[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Sergio Mies Padilla\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":84},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,54],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100650224","digital-prenatal-education-to-reduce-fear-of-childbirth-in-term-pregnancy-100650224",false,"NCT07743502","Digital Prenatal Education to Reduce Fear of Childbirth in Term Pregnancy","Impact of a Digital Prenatal Education Intervention on Fear of Childbirth in Term Pregnant Women: A Randomized Controlled Trial","FEARLESS-BIRTH","Inclusion Criteria:\n\n* Aged 18 years or older\n* Nulliparous or multiparous\n* Singleton pregnancy\n* Pregnancy classified as low obstetric risk according to current local protocols\n* Antenatal care provided at primary or specialised care centres within the catchment area of the Complejo Hospitalario Universitario Insular Materno Infantil (CHUIMI)\n* Access to an internet-connected electronic device (smartphone, tablet or computer) allowing use of the web-based educational platform\n* Able to understand, read and write in Spanish\n* Written informed consent\n* Gestational age between 37+0 and 42+0 weeks at the time of definitive eligibility confirmation, baseline questionnaire completion and randomisation\n\nExclusion Criteria:\n\n* Estimated date of delivery, calculated by first-trimester ultrasound, later than 31 January 2027\n* Risk of preterm birth or medical indication for early termination of pregnancy at the time of recruitment\n* Elective caesarean section scheduled at the time of recruitment\n* Known major structural fetal anomaly requiring specialised obstetric or neonatal management\n* Previous or current diagnosis of an anxiety disorder, depression or other relevant psychopathology that, in the judgement of the recruiting clinician, could interfere with study participation\n* Concurrent participation in another structured intervention study specifically targeting fear of childbirth\n* Planned relocation outside the CHUIMI catchment area before the estimated date of delivery, precluding postpartum data collection",true,"FEMALE","18 Years",{"count":21,"type":22},176,"ESTIMATED","INTERVENTIONAL",[25],"NA","Many pregnant women feel afraid of giving birth. This fear is common and can affect how a woman experiences labour, the type of birth she has, and how she feels afterwards.\n\nAntenatal education helps women prepare for birth, but not everyone can attend the classes offered at health centres. Work schedules, family duties or travel distance often get in the way.\n\nThis study looks at whether an online education programme can help. The programme is a website that women can use at home, at any time, from a phone, tablet or computer. It explains how labour works, what pain relief and other options are available, how to prepare a birth plan, and how to manage difficult feelings. It also includes videos filmed in the hospital where the women will give birth, so the place feels familiar before they arrive.\n\nWomen taking part will be pregnant with one baby, will have a pregnancy considered low risk, and will be at least 37 weeks pregnant when they start. Half of the women will be given access to the website, chosen at random, like tossing a coin. The other half will receive the usual antenatal care offered by their midwife and doctor. All women continue with their normal pregnancy care.\n\nWomen will answer a questionnaire about their feelings towards birth when they join the study, and a second questionnaire in the first two weeks after their baby is born. The researchers will compare the answers of the two groups to see whether the website made a difference. Information about the birth will also be collected from the medical records.\n\nThe study will take place in Gran Canaria, Spain, and will include 176 women. It is run by midwives as part of a specialist training programme and has no commercial funding.",[28,29,30],"Fear of Childbirth","Tocophobia","Pregnancy Related Anxiety",[32,33,34,35,36,37,38,39,40],"fear of childbirth","tocophobia","antenatal education","prenatal education","digital health","web-based intervention","midwifery","term pregnancy","randomized controlled trial","NOT_YET_RECRUITING","2026-07-30",{"date":44,"type":45},"2026-08-04","ACTUAL",{"date":47,"type":22},"2026-10-01",{"date":49,"type":22},"2027-01-30",{"name":51,"class":52},"Sergio Mies Padilla","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":60,"minAge":19,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":63,"briefSummary":64,"conditions":65,"keywords":67,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":53},"100623900","effect-of-early-educational-intervention-on-cardiovascular-risk-factors-after-acute-coronary-syndrome-100623900","NCT07402642","Effect of Early Educational Intervention on Cardiovascular Risk Factors After Acute Coronary Syndrome","Inclusion Criteria:\n\n* Patients must have suffered an Acute Myocardial Infarction.\n* Participants must have undergone an urgent cardiac catheterization.\n* Specifically, this includes patients who received coronary reperfusion strategies following the activation of the CODICAN protocol (assistance for ST-segment elevation myocardial infarction) within the study environment.\n\nExclusion Criteria:\n\n* Patients with little or no knowledge of the Spanish language that prevents effective communication or reading of educational resources.\n* Patients unable to understand their participation or follow health recommendations independently.\n* Patients with an unfavorable clinical prognosis or those requiring hospitalization for a period exceeding established limits.\n* Patients unable to attend in-person nursing consultations due to personal reasons or place of residence","ALL",{"count":62,"type":22},256,[25],"Early Education After a Heart Attack What is the purpose of this study? The main goal is to evaluate if a special nursing education and support program helps patients who have suffered a heart attack feel more confident in managing their own health. Researchers want to see if this extra support improves how patients care for their hearts through diet, physical activity, and quitting smoking. The study compares this new nursing strategy against the standard care patients usually receive.\n\nWho can participate? Participants must be 18 years of age or older. People who have recently had a heart attack requiring an urgent heart catheterization at the Complejo Hospitalario Universitario Insular Materno Infantil.\n\nExclusions: People with significant language barriers (Spanish), mental incapacity to follow recommendations, or those unable to attend in-person consultations cannot participate.\n\nWhat will happen during the study? Participants will be divided into two groups: Standard Care Group (Control): These participants will receive the usual medical follow-up and standard cardiac rehabilitation sessions (an average of 17 sessions focused on exercise and group education). Special Support Group (Experimental): In addition to standard care, these participants will have a specific nursing consultation consisting of 4 scheduled visits.\n\nThese visits are a mix of in-person and telephone appointments.Nurses will provide personalized educational materials, such as infographics, and teach techniques to control blood pressure, improve diet, exercise safely, and manage emotions after a heart attack.\n\nDuration and Follow-up Each participant will be followed for approximately 8 months. During this time, they will be asked to complete several surveys about their lifestyle.\n\nResearchers will also review blood test results (cholesterol levels) from their medical records to track progress.",[66],"Myocardial Infarction",[68,69,70,71,72,73,74],"Patient Education","Secondary Prevention","Nursing Care","Self Efficacy","risk factors","Healthy Lifestyle","Cardiovascular Diseases","RECRUITING","2026-02-04",{"date":78,"type":45},"2026-02-11",{"date":80,"type":45},"2026-01-12",{"date":82,"type":22},"2027-01-01",{"name":51,"class":52},""]