Pain","Patient Education","Informative Video","State-Trait Anxiety Inventory","STAI","Women's Health","Obstetrics","Adherence","2025-09-03",{"date":254,"type":42},"2025-09-11",{"date":256,"type":22},"2025-10-15",{"date":258,"type":22},"2027-10-15",{"name":260,"class":261},"Wolfson Medical Center","OTHER_GOV",{"id":263,"slug":264,"hasResults":11,"nctId":265,"briefTitle":266,"officialTitle":267,"acronym":4,"eligibilityCriteria":268,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":269,"enrollmentInfo":270,"targetDuration":4,"studyType":23,"phases":272,"briefSummary":273,"conditions":274,"keywords":277,"overallStatus":213,"whyStopped":4,"lastUpdateSubmitDate":279,"lastUpdatePostDateStruct":280,"startDateStruct":282,"completionDateStruct":284,"leadSponsor":285,"locationsCount":4},"100604381","effectiveness-of-chatbot-supported-web-program-in-postpartum-care-100604381","NCT07148778","Effectiveness of Chatbot-Supported Web Program in Postpartum Care","Evaluation of the Effectiveness of a Chatbot-Supported Web-Based Postpartum Care Package Program for Postpartum Women","Inclusion Criteria: Women who will be included in the study.\n\n* Have given birth between the 37th and 41st weeks of pregnancy,\n* Be primigravida,\n* Have not been diagnosed with a high-risk pregnancy,\n* Have an educational level of primary school or above,\n* Have no communication difficulties or mental disabilities,\n* Have access to equipment (mobile phone, computer, tablet, internet) for web-based education,\n* Have experienced no complications in the mother or baby during pregnancy, childbirth, or the postpartum period,\n* Voluntarily agree to participate in the study,\n\nExclusion Criteria:\n\n* Women who moved outside the province where the study was conducted during the implementation period,\n* Women who voluntarily withdrew from the study,\n* Women who did not participate in any phase of the study will not be included in the study.","35 Years",{"count":271,"type":22},102,[25],"The purpose of this clinical study was to evaluate the effectiveness of a web-based \"Postpartum Care Package\" program developed for postpartum women and delivered via a chatbot, and to examine its effects on the postpartum health of mothers and newborns.\n\nThe key questions it aims to answer are:\n\n* What is the impact of the chatbot-supported web-based \"Postpartum Care Package\" program on the postpartum health of mothers and newborns?\n* Does the chatbot-supported web-based \"Postpartum Care Package\" program increase women's accessibility and availability of postpartum care resources?",[30,275,276],"Web-based Training","Chatbot-Based Training",[278],"postpartum care","2025-08-23",{"date":281,"type":42},"2025-08-29",{"date":283,"type":22},"2025-10-01",{"date":220,"type":22},{"name":286,"class":49},"Emine Ilkin Aydin"]