[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"psychological-factors\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:psychological-factors":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,53,86],{"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":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100596464","body-awareness-therapy-in-high-stressed-young-adults-effects-on-function-balance-sleep-and-mood-100596464",false,"NCT07045792","Body Awareness Therapy in High Stressed Young Adults: Effects on Function, Balance, Sleep and Mood","Investigating the Effects of Body Awareness Therapy on Functional Capacity, Balance, Sleep Quality and Psychological State in Young Adults With High Stress Levels: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Be between 20 and 30 years old\n* Be literate\n* Score 10 or above on the stress subscale of the Depression Anxiety Stress Scale -21\n* Be willing to participate in the study voluntarily\n\nExclusion Criteria:\n\n* Individuals with orthopedic, neurological, rheumatological, psychiatric, mental, or any systemic chronic diseases\n* Those with cardiac problems that may prevent exercise\n* Those suspected of being pregnant\n* Individuals with malignancy\n* Individuals with active infection\n* Those who do not regularly attend the treatment program",true,"ALL","20 Years","30 Years",{"count":21,"type":22},30,"ESTIMATED","INTERVENTIONAL",[25],"NA","Body Awareness Therapy (BAT) is a holistic approach to human movement that considers the physical, physiological, psychological, and existential aspects of human existence. This planned randomized controlled study will be conducted on young adults with high stress levels. One group will be subjected to BAT and the other group will be the control group. The BAT exercises will be performed in supine, sitting and standing positions. In the BAT group, the exercises will be performed as a group exercise, not individually. After the initial evaluations in both the BAT and control groups, a re-evaluation will be performed at the end of 8 weeks. Functional capacity will be assessed with the 6-minute walk test, static balance with the single-leg balance test (eyes open-eyes closed), dynamic balance with the Y-balance test, psychological status with the Depression-Anxiety-Stress Scale-21 (DASS-21), and sleep quality with the Pittsburgh Sleep Quality Scale. BAT will be performed 2 days per week for 8 weeks and will be continued progressively. This study will examine the effects of BaT on functional capacity, balance, sleep quality, and psychological state in young adults with high stress levels.",[28,29,30,31],"Stress","Psychological Factors","Sleep","Postural Balance",[33,34,35,36,37,38,39,31],"Body Awareness Therapy","Stress Levels","Psychological Stress","Balance","Sleep Quality","Functional Capacity","Physical Therapy","RECRUITING","2026-06-29",{"date":43,"type":44},"2026-07-01","ACTUAL",{"date":46,"type":44},"2025-05-30",{"date":48,"type":22},"2026-06-28",{"name":50,"class":51},"Mustafa Kemal University","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":63,"briefSummary":64,"conditions":65,"keywords":70,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":52},"100641903","an-ecological-momentary-intervention-for-the-reduction-of-impairment-in-somatic-symptom-disorder-100641903","NCT07646509","An Ecological Momentary Intervention for the Reduction of Impairment in Somatic Symptom Disorder","Inclusion Criteria:\n\n* Somatic Symptom Disorder\n\nExclusion Criteria:\n\n* chronic physical illnesses that fully explain the somatic symptoms\n* current psychotic disorder\n* current bipolar disorder\n* current self-harming behavior\n* current suicidality\n* current psychotherapy\n* alcohol, drug, or medication dependence within the past 6 months","18 Years","65 Years",{"count":62,"type":22},40,[25],"Persistent somatic symptoms significantly impair the daily lives of individuals with Somatic Symptom Disorder (SSD). Negative psychological factors (NPFs), such as catastrophizing and negative affectivity, further compound this impairment. Yet, few studies have examined strategies in daily life that directly target somatic symptoms and their dynamic relationship with NPFs. The goal of this clinical trial is to investigate if an Ecological Momentary Intervention (EMI) using music listening and cognitive reappraisal can reduce the intensity of and impairment due to somatic symptoms in 40 individuals with Somatic Symptom Disorder (SSD), aged 18-65 years.\n\nParticipants will report symptom intensity, impairment, and NPFs up to four times daily via a smartphone app over a six-week period. Using an intraindividual randomized controlled design, during weeks two to five, participants will be randomly assigned in the ratio of 50:25:25 to no intervention, music listening, and cognitive reappraisal, both at fixed times (evening measurement) and during episodes of acute somatic impairment.",[66,67,29,68,69],"Somatic Symptom Disorder (DSM-5)","Impairment","Persistent Physical Symptoms","Medically Unexplained Symptoms",[71,72,73,74,75,76],"Ecological Momentary Intervention","Persistent Somatic Symptoms","Daily Life","Music","Cognitive reappraisal","Somatic Symptom disorder","2026-06-09",{"date":79,"type":44},"2026-06-12",{"date":81,"type":44},"2025-06-26",{"date":83,"type":22},"2026-10",{"name":85,"class":51},"University of Vienna",{"id":87,"slug":88,"hasResults":11,"nctId":89,"briefTitle":90,"officialTitle":91,"acronym":92,"eligibilityCriteria":93,"healthyVolunteers":16,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":94,"targetDuration":4,"studyType":23,"phases":96,"briefSummary":97,"conditions":98,"keywords":106,"overallStatus":113,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":123},"100605106","optical-diagnosis-of-neoplasia-using-artificial-intelligence-100605106","NCT07158203","Optical Diagnosis of Neoplasia Using Artificial Intelligence","Assistance for Optical Diagnosis of Neoplasia Using Artificial Intelligence (FAIR Study)","FAIR","Endoscopists who meet the following inclusion\u002Fexclusion criteria Inclusion criteria\n\n* Endoscopists experienced with more than 100 colonoscopies. Exclusion criteria\n* Endoscopists who are involved in the development of the protocol of the present study.\n\nInclusion and exclusion criteria for the study videos. Inclusion criteria.\n\n* Videos with a duration of 15 seconds including both WL and NBI.\n* Videos with diminutive polyps with confirmed pathology. Exclusion criteria.\n* Videos with no clear image of the polyps.\n* Videos with more than one polyp on-screen.\n* Inflammatory bowel disease\n* Polyposis\n* Hereditary colorectal disease\n* Videos which CADx cannot provide sufficient number of outputs.",{"count":95,"type":22},70,[25],"Computer-aided diagnosis (CADx) for colonoscopy aims to enhance optical diagnosis but often underperforms when used alongside humans due to under-reliance on AI. Psychological interventions like cognitive forcing, such as delaying CADx suggestions, may improve human-AI interaction by fostering critical assessment. However, their impact on patient-important outcomes remains unexplored.\n\nThe investigators will conduct an ex-vivo randomized study with 70 endoscopists assessing 100 polyp videos (≤5 mm) using a CADx tool (GI Genius, Medtronic). Participants will be randomized to either:\n\n* Intervention group: CADx suggestions will be shown in the last 3 seconds of the 15 second polyp video.\n* Control group: CADx suggestions will be shown in real-time throughout the playback of the 15 second polyp video.\n\nThe primary endpoint is sensitivity for high-confidence neoplasia detection, with secondary endpoints assessing endoscopists' reliance on AI.\n\nCADx systems on the market function in various ways, such as real-time, delayed, or on-demand diagnosis. Our study aims to inform users and manufacturers whether cognitive forcing through delayed CADx suggestions enhances human-AI interaction, leading to improved clinical outcomes.",[99,100,101,102,103,104,29,105],"Polyps Colorectal","Colonoscopy","Optical Biopsy","Colorectal Cancer Control and Prevention","Colorectal Cancer Screening","Behavior Change","Psychological Intervention",[107,108,109,110,111,112],"behaviour","optical biopsy","colonoscopy","CADx system","colorectal polyps","psychological intervention","NOT_YET_RECRUITING","2025-08-28",{"date":116,"type":44},"2025-09-05",{"date":118,"type":22},"2025-09",{"date":120,"type":22},"2025-12",{"name":122,"class":51},"Fundacin Biomedica Galicia Sur",2]