[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"body-image-disturbance\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:body-image-disturbance":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,50,85,113,151,180,207],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100632774","relationships-between-nomophobia-levels-and-perceived-stress-body-image-and-food-addiction-among-university-students-100632774",false,"NCT07518056","Relationships Between Nomophobia Levels and Perceived Stress, Body Image and Food Addiction Among University Students","An Investigation of the Relationships Between Nomophobia Levels and Stress, Body Image and Food Addiction Among University Students","Inclusion Criteria:\n\n* Being an active smartphone user\n* Reading and providing consent via the Informed Consent Form\n* Absence of conditions such as pacemaker implantation, metallic prostheses in the body, or pregnancy\n* Not having a diagnosed metabolic disorder (e.g., Cushing's syndrome, diabetes, thyroid disorders) or any acute\u002Fchronic psychiatric condition that may affect eating behavior\n\nExclusion Criteria:\n\n* Individuals with a current diagnosis of an eating disorder (e.g., anorexia nervosa, bulimia nervosa, binge eating disorder, etc.)\n* Individuals with a psychiatric diagnosis of severe depression, bipolar disorder, psychotic disorder, or an anxiety disorder requiring treatment\n* Individuals who regularly use psychiatric medications (e.g., SSRIs, SNRIs, antipsychotics, mood stabilizers, etc.)\n* Individuals who have used corticosteroids or similar hormone-regulating medications in the past 3 months\n* Pregnant or breastfeeding individuals\n* Participants who did not complete the questionnaires or the measurement procedures","ALL","18 Years","30 Years",{"count":20,"type":21},150,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to examine the effects of nomophobia levels on stress, food addiction, and body image among undergraduate students aged 18-30 at Bahçeşehir University, Faculty of Health Sciences. The primary questions it aims to answer are:\n\n* Is there a statistically significant relationship between nomophobia levels and perceived stress, food addiction, and body image among university students?\n* Is there a correlation between objective anthropometric data (body fat percentage, skeletal muscle mass) measured via Bioelectrical Impedance Analysis (BIA), waist\u002Fhip circumference measurements, and the individual's perceived body image?",[25,26,27,28,29,30,31],"Nomofobia","Body Image Disturbance","Body Image","Body Image Disorder","Eating Behavior Disorders","Food Addiction","Stress",[33,34,35,36],"nomophobia","stress","body image","food addiction","RECRUITING","2026-04-15",{"date":40,"type":41},"2026-04-17","ACTUAL",{"date":43,"type":41},"2026-02-10",{"date":45,"type":21},"2026-05-01",{"name":47,"class":48},"Bahçeşehir University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":69,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":49},"100628778","lifestyle-intervention-for-obesity-and-eating-disorder-prevention-in-transgender-adolescents-100628778","NCT07466069","Lifestyle Intervention for Obesity and Eating Disorder Prevention in Transgender Adolescents","Lifestyle Intervention to Prevent Obesity and Eating Disorders in Transgender and Gender-Diverse Adolescents: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 10-14 years\n* Self-identified as transgender or gender-diverse\n\nExclusion Criteria:\n\n* Current diagnosis of eating disorder requiring specialized treatment\n* Severe psychiatric instability\n* Cognitive impairment limiting participation","10 Years","14 Years",{"count":60,"type":21},24,"INTERVENTIONAL",[63],"NA","Transgender and gender-diverse adolescents are at increased risk for obesity, disordered eating behaviors, body dissatisfaction, and reduced quality of life due to minority stress and structural inequities. However, no structured lifestyle interventions specifically tailored to this population have been developed.\n\nThis randomized controlled trial aims to evaluate the effectiveness of a 6-month interdisciplinary lifestyle intervention designed to prevent obesity and eating disorders in transgender and gender-diverse adolescents aged 10-14 years. Participants will be randomized (1:1) to either an intervention group receiving monthly group sessions (for adolescents and caregivers separately) and weekly supportive messages, or a control group receiving standard outpatient care and general health recommendations.\n\nThe primary outcome is quality of life measured by the WHOQOL-BREF. Secondary outcomes include eating disorder symptoms, body image, diet quality, physical activity levels, sedentary behavior, body composition, and anthropometric measures.",[66,67,26,68],"Obesity & Overweight","Eating Disorders","Gender Diverse Populations",[70,71,72,73,74,75],"Transgender","Adolescent","Gender-diverse","Lifestyle","Eating disorders","Obesity","2026-03-06",{"date":78,"type":41},"2026-03-12",{"date":80,"type":21},"2026-03",{"date":82,"type":21},"2026-12",{"name":84,"class":48},"University of Sao Paulo",{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":92,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":93,"targetDuration":4,"studyType":61,"phases":95,"briefSummary":96,"conditions":97,"keywords":99,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":49},"100606708","acceptability-and-feasibility-of-a-single-session-online-parent-focused-intervention-targeting-child-body-image-development-100606708","NCT07179068","Acceptability and Feasibility of a Single-Session Online Parent-Focused Intervention Targeting Child Body Image Development","Protocol for a Pilot Randomized Trial Assessing the Acceptability, Feasibility, and Initial Efficacy of a Single-session Online Parent-focused Intervention Targeting Predictors of Body Image Disturbance in Young Children","Inclusion Criteria: Must be at least 18 years old and reside in the US. They must also be the parent of a young child between the ages of 2-6.\n\nExclusion Criteria: None beyond not meeting inclusion criteria.",true,{"count":94,"type":21},100,[63],"Body image concerns have been linked to diverse mental health issues, including depression and disordered eating. Disordered eating can develop into clinically significant eating disorders, which are associated with serious negative impacts on psychological and physical well-being, and can adversely impact developmental trajectories in children and adolescents. Given limitations in the eating disorder intervention literature, it is important to invest in effective eating disorder prevention programs. Evidence suggests that children can recognize the existence of societal appearance ideals as early as age 3; thus, this study examines the acceptability and feasibility of a single-session, online, parent-focused intervention targeting predictors of body image disturbance in young children.",[67,26,98],"Weight Bias",[100,101,102,27,103],"Eating Disorder Prevention","Restriction","Loss of Control Eating","Single Session Intervention","2025-12-11",{"date":106,"type":41},"2025-12-18",{"date":108,"type":41},"2025-11-01",{"date":110,"type":21},"2026-01",{"name":112,"class":48},"University at Albany",{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":118,"acronym":119,"eligibilityCriteria":120,"healthyVolunteers":11,"sex":121,"minAge":17,"maxAge":4,"enrollmentInfo":122,"targetDuration":4,"studyType":61,"phases":124,"briefSummary":125,"conditions":126,"keywords":130,"overallStatus":141,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":49},"100609689","testing-shape-a-single-session-intervention-targeting-binge-eating-in-women-through-assessment-and-values-based-strategies-100609689","NCT07217847","Testing SHAPE: A Single-Session Intervention Targeting Binge Eating in Women Through Assessment and Values-Based Strategies","Testing a Single-session Consultation for Reducing Binge Eating","SHAPE","Inclusion Criteria:\n\n* ≥ 18 years old\n* Identify as cisgender female\n* self-reported BMI ≥ 18.5 kg\u002Fm²\n* Rate the extent to which their weight or shape influences how they feel about themselves as a \"4\" or higher on a 7-point Likert scale on screening measures\n* ≥1 binge eating episode every 2 weeks (i.e., ≥ six episodes over 3 months) at the time of screening\n\nExclusion Criteria:\n\n* \\\u003C 18 years old\n* Assigned male at birth\n* Gender identity different from biological sex indicated on birth certificate\n* Purging behaviors (i.e., self-induced vomiting, laxative misuse, or diuretic misuse) ≥ 1x\u002Fweek in the last 3 months at the time of screening.\n* Engaged in structured psychological therapy or counseling (defined as attending sessions \\> 1x\u002Fmonth in the past 3 months)\n* Prior participation in studies that include administration of the EDE interview at Ohio University (IRB-FY24-403, IRB-FY25-330, and IRB-21-F-14).","FEMALE",{"count":123,"type":21},56,[63],"The goal of this controlled trial is to learn whether a brief single-session intervention (SSI) can reduce binge eating symptoms by targeting overvaluation of weight\u002Fshape in women with recurrent binge eating.\n\nThe main questions it aims to answer are:\n\n* Does assessment alone reduce binge eating severity and overvaluation of weight\u002Fshape compared to a control group undergoing minimal assessment?\n* Does adding a values-based reflection and goal-setting component (the full SHAPE intervention) add benefits beyond the assessment alone?\n\nResearchers will compare three groups:\n\n1. assessment-only,\n2. full SHAPE intervention, and\n3. minimal assessment control to see if both active conditions outperform the control, and whether the full intervention adds any benefits beyond the assessment itself\n\nParticipants will:\n\n* Complete a semi-structured eating disorder assessment (Eating Disorder Examination)\n* Depending on assignment, also complete a values-based reflection and goal-setting exercise with psychoeducation\n* Complete follow-up assessments evaluating binge eating severity, overvaluation of weight\u002Fshape, clinical impairment, binge frequency, and related outcomes.",[127,128,129,27,26],"Binge Eating","Binge Eating Behaviour","Binge Eating\u002FLoss of Control Eating",[131,132,133,134,135,136,35,137,138,139,140],"single session","single-session consultation","single-session intervention","binge eating","disordered eating","binge-spectrum disorder","body image concerns","weight\u002Fshape concerns","overvaluation","loss of control eating","NOT_YET_RECRUITING","2025-10-14",{"date":144,"type":41},"2025-10-20",{"date":146,"type":21},"2025-10",{"date":148,"type":21},"2027-05",{"name":150,"class":48},"Taylor Rezeppa",{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":155,"acronym":4,"eligibilityCriteria":156,"healthyVolunteers":11,"sex":121,"minAge":157,"maxAge":158,"enrollmentInfo":159,"targetDuration":4,"studyType":61,"phases":161,"briefSummary":162,"conditions":163,"keywords":166,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":171,"lastUpdatePostDateStruct":172,"startDateStruct":174,"completionDateStruct":176,"leadSponsor":178,"locationsCount":49},"100541676","interoceptive-mechanisms-of-body-image-disturbance-in-anorexia-nervosa-100541676","NCT06332963","Interoceptive Mechanisms of Body Image Disturbance in Anorexia Nervosa","Inclusion Criteria:\n\n1. Primary diagnosis of anorexia nervosa\n2. Photographic Figure Rating Scale (PFRS) body dissatisfaction score greater than or equal to 1\n3. Eating Disorder Examination Questionnaire (EDE-Q6) Shape Concern Subscale score greater than or equal to 3\n4. Weight restored to body mass index (BMI) greater than or equal to 17.5\n5. No current evidence of orthostatic hypotension or if there is no evidence of additional fall risk as determined by their provider\n6. Clinical status transition from acute to residential status\n7. No new psychiatric medications in the week prior to randomization\n8. Female sex assigned at birth\n9. Ages 13 to 50 years\n10. Independently ambulatory\n11. Ability to lay flat comfortably\n12. English proficiency\n13. Willingness and ability to participate in study procedures\n14. Provision of informed consent (parent consent and minor assent if less than 18 years of age).\n\nExclusion Criteria:\n\n1. Active suicidal ideation with plan and intent\n2. Active cutting or skin lacerating behaviors\n3. Pregnancy as defined by urine screening\n4. Acute intoxication as indicated by urine drug screen or breathalyzer\n5. Orthostatic hypotension as determined by medical provider, evidenced in chart (defined as a drop of ≥ 20 mmHg in systolic blood pressure (BP) or a drop of ≥ 10 mm Hg in diastolic blood pressure (BP) when measured shortly after transitioning from lying down to standing). If evidence of orthostasis is present in chart consultation with provider to determine if status creates additional fall risk. If participant is determined to be at increased fall risk (e.g., dizziness upon standing) they will be excluded.\n6. Seizure reported within the previous 12 months\n7. Co-morbid diagnoses of Diagnostic and Statistical Manual of Mental Disorders, 5th ed. (DSM-5) bipolar disorder, schizophrenia, or other psychosis spectrum disorder\n8. Systolic blood pressure \\> 160 mmHg\n9. Diastolic blood pressure \\>100 mmHg\n10. Resting heart rate \\<50 beats per minute.","13 Years","50 Years",{"count":160,"type":21},102,[63],"The proposed study utilizes a randomized experimental therapeutics design to test a mechanistic framework linking interoceptive processing and disturbed body image, with the purpose of informing the development of future therapies for body image dissatisfaction in anorexia nervosa (AN). A sample of 102 participants will be recruited from the Laureate Eating Disorder Program (LEDP). After being randomized, participants will all receive a one-hour session of acceptance- and mindfulness-based training with a therapist (the introduction session). They will then receive either the interoceptively focused treatment (IFT) or exteroceptively focused treatment (EFT) condition based on randomization. In the IFT condition participants will engage in floatation-REST (Reduced Environmental Stimulation Therapy) while practicing acceptance and mindfulness-based principles. The EFT condition is an exteroceptive intervention in which participants will be asked to view pre-recorded videos of acceptance and mindfulness-based skills to aid in the practice of these skills. Each condition will consist of one introduction session and three experimental sessions. All participants will then return for follow-up measures. Assessed outcomes will include acute changes in body image disturbance (BID) and interoception. Further, longitudinal intervention effects on self-reported eating disorder symptoms, body image dissatisfaction, and interoception; behavioral measures of interoception and body image dissatisfaction; and resting state and interoceptive functioning during functional magnetic resonance imaging (fMRI) will be explored.",[164,26,165],"Anorexia Nervosa","Interoception",[164,26,167,165,168,169,170],"Perceptual Body Image","Acceptance Based Intervention","Mindfulness Based Intervention","Randomized Clinical Trial","2025-09-25",{"date":173,"type":41},"2025-09-26",{"date":175,"type":41},"2024-04-19",{"date":177,"type":21},"2028-12",{"name":179,"class":48},"Laureate Institute for Brain Research, Inc.",{"id":181,"slug":182,"hasResults":11,"nctId":183,"briefTitle":184,"officialTitle":185,"acronym":186,"eligibilityCriteria":187,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":188,"targetDuration":4,"studyType":61,"phases":190,"briefSummary":191,"conditions":192,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":197,"lastUpdatePostDateStruct":198,"startDateStruct":200,"completionDateStruct":202,"leadSponsor":204,"locationsCount":206},"100473289","building-a-renewed-image-after-head--neck-cancer-treatment-bright-multi-site-rct-100473289","NCT05442957","Building a Renewed ImaGe After Head & Neck Cancer Treatment (BRIGHT) Multi-Site RCT","A Multi-Site, Parallel-Group, Randomized Clinical Trial Comparing a Brief Tele-Cognitive Behavioral Therapy Intervention (BRIGHT) With Attention Control for the Reduction of Body Image-Related Distress Among Head and Neck Cancer Survivors","BRIGHT","Inclusion Criteria:\n\n1. Age \\> 18 years on the day of informed consent\n2. History of pathologically confirmed squamous cell carcinoma (or histologic variant) of the oral cavity, pharynx, larynx, nose\u002Fparanasal sinuses, carcinoma of a major or minor salivary gland, or cutaneous malignancy of the face or neck\n3. History of curative intent surgery with or without adjuvant therapy, with or without reconstruction\n4. Completion of oncologic treatment within 12 months of study enrollment (but no sooner than 6 weeks post-treatment completion)\n\n   1. Patients who complete definitive HNC-directed therapy (e.g., surgery or radiation therapy) but are on adjuvant immunotherapy are considered eligible\n   2. Oncologic treatment refers to cancer-directed therapy; non-cancer surgery (e.g., trachea-esophageal puncture, flap debulking, etc) are not relevant for the purposes of determining eligibility vis a vis completing oncologic treatment within 6-week to 12 months of enrollment\n5. Cancer-free at the time of accrual\n\n   -patients with known indolent malignancies (e.g., non-melanoma skin cancer, low risk thyroid cancer, untreated prostate cancer, etc) would not exclude a patient from the study\n6. No planned significant HNC ablative or reconstructive surgery (defined by a postoperative inpatient stay of at least three days) during the study intervention or follow-up period as determined by the HNC oncologic surgeon at the time of study accrual\n7. Willingness to be randomized to either BRIGHT or AC\n8. IMAGE-HN score ≥ 22\n\nExclusion Criteria:\n\n1. Inability to speak or read English\n2. Pre-existing, ongoing psychotherapy services for any disorder and the participant is not willing to discontinue the prior therapy for the duration of the proposed trial\n3. Severe mental illness that would prevent trial participation",{"count":189,"type":21},180,[63],"In this multi-center randomized clinical trial, head and neck cancer (HNC) survivors with clinically significant body image distress (BID) (N=180) will be randomized to BRIGHT (a brief video tele-cognitive behavioral therapy intervention) or Attention Control (AC, a manualized tele-supportive care intervention that controls for professional attention, dose, delivery method, and common factors). HNC survivors will complete IMAGE-HN (a validated patient-reported outcome measure \\[PROM\\] of HNC-related body image distress \\[BID\\]; primary endpoint), measures of psychological and social well-being and quality of life (QOL), and measures of theory-derived mechanisms of change underlying BRIGHT (mediators).",[193,26,27,194,195,196],"Head and Neck Cancer","Survivorship","Psychosocial Impairment","Mental Health Issue","2025-09-18",{"date":199,"type":41},"2025-09-24",{"date":201,"type":41},"2023-02-14",{"date":203,"type":21},"2027-03-30",{"name":205,"class":48},"Medical University of South Carolina",5,{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":212,"acronym":213,"eligibilityCriteria":214,"healthyVolunteers":11,"sex":16,"minAge":157,"maxAge":215,"enrollmentInfo":216,"targetDuration":4,"studyType":61,"phases":218,"briefSummary":220,"conditions":221,"keywords":223,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":230,"lastUpdatePostDateStruct":231,"startDateStruct":233,"completionDateStruct":235,"leadSponsor":237,"locationsCount":49},"100600208","phase-2-adolescent-chatbot-100600208","NCT07094503","Adolescent Chatbot","Improving Access to Services, Preventing Eating Disorders, and Addressing Comorbid Depression and Anxiety in Diverse Adolescents","EMBody","Inclusion Criteria\n\n1. 13 - 17 years old\n2. Owns a smartphone\n3. Speaks English\n4. US resident\n5. Screens as at-risk for an eating disorder\n6. Not currently in treatment for an eating disorder\n\nExclusion Criteria:\n\n1. Below 13 or older than 17 years of age\n2. Does not own a smartphone\n3. Does not speak English\n4. Lives outside the US\n5. Screens as:\n\n   1. Having a subclinical or clinical ED\n   2. Not at risk for an ED\n   3. In treatment for an ED","17 Years",{"count":217,"type":21},400,[219],"PHASE2","The purpose of this study is to test an eating disorders prevention digital chatbot program in a diverse group of adolescents.",[26,222,100],"Disordered Eating Behaviors",[224,222,225,226,227,27,26,228,229],"Adolescents","Eating Disorder Symptoms","Eating Pathology","Eating disorder Prevention","Digital Mental Health","Chatbot","2025-07-29",{"date":232,"type":41},"2025-07-31",{"date":234,"type":41},"2024-06-18",{"date":236,"type":21},"2026-05-30",{"name":238,"class":48},"Washington University School of Medicine"]