[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"body-image\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:body-image":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,24,0,[8,54,86,118,145,165,194,221,251,279,311,338,379,405,427,463,490,517,550,592,616,647,667,701],{"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":33,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100645213","overvaluation-of-weight-and-shape-intervention-vs-the-body-project-100645213",false,"NCT07678554","Overvaluation of Weight and Shape Intervention vs The Body Project","Pilot Testing Overvaluation of Weight and Shape Intervention vs The Body Project","Inclusion Criteria:\n\n* Female-identifying\n* High School\n* College Adolescents\n* Ages 14-22\n\nExclusion Criteria:\n\n* Non-female identifying\n* Outside of the United States",true,"FEMALE","14 Years","22 Years",{"count":21,"type":22},90,"ESTIMATED","INTERVENTIONAL",[25],"NA","Priorities aims to reduce body image concerns, prevent eating disorders, bolster self-esteem, and promote mental and emotional health by helping participants identify and nurture alternative sources of self-worth. Priorities would use group discussions, role-plays \\& behavioral challenges, homework assignments \\& letter-writing, and self-worth activism to achieve this. The Priorities intervention will be compared to The Body Project (an existing and successful harm reduction and eating disorder prevention program) for its effectiveness of reducing body image concerns and eating disorder outcomes. This study aims to evaluate whether there is a more effective eating disorder prevention program than The Body Project.",[28,29,30,31,32],"Body Image","Mental Health Outcomes","Eating Disorders","Body Dysmorphic Disorders","Self-esteem",[34,35,36,37,38,39,40,41],"Eating disorder","Female","Body project","Priorities","self-esteem","adolescent mental health","Body dysmorphia","Disordered eating","NOT_YET_RECRUITING","2026-06-28",{"date":45,"type":46},"2026-07-01","ACTUAL",{"date":45,"type":22},{"date":49,"type":22},"2027-06-01",{"name":51,"class":52},"Stanford University","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":23,"phases":66,"briefSummary":67,"conditions":68,"keywords":72,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":53},"100643847","3d-reconstruction-vr-and-machine-learning-in-body-image-in-bariatrics-100643847","NCT07668492","3D Reconstruction, VR and Machine Learning in Body Image in Bariatrics","The Use of 3D Reconstruction, Virtual Reality, and Machine Learning in Addressing Body Image in Bariatric Metabolic Surgery.","Inclusion Criteria:\n\n* Tier 4 bariatric group\n* On waiting list for bariatric metabolic surgery\n* Able to stand unaided for at least 5 minutes\n\nExclusion Criteria:\n\n* Anyone who cannot provide informed consent\n* Anyone who is involved in current research or has recently been involved in any research prior to recruitment.","ALL","18 Years","75 Years",{"count":65,"type":22},80,[25],"Studies have shown that following bariatric metabolic surgery (BMS), patients continue to experience dissatisfaction with their new body image and identity). The reason for this is poorly understood but negative body image perception after surgery is linked to poor psychological and clinical outcomes. Our pilot study looking at the acceptability and feasibility of 3D reconstruction and virtual reality (VR) in addressing body image in BMS found that participants felt better informed about how their body will change following significant weight loss and agreed this novel intervention would be beneficial in helping patients adjust to changes in their body after BMS.\n\nThe investigators propose a randomised control trial comparing group body image counselling and group body image counselling with 3D reconstruction and VR in addressing body image in BMS. The study aims to enrol 80 participants from the Tier 4 bariatric group at St Mary's Hospital and Chelsea \\& Westminster Hospital. After consent, participants will be divided into two groups: the control group will receive traditional group body image counselling, and the intervention group will receive the same counselling supplemented with VR and 3D reconstructed images depicting 15% and 25% total less body weight. Both groups will undergo four sessions over six months.\n\nThe investigators will collect data including body measurements and 3D images of the participant in their underwear using a secure password protected device at baseline and follow participants at 3, 6, 9, 12, 18, 24, and 36 months post-BMS. Patient reported outcomes will be assessed through patient-reported questionnaires.\n\nThis trial seeks to determine if integrating 3D reconstruction and VR technology into body image counselling can provide better support for patients adjusting to body image changes post-BMS, potentially leading to improved psychological and clinical outcomes.",[69,28,70,71],"Obesity (Disorder)","Mental Health","Bariatric Surgery",[73,74,28,75,76],"3D Reconstruction","Virtual Reality","Machine Learning","Bariatric Metabolic Surgery","2026-06-19",{"date":79,"type":46},"2026-06-25",{"date":81,"type":22},"2026-06",{"date":83,"type":22},"2030-03",{"name":85,"class":52},"Imperial College London",{"id":87,"slug":88,"hasResults":11,"nctId":89,"briefTitle":90,"officialTitle":91,"acronym":4,"eligibilityCriteria":92,"healthyVolunteers":16,"sex":61,"minAge":93,"maxAge":62,"enrollmentInfo":94,"targetDuration":4,"studyType":23,"phases":96,"briefSummary":97,"conditions":98,"keywords":104,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":53},"100641968","the-effects-of-game-based-exercise-programs-100641968","NCT07660822","THE EFFECTS OF GAME-BASED EXERCISE PROGRAMS","THE EFFECTS OF VIRTUAL REALITY AND VIDEO GAME-BASED EXERCISE PROGRAMS ON PHYSICAL FITNESS AND ATTENTION LEVELS IN HEALTHY ADOLESCENTS","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* Being an adolescent aged 10-18 years\n* Having a score below 4 on the Physical Activity Scale for Adolescents\n\nExclusion Criteria:\n\n* Having any physical disability that would prevent participation in the exercise program\n* Having upper or lower extremity orthopedic disease\n* Having a score above 4 on the Physical Activity Scale for Adolescents","10 Years",{"count":95,"type":22},48,[25],"Studies comparing aerobic exercise with virtual reality or video game technologies to traditional games and classical exercise have been conducted in healthy adolescents, but no studies comparing virtual reality and video game technologies have been found. Based on all this, we aimed to investigate the effect of virtual reality and video game-based exercise programs on physical fitness and attention levels in healthy adolescents. The study was planned as a quantitative experimental randomized controlled trial. Healthy individuals aged 10-18 years who meet the inclusion criteria will be evaluated during the dates of the study. Individuals will be divided into 3 groups: a classical physical activity group, a virtual reality group, and a video-based game group. Each program will be implemented for 20-30 minutes, three days a week for eight weeks. The Physical Activity Scale for Adolescents was used to evaluate the physical activity of the individuals, the Multidimensional Body-Self Relationship Scale was used to measure body image, and the Exercise Benefit\u002FBarrier Scale was used to measure exercise perception. To measure attention, balance, and reaction time, the D2 Attention Test, Y-Balance Test, and Nelson's Hand Reaction Test will be administered, respectively. In the virtual reality and video-based game group, the games played by participants will be similar to the physical activities performed in the classic exercise group. One or more games incorporating these physical activities will be selected.",[99,28,100,101,102,103],"Physical Activity","Exercise Perception","Balance","Reaction Time","Attention",[105,106,107],"Healthy adolescent","virtual reality","attention level)","RECRUITING","2026-06-16",{"date":111,"type":46},"2026-06-22",{"date":113,"type":46},"2025-11-15",{"date":115,"type":22},"2026-08-30",{"name":117,"class":52},"Gaziantep Islam Science and Technology University",{"id":119,"slug":120,"hasResults":11,"nctId":121,"briefTitle":122,"officialTitle":123,"acronym":4,"eligibilityCriteria":124,"healthyVolunteers":11,"sex":61,"minAge":125,"maxAge":126,"enrollmentInfo":127,"targetDuration":4,"studyType":23,"phases":129,"briefSummary":130,"conditions":131,"keywords":132,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":141,"leadSponsor":143,"locationsCount":53},"100643268","a-study-testing-a-digital-gamified-early-intervention-for-eating-disorders-flexed-100643268","NCT07632248","A Study Testing a Digital, Gamified Early Intervention for Eating Disorders (\"FlexED\")","A Randomized Controlled Trial Testing Mechanism Engagement and Clinical Impact of FlexED: A Digital, Gamified Early Intervention for Eating Disorders","Inclusion Criteria:\n\n* Female between the age of 15-25 years old.\n* Weight Concerns Scale score of \\>=47.\n* Endorses one or more eating disorder behaviors (e.g., extreme dieting or exercise, subjective or objective binge eating, purging behaviors).\n\nExclusion Criteria:\n\n* Currently meets the DSM-5 diagnostic criteria for full threshold anorexia nervosa, bulimia nervosa or binge eating disorder, or for an eating or feeding disorder that does not include body-image or weight related distress and is not the focus of study (e.g., ARFID, PICA) or a past diagnosis of one of these disorders.\n* Change in psychotropic medications in the past month.\n* Active suicidal ideation, current substance use disorder or diagnosed psychotic disorder.\n* Bipolar disorder not being treated with medication.\n* Currently in treatment for an eating disorder.\n* Non-English speaking.","15 Years","25 Years",{"count":128,"type":22},128,[25],"The goal of this clinical trial is to test whether a new digital intervention decreases eating disorder symptoms in young women and girls at risk by changing how they experience thoughts and feelings about their body.\n\nThe digital intervention is based on Acceptance and Commitment Therapy (ACT). Participants will be randomly assigned (like a coin toss) to either the new digital intervention or education modules completed online.\n\nThe main questions are:\n\nDoes the digital intervention change how participants experience thoughts and feelings about their body or how they react to eating disorder triggers (e.g., images of idealized bodies)? Do these changes lead to decreases in eating disorder symptoms? Is the intervention acceptable and at the right dose?\n\nParticipants will:\n\nComplete seven brief digital sessions over about 8 weeks. Complete interviews, surveys and lab assessments of reaction to body-related words and images.\n\nParticipants are followed for about 1 year.",[30,28],[30,133,134,135,136],"Body Image Flexibility","Acceptance and Commitment Therapy","Psychological Flexibility","Early Intervention","2026-06-01",{"date":139,"type":46},"2026-06-08",{"date":137,"type":22},{"date":142,"type":22},"2028-07-31",{"name":144,"class":52},"Duke University",{"id":146,"slug":147,"hasResults":11,"nctId":148,"briefTitle":149,"officialTitle":149,"acronym":4,"eligibilityCriteria":150,"healthyVolunteers":16,"sex":61,"minAge":62,"maxAge":4,"enrollmentInfo":151,"targetDuration":4,"studyType":23,"phases":153,"briefSummary":154,"conditions":155,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":156,"lastUpdatePostDateStruct":157,"startDateStruct":159,"completionDateStruct":161,"leadSponsor":163,"locationsCount":53},"100640206","brief-single-session-body-neutrality-program-for-lgbtq-adults-in-central-alabama-100640206","NCT07621081","Brief Single-Session Body Neutrality Program for LGBTQ+ Adults in Central Alabama","Inclusion Criteria:\n\n* At least 18 years old,\n* Identify as LGBTQ+,\n* Currently living in one of the following AL counties: Lee, Dallas, Lowndes, Autauga, Coosa, Elmore, Tallapoosa, Macon, or Russell\n* Have internet access (either via computer\u002Ftablet, mobile phone, or community center \\[e.g., library\\])\n\nExclusion Criteria:\n\n* Being less than 18 years old,\n* Identifying as cisgender and heterosexual,\n* Not living in central AL,\n* Not having internet access.",{"count":152,"type":22},40,[25],"LGBTQ+ individuals tend to have elevated risks for eating disorders (ED), possibly due to minority stress. For LGBTQ+ individuals living in rural Alabama, they tend to experience high levels of anti-LGBTQ+ structural stigma and limited access to LGBTQ+-specific resources, which engender compounded risk for ED development and reduced access to care. Brief digital single-session intervention that incorporates psychoeducation about minority stress and body neutrality may be efficacious in reducing ED risk and improve positive body image among LGBTQ+ adults in rural areas. Prior research from another lab developed a single-session intervention (Project Body Neutrality) among LGBTQ+ adolescents indicated immediate positive changes in body image constructs and psychological well-being. The present project evaluates and adapts Project Body Neutrality, specifically for LGBTQ+ adults in a rural high-stigma, low-resource region.",[28],"2026-05-27",{"date":158,"type":46},"2026-06-02",{"date":160,"type":22},"2026-08-02",{"date":162,"type":22},"2028-08-02",{"name":164,"class":52},"Auburn University",{"id":166,"slug":167,"hasResults":11,"nctId":168,"briefTitle":169,"officialTitle":170,"acronym":4,"eligibilityCriteria":171,"healthyVolunteers":16,"sex":61,"minAge":172,"maxAge":173,"enrollmentInfo":174,"targetDuration":4,"studyType":23,"phases":176,"briefSummary":177,"conditions":178,"keywords":179,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":186,"lastUpdatePostDateStruct":187,"startDateStruct":189,"completionDateStruct":190,"leadSponsor":192,"locationsCount":53},"100639155","assessing-the-efficacy-of-a-song-to-improve-body-appreciation-among-young-children-100639155","NCT07586852","Assessing the Efficacy of a Song to Improve Body Appreciation Among Young Children","Assessing the Efficacy of a Song to Improve Body Appreciation Among Young Children: A Cluster Randomised Controlled Trial in UK Primary Schools","Inclusion Criteria:\n\n\\- Child in Reception or Year 1 at a recruited school.\n\nExclusion Criteria:\n\n* Parent\u002Fguardian opted out of the research.","4 Years","6 Years",{"count":175,"type":22},200,[25],"The goal of this randomised controlled trial has two aims: Do UK-based children ages 4 to 6 years understand a evidence-informed song with body confidence messaging without visual aids? and Does children's body appreciation improve after listening to the intervention song, relative to an active control? Children in primary school will be randomised to an intervention condition or active control condition at the individual level. Assessments will occur through one-on-one structured play-based questions assessing body appreciation, message comprehension, and intervention acceptability.",[28],[180,181,182,183,184,185],"body image","body appreciation","children","randomized controlled trial","song","intervention","2026-05-18",{"date":188,"type":46},"2026-05-20",{"date":111,"type":22},{"date":191,"type":22},"2026-09",{"name":193,"class":52},"University of the West of England",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":16,"sex":17,"minAge":201,"maxAge":202,"enrollmentInfo":203,"targetDuration":4,"studyType":23,"phases":205,"briefSummary":206,"conditions":207,"keywords":210,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":186,"lastUpdatePostDateStruct":214,"startDateStruct":216,"completionDateStruct":217,"leadSponsor":219,"locationsCount":4},"100619459","mbsr-effects-on-aging-anxiety-and-body-image-100619459","NCT07344896","MBSR Effects on Aging Anxiety and Body Image","Effects of a Mindfulness-Based Stress Reduction Program on Aging Anxiety and Body Image in Middle-Aged Women: A Randomized Controlled Trial","Inclusion Criteria:\n\n* At least primary school graduate,\n* Being between 40-59 years old,\n* Living in Çumra district center,\n* Being open to communication and cooperation\n\nExclusion Criteria:\n\n* Those with chronic illnesses (self-report)\n* Foreign nationals Those with psychiatric illnesses (self-report) Those with physical disabilities and limited mobility","40 Years","59 Years",{"count":204,"type":22},58,[25],"This study was designed to determine the effect of a mindfulness-based stress reduction (MBSR) program on aging anxiety and body image among middle-aged women. The primary hypotheses to be tested are as follows:\n\nH0a: There is no difference in the mean scores of the Aging Anxiety Scale between the women in the experimental group who receive the mindfulness-based stress reduction program and the women in the control group.\n\nH0b: There is no difference in the mean scores of the Body Image Scale between the women in the experimental group who receive the mindfulness-based stress reduction program and the women in the control group.\n\nH0c: There is no difference between the pre-intervention and post-intervention mean scores of the Aging Anxiety Scale among the women in the experimental group who receive the mindfulness-based stress reduction program.\n\nH0d: There is no difference between the pre-intervention and post-intervention mean scores of the Body Image Scale among the women in the experimental group who receive the mindfulness-based stress reduction program.\n\nThe researchers will compare the experimental group with the control group in order to assess the effect of the mindfulness-based stress reduction program on aging anxiety and body image among middle-aged women.\n\nParticipants:\n\n* They will attend an 8-session mindfulness-based stress reduction program.\n* They will participate in one silent mindfulness retreat session.",[28,208,209],"Mindfulness Based Stress Reduction","Middle Aged",[211,212,213,180],"aging anxiety","middle age woman","mindfulness",{"date":215,"type":46},"2026-05-19",{"date":137,"type":22},{"date":218,"type":22},"2027-05-30",{"name":220,"class":52},"KTO Karatay University",{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":226,"acronym":4,"eligibilityCriteria":227,"healthyVolunteers":16,"sex":17,"minAge":62,"maxAge":4,"enrollmentInfo":228,"targetDuration":4,"studyType":23,"phases":230,"briefSummary":231,"conditions":232,"keywords":237,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":243,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":249,"locationsCount":53},"100637653","prenatal-yoga-intervention-in-pregnant-women-100637653","NCT07585916","Prenatal Yoga Intervention in Pregnant Women","Effects of a Prenatal Yoga Intervention on Traumatic Childbirth Perception, Self-Perception, and Delivery Preferences in Pregnant Women","Inclusion Criteria:\n\n* Being at or beyond the 16th week of gestation (second trimester or later)\n* Being aged 18 years or older\n* Having no diagnosis of high-risk pregnancy based on obstetric evaluation\n* Having no medical restriction on physical activity or yoga practice as determined by a physician\n* Providing written informed consent after being informed about the study\n\nExclusion Criteria:\n\n* Diagnosis of high-risk pregnancy (e.g., preeclampsia, placenta previa, premature rupture of membranes, risk of preterm birth, or other serious obstetric complications)\n* Physician-imposed restriction on physical activity\n* Presence of serious systemic conditions that would prevent participation in yoga practice\n* Inability to complete the questionnaires reliably due to psychiatric or cognitive conditions\n* Declining to participate or not providing informed consent",{"count":229,"type":22},46,[25],"The aim of this study is to determine the effects of a prenatal yoga intervention on traumatic childbirth perception, self-perception, and delivery preferences in pregnant women.",[233,234,235,28,236],"Pregnant Women","Prenatal Yoga","Trauma","Delivery",[238,180,239,240,241],"perception of traumatic childbirth","preferred mode of delivery","pregnant women","prenatal yoga","2026-05-09",{"date":244,"type":46},"2026-05-14",{"date":246,"type":22},"2026-05-15",{"date":248,"type":22},"2026-12-30",{"name":250,"class":52},"Saglik Bilimleri Universitesi",{"id":252,"slug":253,"hasResults":11,"nctId":254,"briefTitle":255,"officialTitle":256,"acronym":4,"eligibilityCriteria":257,"healthyVolunteers":16,"sex":17,"minAge":62,"maxAge":4,"enrollmentInfo":258,"targetDuration":4,"studyType":23,"phases":260,"briefSummary":261,"conditions":262,"keywords":266,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":271,"lastUpdatePostDateStruct":272,"startDateStruct":274,"completionDateStruct":275,"leadSponsor":277,"locationsCount":53},"100637032","effects-of-mindful-eating-on-female-nutrition-students-100637032","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",{"count":259,"type":22},88,[25],"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",[70,28,263,264,265],"Feeding Behavior","Feeding and Eating Disorders","Stress and Anxiety",[267,268,269,270],"mindful eating","feeding behavior","Students","mental health","2026-05-06",{"date":273,"type":46},"2026-05-11",{"date":137,"type":22},{"date":276,"type":22},"2027-12-01",{"name":278,"class":52},"Federal University of Uberlandia",{"id":280,"slug":281,"hasResults":11,"nctId":282,"briefTitle":283,"officialTitle":284,"acronym":4,"eligibilityCriteria":285,"healthyVolunteers":11,"sex":61,"minAge":62,"maxAge":286,"enrollmentInfo":287,"targetDuration":4,"studyType":289,"phases":4,"briefSummary":290,"conditions":291,"keywords":298,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":302,"lastUpdatePostDateStruct":303,"startDateStruct":305,"completionDateStruct":307,"leadSponsor":309,"locationsCount":53},"100632774","relationships-between-nomophobia-levels-and-perceived-stress-body-image-and-food-addiction-among-university-students-100632774","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","30 Years",{"count":288,"type":22},150,"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?",[292,293,28,294,295,296,297],"Nomofobia","Body Image Disturbance","Body Image Disorder","Eating Behavior Disorders","Food Addiction","Stress",[299,300,180,301],"nomophobia","stress","food addiction","2026-04-15",{"date":304,"type":46},"2026-04-17",{"date":306,"type":46},"2026-02-10",{"date":308,"type":22},"2026-05-01",{"name":310,"class":52},"Bahçeşehir University",{"id":312,"slug":313,"hasResults":11,"nctId":314,"briefTitle":315,"officialTitle":316,"acronym":317,"eligibilityCriteria":318,"healthyVolunteers":11,"sex":61,"minAge":62,"maxAge":319,"enrollmentInfo":320,"targetDuration":4,"studyType":23,"phases":322,"briefSummary":323,"conditions":324,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":302,"lastUpdatePostDateStruct":330,"startDateStruct":331,"completionDateStruct":333,"leadSponsor":335,"locationsCount":337},"100628661","effects-of-stoma-education-on-patients-100628661","NCT07464548","Effects of Stoma Education on Patients","Determining the Effects of Stoma Education on Patients' Self-Efficacy, Body Image, and Stoma Adherence","Stoma","Inclusion Criteria:\n\n* Adults who have undergone colostomy or ileostomy surgery.\n* Willingness to participate voluntarily in the study.\n* Elective surgery patients.\n* No diagnosed psychological disorders.\n\nExclusion Criteria:\n\n* Emergency surgery cases.\n* Patients with cognitive impairment or psychiatric disorders preventing participation.\n* Patients unwilling to participate or unable to comply with study follow-ups.","90 Years",{"count":321,"type":22},100,[25],"tomas are classified according to the anatomical region in which they are created and the surgical technique used. Stomas that open into the large intestine are called colostomies, those that open into the small intestine are called ileostomies, and the creation of an anastomosis of the ureters to the abdominal wall is called a urostomy. Stomas are commonly used in the treatment of gastrointestinal diseases. Ileostomy and colostomy are the most frequently encountered types of stomas. While colorectal cancer is the primary reason for intestinal stoma creation, inflammatory bowel diseases, penetrating abdominal injuries, congenital anomalies, obstructions due to diverticular disease, ischemic colitis, radiation injury, sigmoid colon volvulus, and fecal incontinence are also among the indications for stoma creation. Despite advances in surgical techniques, complications are commonly seen in individuals with stomas. Incorrect stoma placement, the use of inappropriate bags and adapter systems, and a lack of knowledge and skills among patients and caregivers play a significant role in the development of complications. Depending on these conditions, patients may encounter problems such as edema, bleeding, ischemia, and mucocutaneous dehiscence in the early postoperative period. These complications negatively affect not only physical health but also the individual's social life, psychological state, and overall quality of life. Symptoms such as peristomal skin problems, uncontrolled gas release, fecal incontinence, and pain can hinder participants' adaptation to daily life and lead to social isolation. Nursing care and patient education are of great importance in managing these problems faced by individuals with stomas. The nursing process requires a comprehensive approach extending from the pre-operative period to the post-discharge phase. In this process, individualized education programs addressing fundamental issues such as nutrition, elimination, sexuality, social participation, and privacy should be implemented to improve quality of life, develop self-care skills, and prevent complications. In this context, the investigators have planned this study to determine the effects of the education provided to patients on stoma adaptation, body image, and self-efficacy.",[325,326,327,28,328,329],"Colostomy - Stoma","Ileostomy - Stoma","Patient Education","Self Efficacy","Adjustment",{"date":304,"type":46},{"date":332,"type":46},"2026-03-10",{"date":334,"type":22},"2026-08-10",{"name":336,"class":52},"Ataturk University",2,{"id":339,"slug":340,"hasResults":11,"nctId":341,"briefTitle":342,"officialTitle":343,"acronym":344,"eligibilityCriteria":345,"healthyVolunteers":11,"sex":17,"minAge":346,"maxAge":347,"enrollmentInfo":348,"targetDuration":4,"studyType":23,"phases":350,"briefSummary":351,"conditions":352,"keywords":355,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":369,"lastUpdatePostDateStruct":370,"startDateStruct":372,"completionDateStruct":374,"leadSponsor":376,"locationsCount":53},"100618092","effect-of-skin-closure-techniques-on-body-image-in-women-undergoing-gynecologic-surgery-100618092","NCT07327125","Effect of Skin Closure Techniques on Body Image in Women Undergoing Gynecologic Surgery","Effect of Skin Closure Techniques on Body Image and Mood in Gynecologic Oncology Patients","BISGO","Inclusion Criteria:\n\n* Female participants aged 18 years or older.\n* Patients scheduled for elective open gynecologic surgery for suspected or confirmed gynecologic malignancy.\n* Surgery planned to be performed via a vertical midline laparotomy incision.\n* Literate patients capable of reading, understanding, and completing the Body Image Scale (BIS) and Hospital Anxiety and Depression Scale (HADS).\n* Patients who provide written informed consent to participate in the study.\n\nExclusion Criteria:\n\n* History of prior radiotherapy to the abdominal or pelvic region.\n* Patients currently receiving chronic immunosuppressive therapy.\n* Body Mass Index (BMI) less than 18 kg\u002Fm\\^2 or greater than 40 kg\u002Fm\\^2.\n* Presence of cognitive impairment, dementia, or Alzheimer's disease.\n* Major psychiatric disorders that prevent the patient from understanding or completing the questionnaires.\n* Patients undergoing emergency surgery.","17 Years","60 Years",{"count":349,"type":22},140,[25],"This randomized clinical trial investigates the impact of two different skin closure techniques on body image and mood in women undergoing surgery for gynecologic cancers.\n\nPatients undergoing elective surgery with a midline abdominal incision will be randomly assigned to one of two groups: 1. Interrupted Closure Group: The surgical incision is closed using either metal clips (staples) or separate mattress sutures (individual stitches). 2. Subcuticular Sutures Group: The surgical incision is closed using continuous stitches placed under the skin surface (aesthetic stitching).\n\nThe main goal of the study is to determine whether the method of wound closure affects a patient's perception of their body image, cosmetic satisfaction, and levels of anxiety or depression.\n\nAdditionally, the study aims to prove that the subcuticular suture technique is safe and does not increase the risk of wound complications (such as infection or wound separation) compared to the other method.\n\nParticipants will be asked to complete questionnaires before surgery, and again at 1, 3 and 6 months after surgery to track changes in their feelings and satisfaction with the scar.",[353,354,28],"Gynecologic Cancers","Surgical Wound Closure Techniques",[356,357,358,359,28,360,361,362,363,364,365,366,367,368],"surgical staples","Subcuticular Sutures","Gynecologic Oncology","Skin Closure Techniques","Surgical Wound","Laparotomy","Cicatrix","Anxiety","Depression","Midline Incision","Wound Dehiscence","Wound Complications","Surgical Site Infection","2026-04-12",{"date":371,"type":46},"2026-04-14",{"date":373,"type":46},"2026-01-01",{"date":375,"type":22},"2028-03-01",{"name":377,"class":378},"Başakşehir Çam & Sakura City Hospital","OTHER_GOV",{"id":380,"slug":381,"hasResults":11,"nctId":382,"briefTitle":383,"officialTitle":384,"acronym":385,"eligibilityCriteria":386,"healthyVolunteers":16,"sex":17,"minAge":62,"maxAge":126,"enrollmentInfo":387,"targetDuration":4,"studyType":23,"phases":389,"briefSummary":390,"conditions":391,"keywords":392,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":396,"lastUpdatePostDateStruct":397,"startDateStruct":399,"completionDateStruct":401,"leadSponsor":403,"locationsCount":4},"100631873","sdt-based-intervention-for-exercise-motivation-in-female-students-100631873","NCT07506343","SDT-Based Intervention for Exercise Motivation in Female Students","Study Protocol for a Randomized Controlled Trial of a Self-determination Theory-Based Psychoeducational Intervention to Enhance Autonomous Motivation for Exercise in Female University Students","No acronym use","Inclusion Criteria:\n\n* Female sex\n* Age between 18 and 25 years\n* Enrolled in Health Sciences programs (Physical Activity and Sport Sciences, Physiotherapy, Human Nutrition and Dietetics, Nursing) at Universidad Francisco de Vitoria\n* Provision of written informed consent\n\nExclusion Criteria:\n\n* Current or previous diagnosis of an eating disorder\n* Failure to complete baseline or post-intervention questionnaires\n* Identification of an eating disorder after enrollment, which triggers referral according to the well-being protocol",{"count":388,"type":22},194,[25],"Physical inactivity, maladaptive exercise motives, and body image concerns are highly prevalent among young adult women and are associated with reduced psychological well-being and increased risk for disordered eating. This study protocol describes a randomized controlled trial designed to evaluate a multi-component psychoeducational intervention integrating Self-Determination Theory principles with functionality-oriented body image strategies to enhance autonomous motivation for exercise and promote psychological well-being among female university students. Female Health Sciences students aged 18-25 will be randomly allocated (1:1) to an experimental or control group following baseline assessment, and outcomes will be evaluated at baseline, post-intervention, and six-week follow-up. The six-session face-to-face intervention incorporates autonomy-supportive communication, competence-building activities, meaningful rationales, choice provision, and supportive relational climates, combined with functionality-based body image content. The primary outcome is autonomous motivation for exercise (BREQ-3; Relative Autonomy Index), and secondary outcomes include basic psychological need satisfaction and frustration, physical activity levels, positive body image, and eating disorder risk. Linear mixed-effects models will be used under an intention-to-treat approach, and mediation analyses will test whether changes in psychological need satisfaction underlie improvements in motivational quality. The intervention is expected to promote healthier motivational regulation, increase physical activity engagement, strengthen positive body image, and reduce maladaptive exercise drivers. Findings aim to inform scalable, theory-driven preventive strategies for improving health and well-being among young women in university settings.",[28,99],[393,394,395],"SDT theory","Gender gap","ED risk","2026-03-27",{"date":398,"type":46},"2026-04-01",{"date":400,"type":22},"2026-10-01",{"date":402,"type":22},"2027-04-30",{"name":404,"class":52},"Universidad Francisco de Vitoria",{"id":406,"slug":407,"hasResults":11,"nctId":408,"briefTitle":409,"officialTitle":409,"acronym":410,"eligibilityCriteria":411,"healthyVolunteers":16,"sex":61,"minAge":125,"maxAge":19,"enrollmentInfo":412,"targetDuration":4,"studyType":23,"phases":414,"briefSummary":415,"conditions":416,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":420,"lastUpdatePostDateStruct":421,"startDateStruct":423,"completionDateStruct":424,"leadSponsor":425,"locationsCount":53},"100590105","implementing-an-eating-disorder-prevention-program-for-youth-in-nova-scotia-100590105","NCT06963086","Implementing an Eating Disorder Prevention Program for Youth in Nova Scotia","EDPP-P2","Inclusion Criteria:\n\n* Self-identify as a girl\u002Fwoman.\n* Be between the ages of 15-22 years old.\n* For inclusion in an in-person group, an individual must be currently enrolled as a student at the school where they will participate in sessions.\n* For inclusion in a virtual BP group, an individual must live in and\u002For attend school in Nova Scotia, and have access to a computer (e.g., laptop, desktop computer, cellphone) with internet connection and a webcam that can be used in a private location (if a participant does not have a private location to use when attending sessions, they will be asked to wear headphones).\n* Able to complete English computer-based self-report questionnaires (with adequate accommodation, if necessary).\n* Provides informed consent (or verbal assent with informed consent provided by parent\u002Fguardian).\n\nExclusion Criteria:\n\n* Previous participation in the Body Project.",{"count":413,"type":22},120,[25],"The goal of this study is to evaluate the Body Project, which is an eating disorder prevention program for youth 15-22 years old. The main question it aims to answer is 'Can an eating disorder prevention program, specifically the Body Project, be successfully delivered to youth in Nova Scotia'?\n\nThis study will determine the feasibility of implementing the Body Project in Nova Scotia by assessing the following objectives:\n\n1. Acceptability (how well the Body Project is received by, and the extent to which it is perceived as meeting the needs of, youth in Nova Scotia).\n2. Demand (the extent to which youth in Nova Scotia are interested in and willing to engage with the program).\n3. Integration (the extent to which the Body Project is judged as feasible by the group facilitators).\n4. Effectiveness (the extent to which the Body Project reduces eating disorder risk factors in youth in Nova Scotia).\n\nParticipants will:\n\n* Attend a total of 4-4.5 hours of Body Project group sessions, which are led by peer mentors.\n* Complete outcome measure questionnaires before their first session and after their last session.\n* Participate in a focus group with their session group members after their last session.",[28,417,418,419],"Body Dissatisfaction","Dietary Restraint","Negative Affect","2026-01-14",{"date":422,"type":46},"2026-01-15",{"date":420,"type":46},{"date":191,"type":22},{"name":426,"class":52},"Susan Gamberg",{"id":428,"slug":429,"hasResults":11,"nctId":430,"briefTitle":431,"officialTitle":432,"acronym":433,"eligibilityCriteria":434,"healthyVolunteers":11,"sex":17,"minAge":62,"maxAge":4,"enrollmentInfo":435,"targetDuration":4,"studyType":23,"phases":437,"briefSummary":438,"conditions":439,"keywords":443,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":454,"lastUpdatePostDateStruct":455,"startDateStruct":457,"completionDateStruct":459,"leadSponsor":461,"locationsCount":53},"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).",{"count":436,"type":22},56,[25],"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.",[440,441,442,28,293],"Binge Eating","Binge Eating Behaviour","Binge Eating\u002FLoss of Control Eating",[444,445,446,447,448,449,180,450,451,452,453],"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","2025-10-14",{"date":456,"type":46},"2025-10-20",{"date":458,"type":22},"2025-10",{"date":460,"type":22},"2027-05",{"name":462,"class":52},"Taylor Rezeppa",{"id":464,"slug":465,"hasResults":11,"nctId":466,"briefTitle":467,"officialTitle":468,"acronym":469,"eligibilityCriteria":470,"healthyVolunteers":11,"sex":61,"minAge":62,"maxAge":4,"enrollmentInfo":471,"targetDuration":4,"studyType":23,"phases":473,"briefSummary":474,"conditions":475,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":480,"lastUpdatePostDateStruct":481,"startDateStruct":483,"completionDateStruct":485,"leadSponsor":487,"locationsCount":489},"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":472,"type":22},180,[25],"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).",[476,293,28,477,478,479],"Head and Neck Cancer","Survivorship","Psychosocial Impairment","Mental Health Issue","2025-09-18",{"date":482,"type":46},"2025-09-24",{"date":484,"type":46},"2023-02-14",{"date":486,"type":22},"2027-03-30",{"name":488,"class":52},"Medical University of South Carolina",5,{"id":491,"slug":492,"hasResults":11,"nctId":493,"briefTitle":494,"officialTitle":495,"acronym":4,"eligibilityCriteria":496,"healthyVolunteers":16,"sex":17,"minAge":497,"maxAge":498,"enrollmentInfo":499,"targetDuration":4,"studyType":23,"phases":501,"briefSummary":502,"conditions":503,"keywords":504,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":510,"lastUpdatePostDateStruct":511,"startDateStruct":513,"completionDateStruct":515,"leadSponsor":516,"locationsCount":53},"100601683","the-impact-of-a-podcast-based-body-image-intervention-among-millennial-women-100601683","NCT07113678","The Impact of a Podcast-based Body Image Intervention Among Millennial Women","Efficacy of a Podcast-based Body Image Intervention for Millennial Women: A Three-Arm Randomised Controlled Trial","Inclusion Criteria:\n\n* Be fluent in English\n* Identify as a woman between 29 and 44 years\n* Be based in the UK\n* Has a personal device to complete the study\n\nExclusion Criteria:\n\n* Never listens to podcasts\n* Has listened to part or all of the How To Fail podcast episode featuring Pamela Anderson","29 Years","44 Years",{"count":500,"type":22},1800,[25],"The goal of this three-arm randomized controlled trial is to evaluate the acceptability and efficacy of two podcast-based interventions -- a podcast with an accompanying journal and the same podcast without a journal -- which aim to improve body confidence among millennial-aged women (29-44 years of age) in the United Kingdom.\n\nA total of 1800 women in the UK (29-44 years), who are podcast listeners, will be recruited by a research agency. Participants will be randomised to one of three groups: body confidence podcast episode with journal; body confidence podcast episode alone; a non-body confidence-related podcast episode from the same series as the intervention podcast.\n\nThe research aims are to determine the following:\n\n1. Are the two versions of the intervention (i.e., podcast with and without a journal) effective in improving appearance esteem (primary outcome), internalisation of appearance ideals, self-objectification, and weight esteem among UK-based women (i) 1 day post-intervention and (ii) 1 week post-intervention, compared to a control podcast?\n2. Are the two interventions (i.e., podcast with and without a journal) effective in generating immediate change in state body satisfaction and state mood, compared to a control podcast?\n3. Are the two versions of the intervention acceptable to women?",[28],[505,506,185,507,508,509],"Body image","podcast","women","Randomized controlled trial","millennial women","2025-08-20",{"date":512,"type":46},"2025-08-21",{"date":514,"type":46},"2025-08-19",{"date":113,"type":22},{"name":193,"class":52},{"id":518,"slug":519,"hasResults":11,"nctId":520,"briefTitle":521,"officialTitle":522,"acronym":4,"eligibilityCriteria":523,"healthyVolunteers":16,"sex":17,"minAge":524,"maxAge":525,"enrollmentInfo":526,"targetDuration":4,"studyType":23,"phases":528,"briefSummary":529,"conditions":530,"keywords":534,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":542,"lastUpdatePostDateStruct":543,"startDateStruct":545,"completionDateStruct":547,"leadSponsor":548,"locationsCount":53},"100601564","non-diet-nutrition-education-and-its-effects-on-eating-behavior-body-image-and-well-being-in-adult-women-100601564","NCT07112131","Non-Diet Nutrition Education and Its Effects on Eating Behavior, Body Image, and Well-Being in Adult Women","The Effect of Non-Diet Nutrition Education on Eating Behavior, Body Image, and Well-Being in Adult Women: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Female,\n* Aged between 19-35 years,\n* Body Mass Index (BMI) between 18.5-24.9,\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding,\n* Diagnosed eating disorder or other psychiatric condition,\n* Currently enrolled in a weight loss program,\n* Following a restrictive diet due to medical conditions.","19 Years","35 Years",{"count":527,"type":22},52,[25],"The goal of this clinical trial is to evaluate whether a non-diet nutrition education program can improve eating behaviors, body image, and well-being in normal-BMI women aged 19-35 years. The main questions it aims to answer are:\n\n* Does participation in an 8-week non-diet nutrition education program improve eating behavior, body image, and well-being over time in the intervention group compared to the control group?\n* Is there a significant difference between the intervention and control groups in eating behavior, body image, and well-being after the intervention?\n\nResearchers will compare an intervention group receiving an 8-week non-diet nutrition education with a control group receiving no intervention, to see if the program leads to improvements in psychological and behavioral outcomes without focusing on weight loss.\n\nParticipants will:\n\n* Complete pre- and post-intervention assessments, including validated questionnaires on eating behavior (DEBQ, FCQ, IES-2), body image (BAS, Stunkard Figure Rating Scale), and psychological well-being (WHO-5, Rosenberg Self-Esteem Scale), as well as a 3-day food diary.\n* Be randomly assigned to either the intervention group (8-week online non-diet nutrition education sessions) or the control group (no intervention).\n* Engage in 8 weekly, 60-minute sessions focused on intuitive eating, body acceptance, and health-promoting nutrition.",[531,28,532,533],"Eating Behaviors","Well-Being, Psychological","Young Adult Females",[535,536,537,505,538,539,540,541,508],"Non-diet approach","Intuitive eating","Body acceptance","Eating behavior","Psychological well-being","Young adult women","Nutrition education","2025-08-01",{"date":544,"type":46},"2025-08-08",{"date":546,"type":46},"2025-07-21",{"date":458,"type":22},{"name":549,"class":52},"Tuğba TÜRKCAN",{"id":551,"slug":552,"hasResults":11,"nctId":553,"briefTitle":554,"officialTitle":554,"acronym":555,"eligibilityCriteria":556,"healthyVolunteers":11,"sex":17,"minAge":62,"maxAge":4,"enrollmentInfo":557,"targetDuration":4,"studyType":23,"phases":559,"briefSummary":560,"conditions":561,"keywords":575,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":583,"lastUpdatePostDateStruct":584,"startDateStruct":586,"completionDateStruct":588,"leadSponsor":590,"locationsCount":53},"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":558,"type":22},138,[25],"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.",[562,563,564,565,566,567,568,569,570,571,28,572,573,574],"Breast Neoplasms","Mastectomy","Mammaplasty","Nipple Disorder","Tattooing","Hyaluronic Acid","Dermal Fillers","Reconstructive Surgical Procedures","Quality of Life","Self Concept","Patient Satisfaction","Breast Reconstruction","Nipple Reconstruction",[576,563,573,577,574,578,567,568,579,566,28,570,580,581,572,582],"Breast Cancer","Nipple-Areola Complex Reconstruction","Areola Reconstruction","Micropigmentation","Postmastectomy Reconstruction","Cross-linked Hyaluronic Acid","Breast Cancer Survivors","2025-06-04",{"date":585,"type":46},"2025-06-06",{"date":587,"type":46},"2023-06-02",{"date":589,"type":22},"2029-07-02",{"name":591,"class":52},"Germans Trias i Pujol Hospital",{"id":593,"slug":594,"hasResults":11,"nctId":595,"briefTitle":596,"officialTitle":597,"acronym":598,"eligibilityCriteria":599,"healthyVolunteers":16,"sex":17,"minAge":62,"maxAge":525,"enrollmentInfo":600,"targetDuration":4,"studyType":23,"phases":602,"briefSummary":603,"conditions":604,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":607,"lastUpdatePostDateStruct":608,"startDateStruct":610,"completionDateStruct":612,"leadSponsor":614,"locationsCount":53},"100589919","nature-for-body-image-100589919","NCT06960668","Nature for Body Image","Look at the Bright (Nature) Side: Improving Body Image and Associated Protective Factors and Reducing Body Image Threats With the Nature for Body Image (NBI) Project","NBI","Inclusion Criteria:\n\n* Females\n* Age 18-35 years old\n\nExclusion Criteria:\n\n* Full-blown body image disorder",{"count":601,"type":22},60,[25],"Nature exposure has been found to be particularly beneficial for body image, as recent studies have identified a positive association between time spent in nature and positive body image. Positive body image, defined as the ability to accept and respect one's body, has been linked to greater life satisfaction and engagement in healthy behaviors. Conversely, negative body image is recognized as a public health concern due to its detrimental effects on both physical and mental health. It has been associated with symptoms of Body Image Disorders (BIDs), including Eating Disorders (EDs) and Body Dysmorphic Disorder (BDD).\n\nThe Nature for Body Image (NBI) project aimed to examine the impact of a structured nature exposure intervention on improving body image among young women aged 18-35 years.",[28,531,605,606],"Self-Compassion","Interoception","2025-05-15",{"date":609,"type":46},"2025-05-16",{"date":611,"type":46},"2025-05-01",{"date":613,"type":22},"2026-02-28",{"name":615,"class":52},"University of Padova",{"id":617,"slug":618,"hasResults":11,"nctId":619,"briefTitle":620,"officialTitle":621,"acronym":4,"eligibilityCriteria":622,"healthyVolunteers":16,"sex":61,"minAge":62,"maxAge":623,"enrollmentInfo":624,"targetDuration":625,"studyType":289,"phases":4,"briefSummary":626,"conditions":627,"keywords":634,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":638,"lastUpdatePostDateStruct":639,"startDateStruct":641,"completionDateStruct":643,"leadSponsor":645,"locationsCount":4},"100591815","3-dimensional-evaluation-of-body-perception-100591815","NCT06985329","3-Dimensional Evaluation of Body Perception","Evaluation of Neurocognitive Skills, VisuoSpatial Perception and Perspective Perception in Amputees","Inclusion criteria for the amputee group:\n\n* Acquired amputees\n* Aged 18-65 years\n* Using a prosthesis for at least six months\n* At least a primary school graduate\n* Individuals who can adapt to prolonged, attention-demanding activities will be included.\n* Standardised Mini Mental State Examination score of \\>24.\n\nFollowing the recruitment of the amputee group, a healthy control group will be recruited to match it in terms of age, gender and educational status.\n\nInclusion criteria for the healthy control group:\n\n* Age range: 18-65 years\n* At least a primary school graduate\n* Individuals who can adapt to prolonged, attention-demanding activities will be included.\n* Standardised Mini Mental State Examination score of \\>24.\n\nExclusion criteria for the amputee group:\n\n* Individuals with congenital amputation\n* Those with phantom limb pain and\u002For sensation\n* Those with an open wound on the stump\n* Bilateral amputation\n* Any neurological or psychiatric diagnosis\n* Those using sedative medication and\u002For its derivatives\n* Have vision and related problems\n* Individuals who are illiterate\n* Individuals participating in treatments targeting body representation (e.g. imagery-based treatments or progressive motor visualisation) will not be included in the study.\n\nExclusion criteria for the Healthy Control Group:\n\n* Having any neurological or psychiatric diagnosis\n* Using sedative medication and\u002For its derivatives\n* People with vision and related problems\n* Illiterate individuals will not be included in the study.","65 Years",{"count":601,"type":22},"15 Days","The goal of this observational study is to evaluate the changing body perception of amputees aged 18-65 years using prostheses through different personal perspectives of the right-left distinction. In addition, we aimed to examine the relationship between possible changes in body perception and visual spatial perception and neurocognitive performances. The main questions that this study aimed to answer are as follows:\n\n1. Is there a difference between the amputee group and the control group in terms of parameters related to body perception?\n2. Is there a difference between the amputee group and the control group in terms of neurocognitive skills?\n3. Is there any difference between the amputee group and the control group in terms of visual spatial perception abilities?\n\nTo examine whether changes in body perception in amputees affect neurocognitive performance, visuospatial perception and perspective perception and the relationship between them will be compared with a healthy control group.\n\nThe assessments to be applied to both groups can be summarised as follows:\n\n* Demographic information such as age, gender, and education level will be recorded.\n* Mini-mental state test will be used to assess the cognitive level.\n* Edinburgh Handedness Scale will be used to determine the dominant side.\n* Right-left discrimination and personal perspective perception will be assessed using a desktop programme.\n* The clock drawing test and Benton line orientation test will be used to visual spatial perception.\n* A computer based program called The Central Nervous System (CNS) Vital Signs Neurocognitive Test Battery will be used to asesses neurocognitive abilities.",[28,628,629,630,631,632,633],"Cognition","Decision Making","Visuospatial\u002FPerceptual Abilities","Neurocognitive Function","Executive Function (Cognition)","Amputation",[28,628,635,633,636,629,637],"Neuropsychological Test","Executive Function","Visuospatial Skills","2025-05-14",{"date":640,"type":46},"2025-05-22",{"date":642,"type":22},"2025-06",{"date":644,"type":22},"2026-06-15",{"name":646,"class":52},"Trakya University",{"id":648,"slug":649,"hasResults":11,"nctId":650,"briefTitle":651,"officialTitle":652,"acronym":653,"eligibilityCriteria":654,"healthyVolunteers":16,"sex":17,"minAge":62,"maxAge":525,"enrollmentInfo":655,"targetDuration":4,"studyType":23,"phases":656,"briefSummary":657,"conditions":658,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":659,"lastUpdatePostDateStruct":660,"startDateStruct":662,"completionDateStruct":664,"leadSponsor":666,"locationsCount":53},"100571787","yoga-4-body-image-y4bi-investigating-the-impact-of-yoga-on-body-image-and-eating-behaviours-100571787","NCT06724796","Yoga 4 Body Image (Y4BI): Investigating the Impact of Yoga on Body Image and Eating Behaviours","Yoga 4 Body Image (Y4BI): Investigating the Impact of Yoga on Body Image and Eating Behaviours in Young Women","Y4BI","Inclusion Criteria:\n\n* Females\n* Age 18-35 years old\n\nExclusion Criteria:\n\n* Regular yoga practice\n* Pregnancy\n* Medical conditions that preclude yoga practice (e.g., neurodegenerative diseases, recent injuries, rheumatic conditions)\n* Full-blown body image disorder",{"count":321,"type":22},[25],"The practice of yoga can positively impact body image, a psychological construct encompassing perceptual, emotional, cognitive, and behavioral aspects, which can be either positive or negative. Negative body image manifests as extreme dissatisfaction with one's body-a condition particularly common among young women-that places them at significant risk for developing Body Image Disorders (BIDs). In contrast, positive body image is characterized by an overall respect for one's body.\n\nCurrent research on the impact of yoga on body image has several limitations, making it challenging to determine whether yoga practice truly has a positive effect on body image and to identify the mechanisms underlying this impact. To address these gaps, the present project aims to overcome the limitations of existing studies by investigating the impact of yoga on body image through quantitative methodologies and by exploring the mechanisms that drive this effect.\n\nThe project consists of two phases:\n\n1. Investigating the impact of yoga on body image (both positive and negative) and eating behaviours in a population characterized by high levels of body dissatisfaction-young women.\n2. Examining the psychological mechanisms underlying yoga's impact on body image, including increased interoceptive awareness, embodiment, and self-compassion, as well as a reduction in self-objectification.",[417,28,531],"2025-03-24",{"date":661,"type":46},"2025-03-25",{"date":663,"type":46},"2024-11-30",{"date":665,"type":22},"2026-07-31",{"name":615,"class":52},{"id":668,"slug":669,"hasResults":11,"nctId":670,"briefTitle":671,"officialTitle":672,"acronym":4,"eligibilityCriteria":673,"healthyVolunteers":11,"sex":61,"minAge":62,"maxAge":4,"enrollmentInfo":674,"targetDuration":4,"studyType":289,"phases":4,"briefSummary":676,"conditions":677,"keywords":681,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":693,"lastUpdatePostDateStruct":694,"startDateStruct":696,"completionDateStruct":697,"leadSponsor":699,"locationsCount":4},"100577662","the-weight-of-victory-exploring-short--and-long-term-health-outcomes-in-former-male--female-elite-athletes-from-weight-sensitive-sports-100577662","NCT06801210","The Weight of Victory: Exploring Short- and Long-term Health Outcomes in Former Male & Female Elite Athletes from Weight-sensitive Sports","The Weight of Victory: Exploring Short- and Long-term Health Outcomes in Former Male & Female Elite Atheltes from Weight-sensitive Sports","Inclusion Criteria:\n\n* Represented the national team at senior and\u002For junior level, (Non-organized sports) competed at national and\u002For international level. , \\>1 year since retirement , \\>18 years old,and a proficient level of Norwegian reading and writing skills\n\nExclusion Criteria:\n\n\\-",{"count":675,"type":22},1500,"The health of former elite athletes has been identified as a critical research gap where there is limited knowledge about both short- and long-term consequences after ending their careers. The transition phase from an active elite career to everyday life has been shown to be particularly problematic, yet this issue has been little studied among former Norwegian elite athletes. Furthermore, questions remain regarding the health of athletes from weight-sensitive sports, such as weight-class, aesthetic, and certain endurance sports. These athletes face specific challenges related to maintaining a certain physique and frequent changes in body weight during their active careers. This group has been shown to be vulnerable to a range of problematic health outcomes related to low energy availability, and little is known about the long-term effects of a career involving this.\n\nTherefore, the overall purpose of the project is to map the mental and physical health of former elite athletes. At the same time, there will be a particular focus on the differences between weight-sensitive and less weight-sensitive sports, different types of sports, gender, as well as previous dieting and eating behaviors.",[678,679,70,570,28,680],"Musculoskeletal Health","Fertility","Disordered Eating",[682,683,684,41,685,686,687,688,689,679,690,537,691,692],"Elite athletes","Mental health","Somatic health","Musculoskeletal health","Quality of life","Anxiety and depression","Behavioral","Reproductive health","Harassment","Personality traits","Weight regulation","2025-01-23",{"date":695,"type":46},"2025-01-30",{"date":695,"type":22},{"date":698,"type":22},"2025-06-30",{"name":700,"class":52},"Norwegian School of Sport Sciences",{"id":702,"slug":703,"hasResults":11,"nctId":704,"briefTitle":705,"officialTitle":706,"acronym":4,"eligibilityCriteria":707,"healthyVolunteers":11,"sex":17,"minAge":62,"maxAge":708,"enrollmentInfo":709,"targetDuration":4,"studyType":289,"phases":4,"briefSummary":711,"conditions":712,"keywords":715,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":719,"lastUpdatePostDateStruct":720,"startDateStruct":722,"completionDateStruct":724,"leadSponsor":726,"locationsCount":337},"100572249","body-image-and-physical-activity-of-women-with-breast-cancer-100572249","NCT06730815","Body Image and Physical Activity of Women with Breast Cancer","Body Image and Physical Activity of Women with Breast Cancer Self-developed Questionnaire-based Follow-up Clinical Trial","Inclusion Criteria:\n\n* Adult women diagnosis of breast carcinoma\n\nExclusion Criteria:\n\n* neuromuscular diseases\n* severe congenital musculoskeletal and other disorders\n* other surgical procedures within 1 year","80 Years",{"count":710,"type":22},300,"The goal of this self-initiated questionnaire-based follow-up clinical trial is to map the body image and physical activity of Hungarian women treated for breast cancer.\n\nThe main questions it aims to answer are:\n\n1. How body image changes during different treatments among women treated for breast cancer?\n2. How is physical activity among Hungarian women treated for breast cancer?",[713,714,570,28],"Breast Cancer Female","Physical Inactivity",[716,717,718],"body image after breast cancer","physical activity","life quality","2024-12-16",{"date":721,"type":46},"2024-12-19",{"date":723,"type":46},"2024-09-01",{"date":725,"type":22},"2025-08-31",{"name":727,"class":52},"University of Pecs"]