[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"self-concept\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:self-concept":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,51,80,122],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":33,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100632286","using-real-time-lung-visuals-to-reduce-mental-strain-and-improve-diagnosis-speed-100632286",false,"NCT07511712","Using Real-Time Lung Visuals to Reduce Mental Strain and Improve Diagnosis Speed","Effect of Real-Time Respiratory Mechanics Visualization (\"Digital Twin\") on Clinician Cognitive Workload and Diagnostic Latency: A Randomized Crossover Simulation Trial","VERDICT","Inclusion Criteria:\n\n* Licensed physicians currently practicing in intensive care units (ICU), neuro-intensive care units (NICU), or respiratory departments.\n* For the Junior Stratum: Physicians currently in a standardized residency training program or in their first two years of a sub-specialty fellowship. For the Senior Stratum: Senior attending physicians or senior fellows with more than 5 years of experience in intensive care medicine.\n* Basic proficiency in operating the mechanical ventilators used in the study (e.g., Hamilton, Dräger, or Puritan Bennett).\n* Willingness to participate in two simulation sessions separated by a 14-day interval.\n\nExclusion Criteria:\n\n* Prior formal training or significant experience using the ASL 5000 \u002F RespiSim \"Digital Twin\" or Aurora interface.\n* Physical limitations that prevent the operation of a mechanical ventilator or the viewing of a digital monitor.\n* Refusal to provide informed consent for video recording of the simulation session for data adjudication.",true,"ALL","18 Years","65 Years",{"count":22,"type":23},34,"ESTIMATED","INTERVENTIONAL",[26],"NA","The goal of this clinical simulation study is to learn if a \"Digital Twin\" graphical lung display reduce the mental workload of clinicians. The study also evaluates if this helps physicians diagnose and manage ventilator-related crises more effectively than standard ventilator screens.\n\nThe main questions it aims to answer are:\n\nDoes the Digital Twin display lower the cognitive stress (mental workload) experienced by clinicians during a crisis? Does the Digital Twin display reduce the time it takes for clinicians to identify specific respiratory complications? Does the use of real-time physiological visualization improve the accuracy of clinical decision-making? Researchers will compare the performance of clinicians using a standard ventilator display (the \"Black Box\" condition) to their performance when provided with an additional synchronized 3D lung and advanced waveform display (the \"Digital Twin\" condition).\n\nParticipants will:\n\nComplete four randomized mechanical ventilation crisis scenarios using a high-fidelity lung simulator (ASL 5000).\n\nManage scenarios involving high airway resistance, low lung compliance, auto-PEEP, and patient-ventilator asynchrony.\n\nUndergo a 14-day \"washout\" period between sessions to ensure no memory bias between the control and intervention groups.\n\nComplete a NASA-TLX survey after each scenario to measure their perceived mental, physical, and temporal demand.",[29,30,31,32],"Mechanical Ventilation","Clinical Competence","Education Curriculum","Self Concept",[34,35,36,37],"medical simulation","mechanical ventilation","clinical competence","mental pressure load","NOT_YET_RECRUITING","2026-04-06",{"date":41,"type":42},"2026-04-13","ACTUAL",{"date":44,"type":23},"2026-04-15",{"date":46,"type":23},"2026-07-31",{"name":48,"class":49},"Second Affiliated Hospital, School of Medicine, Zhejiang University","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":24,"phases":61,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":50},"100606693","psychosocial-teleassistance-programme-for-adults-with-spina-bifida-100606693","NCT07178873","Psychosocial Teleassistance Programme for Adults With Spina Bifida","Effects of a Psychosocial Teleassistance Programme for Adults With Spina Bifida","Inclusion Criteria:\n\n* To be diagnosed with spina bifida by a specialist.\n* Being between 18 and 75 years old.\n* Having their informed consent or the informed consent of their legal guardians.\n* Having Spanish as one of their main languages.\n* Having access to a computer (with a camera, microphone and speakers integrated) and Internet connection to take part in the videoconferences.\n\nExclusion Criteria:\n\n* Age that is inconsistent with the established range.\n* The presence of any comorbid diagnosis or sensory deficit that would impede the effective execution of the intervention's activities.","75 Years",{"count":60,"type":23},35,[26],"This clinical trial assesses the effect of a telecare psychosocial intervention designed for adults with spina bifida. The intervention consists of 10 weekly 1.5-hour group sessions, followed by two 3-month follow-up sessions. Each group will consist of 6 to 7 individuals. The intervention is aimed at strengthening aspects of self-concept, self-esteem, social skills and aims at a reduction of symptomatology and a general improvement of psychological well-being.",[64,65,66,32,67,68,69],"Spina Bifida","Self Esteem","Quality of Life (QOL)","Anxiety","Depression","Interpersonal Needs","RECRUITING","2025-12-02",{"date":73,"type":42},"2025-12-10",{"date":75,"type":42},"2024-06-25",{"date":77,"type":23},"2027-01",{"name":79,"class":49},"University of Deusto",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":87,"minAge":88,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":24,"phases":92,"briefSummary":93,"conditions":94,"keywords":102,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":121},"100589168","contemplative-practice-for-well-being-and-self-deconstruction-in-women-100589168","NCT06950905","Contemplative Practice for Well-being and Self-Deconstruction in Women","Effectiveness of a Contemplative Practice on Psychological Well-Being, Self-Deconstruction, Body Image, Body Acceptance, and Compassion in Women","Inclusion Criteria:\n\n* Sex assigned female at birth and self-identifies as a woman\n* Aged between 30 and 60 years\n* Spanish nationality, or residency in Spain for more than 5 years\n* Fluent in Spanish\n* At least one month of experience with meditation or mindfulness practices, with a regular practice of more than 15 minutes per session\n* Provides informed consent\n\nExclusion Criteria:\n\n* Indicators of eating disorders (ED) or mental health deterioration, determined by the following cut-off points: SCOFF ≥ 2 and PHQ-9 ≥ 10\n* Formal diagnosis of an eating disorder or any psychiatric condition\n* Substance use disorder\n* History of neurological disease diagnosis\n* Participant's decision to withdraw from the study at any point","FEMALE","30 Years","60 Years",{"count":91,"type":23},122,[26],"This randomized controlled trial aims to evaluate the effectiveness of a contemplative practice called Feeding Your Demons (FYD), based on a secular adaptation of Tibetan Buddhism, in improving psychological well-being, body image, body acceptance, compassion, and self-deconstruction in adult women. Participants will be randomly assigned to either FYD or an active control group practicing mindfulness meditation. Psychological variables will be assessed before and after the intervention, and at a six-month follow-up. Additionally, a qualitative exploration will be conducted through interviews with a subgroup of participants.",[95,32,96,97,98,99,100,101],"Mental Health","Body Dissatisfaction","Compassion","Self-Perception","Mindfulness Meditation","Meditation","Psychological Well-being",[103,104,105,106,100,97,107,108,109,110,111],"Feeding Your Demons","Self-Deconstruction","Selflessness","Contemplative Practices","Body Image","Women's Mental Health","Randomized Controlled Trial (RCT)","mindfulness","psychological well-being","2025-09-09",{"date":114,"type":42},"2025-09-10",{"date":116,"type":42},"2025-06-18",{"date":118,"type":23},"2028-06-30",{"name":120,"class":49},"Hospital Miguel Servet",2,{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":126,"acronym":127,"eligibilityCriteria":128,"healthyVolunteers":11,"sex":87,"minAge":19,"maxAge":4,"enrollmentInfo":129,"targetDuration":4,"studyType":24,"phases":131,"briefSummary":132,"conditions":133,"keywords":146,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":50},"100593584","impact-of-nipple-reconstruction-in-mastectomized-patients-using-cross-linked-hyaluronic-acid-injection-100593584","NCT07008339","Impact of Nipple Reconstruction in Mastectomized Patients Using Cross-Linked Hyaluronic Acid Injection.","RECHIAL","* Quantitative Phase\n* Inclusion Criteria:\n\nWomen over 18 years of age, or with parental or legal guardian consent.\n\nAt least one of the following criteria:\n\nWomen undergoing their first nipple-areola complex (NAC) reconstruction through micropigmentation and\u002For:\n\nNo previous neo-nipple surgery, either unilaterally or bilaterally.\n\nSurgical reconstruction of the areola.\n\nSurgical reconstruction of the NAC with subsequent retraction of the neo-nipple.\n\nMore than 6 months since their last surgery.\n\n\\- Exclusion Criteria:\n\nAllergy to hyaluronic acid.\n\nPoor tolerance to needle injections.\n\nWithdrawal Criteria:\n\nParticipant's voluntary decision.\n\nComplications associated with the technique (allergy, hematoma, etc.).\n\nClinical deterioration preventing the woman from continuing in the study.\n\n\\- Qualitative Phase\n\nParticipant Profile Characteristics: For the qualitative phase, women who have received NAC reconstruction with HA will be invited to participate, following the maximum variation criterion. To ensure the inclusion of participants with diverse characteristics and capture a wide range of perspectives and experiences on the phenomenon under study, women of varying ages, with different breast cancer diagnoses, and histories of various oncological, surgical, and therapeutic treatments will be selected.",{"count":130,"type":23},138,[26],"This study evaluates the impact of hyaluronic acid (HA) injection for nipple projection following mastectomy, as a complement to areola micropigmentation. While micropigmentation is standard in nipple-areola complex (NAC) reconstruction, HA use remains novel, with limited data on psychosocial, sexual, and aesthetic outcomes.\n\nA sequential explanatory mixed-methods design will be used. In Phase 1, a randomized controlled trial will compare two groups: one receiving NAC micropigmentation alone (control) and the other receiving micropigmentation plus HA-based nipple projection (intervention). A total of 138 participants will be recruited at the Areolar Micropigmentation Unit of Germans Trias i Pujol University Hospital (Barcelona) over 36 months. Outcomes will include psychosocial and sexual well-being, satisfaction with breast and nipple appearance, and nipple projection, measured using the Spanish BREAST-Q, a custom satisfaction tool, and calipers.\n\nPhase 2 will involve a qualitative phenomenological study using semi-structured interviews with a purposive sample from the intervention group. Thematic analysis will explore body image, emotional and social well-being, and overall satisfaction, using NVivo software.\n\nThis is the first study assessing HA nipple reconstruction by advanced practice nurses using validated patient-reported outcomes. While the BREAST-Q is appropriate, it may not fully capture emotional nuances, justifying qualitative exploration. HA durability is estimated at 6-9 months, but residual volume and satisfaction over time remain underexplored. HA's aesthetic footprint may allow reduced dosages in future applications.\n\nThis minimally invasive technique may reduce the need for surgical nipple reconstruction. Conducting the procedure in a nurse-led setting is novel and may enhance patient-centered care and the role of nursing in post-mastectomy recovery.\n\nThe study complies with the Declaration of Helsinki and Spanish biomedical regulations. Ethical approval was obtained. Participants will provide informed consent, and data will be anonymized and securely stored.",[134,135,136,137,138,139,140,141,142,32,107,143,144,145],"Breast Neoplasms","Mastectomy","Mammaplasty","Nipple Disorder","Tattooing","Hyaluronic Acid","Dermal Fillers","Reconstructive Surgical Procedures","Quality of Life","Patient Satisfaction","Breast Reconstruction","Nipple Reconstruction",[147,135,144,148,145,149,139,140,150,138,107,142,151,152,143,153],"Breast Cancer","Nipple-Areola Complex Reconstruction","Areola Reconstruction","Micropigmentation","Postmastectomy Reconstruction","Cross-linked Hyaluronic Acid","Breast Cancer Survivors","2025-06-04",{"date":156,"type":42},"2025-06-06",{"date":158,"type":42},"2023-06-02",{"date":160,"type":23},"2029-07-02",{"name":162,"class":49},"Germans Trias i Pujol Hospital"]