[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"emotional-eating\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:emotional-eating":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,57,87,122,153],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":30,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":45,"lastUpdatePostDateStruct":46,"startDateStruct":49,"completionDateStruct":51,"leadSponsor":53,"locationsCount":56},"100650370","just-in-time-support-for-smoking-vaping-and-eating-urges-during-high-stress-moments-among-gender-and-sexual-minority-adults-in-dhaka-100650370",false,"NCT07746492","Just-in-Time Support for Smoking, Vaping, and Eating Urges During High-Stress Moments Among Gender and Sexual Minority Adults in Dhaka","A Digital Real-Time Support for Stress-Induced Smoking and Unhealthy Eating Among Gender and Sexual Minorities in Dhaka","Inclusion Criteria:\n\n* Age 18 years or older\n* Self-identifies as a gender and\u002For sexual minority person\n* Resides in Dhaka at enrolment and expects to remain in Dhaka throughout the 24-day assessment period\n* Reports at least one qualifying behaviour on average at least 3 days per week during the past month: (a) smoking or vaping, or (b) eating primarily in response to stress, anxiety, or emotional distress\n* Owns a personal Android or iOS smartphone compatible with the study platform that is used solely by the participant and is not shared with others\n* Able to read, understand, and respond to simple Bangla text\n* Able to operate the study app independently after a structured onboarding session\n* Willing to complete five scheduled app-based momentary assessments per day for 24 days and additional brief follow-up assessments after randomized decision points\n* Provides written informed consent\n\nExclusion Criteria:\n\n* Currently participating in another behavioural or pharmacological intervention study targeting smoking, vaping, or eating behaviour\n* Has a severe or unstable psychiatric condition that, based on screening and review by the study clinician, would make participation in the repeated daily assessment protocol unsafe\n* Is unable to operate the study app independently after structured onboarding","ALL","18 Years",{"count":19,"type":20},115,"ESTIMATED","INTERVENTIONAL",[23],"NA","Gender and sexual minority adults in Bangladesh experience high levels of stigma-related stress. Acute stress can trigger strong, affect-driven urges to smoke, vape, or engage in stress-attributed eating. These urges can rise and fall within minutes to hours, operating outside the reach of conventional clinic-based interventions delivered days or weeks later.\n\nThis pilot micro-randomized trial (MRT) evaluates whether delivering a brief, culturally adapted support message via smartphone during moments of high self-reported stress reduces the intensity of the urge for the participant's pre-specified target behaviour, relative to no message. Over a 24-day period, 115 participants will be scheduled for up to 5 ecological momentary assessments (EMA) per day. Whenever a participant reports an acute stress level of 5 or higher (0 to 10 scale) and satisfies pre-specified privacy, safety, behavioural, and spacing criteria, the app randomizes with probability 0.5 to deliver either a brief support message or no message. By contributing multiple randomized decision points over time, each participant serves as their own micro-control.\n\nThe primary outcome is the intensity of the urge for the participant's pre-specified target behaviour, measured 45 to 60 minutes after randomization. An exploratory urge assessment is also collected 10 minutes after randomization; comparing the two time points will help establish whether the support message's effect is immediate, delayed, or both, and will inform the choice of follow-up window for a future, fully powered trial. Prior to trial launch, all EMA items, message content, notification logic, and digital safety protocols will be developed and tested with community members, reviewed by a Community Advisory Board, and locked.\n\nAs a pilot optimization trial, its objectives are to estimate the short-term causal effect of the prompt, to identify the contexts in which that effect is larger or smaller, and to establish whether momentary assessment and just-in-time intervention research can be delivered safely, privately, and acceptably in this high-stigma setting. The study does not evaluate long-term behavioural maintenance and does not claim to address the underlying structural stigma and discrimination that produce minority stress.",[26,27,28,29],"Tobacco Use","Electronic Cigarette Use","Emotional Eating","Stress, Psychological",[31,32,33,34,35,36,37,38,39,40,41,42,43],"micro-randomized trial","just-in-time adaptive intervention","ecological momentary assessment","mHealth","digital health","minority stress","smoking","vaping","stress-attributed eating","urge","Bangladesh","gender and sexual minority","pilot optimization trial","NOT_YET_RECRUITING","2026-07-30",{"date":47,"type":48},"2026-08-05","ACTUAL",{"date":50,"type":20},"2026-09-01",{"date":52,"type":20},"2027-02-06",{"name":54,"class":55},"International Centre for Diarrhoeal Disease Research, Bangladesh","OTHER",1,{"id":58,"slug":59,"hasResults":11,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":4,"eligibilityCriteria":63,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":64,"enrollmentInfo":65,"targetDuration":4,"studyType":67,"phases":4,"briefSummary":68,"conditions":69,"keywords":76,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":56},"100624560","emotional-eating-sleep-quality-mental-state-and-metabolic-syndrome-100624560","NCT07411222","Emotional Eating, Sleep Quality, Mental State and Metabolic Syndrome","The Mediating Role of Emotional Eating and Sleep Quality in the Relationship Between Mental State and Metabolic Syndrome in Individuals With Schizophrenia and Bipolar Disorder","Inclusion Criteria:\n\n* Being registered with the Bolu İzzet Baysal Mental Health and Diseases Hospital Community Mental Health Center,\n* Having a severe chronic psychiatric illness (Schizophrenia Spectrum and Other Psychotic Disorders and Bipolar Disorder) followed by the Bolu İzzet Baysal Mental Health and Diseases Hospital Community Mental Health Center for at least 6 months,\n* Being in remission (Complete Remission (Pre-Remission): Symptoms remaining below threshold values for at least 2 months (8 weeks). A state of improvement lasting more than 2 months is generally referred to as \"remission\"),\n* Schizophrenia remission definition: 8 diagnostically significant symptoms were selected from the Positive and Negative Syndrome Scale.\n* Bipolar disorder remission definition: Complete remission is defined as the absence of acute attacks and the presence of minimal\u002Fvery mild symptoms.\n* Being between 18-65 years of age,\n* Being able to understand what is read and give written consent.\n\nExclusion Criteria:\n\n* Having a diagnosis of mental retardation,\n* Having other neurocognitive disorders, primarily dementia, according to DSM-V (as it can affect the ability to make decisions and give correct answers),\n* Not being able to speak or understand Turkish.","65 Years",{"count":66,"type":20},78,"OBSERVATIONAL","In predominantly medication-naïve schizophrenic patients, those exhibiting partial metabolic disorders have significantly worse sleep quality and sleep onset time; poor sleep predicted metabolic dysregulation even after controlling for confounding factors. Mental health, sleep, and eating behavior interact in ways that strongly influence the risk of obesity and MetS. Emotional eating (eating in response to emotions rather than hunger) is central to this network and appears to be closely associated with psychiatric illnesses, particularly depression, anxiety, and sleep disorders. There is a continuing need to elucidate the frequency, level, and relationship of emotional eating with other factors in individuals with SMI. Therefore, this study aims to elucidate this complex relationship, thereby shedding light on new ways to reduce metabolic risks in psychiatric patients.",[70,71,72,73,28,74,75],"Schizophrenia","Bipolar Disorder","Psychiatric Issue","Metabolic Syndrome","Sleep","Mediating",[70,71,73,28,74],"RECRUITING","2026-07-24",{"date":80,"type":48},"2026-07-27",{"date":82,"type":48},"2026-05-30",{"date":84,"type":20},"2026-12",{"name":86,"class":55},"Abant Izzet Baysal University",{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":92,"acronym":4,"eligibilityCriteria":93,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":94,"targetDuration":4,"studyType":21,"phases":96,"briefSummary":97,"conditions":98,"keywords":102,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":4},"100645554","online-group-programme-on-mindful-eating-during-medication-supported-weight-loss-100645554","NCT07701291","Online Group Programme on Mindful Eating During Medication-Supported Weight Loss","Feasibility and Acceptability of a Digital Mindfulness-Based Nutrition Group Intervention During Pharmacological Treatment for Weight Reduction","Inclusion Criteria: Sufficient German language skills, informed consent, and willingness to participate in a 16-week online program.\n\nExclusion Criteria:\n\nRecent diagnosis of diabetes, pregnancy or intention to become pregnant, breastfeeding, substance use, untreated thyroid disorders and severe psychiatric conditions (e.g., psychosis, major depression, binge eating disorder) and the previous participation of a mindfulness intervention. No vulnerable populations are specifically targeted or expected to be included.",{"count":95,"type":20},28,[23],"The goal of this clinical trial is to evaluate the feasibility and acceptability of a digitally delivered, mindfulness-based nutrition group program for adults with obesity who are taking GLP-1 receptor agonist medication and receiving usual medical care, including dietetic counselling.\n\nThe main questions this study aims to answer are:\n\nCan this online group program be successfully delivered to adults receiving GLP-1 treatment? Do participants find the program useful, acceptable, and easy to engage with? Are participants willing to attend the online sessions, complete the home exercises, and complete the study questionnaires?\n\nResearchers will compare participants who receive the online mindfulness-based nutrition group program in addition to usual care with participants who receive usual care alone.\n\nParticipants in the intervention group will take part in a 16-week online program consisting of nine live group sessions delivered via videoconference. They will practice mindful eating, mindfulness exercises, reflective journaling, and peer discussion. All participants will complete online questionnaires and body measurements at baseline, after 16 weeks, and 12 months after the start of the study.\n\nThis study does not evaluate a new drug or medical device. The study team will not make decisions regarding participants' GLP-1 medication. All medication management remains part of routine medical care.",[99,28,100,101],"Obesity & Overweight","Emotional Eating Behaviour","Online Intervention",[103,104,105,106,107,108,109,110,111,112],"obesity","mindfulness","midnful eating","online intervention","group therapy","feasibility study","incretin-based therapy","dietetic counselling","acceptability","recruitement rate","2026-07-08",{"date":115,"type":48},"2026-07-14",{"date":117,"type":20},"2026-08-15",{"date":119,"type":20},"2027-08-15",{"name":121,"class":55},"Bern University of Applied Sciences",{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":127,"acronym":128,"eligibilityCriteria":129,"healthyVolunteers":130,"sex":16,"minAge":17,"maxAge":64,"enrollmentInfo":131,"targetDuration":4,"studyType":21,"phases":132,"briefSummary":133,"conditions":134,"keywords":138,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":149,"leadSponsor":151,"locationsCount":56},"100635966","act-based-group-therapy-and-mobile-application-intervention-for-emotional-eating-100635966","NCT07559552","ACT-Based Group Therapy and Mobile Application Intervention for Emotional Eating","The Effect of Acceptance and Commitment Therapy and a Mobile App on Emotional Eating, Emotion Regulation, and Psychological Flexibility in Overweight Individuals","ACT-EE","Inclusion Criteria:\n\n* Agreeing to participate in the study,\n* Being between 18-65 years of age,\n* Having a body mass index ≤ 25 (BMI ≤ 29.9),\n* Being able to read and write,\n* Having an iOS or Android smartphone,\n* Having internet access,\n* Having a home environment suitable for online sessions (having a computer\u002Fsmartphone, internet access at home, the patient being able to be alone in the room during the session, etc.),\n\nExclusion Criteria:\n\n* Having communication problems that would prevent the interview,\n* Having a diagnosis of a mental disorder, including an eating disorder, that would prevent participation in the study, or having concomitant serious medical conditions that could potentially jeopardize study participation.\n* Having undergone bariatric surgery. • Being on the waiting list for bariatric surgery.\n* Being pregnant, breastfeeding, or planning to become pregnant within the next 6 months.\n* Receiving therapy\u002Fcounseling for emotional eating and emotion regulation problems,\n* Using a mobile application for emotional eating and emotion regulation problems,",true,{"count":66,"type":20},[23],"This study aims to evaluate the effects of an Acceptance and Commitment Therapy (ACT)-based group therapy program, combined with an ACT-based mobile app, on emotional eating, emotion regulation, and psychological flexibility in overweight individuals. Emotional eating is a condition in which individuals frequently use eating behavior as a coping mechanism for negative emotions.\n\nParticipants will be randomly assigned to intervention groups receiving ACT-based group therapy, ACT-based group therapy combined with an ACT-based mobile app, or a control group. The intervention will last six weeks and will include structured group sessions as well as mobile-based exercises, reminders, and coping strategies.\n\nOutcome measures will include emotional eating, emotion regulation, and psychological flexibility. Assessments will be conducted at baseline, post-intervention, and during the follow-up phase. The findings of this study are expected to contribute to the development of accessible and effective interventions for emotional eating.",[28,135,136,137],"Emotion Regulation","Overweight","Psychological Flexibility",[139,28,135,137,140,141,142,136,143],"Acceptance and Commitment Therapy","Mobile Health (mHealth)","Mobile Application","Group Therapy","Digital Intervention","2026-04-22",{"date":146,"type":48},"2026-04-30",{"date":148,"type":20},"2026-06-15",{"date":150,"type":20},"2026-12-30",{"name":152,"class":55},"Saglik Bilimleri Universitesi",{"id":154,"slug":155,"hasResults":11,"nctId":156,"briefTitle":157,"officialTitle":157,"acronym":158,"eligibilityCriteria":159,"healthyVolunteers":130,"sex":160,"minAge":17,"maxAge":161,"enrollmentInfo":162,"targetDuration":4,"studyType":21,"phases":164,"briefSummary":165,"conditions":166,"keywords":169,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":183},"100582496","study-of-emotional-regulation-and-underlying-prefrontal-activity-in-binge-eating-disorder-100582496","NCT06864065","Study of Emotional Regulation and Underlying Prefrontal Activity in Binge Eating Disorder","EmoBED","Inclusion Criteria:\n\n* Women between 18 and 60 years old (including 60)\n* Right-handed.\n* For patients only : diagnosed with Binge Eating Desordors according to DSM criteria.\n* Membership of a French social security scheme or beneficiary of such a scheme.\n* Non-opposition of the subject to participate in the study.\n\nNon inclusion Criteria:\n\nHealthy volunteers only :\n\n* Suffering from an eating disorder or any other psychiatric disorder.\n* History of bariatric surgery.\n\nAll subjects (healthy volunteers and patients) :\n\n* Rare obesity (genetic or syndromic).\n* Specific addictions (substances or behaviors).\n* Neurological disorders and\u002For history of stroke or head trauma.\n* Presence of lesions, wounds or dermatitis at the sites where the recording devices are applied.\n* Any serious acute or chronic illness other than the pathology under study, or any treatment likely to interfere with the evaluation of the parameter under study.\n* Inability to follow protocol requirements.\n* Subject unlikely to cooperate with the study and\u002For poor cooperation anticipated by the investigator.\n* Subject unable to speak French and\u002For unable to read.\n* Pregnant or breast-feeding women.\n* Persons deprived of their liberty by judicial or administrative decision; persons under compulsory psychiatric care; persons admitted to a health or social institution for purposes other than research.","FEMALE","60 Years",{"count":163,"type":20},80,[23],"The goal of this exploratory, interventional, multicentre study is to compare the prefrontal activity during a negative emotion regulation task in women with Binge-Eating Disorder (BED) and healthy women with and without Emotional Eating (EE).\n\nThe aim of this study is to compare the prefrontal processing of cognitive control of emotions between BED and EE and to compare the emotional processing and emotional experience between BED and EE.\n\nThe study will thus compare four experimental groups: patients with BED, BMI-matched healthy volunteers with EE, BMI-matched healthy volunteers, and healthy volunteers of normal weight without BED.\n\nParticipants will perform a down-regulation task of negative emotions elicited by negative pictures. During this task, their cerebral activity will be recorded using functional near-infrared spectroscopy (fNIRS), as well as their autonomous activity (skin conductance, pulse rate, respiration rate).",[167,28,168],"Binge-Eating Disorder","Healthy Volunteers",[167,170,171,172,173,28],"Emotion regulation","fNIRS","Prefrontal cortex","Eating disorder","2025-07-21",{"date":176,"type":48},"2025-07-22",{"date":178,"type":48},"2025-06-24",{"date":180,"type":20},"2026-10-30",{"name":182,"class":55},"Centre Hospitalier Universitaire de Besancon",3]