[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"eating-disorders-excluding-anorexia-nervosa\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:eating-disorders-excluding-anorexia-nervosa":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,77],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100576657","enhancing-social-connections-among-rural-community-members-with-disordered-eating-100576657",false,"NCT06788145","Enhancing Social Connections Among Rural Community Members With Disordered Eating","Inclusion Criteria:\n\n* Adult (18+ years old)\n* disordered eating\n* live in the United States of America\n\nExclusion Criteria:\n\n* BMI below 18.5","ALL","18 Years","100 Years",{"count":19,"type":20},111,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study is about testing a short program that uses social support to help people with disordered eating. The goal is to see if this program can help people build better habits and feel better about eating while reducing harmful symptoms. In the long run, this project wants to make it easier for people with eating problems to get help and recover, especially for those in rural areas or other groups who don't often get the care they need. Participants will complete self-report measures online, and complete a digital single-session program.",[26,27,28,29],"Eating Disorders (Excluding Anorexia Nervosa)","Disordered Eating","Disordered Eating Behaviors","Eating Disorder Symptom",[31,32],"eating disorder","disordered eating","NOT_YET_RECRUITING","2026-04-29",{"date":36,"type":37},"2026-05-01","ACTUAL",{"date":39,"type":20},"2026-07-01",{"date":41,"type":20},"2027-06-30",{"name":43,"class":44},"University of Montana","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100597595","building-healthy-eating-and-self-esteem-together-for-university-students-100597595","NCT07060534","Building Healthy Eating and Self-Esteem Together for University Students","Building Healthy Eating and Self-Esteem Together for University Students (BEST-U): A Pilot Randomized Controlled Trial of an mHealth Intervention for Binge-Spectrum Disorders","BEST-U","Inclusion Criteria:\n\n* Age ≥ 18 years.\n* Student enrolled at KU.\n* Bulimia nervosa (BN) or binge-eating disorder (BED) (or sub-threshold BN or BED).\n* Access to a smartphone.\n* No uncorrected vision problems that would interfere with ability to participate in the study.\n* Students taking psychotropic medications must be on a stable therapeutic dose for four weeks prior to study enrollment.\n* Able to read and speak fluent English.\n\nExclusion Criteria:\n\n* Presence of current moderate\u002Fsevere suicidal ideation with active intent.\n* Significant psychopathology that could interfere with treatment (e.g., current substance-use disorder or psychosis).\n* Medical conditions or medications that could interfere with treatment (e.g., Type 1 diabetes mellitus, cancer, current pregnancy or nursing, taking corticosteroids, etc.).\n* Lab abnormalities indicating medical instability (e.g., low heart rate, electrolyte disturbance, acute medical complications of malnutrition) or another medical problem that would prevent outpatient care as determined through physical health assessment by the student's local clinician.\n* Already receiving therapy for an ED.\n* Positive screen for anorexia nervosa (AN), atypical AN (AAN), and\u002For low body weight (i.e., BMI \\\u003C 19.5) or avoidant and restrictive food intake disorder (ARFID).","65 Years",{"count":55,"type":20},74,[23],"Eating disorders (EDs) are a critical concern on college campuses. Moreover, since the COVID-19 pandemic, ED prevalence has increased by 62% in university women and 140% in university men. Resources are inadequate to meet demand, leading to delays in students' access to treatment. Untreated (or poorly treated) EDs result in greater healthcare utilization and costs to students, as well as lower academic achievement and increased psychiatric disability and mortality, suggesting a critical need for quality ED treatment on university campuses and to rethink treatment delivery. One way to address this gap in care delivery is to improve treatment accessibility and scalability, such as dissemination via mobile apps. Guided self-help Cognitive Behavior Therapy (CBT-gsh) is a cost-effective option that can be delivered by non-traditional service providers, such as nurses and physicians. Our scientific premise is that the mHealth CBT-gsh app, Building Healthy Eating and Self-Esteem Together for University Students (BEST-U), will lead to reductions in binge eating (primary outcome) through reductions in dietary restraint and weight\u002Fshape concerns (target mechanisms). Prior to implementing BEST-U at other universities, we need to test the intervention in a real-world setting with the end goal of disseminating at scale. Our objectives are to: 1) conduct an effectiveness test of BEST-U compared to a similar dose of present-centered therapy (PCT) in students with non-low weight binge-spectrum EDs and 2) test target mechanisms that lead to changes in binge eating. To accomplish our objectives, we will test the following specific aims: 1) conduct an RCT of BEST-U (N=37) compared to a similar dose of PCT (N=37) in students with non-low weight binge-spectrum EDs; 2) test target mechanisms that lead to changes in binge eating and other ED symptoms; and 3) characterize barriers and facilitators to implementation across two campuses. Our exploratory aim will test food reinforcement and food-choice impulsivity as potential target mechanisms or response moderators of rapid response in binge eating. Given that few studies have identified underlying mechanisms that explain how CBT-gsh works and for whom, this study may lead to improved ability to tailor or modify existing CBT-gsh or lead to novel intervention development for students who are unlikely to respond rapidly (or at all) to first line CBT interventions for EDs.",[26,59],"Binge-Eating Disorder",[61,62,63,64,65],"Eating disorders","Bulimia nervosa","Binge-eating disorder","College Students","Purging disorder","RECRUITING","2026-01-13",{"date":69,"type":37},"2026-01-14",{"date":71,"type":20},"2026-06-23",{"date":73,"type":20},"2027-12-31",{"name":75,"class":44},"University of Kansas",1,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":84,"minAge":16,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":21,"phases":88,"briefSummary":89,"conditions":90,"keywords":91,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":76},"100595789","cbt-effects-on-neural-physiological-and-attentional-responses-in-anorexia-nervosa-100595789","NCT07037017","CBT Effects on Neural, Physiological, and Attentional Responses in Anorexia Nervosa","Neurophysiological Effects of Cognitive-Behavioral Therapy in Anorexia Nervosa: A Pre-Post EEG, GSR, and Eye-Tracking Study","Inclusion Criteria:\n\n* Female participants aged 18 to 35\n* Meeting DSM-5 diagnostic criteria for restrictive-type anorexia nervosa\n* Body Mass Index (BMI) between 15.0 and 18.5\n* Medically stable to participate in psychological and neurophysiological assessments\n* Willingness to participate in weekly therapy sessions (for the CBT group) and to complete pre- and post-assessments\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Current or past diagnosis of bulimia nervosa, binge-eating disorder, or other eating disorders\n* Presence of comorbid severe psychiatric disorders (e.g., psychosis, bipolar disorder, substance use disorder)\n* History of neurological illness or traumatic brain injury\n* Use of psychotropic medication within the last 6 weeks\n* Prior participation in structured Cognitive-Behavioral Therapy for an eating disorder\n* Pregnancy\n* Visual or neurological impairments that would prevent accurate EEG, GSR, or eye-tracking recordings","FEMALE","35 Years",{"count":87,"type":20},60,[23],"This randomized controlled trial investigates the neurophysiological, physiological, and attentional effects of Cognitive-Behavioral Therapy (CBT) in individuals with restrictive-type anorexia nervosa (AN). The study compares two groups: one receiving a 12-week CBT intervention, and one placed on a waitlist (no active treatment during the study period). All participants undergo pre- and post-intervention assessments using electroencephalography (EEG), galvanic skin response (GSR), and eye-tracking while exposed to visual stimuli related to food, body image, and self-appearance. The primary outcomes include neural changes in attention and emotional processing (P300, LPP, frontal alpha asymmetry), physiological arousal (skin conductance), and visual attention biases (fixation duration and gaze distribution). The aim is to determine whether CBT leads to measurable improvements in neurobiological and attentional mechanisms related to body image disturbance and food-related anxiety in AN, contributing to biomarker-informed psychotherapy approaches.",[26],[92,93,94,95,96],"Cognitive Behavioral Therapy (CBT)","EEG","Eye-Tracking","Galvanic Skin Response (GSR)","Body Image","2025-06-17",{"date":99,"type":37},"2025-06-25",{"date":101,"type":37},"2025-05-15",{"date":103,"type":20},"2025-10-15",{"name":105,"class":44},"Istanbul Nisantasi University"]