[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"perinatal-loss\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:perinatal-loss":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,70,94],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100648519","comparison-of-social-media-based-and-online-training-in-grief-counseling-education-100648519",false,"NCT07723170","Comparison of Social Media-Based and Online Training in Grief Counseling Education","Comparison of Social Media-Based and Online Training in Grief Counseling Education: A Randomized Controlled Head-to-Head Study","Inclusion Criteria:\n\n* Midwives or nurses currently working in perinatal care settings in Türkiye.\n* Aged 18 years or older.\n* Own a smartphone and have regular internet access.\n* Able to actively use Instagram and Zoom.\n* Provide informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Previous training in perinatal grief counseling.\n* Failure to participate regularly in the educational intervention.\n* Failure to complete the study assessments.",true,"ALL","18 Years",{"count":20,"type":21},72,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized trial aims to compare the effectiveness of two digital educational approaches for perinatal grief counseling training among midwives and nurses working in perinatal care settings in Türkiye: a social media-based education program delivered through Instagram and an online education program delivered through Zoom. Both groups will receive the same six-module perinatal grief counseling education content, but through different delivery methods.\n\nParticipants will be randomly assigned to one of the two study groups. Outcomes will be assessed before the intervention, immediately after completion of the 6-week training program, and 4 weeks after the intervention. The study will evaluate changes in participants' competency and confidence in providing perinatal grief care and compare the sustainability of learning outcomes between the two digital education models.",[27,28,29],"Perinatal Grief","Perinatal Loss","Bereavement","NOT_YET_RECRUITING","2026-07-23",{"date":33,"type":34},"2026-07-24","ACTUAL",{"date":36,"type":21},"2026-07-27",{"date":38,"type":21},"2026-12-30",{"name":40,"class":41},"Istinye University","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":58,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":42},"100634309","effects-of-a-acceptance-and-commitment-therapy-based-psychosocial-intervention-on-mental-health-of-women-with-perinatal-loss-a-pilot-randomised-controlled-trial-100634309","NCT07538011","Effects of a Acceptance and Commitment Therapy-Based Psychosocial Intervention on Mental Health of Women With Perinatal Loss: A Pilot Randomised Controlled Trial","Effects of an Acceptance and Commitment Therapy-Based Psychosocial Intervention on Mental Health of Women With Perinatal Loss: A Pilot Study","Inclusion Criteria:\n\n* Women aged ≥18 years\n* Experienced perinatal loss (including miscarriage, stillbirth, or early neonatal death) within the past 12 months\n* Spouse\u002Fpartner willing to participate throughout the entire study\n* Able to read and communicate in Chinese\n* Willing and able to provide written informed consent\n\nExclusion Criteria:\n\n* Current diagnosis of severe mental illness (e.g., schizophrenia, bipolar disorder acute episode, psychotic disorder)\n* Active suicidal ideation with plan or intent, as assessed by clinical judgment or PHQ-9 item 9 score ≥1\n* Concurrent participation in other systematic psychotherapy or psychosocial intervention\n* Cognitive impairment that precludes understanding of the intervention content","FEMALE",{"count":52,"type":21},88,[24],"The purpose of this pilot study is to evaluate the feasibility, acceptability, and preliminary effects of an Acceptance and Commitment Therapy (ACT)-based psychosocial intervention for women who have experienced perinatal loss (miscarriage, stillbirth, or neonatal death). The intervention is a 4-week programme delivered in a mixed format: four in-person sessions (hospital setting, one-on-two with spouse\u002Fsignificant other) and two videoconferencing sessions (post-discharge, one-on-one), plus a 30-minute booster session one month after completion. Outcome assessments will occur at baseline (pre-intervention), immediately post-intervention, and three months post-intervention. Primary feasibility and acceptability metrics include recruitment, retention, session attendance, and participant-rated satisfaction. Preliminary effectiveness outcomes include perinatal grief, post-traumatic stress, depression, anxiety, psychological flexibility, and perceived social support. A qualitative component (semi-structured interviews) will explore participants' experiences and suggestions for refinement.",[56,28,57],"ACT","Mental Health",[56,57,59,60],"perinatal loss","Pilot RCT","2026-04-26",{"date":63,"type":34},"2026-04-30",{"date":65,"type":21},"2026-06-01",{"date":67,"type":21},"2027-06-30",{"name":69,"class":41},"Second Xiangya Hospital of Central South University",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":80,"conditions":81,"keywords":82,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":4},"100597613","the-effect-of-mandala-coloring-on-perinatal-grief-and-psychological-resilience-levels-in-women-experiencing-perinatal-loss-100597613","NCT07060768","The Effect of Mandala Coloring on Perinatal Grief and Psychological Resilience Levels in Women Experiencing Perinatal Loss","The Effect of Mandala Coloring on Perinatal Grief and Psychological Resilience Levels in Women Experiencing Perinatal Loss: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Experienced perinatal loss (neonatal death, fetal death, abortion) within the last six weeks\n\nExclusion Criteria:\n\n* Serious psychological problem that requires intervention with the recommendation of a psychiatrist, such as having a previous mental disorder or use of antidepressants.\n* Practicing alternative methods such as yoga, meditation, acupuncture",{"count":78,"type":21},60,[24],"The goal of this clinical trial is to evaluate if mandala colouring helps to decrease grief symptoms and increase resilience in women who experienced perinatal loss.\n\nThe main questions are:\n\nDoes mandala coloring decrease perinatal grief symptoms? Does mandala coloring increase resilience?\n\nResearchers will compare mandala coloring intervention with standard perinatal loss nursing care to evaluate if mandala coloring works to decrease grief symptoms.\n\nParticipants will:\n\nAnswer some questionnaires and scales, and do mandala coloring at least for 20 minutes for 10 days after perinatal loss experience.",[28],[59,83,84],"resilience","perinatal grief","2025-08-11",{"date":87,"type":34},"2025-08-15",{"date":89,"type":21},"2025-09-01",{"date":91,"type":21},"2026-09-30",{"name":93,"class":41},"University of Yalova",{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":99,"acronym":4,"eligibilityCriteria":100,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":101,"enrollmentInfo":102,"targetDuration":4,"studyType":22,"phases":104,"briefSummary":105,"conditions":106,"keywords":107,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":4},"100584965","the-effect-of-nursing-care-with-peri-natal-loss-100584965","NCT06896214","The Effect of Nursing Care With Peri-Natal Loss","The Effect of Standardised Nursing Care Given to Women With Peri-Natal Loss on Peri-Natal Grief, Posttraumatic Stress, Postpartum Depression","Inclusion Criteria:- To be over 18 years old\n\n* Being married (according to the woman's declaration)\n* Not having an existing psychiatric illness (according to the woman's declaration)\n* Not having communication problems (knowing Turkish, being literate, not having vision, speech or hearing problems, etc.)\n* Spontaneous conception\n* Singleton pregnancy\n* No substance addiction\n\nExclusion Criteria:Women who agreed to participate in the study but did not want to receive post-discharge care, who were hospitalised for any reason, who became pregnant again, who did not want to complete the last tests or who wanted to leave the study at any stage of the study will be excluded from the sample.","50 Years",{"count":103,"type":21},58,[24],"This study was planned to evaluate the effect of standardised nursing care given to women with perinatal loss using the nursing process on perinatal grief, posttraumatic stress and postpartum depression.\n\nH01: There is no difference between pre-test, post-test and follow-up tests in terms of perinatal grief scale mean scores in the intervention group.\n\nH02: There is no difference between pre-test, post-test and follow-up tests in terms of IES-R mean scores in the intervention group.\n\nH03: There is no difference between pre-test, post-test and follow-up tests in terms of EPDS mean scores in the intervention group.\n\nH04: There is no difference between the pre-test post-test and follow-up tests in terms of the mean scores of the Complicated Grief Scale in the intervention group.\n\n* At the first encounter with women, the mean scores of PMI, IESR and EPDS will be evaluated.\n* The mean EPDS score will be evaluated on the 10th postpartum day, 1st, 3rd and 6th month.\n* The mean I-ESR scale score will be evaluated at postpartum 1st, 3rd and 6th month.\n* At postpartum 1st and 3rd month, the mean score of PMS will be evaluated.\n* At the postpartum 6th month, the mean score of the PBI scale will be evaluated.",[28,27],[108,109,110],"perinatal grief, perinatal loss,","Postpartum Depression","post-traumatic stress disorder","2025-03-19",{"date":113,"type":34},"2025-03-26",{"date":115,"type":21},"2025-04-15",{"date":117,"type":21},"2025-12-30",{"name":119,"class":41},"Gazi University"]