[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"postnatal-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:postnatal-care":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,93,123],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100616283","mom-multi-postnatal-supplementation-trial-100616283",false,"NCT07303595","Mom Multi Postnatal Supplementation Trial","Effect of a Postpartum Multivitamin-Mineral Supplement on Maternal Nutrient Status and Wellbeing","Inclusion criteria:\n\n* Healthy, postpartum women (\\~4 weeks \\[± 2 weeks\\]) with infants born term and singleton\n* Not pregnant during the study period\n* Able to understand (written and spoken) English or Spanish.\n\nExclusion criteria:\n\n* Cardiometabolic disease\n* Past pregnancy complications (gestational diabetes, hypertension)\n* malabsorption syndromes (IBS, IBD, Crohn's, Colitis, Celiac)\n* Caily use of medications which may affect nutrient absorption\n* chronic alcohol use (\\> 4 alcoholic drinks\u002Fday)\n* those prescribed postnatal MVM supplements by their physician\n* unwilling to discontinue dietary supplementation containing any of the active components in the study product over the study period\n* Women should not have an allergy or intolerance to active or inactive product ingredients.","FEMALE","18 Years",{"count":19,"type":20},80,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to learn if a vitamin and mineral supplement designed specifically for women after childbirth can improve their nutrition and health in women who are pregnant or have recently given birth (within 6 weeks).\n\nThe main question it aims to answer is:\n\nCan a postpartum-specific vitamin and mineral supplement help improve nutritional status and health outcomes in women after giving birth?\n\nResearchers will compare women who take the new postpartum vitamin and mineral supplement to women who take a placebo (fake pills without active ingredients) to see if the supplement improves their nutritional health.\n\nParticipants will:\n\nAttend 2 visits at University of Georgia (1-1.5 hours each) over 12 weeks Participate in 2 phone calls between visits Stop taking other vitamin\u002Fmineral supplements during the study Have blood drawn to test vitamin and mineral levels Provide urine samples and breastmilk samples if breastfeeding (optional) Have height, weight, and skin color measured Complete questionnaires about health, pregnancy, and mental wellness Answer questions about daily food and drink intake Take either the study supplement or placebo daily",[26],"Postnatal Care",[28,29],"Postnatal","multivitamin dietary supplement","RECRUITING","2025-12-10",{"date":33,"type":34},"2025-12-26","ACTUAL",{"date":36,"type":34},"2025-11-10",{"date":38,"type":20},"2026-10",{"name":40,"class":41},"Perelel Inc.","INDUSTRY",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":74,"overallStatus":82,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":42},"100598934","comparing-integrative-midwife-led-vs-fragmented-inpatient-postpartum-care-impact-on-satisfaction-and-transition-to-motherhood-100598934","NCT07077941","Comparing Integrative Midwife-led vs. Fragmented Inpatient Postpartum Care: Impact on Satisfaction and Transition to Motherhood","Supporting Mothers With Integrative Care by Midwives for Lifelong Empowerment (SMILE): A Randomized Controlled Trial Comparing Midwife-led Integrative and Fragmented Standard Inpatient Postpartum Care Models on Maternal Satisfaction and Transition to Motherhood","SMILE","Inclusion Criteria:\n\n* Women aged 18 to 50 years at the time of delivery\n* Classified as \"low-risk\" by the obstetric team in the delivery room\n* Gestational age at birth between 36+0 and 42+0 weeks\n* Singleton birth (only one child born)\n* Intent to breastfeed\n* Consent to participate in the study\n\nExclusion Criteria:\n\n* Women younger than 18 or older than 50 at the time of delivery\n* Classified as \"high-risk\" by the obstetric team\n* Multiple birth (e.g., twins, triplets)\n* No intention or ability to breastfeed the newborn","50 Years",{"count":53,"type":20},784,[23],"The goal of this clinical trial is to compare two different forms of postnatal care to find out which is most beneficial for mothers and their children after birth and with which they are most satisfied. One is a nurse-led, seperate model of care and the other is a midwife-led, integrative model of care. Participants are healthy women between the ages of 18 and 50. They gave birth between 36+0 and 42+0 weeks of pregnancy and had a child. The type of birth is not an inclusion or exclusion criteria. Our hypotheses are: i) that maternal satisfaction with care in a midwife-led, integrative care model is higher than in separate maternal and infant care; ii) that a positive postpartum experience leads to earlier and increased maternity competence; iii) that a higher breastfeeding rate at the time of the survey in the fourth month can be achieved through integrative care. Participants will be randomly assigned, after birth of their child, to either the group cared for by a nurse or the group cared for by a midwife.",[57,58,26,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73],"Maternal Health Services","Infant, Newborn","Breast Feeding","Maternal-Child Relations","Postpartum Depression (PPD)","Mental Health","Lactation","Breast Feeding, Exclusive","Patient Satisfaction and Experience With Integrative Therapies","Neonatal Jaundice","Maternal Behavior","Body Weight Decreased","Breast Feeding of Healthy Full Term Infants","Lactation Mastitis","Lactation Disorder - Postpartum Condition or Complication","Lactation Disorder With Baby Delivered","Lactation; Insufficient, Partial",[75,76,77,78,79,80,81],"Postnatal care","inpatient","maternity competence","satisfaction","integrative care","breastfeeding","maternal behavior","NOT_YET_RECRUITING","2025-07-12",{"date":85,"type":34},"2025-07-22",{"date":87,"type":20},"2025-10-01",{"date":89,"type":20},"2026-12-31",{"name":91,"class":92},"Medical University of Vienna","OTHER",{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":97,"acronym":4,"eligibilityCriteria":98,"healthyVolunteers":99,"sex":16,"minAge":17,"maxAge":100,"enrollmentInfo":101,"targetDuration":4,"studyType":21,"phases":103,"briefSummary":104,"conditions":105,"keywords":107,"overallStatus":82,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":4},"100573007","effects-of-ve-focus-expressive-touch-on-pain-anxiety-breastfeeding-and-mobilization-in-women-delivering-by-cesarean-section-100573007","NCT06740669","Effects of VE, Focus, Expressive Touch on Pain, Anxiety, Breastfeeding and Mobilization in Women Delivering by Cesarean Section","Inclusion Criteria:\n\n\\- Women who do not have any psychiatric illness,\n\n* Those who do not have any vision, hearing or perception problems,\n* Those who do not have any communication problems (can speak Turkish),\n* Those who accept to participate in the study verbally and in writing were included in the study.\n* Those who are between the ages of 18-35,\n* Those who have had a singleton birth,\n* Those who have had the operation with regional anesthesia (spinal or epidural anesthesia),\n\nExclusion Criteria:\n\n* Exclusion Criteria from the Study\n\n  * Receiving controlled analgesia after cesarean section\n  * Having a psychiatric diagnosis such as anxiety and depression\n  * Those who develop postpartum complications\n  * Women who want to leave the study at any stage of the study will be excluded from the study",true,"35 Years",{"count":102,"type":20},208,[23],"Cesarean section is one of the most common surgical interventions in many countries. It is seen that 21.1% of women worldwide, 57.5% in Turkey, give birth by cesarean section. 99.6% of women have pain in the first 24 hours after cesarean section and oral analgesia is not sufficient for pain. It is seen that pain has an effect on recovery and breastfeeding after CS.This study will be conducted to determine the effects of non-pharmacological methods, virtual reality glasses, focusing and expressive touch on pain, anxiety, breastfeeding and mobilization in women giving birth by cesarean section. The ınvestigators aim to contribute to the midwifery and nursing care literature with the findings and results of the study.",[106,26],"Women",[108,109,110,111,112,113],"Virtual reality,","Focus","Expressive touch","Pain","Anxiety","Breastfeeding","2024-12-17",{"date":116,"type":34},"2024-12-18",{"date":118,"type":20},"2024-12-20",{"date":120,"type":20},"2025-05-30",{"name":122,"class":92},"Burdur Mehmet Akif Ersoy University",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":128,"acronym":4,"eligibilityCriteria":129,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":100,"enrollmentInfo":130,"targetDuration":4,"studyType":21,"phases":132,"briefSummary":133,"conditions":134,"keywords":135,"overallStatus":82,"whyStopped":4,"lastUpdateSubmitDate":141,"lastUpdatePostDateStruct":142,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":4},"100573008","the-effect-of-potcost-stories-on-childbirth-fear-100573008","NCT06740682","The Effect of Potcost Stories on Childbirth Fear,","The Effect of Potcost Stories on Childbirth Fear, Pain and Delivery Method","Inclusion Criteria:\n\nThose who have completed at least primary school education\n\n* Those who can speak, understand and write Turkish\n* Those between the ages of 18-35\n* Those who have spontaneous pregnancy\n* Those who volunteer to participate in the study\n* Those who are in the 24th week of pregnancy according to their last menstrual period (LMT) or ultrasound (USG) records\n* Those who have no risk factors\n* Those who have a phone number that can be used for educational interviews\n* Those who attend a pregnancy school\n\nExclusion Criteria:\n\n* Those who have fear of childbirth\n\n  * Those who have chronic and\u002For psychiatric health problems\n  * Those who did not attend at least three sessions of the education program\n  * Those who were at risk during the pregnancy at any stage of the study\n  * Those who could not be interviewed within the first 24 hours after birth were excluded from the study.",{"count":131,"type":20},96,[23],"Birth is an important period that affects a woman's life physically, psychologically and socially. Although this experience can bring joy, it can also be accompanied by anxiety and fear. Fear of birth is affected by people's past traumatic birth experiences, lack of information, and the transfer of birth experiences experienced by individuals . Birth stories are one of the most accessible and frequently used tools for women to learn about birth. These stories are seen to affect women's fears of birth and their birth preferences .This study will evaluate the impact of Potcost Stories on childbirth-related fear, pain, experiences and mode of delivery.",[26],[136,137,138,139,140],"Potcost Stories","fear","pain","experiences","birth","2024-12-14",{"date":116,"type":34},{"date":144,"type":20},"2025-01-01",{"date":146,"type":20},"2025-08-30",{"name":122,"class":92}]