[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"feeding-and-eating-disorders\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:feeding-and-eating-disorders":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,50,80,112,146,174,197,225,250,279,306],{"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":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100637032","effects-of-mindful-eating-on-female-nutrition-students-100637032",false,"NCT07573410","Effects of Mindful Eating on Female Nutrition Students","Efficacy of a Mindful Eating Intervention on Eating Behavior, Body Image, and Mental Health in Female Nutrition Students: a Pilot Randomized Clinical Trial","Inclusion Criteria:\n\n* Female gender\n* Active enrollment in the Nutrition undergraduate program at the time of data collection\n* Agreement to participate in the study\n\nExclusion Criteria:\n\n* Diagnosis of severe cognitive or mental disorders; Regular practice (at least once a week in the last six months) of meditation, yoga, or mindfulness\n* Regular practice (at least once a week in the last six months) of meditation, yoga, or mindfulness",true,"FEMALE","18 Years",{"count":20,"type":21},88,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this pilot randomized clinical trial is to evaluate the efficacy of a mindful eating intervention (\"Eat for Life\") on eating behavior, body image, and mental health in female nutrition students. The main questions it aims to answer are: Does a mindful eating intervention reduce disordered eating behaviors in female nutrition students? Does the intervention improve body appreciation, mindfulness levels, and mental health?\n\nResearchers will compare an active control group receiving nutritional guidance to an intervention group participating in the \"Eat for Life\" mindful eating program to see if the mindful eating intervention reduces disordered eating behaviors and improves overall psychological well-being and body appreciation.\n\nParticipants will: Complete online questionnaires evaluating eating behavior, mindfulness, mental health, and body image at three distinct time points: before the intervention (baseline), post-intervention, and at a 3-month follow-up.\n\nIf assigned to the intervention group, attend 12 weekly face-to-face mindful eating sessions lasting approximately two hours each. If assigned to the active control group, receive weekly informative leaflets via WhatsApp with nutritional guidance based on the Dietary Guidelines for the Brazilian Population for 12 weeks",[27,28,29,30,31],"Mental Health","Body Image","Feeding Behavior","Feeding and Eating Disorders","Stress and Anxiety",[33,34,35,36],"mindful eating","feeding behavior","Students","mental health","NOT_YET_RECRUITING","2026-05-06",{"date":40,"type":41},"2026-05-11","ACTUAL",{"date":43,"type":21},"2026-06-01",{"date":45,"type":21},"2027-12-01",{"name":47,"class":48},"Federal University of Uberlandia","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":49},"100639374","understanding-and-targeting-self-regulatory-control-in-bulimia-nervosa-100639374","NCT07581158","Understanding and Targeting Self-Regulatory Control in Bulimia Nervosa","Understanding and Targeting Self-Regulatory Control in Bulimia Nervosa Via a Combined Real-Time Neurofeedback and Smartphone Intervention","Inclusion criteria:\n\n* Female\n* Aged 18 to 55 years\n* Meet diagnostic criteria for bulimia nervosa (BN) or BN of low frequency and\u002For limited duration\n* Current body mass index greater than or equal to 18.5kg\u002Fm2 but under 40kg\u002Fm2\n* English-speaking\n\nExclusion criteria:\n\n* Ongoing medical treatment or planned\u002Frecent change in medical treatment, major medical condition, or psychiatric disorder that may interfere with study variables or participation\n* Current psychotherapy focused primarily on eating disorder symptoms\n* Pregnancy or planned pregnancy, or lactation during the study period\n* Allergy to ingredients in the shake","55 Years",{"count":59,"type":21},40,[24],"The purpose of this study is to examine the effects of noninvasive prefrontal cortex (PFC) neurofeedback during eating in women with bulimia nervosa (BN) using wearable brain imaging, functional near-infrared spectroscopy (fNIRS), together with a brain-based 4-week text-messaging intervention. The investigators will examine how these interventions may influence inhibitory control and eating disorder symptoms in women with bulimia nervosa.",[63,30,64],"Bulimia Nervosa","Mental Disorders",[66,67,68,69,70,71],"fNIRS","fNIRS neurofeedback","smartphone intervention","eating disorders","bulimia nervosa","bulimia",{"date":73,"type":41},"2026-05-12",{"date":75,"type":21},"2026-04-25",{"date":77,"type":21},"2028-12-14",{"name":79,"class":48},"Icahn School of Medicine at Mount Sinai",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":17,"minAge":88,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":92,"phases":4,"briefSummary":93,"conditions":94,"keywords":95,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":49},"100577631","metacognitive-beliefs-in-adolescents-with-eating-and-nutrition-disorders-100577631","NCT06800807","Metacognitive Beliefs in Adolescents With Eating and Nutrition Disorders","Metacognitive Beliefs and Eating and Nutrition Disorders in Adolescents With Eating and Nutrition Disorders","METAED","Eating and nutrition disorders (END)\n\nInclusion Criteria:\n\n* Female sex\n* Age: 12 to 17 years\n* Italian nationality\n* Diagnosis relating to the END framework according to the diagnostic criteria of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5).\n\nExclusion Criteria:\n\n* Absence of signed Informed Consent\n\nControl group\n\nInclusion Criteria:\n\n* Female sex\n* Age: 12 to 17 years\n* Italian nationality\n\nExclusion Criteria:\n\n* Absence of signed Informed Consent","12 Years","17 Years",{"count":91,"type":21},72,"OBSERVATIONAL","The present study aims to study the presence of metacognitive beliefs in adolescent subjects with eating and nutrition disorders (END) compared with a control group composed of subjects of the same sex and age belonging to the general population.",[30],[96,97,98,99,100,70,101],"metabeliefs","metacognition","brooding","rumination","anorexia nervosa","binge eating disorder","RECRUITING","2026-03-25",{"date":105,"type":41},"2026-03-30",{"date":107,"type":41},"2024-06-26",{"date":109,"type":21},"2026-06-30",{"name":111,"class":48},"Istituto Auxologico Italiano",{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":116,"acronym":117,"eligibilityCriteria":118,"healthyVolunteers":11,"sex":119,"minAge":18,"maxAge":4,"enrollmentInfo":120,"targetDuration":4,"studyType":22,"phases":122,"briefSummary":123,"conditions":124,"keywords":126,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":142,"leadSponsor":144,"locationsCount":4},"100620094","artificial-intelligence-based-virtual-reality-application-to-provide-data--driven-patient-centred-treatment-for-people-with-eating-disorders-100620094","NCT07353151","Artificial Intelligence-based, Virtual Reality Application to Provide Data- Driven, Patient-centred Treatment for People With Eating Disorders","OASIS","Inclusion Criteria:\n\n* Adults ≥18 years.\n* Anorexia nervosa receiving or awaiting treatment as usual (TAU) within South London and Maudsley NHS Foundation Trust (inpatient, day service, or outpatient).\n* Medically stable and clinically suitable to take part in brief VR sessions alongside TAU (as judged by the treating team).\n* Able to give informed consent.\n\nExclusion Criteria:\n\n* Current or recent (within 12 months) serious self-harm with suicidal intent, or behaviour that posed a risk to life (e.g., overdose, deep cutting, swallowing sharp objects), or self-harm likely to cause lasting impairment.\n* Active suicidality or high risk of suicide.\n* Untreated or unstable epilepsy.\n* Psychotic disorder.\n* Outpatient participants with BMI \\\u003C 10.\n* Current participation in another research study or clinical trial.","ALL",{"count":121,"type":21},45,[24],"The goal of this clinical trial is to see if a short virtual reality (VR) program can be used safely and comfortably with people receiving care for anorexia nervosa. The study will also check if people are willing to take part and complete the full week of VR sessions.\n\nThe main questions the study will answer are:\n\nCan the investigators recruit and keep participants in the study? Do participants complete most of the VR sessions? Do they find the experience helpful and acceptable? Are there any side effects, like nausea or dizziness?\n\nParticipants will:\n\n* Take part in one VR session each weekday (about 20 to 30 minutes) for one week\n* Continue their usual care during this time\n* Answer questions before and after the VR sessions about their anxiety, mood, motivation, and experience\n* Some participants may join a short interview or focus group to share feedback\n\nThe VR program includes scenes for food-related exposure, calming music, motivational phrases, and goal setting. The app was designed with help from people with lived experience of anorexia and based on psychological therapies used in treatment.\n\nWho can take part:\n\n* Adults aged 18 or older\n* People receiving or waiting for care for anorexia nervosa at South London and Maudsley NHS Foundation Trust (SLaM)\n* People who are medically stable and able to give informed consent\n\nWhy this matters:\n\nThis study will help researchers understand if using VR in eating disorder services is practical, safe, and acceptable. The results will help plan a larger trial in the future to see if this type of VR treatment can support recovery from anorexia nervosa. Taking part is voluntary, and participants can stop at any time.",[125,30],"Anorexia Nervosa",[127,128,129,130,131,132,133,134,135,136],"Anorexia nervosa (AN)","Virtual reality (VR)","Eating disorders","Food exposure","Feasibility study","Food-related anxiety","Exposure-based intervention","South London and Maudsley (SLaM)","King's College London (KCL)","United Kingdom","2026-01-19",{"date":139,"type":41},"2026-01-21",{"date":141,"type":21},"2026-01",{"date":143,"type":21},"2027-08",{"name":145,"class":48},"King's College London",{"id":147,"slug":148,"hasResults":11,"nctId":149,"briefTitle":150,"officialTitle":150,"acronym":4,"eligibilityCriteria":151,"healthyVolunteers":16,"sex":119,"minAge":88,"maxAge":4,"enrollmentInfo":152,"targetDuration":4,"studyType":92,"phases":4,"briefSummary":154,"conditions":155,"keywords":161,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":49},"100619731","the-diabeat-study-insulin-delivery-technologies-and-eating-behaviours-in-people-with-type-1-diabetes-100619731","NCT07348432","The diabEAT Study: Insulin dElivery Technologies And eaTing Behaviours in People With Type 1 Diabetes","Inclusion Criteria:\n\n* 12 years of age or older\n* Living in Canada\n* Living with type 1 diabetes for more than 1 year\n* Using at least 2 insulin injections per day or using an insulin pump\n* Using current insulin delivery system for 3 months or more\n\nExclusion Criteria:\n\n* Are pregnant or currently are breastfeeding\n* Don't speak French or English\n* Does not have a smart phone (to download applications)",{"count":153,"type":21},106,"Type 1 diabetes is an autoimmune health condition that requires daily injections of insulin. Insulin allows the body to use energy from carbohydrates in food. Disordered eating behaviours, like restricting food intake to lose body weight, are more common in women and people with type 1 diabetes, compared to those without because they must practice carbohydrate counting. Carbohydrate counting means identifying, measuring, and planning carbohydrate intake to match insulin dosage. New technologies, such as automated insulin delivery (AID) systems adjust insulin delivery in a blood sugar responsive manner. AID is rapidly replacing conventional insulin delivery like injections or non-automated insulin pumps since it reduces management burden and improves blood sugar levels. It is not known if AID reduces food management and disordered eating behaviours. This study aims to: 1. investigate the relationship between AID and eating behaviours according to gender for youth (12 to 17 years), and adults (18 years and older). 2. Determine the limit of carbohydrate counting inaccuracy to maintain stable blood sugar levels according to insulin delivery method (AID, injections, or pumps). It is hypothesized that those who use AID will have lower disordered eating behaviours and will maintain stable blood sugar levels while allowing for higher carbohydrate counting inaccuracy. This will be a cross-sectional cohort study of people with type 1 diabetes who are 12 years of age or over. Participants will be recruited through the BETTER registry and social medias across Canada. This research is needed to improve nutrition guidelines for type 1 diabetes in the context of new technologies like AID. Evidence from this study may reduce food management burden, lower the risk of disordered eating behaviours, and prevent eating disorders and medical complications.",[156,30,157,158,159,160],"Insulin Dependent Diabetes Mellitus","Eating Behavior","Type 1 Diabetes","Autoimmune Diseases","Endocrine System Diseases",[162,163,164,158],"Automated Insulin Delivery","Disordered Eating Behaviours","Nutrition","2026-01-12",{"date":167,"type":41},"2026-01-16",{"date":169,"type":41},"2024-07-29",{"date":171,"type":21},"2026-05-01",{"name":173,"class":48},"McGill University",{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":180,"eligibilityCriteria":181,"healthyVolunteers":11,"sex":119,"minAge":88,"maxAge":18,"enrollmentInfo":182,"targetDuration":4,"studyType":22,"phases":184,"briefSummary":185,"conditions":186,"keywords":4,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":187,"lastUpdatePostDateStruct":188,"startDateStruct":190,"completionDateStruct":192,"leadSponsor":194,"locationsCount":196},"100535788","comparing-enhanced-cognitive-behavior-therapy-and-family-based-treatment-for-adolescents-with-an-eating-disorder-100535788","NCT06256380","Comparing Enhanced Cognitive-behavior Therapy and Family-based Treatment for Adolescents With an Eating Disorder","Comparing Enhanced Cognitive-behavior Therapy and Family-based Treatment for Adolescents With an Eating Disorder: a Non-inferiority Randomized Controlled Trial","CogFam","Inclusion Criteria:\n\n1. Diagnostic and Statistical Manual of Mental Disorders (DSM-5) diagnosed eating disorder\n2. Medically stable for outpatient treatment.\n3. Living with at least one of their parents\n4. At least one of their parents could be actively involved in the treatment\n5. Sufficient knowledge in reading, understanding and speaking Norwegian\n\nExclusion Criteria:\n\n1. Avoidant restrictive food intake disorders\n2. A co-morbid medical condition or disorder known to influence eating or weight, or influence the possibilities to take part in treatment\n3. Psychotic disorders\n4. Acute suicidality\n5. Substance abuse and\u002For substance dependence\n6. Serious traumatic events in the family making treatment following FBT or CBT-E manual not recommended\n7. Unstable psychotropic medication last 6 weeks",{"count":183,"type":21},200,[24],"The goal of this randomized controlled clinical trial is to compare the efficacy of outpatient family-based treatment versus enhanced cognitive behavior therapy for children and adolescents with eating disorders.\n\nBecause of insufficient recruitment, the study design was modified on December 1st, 2025, to a partially randomized preference design.\n\nThe main aim is to determine if enhanced cognitive behavior therapy has a similar efficacy as family-based treatment among children and adolescents with eating disorders receiving treatment in an outpatient setting. The main outcome is improvement in eating disorders psychopathology at the end of treatment.",[30],"2025-12-17",{"date":189,"type":41},"2025-12-24",{"date":191,"type":41},"2024-03-07",{"date":193,"type":21},"2033-12-31",{"name":195,"class":48},"Oslo University Hospital",5,{"id":198,"slug":199,"hasResults":11,"nctId":200,"briefTitle":201,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":11,"sex":119,"minAge":18,"maxAge":4,"enrollmentInfo":204,"targetDuration":4,"studyType":22,"phases":206,"briefSummary":207,"conditions":208,"keywords":4,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":49},"100484368","exposure-based-cbt-for-avoidantrestrictive-food-intake-in-functional-dyspepsia-100484368","NCT05587127","Exposure-Based CBT for Avoidant\u002FRestrictive Food Intake in Functional Dyspepsia","A Randomized Controlled Trial of Exposure-Based Cognitive Behavioral Treatment for Avoidant\u002FRestrictive Food Intake in Functional Dyspepsia","Inclusion Criteria\n\n* Age at least 18 years at screening visit\n* Rome IV Functional Dyspepsia post-prandial distress type (with or without epigastric pain syndrome)\n* Negative upper endoscopy or upper radiographic GI series to rule out structural\u002Forganic cause for FD\n* Avoidant\u002FRestrictive Food Intake Disorder (ARFID) diagnosis (by the Structured Clinical Interview for DSM-5; SCID-5 at Screening visit)\n* ≥5% weight loss from weight after functional dyspepsia symptom onset (at Screening visit)\n* Stable for outpatient care (based on the American Psychiatric Association Practice Guideline for the Treatment of Patients with Eating Disorders)\n* No previous history of CBT for functional dyspepsia or ARFID\n* Computer\u002Finternet webcam access\n* Fluency in English\n* Stable dose for 30 days if on any medication\n\nExclusion Criteria\n\n* Inability to provide informed consent\n* Presence of other conditions that could explain the patient's symptoms by chart:\n\nPyloric or intestinal obstruction (by EGD, UGI, or Abdominal CT) Active H.pylori infection (by CLO test or stool antigen test) Active inflammatory bowel disease Eosinophilic gastroenteritis or eosinophilic esophagitis Acute renal failure Chronic renal failure (serum creatinine \\>3 mg\u002FdL) and\u002For on hemodialysis or peritoneal dialysis Acute liver failure Any acute gastrointestinal process Any plausible structural or metabolic causes Heartburn as predominant symptom History of peptic ulcer\n\n* Symptom resolution with antisecretory therapy (PPI use for other reasons that did not resolve FD symptoms will be allowed)\n* History of gastrointestinal tract surgery (including gastrectomy, gastric bypass surgery, and small or large bowel resection)\n* History of any serious medical condition (e.g., cancer)\n* Use of narcotic analgesics greater than three days per week\n* Current pregnancy or breastfeeding within the last 8 weeks\n* Uncontrolled diabetes (indicated by HbA1c ≥7%) by chart\n* Intellectual disability by history\n* Current substance\u002Falcohol use disorder within the past month\n* Current\u002Fhistory of psychosis (by Mini-International Neuropsychiatric Interview (MINI-Screen)\n* Current mania (by Mini-International Neuropsychiatric Interview (MINI-Screen) (defined as any manic episodes within the past 12 months)\n* Active suicidal ideation (by MINI-Screen)\n* Psychiatric disorder that would warrant independent attention (by Mini-International - Neuropsychiatric Interview (MINI-Screen))\n* Current enteral or parenteral feeding\n* Plans to initiate another psychotherapy or pregnancy in the concurrent study period",{"count":205,"type":21},50,[24],"Randomized controlled trial of an exposure-based behavioral treatment (CBT) in adults with functional dyspepsia who meet criteria for avoidant\u002Frestrictive food intake disorder (ARFID) with weight loss.",[209,210,30,211,212,213,214,215],"Avoidant\u002FRestrictive Food Intake Disorder","Dyspepsia","Cognitive Behavioral Therapy","Appetite Regulation","Functional Dyspepsia","Post-prandial Distress Syndrome","Behavioral Medicine","2025-09-22",{"date":218,"type":41},"2025-09-25",{"date":220,"type":41},"2022-11-30",{"date":222,"type":21},"2027-05",{"name":224,"class":48},"Massachusetts General Hospital",{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":230,"acronym":4,"eligibilityCriteria":231,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":232,"enrollmentInfo":233,"targetDuration":4,"studyType":22,"phases":235,"briefSummary":236,"conditions":237,"keywords":238,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":241,"lastUpdatePostDateStruct":242,"startDateStruct":244,"completionDateStruct":246,"leadSponsor":248,"locationsCount":49},"100588550","mechanisms-of-deep-transcranial-magnetic-stimulation-in-enhancing-cognitive-behavioral-therapy-for-anorexia-nervosa-100588550","NCT06942858","Mechanisms of Deep Transcranial Magnetic Stimulation in Enhancing Cognitive-Behavioral Therapy for Anorexia Nervosa","Mechanisms of Deep Transcranial Magnetic Stimulation Enhances the Efficacy of Cognitive-behavioral Therapy (CBT) by Modulating Anterior Cingulate Cortex in Patients With Anorexia Nervosa","Inclusion Criteria:\n\n* Inclusion Criteria:\n* Female, aged 18-35 years, right handedness.\n* Above primary education.\n* Meet the diagnostic criteria of AN in DSM-V, and13.0 kg\u002Fm2 ≤ body mass index (BMI)\\\u003C18.5 kg\u002Fm2.\n* No systemic nutritional therapy, psychiatric medication or any form of psychotherapy have been received within 1 month before enrollment.\n* Able to understand the nature of this study and sign an informed consent form.\n\nExclusion Criteria:\n\n* Diagnosed with a DSM-5 disease other than anorexia nervosa, or at high risk of suicide, strong impulsive behavior as well as anti-social behavior.\n* With severe physical or cognitive impairment.\n* Not able to undergo MRI.\n* Considered unsuitable for enrollment in this clinical trial for other reasons.","35 Years",{"count":234,"type":21},110,[24],"The goal of this clinical trial is to learn if dTMS targeting the ACC can be used to rapidly and effectively treat AN. A randomized controlled study design is adopted, in which patients with AN are divided into the CBT+dTMS treatment group and CBT+pseudostimulation group by 1:1 randomization, followed by a 6-week intervention and a half-year follow-up to clarify whether CBT combined with dTMS is superior to single CBT treatment for AN.",[30],[100,239,240],"Deep transcranial magnetic stimulation","anterior cingulate cortex","2025-05-06",{"date":243,"type":41},"2025-05-11",{"date":245,"type":21},"2025-04-30",{"date":247,"type":21},"2028-12-31",{"name":249,"class":48},"Shanghai Mental Health Center",{"id":251,"slug":252,"hasResults":11,"nctId":253,"briefTitle":254,"officialTitle":255,"acronym":256,"eligibilityCriteria":257,"healthyVolunteers":11,"sex":119,"minAge":258,"maxAge":259,"enrollmentInfo":260,"targetDuration":4,"studyType":22,"phases":262,"briefSummary":263,"conditions":264,"keywords":267,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":270,"lastUpdatePostDateStruct":271,"startDateStruct":273,"completionDateStruct":275,"leadSponsor":277,"locationsCount":49},"100576959","evaluation-of-radically-open-dialectical-behavior-therapy-for-youth-at-risk-for-developing-severe-and-enduring-eating-disorders-100576959","NCT06792071","Evaluation of Radically Open Dialectical Behavior Therapy for Youth At Risk for Developing Severe and Enduring Eating Disorders","Feasibility and Efficacy of Radically Open Dialectical Behavior Therapy for Youth At Risk for Developing Severe and Enduring Eating Disorders","RO-SEED","Inclusion Criteria:\n\n* Being 14-19 years old\n* Primarily restrictive eating disorder symptoms that remain despite at least one previous treatment attempt.\n* Problems related to maladaptive overcontrol\n* Written informed consent (for minors, this includes consent from all caregivers and the minors themselves).\n\nExclusion criteria:\n\n* Eating disorders symptoms in need of emergency care\n* High risk for suicide\n* An inability to respond to the questionnaires or participate in the skills class, e.g., due to lack of knowledge in Swedish.","14 Years","19 Years",{"count":261,"type":21},18,[24],"The goal of this experimental interventional study is to learn if the psychological treatment Radically Open Dialectical Behavior Therapy (RO-DBT), is feasible to conduct and provide positive effects for adolescents with eating disorders and emotional overcontrol. Participants will be those at risk for developing severe and enduring eating disorder symptoms, as they have not responded fully to previous treatment attempts.\n\nPrimary outcomes are feasibility and changes in eating disorder symptoms. Secondary outcomes are changes in unhelpful behaviors and experiences related to emotional overcontrol; including psychological inflexibility, suppression of emotions, and experience of loneliness.\n\nThe participants will undergo the treatment with RO-DBT, which include an approximately 22 week long treatment consisting of individual psychotherapy and parallel skills training in group.",[265,125,266,30],"Eating Disorders","Anorexia Nervosa, Atypical",[125,129,268,269],"Radically open dialectical behavior therapy","Single-case experimental design study","2025-01-19",{"date":272,"type":41},"2025-01-24",{"date":274,"type":21},"2025-02",{"date":276,"type":21},"2027-07",{"name":278,"class":48},"Uppsala University Hospital",{"id":280,"slug":281,"hasResults":11,"nctId":282,"briefTitle":283,"officialTitle":283,"acronym":284,"eligibilityCriteria":285,"healthyVolunteers":11,"sex":119,"minAge":4,"maxAge":286,"enrollmentInfo":287,"targetDuration":4,"studyType":22,"phases":288,"briefSummary":289,"conditions":290,"keywords":291,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":297,"lastUpdatePostDateStruct":298,"startDateStruct":300,"completionDateStruct":302,"leadSponsor":304,"locationsCount":49},"100520503","improving-gastrointestinal-function-in-high-risk-newborns-by-stimulation-of-the-enteric-nervous-system-100520503","NCT06057415","Improving Gastrointestinal Function In High-Risk Newborns By Stimulation Of The Enteric Nervous System","NeoHemoHapt","Inclusion Criteria:\n\n1. Preterm birth at gestational age \\\u003C 30 weeks or\n2. Diagnosis of Congenital Diaphragmatic Hernia\n3. Born at Amalia Children's Hospital or admitted 1rst day of life\n4. Written informed consent of both parents or representatives\n\nExclusion Criteria:\n\n1. Preterm infant born at gestational age ≥ 30 weeks\n2. Perinatal Asphyxia; (Apgar score at 5' \\\u003C 5 and first pH ≤ 7,0)\n3. Major congenital anomalies or birth defects other than congenital diaphragmatic hernia;\n4. Metabolic disease that necessitates a special diet other than human milk or formula feeding and or has a prognosis of impaired neurological development\n5. Parental refusal of participation","2 Days",{"count":183,"type":21},[24],"The goal of this therapeutical intervention trial is to investigate whether tactile-kinesthaetic and oral sensorimotor stimulation can improve gastrointestional function in preterm infants born before gestational age of 30 weeks and newborns with congenital diaphragmatic hernia. The main question it aims to answer is:\n\n• To determine whether HAPTOS- intervention (Handling Adapted to Postnatal age with Tactile-kinaesthetic and Oral sensorimotor Stimulation) in the particpants results in earlier attainment (postnatal days) of full enteral feeding and\u002For full oral feeding (post menstrual age) compared to standard care. Researchers will compare an intervention group receiving standard of care plus HAPTOS intervention to a group of patients receiving only current standard of care.",[30],[292,293,294,295,296],"preterm infants","high-risk newborns","congenital diaphragmatic hernia","autonomous nervous system","tactile stimulation","2024-08-23",{"date":299,"type":41},"2024-08-27",{"date":301,"type":41},"2024-06-10",{"date":303,"type":21},"2028-05-31",{"name":305,"class":48},"Radboud University Medical Center",{"id":307,"slug":308,"hasResults":11,"nctId":309,"briefTitle":310,"officialTitle":310,"acronym":311,"eligibilityCriteria":312,"healthyVolunteers":11,"sex":119,"minAge":313,"maxAge":314,"enrollmentInfo":315,"targetDuration":4,"studyType":92,"phases":4,"briefSummary":317,"conditions":318,"keywords":319,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":325,"lastUpdatePostDateStruct":326,"startDateStruct":328,"completionDateStruct":330,"leadSponsor":332,"locationsCount":49},"100555620","italian-validation-of-the-state-urge-to-be-physically-active--questionnaire-supaq-i-in-patients-with-eating-disorders-100555620","NCT06514456","Italian Validation of the State Urge to be Physically Active- Questionnaire (SUPAQ-I) in Patients With Eating Disorders","SUPAQ-I","Inclusion criteria:\n\n* age between 16 and 65 years old;\n* diagnosis of ED as per DSM 5 or DSM-5 TR\n* BMI\\* range between 13 and 30 kg\u002Fm2 (depending on ED main diagnosis)\n* for the pediatric population BMI SDS\\*\\* range is set between -3 and +3 SD from expected BMI for age and sex\n\nExclusion criteria:\n\n* presence of other pathologies not associated with ED (i.e., neurodegenerative diseases);\n* severe psychopathologies other than ED (i.e., schizophrenia)\n\n  * BMI will be calculated using the following formula: weight (kg)\u002Fheight (m2) \\*\\*For the pediatric population, BMI SDS will also be calculated to adjust BMI according to growth curve charts for children and adolescents belonging to the Italian population","16 Years","65 Years",{"count":316,"type":21},210,"Eating disorders (EDs) are severe psychiatric conditions that cause significant health and psychosocial issues, with Anorexia Nervosa (AN) and Bulimia Nervosa (BN) having the highest mortality rates. The COVID-19 pandemic has led to an increase in ED cases, especially among children, with heightened restrictive eating and compulsive exercise. Up to 80% of individuals with AN engage in compulsive exercise, which current treatments fail to adequately address.\n\nThe State Urge to be Physically Active Questionnaire (SUPA-Q) is the only validated tool for assessing activity urges in ED patients, covering cognitive, emotional, and behavioral aspects. This study aims to develop and validate an Italian version of the SUPA-Q (SUPAQ-I) in a clinical sample of ED patients.\n\nA mixed-longitudinal study design will be used, with assessments at admission (T0) and discharge (T1) to evaluate the SUPAQ-I's reliability, validity, and sensitivity to change. The sample will include patients aged 16-65 diagnosed with EDs undergoing inpatient rehabilitation. Statistical analyses will include exploratory and confirmatory factor analyses, and internal consistency will be measured using Cronbach's α and McDonald's Ω indices.\n\nValidating the SUPAQ-I will improve the assessment of activity urges in ED patients, enhancing treatment strategies and outcomes.",[30],[265,320,125,63,321,322,323,324],"State Urge to be Physically Active","Binge Eating Disorder","Questionnaire Language Validation","Urge to move","Physical activity","2024-07-16",{"date":327,"type":41},"2024-07-23",{"date":329,"type":41},"2024-05-07",{"date":331,"type":21},"2026-04-15",{"name":111,"class":48}]