[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"eye-tracking\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:eye-tracking":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,53,81,105,132,157,187,212,238],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":4},"100644861","ai-timing-in-chest-x-ray-interpretation-using-eye-tracking-100644861",false,"NCT07675694","AI Timing in Chest X-ray Interpretation Using Eye-Tracking","A Within-Subject Eye-Tracking Study Examining How the Timing of AI Decision Support Influences Visual Search Behaviour, Diagnostic Accuracy, and Trust During Chest X-ray Interpretation","CREAITED","Inclusion Criteria:\n\nMain reader study:\n\n* Healthcare professionals aged 18 years or over\n* Registered to practise in the UK\n* Employed by the NHS or another healthcare service operating in the UK\n* Current or recent, within the last 3 years, clinical experience involving chest X-ray interpretation, review, or use in clinical practice\n* Able to attend two onsite study sessions at University Hospitals of Leicester NHS Trust at mutually agreed times\n* Able and willing to provide written informed consent\n* Compatible with the eye-tracking equipment\n\nSupplementary survey:\n\n* Adults aged 18 years or over\n* Live in the UK or have used the NHS or another UK healthcare service within the last 5 years\n* Able to provide informed electronic consent\n* Belong to one of the following respondent groups: healthcare professionals or healthcare staff, patients or carers, or members of the public\n* Healthcare professional respondents may include adults involved in requesting, interpreting, checking, or acting on chest X-ray findings in clinical practice\n\nExclusion Criteria:\n\nMain reader study:\n\n* Inability to attend both onsite study sessions at University Hospitals of Leicester NHS Trust\n* Eye-tracking incompatibility, such as visual, neurological, or physical conditions preventing adequate gaze tracking or participant comfort\n* Direct involvement in selection, adjudication, or preparation of the chest X-rays used in the study\n* Conflicts of interest, including direct involvement in development of the AI system under evaluation\n* Prior participation in a closely related AI chest X-ray study where overlap in image sets or study procedures may compromise validity, assessed on a case-by-case basis\n\nSupplementary survey:\n\n* Aged under 18 years\n* Does not live in the UK and has not used the NHS or another UK healthcare service within the last 5 years\n* Unable to provide informed electronic consent\n* Does not meet one of the eligible respondent groups for the survey",true,"ALL","18 Years",{"count":21,"type":22},24,"ESTIMATED","INTERVENTIONAL",[25],"NA","Chest X-rays are commonly used to help diagnose and manage chest conditions. Artificial intelligence (AI) tools are increasingly being used to support chest X-ray interpretation. However, it is not yet clear whether the timing of AI information affects how clinicians review images, make decisions, and use AI support.\n\nThis study will look at whether showing AI information before or after a clinician first reviews a chest X-ray changes how they look at the image, how long they take, their interpretation decisions, their confidence, and their trust in AI support.\n\nHealthcare professional participants will complete two chest X-ray interpretation sessions in a controlled NHS research setting. During each session, participants will review de-identified chest X-ray images while wearing eye-tracking equipment. Eye-tracking will record where a participant looks on the image and how long they spend looking at different areas.\n\nIn one session, AI information will be shown before the participant reviews the chest X-ray. In the other session, AI information will be shown after the participant has first reviewed the chest X-ray. The order of these two sessions will be balanced across participants.\n\nThe study uses de-identified chest X-ray images from existing examinations. It does not involve patients directly, does not change clinical care, and no clinical decisions will be made from the study readings. Participants will also complete a short questionnaire about their experience of using AI support. A separate anonymous survey will collect wider views from clinicians, patients, members of the public, and healthcare staff about the use of AI in chest X-ray interpretation.",[28,29,30],"Diagnostic Imaging","Eye Tracking","Artificial Intelligence (AI)",[32,33,34,35,36,37,38,39,40],"Artificial intelligence timing","Chest X-ray interpretation","Visual search behaviour","Diagnostic accuracy","Trust in automation","Automation bias","Clinician confidence","Decision support systems","Human-AI interaction","NOT_YET_RECRUITING","2026-06-29",{"date":44,"type":45},"2026-06-30","ACTUAL",{"date":47,"type":22},"2026-06",{"date":49,"type":22},"2026-12",{"name":51,"class":52},"University Hospitals, Leicester","OTHER",{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":67,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":80},"100430528","eye-tracking-fp-a-pilot-study-of-the-quantitative-evaluation-of-the-attention-paid-to-faces-with-facial-palsy-by-the-eye-tracking-technology-100430528","NCT04886245","Eye-Tracking FP \"A Pilot Study of the Quantitative Evaluation of the Attention Paid to Faces With Facial Palsy by the Eye-tracking Technology.","EyeTrackingFP","Inclusion Criteria:\n\n* for patient with facial paralysis:\n* Patient with peripheral facial palsy, irrespective of grade, whether or not previously treated\n* Patient providing written informed consent\n* Patient aged ≥ 18 years\n* Patient affiliated to a social security system\n* for Healthy voluntary subject :\n* Subject without major facial sequelae\n* Subject who provided written informed consent\n* Major subject ≥ 18 years old\n* Subject affiliated to a social security system\n\nExclusion Criteria:\n\n* for Patient with facial paralysis:\n* Patient with recent peripheral facial palsy whose total recovery is possible\n* Patient unable to provide written informed consent\n* Patient with difficulties to follow instructions and especially to stand in front of a computer screen\n* Minor patient \\\u003C18 years\n* Patient under guardianship or curators or judicial safeguard\n* for Healthy voluntary subject :\n* Subject with major facial sequelae\n* Subject not able to provide written informed consent\n* Subject presenting difficulties in following instructions and in particular in standing still in front of a computer screen\n* Minor subject \\\u003C 18 years old\n* Subject under guardianship or curators or judicial safeguard",{"count":61,"type":22},60,[25],"The facial palsy concerns between 15 and 40 people per 100000 inhabitants. They are of various etiologies such as infectious, tumoral, traumatic or idiopathic.\n\nIt has variable severities with sometimes heavy functional repercussions and different recovery potentials. The proposed palliative treatments are based on surgery, physiotherapy and botulinum toxin injections. However, when recovery is incomplete, acceptance is more difficult, with an impacted quality of life. In this context, patients' expectations and feelings about their care may become difficult for clinicians to apprehend.\n\nThe eye-tracking is widely used in the marketing field, but it also finds medical applications including head and neck lesions and facial palsy in particular. Published studies focus on the gaze of photographs, excluding any notion of dynamics and by the analysis of the gaze of outside observers, ignoring the patient's gaze.The main objective is to evaluate the attention paid to the facial side with abnormal facial movement by patients with facial paralysis compared to healthy volunteers.",[65,66],"Eye-tracking","Facial Palsy",[68,69,66],"facial mimics","eye-tracking","RECRUITING","2026-05-12",{"date":73,"type":45},"2026-05-13",{"date":75,"type":45},"2021-05-06",{"date":77,"type":22},"2027-07",{"name":79,"class":52},"Centre Hospitalier Universitaire, Amiens",1,{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":23,"phases":90,"briefSummary":91,"conditions":92,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":4},"100625981","eye-tracking-interactive-agent-in-non-verbal-icu-patients-100625981","NCT07429695","Eye-Tracking Interactive Agent in Non-verbal ICU Patients","Eye-Tracking Interactive Agent in Non-verbal ICU Patients: A Study Protocol of a Randomized Controlled Trial With an Embedded Qualitative Study","Inclusion Criteria:\n\n* Aged ≥ 18 years\n* Patients in the ICU who are unable to communicate through normal verbal means due to endotracheal intubation\u002Ftracheotomy, muscle or nerve injury, acute\u002Fchronic spinal cord injury, etc.\n* Richmond Agitation-Sedation Scale (RASS) score of -1 to 1\n* Primary caregivers are adults\n* Able to read Chinese characters and follow simple commands\n* Willing to participate in this study.\n\nExclusion Criteria:\n\n* Diseases associated with cognitive impairment, such as pulmonary encephalopathy, hepatic encephalopathy, diabetic hyperosmolar coma, and coma of unknown cause\n* A history of mental disorders, dementia or pre-dementia, or intellectual disability\n* Conditions precluding cooperation with eye-tracking interaction, such as blindness or inability to elevate the eyelids.",{"count":89,"type":22},54,[25],"The goal of this clinical trial is to determine whether an eye-tracking interactive agent can ameliorate communication impairments and reduce the incidence of complications among non-verbal patients in the intensive care unit (ICU). The main questions it aims to answer are:\n\nDoes the eye tracking interactive agent alleviate communication impairments among non-verbal patients in the ICU? Does the eye tracking interactive agent improve communication efficiency among non-verbal patients in the ICU? Does the eye tracking interactive agent m reduce the incidence of negative emotions among non-verbal patients in the ICU? Does the eye tracking interactive agent shorten the ICU length of stay for non-verbal patients in the ICU? Does the eye tracking interactive agent reduce the dosage of analgesic and sedative medications for non-verbal patients in the ICU? Does the eye tracking interactive agent improve family satisfaction for non-verbal patients in the ICU? Does the eye tracking interactive agent alleviate nurses' communication burden among non-verbal patients in the ICU? Researchers will compare eye tracking interactive agent to conventional techniques to see if e eye tracking interactive agent works to alleviate communication impairments.\n\nParticipants will:\n\nUse an eye tracking interactive agent for augmentative communication for 2 consecutive days Document each communication's details, ICU LOS, and analgesic-sedative dosages; assess communication difficulty severity, delirium, anxiety, family satisfaction and nurses' communication burden with validated scales.",[29,93,94,95],"ICU","Communication Barriers","Non-Verbal Communication","2026-02-22",{"date":98,"type":45},"2026-02-24",{"date":100,"type":22},"2026-04-01",{"date":102,"type":22},"2027-12-31",{"name":104,"class":52},"Shanghai Zhongshan Hospital",{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":111,"eligibilityCriteria":112,"healthyVolunteers":17,"sex":18,"minAge":113,"maxAge":114,"enrollmentInfo":115,"targetDuration":4,"studyType":23,"phases":117,"briefSummary":118,"conditions":119,"keywords":123,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":80},"100621946","social-cognition-screening-100621946","NCT07377227","Social COgnition Screening","Evaluation of Social Cognition: A New Screening Approach for Autism","ECoS-A","Inclusion Criteria:\n\n* ASD Group:\n* Boys or girls diagnosed with Autism Spectrum Disorder (based on clinical tools and observations)\n* Aged between 4 and 10 years old\n* Affiliation with a social security scheme\n* Informed consent of those with parental authority\n* DT Group:\n* Boys or girls\n* Aged between 4 and 10\n* Attending school in the Hauts-de-France region\n* Affiliation with a social security scheme\n* Consent of those with parental authority\n\nExclusion Criteria:\n\n* For ASD: Uncorrected visual or auditory impairments.\n* For DT: Intellectual disability, neurological or genetic disorders, autistic traits reported by teachers. The discrepancy between actual age and abilities calculated on the basis of standardised test scores","4 Years","10 Years",{"count":116,"type":22},128,[25],"Social cognition refers to the mental processes involved in social interactions, including social perception, motivation, communication, emotion recognition, and theory of mind. Face perception plays a key role in children's social development, but children with Autism Spectrum Disorder (ASD) tend to look less at social stimuli, especially faces, than typically developing (TD) peers. Eye-tracking studies highlight these visual exploration differences, linked to difficulties in joint attention, emotion recognition, and theory of mind, as well as in executive and memory functions. Standard diagnostic tests often require active participation and sufficient language, which makes assessment challenging for children with ASD and additional cognitive or language impairments.\n\nThis research project investigates how visual activity supports social cognition depending on cognitive and language levels, hypothesizing that eye-tracking can provide useful indicators for ASD screening and diagnosis.",[65,120,121,122],"Autism Spectrum Disorder","Social Cognition","Diagnosis",[65,120,121,122],"2026-02-04",{"date":126,"type":45},"2026-02-06",{"date":128,"type":22},"2026-02",{"date":130,"type":22},"2028-12",{"name":79,"class":52},{"id":133,"slug":134,"hasResults":11,"nctId":135,"briefTitle":136,"officialTitle":136,"acronym":137,"eligibilityCriteria":138,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":139,"enrollmentInfo":140,"targetDuration":4,"studyType":142,"phases":4,"briefSummary":143,"conditions":144,"keywords":146,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":149,"lastUpdatePostDateStruct":150,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":80},"100622268","eye-tracking-study-on-eye-movement-function-and-visual-attention-patterns-in-patients-with-thyroid-associated-ophthalmopathy-100622268","NCT07381413","Eye Tracking Study on Eye Movement Function and Visual Attention Patterns in Patients With Thyroid-Associated Ophthalmopathy","TAO-A","Inclusion Criteria:\n\n* Aged between 18 and 70 years, inclusive.\n* Willing and able to provide written informed consent.\n* Best-corrected visual acuity (BCVA) ≥ 1.0 in both eyes, with no history of ocular diseases or thyroid disorders.\n\nExclusion Criteria:\n\n* Non-TAO Ocular Motility Disorders: History of conditions like myasthenia gravis, cranial nerve palsy, or congenital strabismus.\n* Neurological Diseases: Disorders affecting oculomotor control (e.g., Parkinson's, MS, stroke, or brain tumors).\n* Significant Visual Impairment: BCVA \\\u003C 0.5 due to media opacities or retinopathy, preventing clear visualization of stimuli.\n* Prior Ocular Surgery: History of surgeries affecting extraocular muscle mechanics (e.g., strabismus surgery, scleral buckling).\n* Psychiatric or Cognitive Disorders: Inability to follow instructions or conditions affecting eye movements (e.g., schizophrenia).\n* Medication Interference: Use of drugs affecting reaction time (e.g., sedatives) within 48 hours of testing.","70 Years",{"count":141,"type":22},100,"OBSERVATIONAL","This study focuses on eye health and visual function in patients with Thyroid-Associated Ophthalmopathy (TAO), a condition that often causes bulging eyes and restricted eye movement. The purpose of this study is to use non-invasive eye-tracking technology to evaluate how the disease affects eye movement function. The investigators hypothesize that compared to healthy individuals, patients with TAO will show measurable differences in eye stability and the ability to track moving objects. Additionally, the investigators believe the disease may alter how patients visually scan faces (e.g., avoiding eye contact). The study will enroll 100 participants, including both patients and healthy volunteers. By recording gaze patterns while participants look at a screen, the investigators aim to objectively quantify the physical and social impact of the disease, providing better data for future treatment plans.",[145,29],"Thyroid Associated Ophthalmopathies",[147,148],"TAO","eye tracking","2026-02-03",{"date":126,"type":45},{"date":152,"type":45},"2026-01-31",{"date":154,"type":22},"2029-05",{"name":156,"class":52},"Shanghai Changzheng Hospital",{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":161,"acronym":162,"eligibilityCriteria":163,"healthyVolunteers":17,"sex":18,"minAge":164,"maxAge":4,"enrollmentInfo":165,"targetDuration":4,"studyType":23,"phases":167,"briefSummary":168,"conditions":169,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":179,"lastUpdatePostDateStruct":180,"startDateStruct":182,"completionDateStruct":184,"leadSponsor":185,"locationsCount":80},"100597159","rural-autistic-individuals---supporting-expression-100597159","NCT07054866","Rural Autistic Individuals - Supporting Expression","RAISE","Inclusion Criteria:\n\n* 1.1 Confirmed (preferably) or suspected diagnosis of ASD (autism spectrum disorder), or a receptive language impairment (i.e., difficulties with comprehension, Developmental Language Disorder), or both. Additional diagnoses, including ADHD (Attention Deficit and Hyperactivity Disorder), are acceptable. Siblings and cousins of these individuals are also welcome.\n\nOR 1.2 No diagnoses of ASD or DLD for unrelated control typically-developing participants.\n\n2\\. Normal hearing and normal vision (or corrected to normal with glasses or contacts).\n\n3\\. Ages 2+. 4. English as the dominant language of caregivers. 5. Caregivers who self-identify as living in a rural area. 6. The ability to verbally or physically respond is optional.\n\nExclusion Criteria:\n\n* 1\\. Poor hearing. 2. Inborn or acquired brain damage.","2 Years",{"count":166,"type":22},50,[25],"This research study investigates how hand gestures can support language comprehension and communication skills of hearing speaking, non-speaking, and\u002For minimally verbal individuals with Autism Spectrum Disorders (ASD), who are especially disadvantaged by the lack of accessible services in their rural communities. Individuals with other cognitive profiles, including Developmental Language Disorder (DLD), ADHD, Dyslexia, and others are welcome too. The study uses methods of eye tracking and recording of brain activity to understand how hand gestures adapted from signs from American Sign Language, such as \\[cry\\], can promote successful understanding of words like \"cry\". The overarching goal is to help families effectively utilize gestures to support communication with their children.",[170,171,172,173,174,175,176,29,177,178],"Autism Disorder","Language Development Disorders","ADHD","Typical Development","Rural Health","Children","Neuroimaging","EEG","fNIRS","2025-07-07",{"date":181,"type":45},"2025-07-10",{"date":183,"type":22},"2025-07",{"date":77,"type":22},{"name":186,"class":52},"Montana State University",{"id":188,"slug":189,"hasResults":11,"nctId":190,"briefTitle":191,"officialTitle":192,"acronym":193,"eligibilityCriteria":194,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":195,"targetDuration":4,"studyType":23,"phases":197,"briefSummary":198,"conditions":199,"keywords":201,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":205,"startDateStruct":207,"completionDateStruct":209,"leadSponsor":211,"locationsCount":80},"100483949","multimodal-quantified-analysis-of-facial-movements-comparison-between-pathological-and-control-subjects-100483949","NCT05581680","Multimodal Quantified Analysis of Facial Movements: Comparison Between Pathological and Control Subjects","Multimodal Quantified Analysis of Facial Movements: Comparison Between Pathological","AQ2MF","Inclusion Criteria:\n\n* Subjects with no known facial pathology (healthy volunteers) OR\n* Patients with peripheral facial palsy, irrespective of grade, whether or not previously treated\n* Subject with written informed consent\n* Subject over 18 years of age\n* Subject affiliated to a social security scheme\n\nExclusion Criteria:\n\n* Subjects with severe skin disorders that do not allow the application of electrodes or photo reflective markers\n* Subjects with speech disorders making it impossible to pronounce the sounds \\[o\\] and \\[pu\\]\n* Subject unable to provide written informed consent\n* Subjects under guardianship, curators or safeguard of justice",{"count":196,"type":22},720,[25],"The facial palsy is a frequent disease with a lot of etiologies. It has variable severities with sometimes heavy functional repercussions and different recovery potentials. The proposed treatments are based on surgery, physiotherapy and botulinum toxin injections. However, when recovery is incomplete, acceptance is more difficult, with an impacted quality of life. Thanks to Motion Capture and Electromyography, a quantification of the facial mimicry is now possible with a great precision. In addition with the quantification of the facial mimicry, eye-tracking, wich is widely used in the marketing field, but it also finds medical applications including head and neck lesions and facial palsy in particular, will be used to evaluate the visio of the patients on their pathology in function of the movement quantification measured with MoCap and Electromyography. The aim of this research is to measure in a combined way the action potentials by sEMG and the amplitudes of displacement of the markers in motion capture, for movements determined in a population of patients presenting a facial pathology, in order to compare them with reference values obtained in healthy subjects. In a second step, the aim will be to study if there is a link between the way the patient looks at his pathology and the results of his management (treatment, rehabilitation) which will be quantitatively evaluated thanks to MoCap and sEMG.",[200,65,66],"Electromyography",[68,202,203,69,66],"motion capture","electromyography","2025-05-22",{"date":206,"type":45},"2025-05-28",{"date":208,"type":45},"2022-10-12",{"date":210,"type":22},"2028-10",{"name":79,"class":52},{"id":213,"slug":214,"hasResults":11,"nctId":215,"briefTitle":216,"officialTitle":216,"acronym":217,"eligibilityCriteria":218,"healthyVolunteers":17,"sex":18,"minAge":114,"maxAge":219,"enrollmentInfo":220,"targetDuration":4,"studyType":23,"phases":222,"briefSummary":223,"conditions":224,"keywords":228,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":232,"startDateStruct":233,"completionDateStruct":235,"leadSponsor":237,"locationsCount":80},"100454185","mri-eye-tracking-pairing-a-tool-for-assessing-social-cognition-in-children-with-asd-100454185","NCT05194254","MRI-Eye Tracking Pairing, a Tool for Assessing Social Cognition in Children With ASD","IRM-ET","Inclusion Criteria:\n\nFor the group of people with Autism Spectrum Disorders (experimental group):\n\n* Age between 10 to 20 years old\n* Diagnosis of ASD (CARS) ≥ 30 performed at inclusion\n* IQ test evaluation (regardless of the result) performed by a trained psychologist\n* Obtaining informed oral and written consent after appropriate information\n* Obtaining informed oral and written consent from the legal guardian after information\n* Be affiliated with social security\n* No contraindication to magnetic resonance imaging\n\nFor the TD (Typical Development) group of people (control group):\n\n* Age between 10 to 20 years old\n* Diagnosis of ASD (CARS) \\\u003C30 performed at inclusion\n* IQ test evaluation (regardless of the result) performed by a trained psychologist\n* Obtaining informed oral and written consent after appropriate information\n* Obtaining informed oral and written consent from the legal guardian after information\n* Be affiliated with social security\n* No contraindication to magnetic resonance imaging\n\nExclusion Criteria:\n\nFor all groups:\n\n* Age outside the range 10 to 20 years\n* Person with a contraindication to MRI (including claustrophobia, pace maker, neurosurgical clips, vascular clips, heart valves, ventriculoperitoneal valves, cochlear implant, neurostimulator, intraocular metal shards, joint prosthesis, etc.)\n* Person suffering from major obesity (\\> 140 kg) not allowing him to enter the tunnel of the MRI machine (diameter \\\u003C70cm)\n* Pregnant or breastfeeding woman\n* Person under guardianship or guardianship or deprived of liberty by a judicial or administrative decision\n\nFor TD people (control group):\n\n* Person with psychiatric disorders such as attention disorder with or without hyperactivity, depression, bipolar disorder and schizophrenia.\n* Person with a neurological history such as epilepsy and \u002F or neurovascular accident.","20 Years",{"count":221,"type":22},68,[25],"Most studies use static visual percepts that are less representative of joint attention versus an ecological environment. This has the consequence of decreasing the perception of an interaction with a social partner, which is an essential step in achieving joint attention. The originality of this study is to improve the design of visual percepts (in the form of video) in order to mimic an ecological environment as much as possible by using MRI-ET coupling. The second originality of this study is the longitudinal exploration of the neurodevelopment of social cognition in autistic children. Studies by the Redcay and Oberwelland teams observe different activations at different ages. The hypothesis is that the perception of joint attention varies over time in people with ASD. To date, there are no studies to determine the influence of childhood neurodevelopment in autistic people on the perception of joint attention. It would be unprecedented to use the MRI-ET pairing as a tool for assessing social cognition as a function of the development of children with ASD.",[225,226,29,121,227],"ASD","Functional Magnetic Resonance Imaging","Joint Attention",[225,229,29,230,231],"Functional magnetic resonance imaging","social cognition","joint attention",{"date":206,"type":45},{"date":234,"type":45},"2022-01-04",{"date":236,"type":22},"2025-06",{"name":79,"class":52},{"id":239,"slug":240,"hasResults":11,"nctId":241,"briefTitle":242,"officialTitle":243,"acronym":244,"eligibilityCriteria":245,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":246,"targetDuration":4,"studyType":23,"phases":247,"briefSummary":248,"conditions":249,"keywords":253,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":257,"startDateStruct":259,"completionDateStruct":261,"leadSponsor":263,"locationsCount":80},"100554101","quantitative-evaluation-of-attention-to-faces-after-orthognathic-surgery-with-eye-tracking-100554101","NCT06494709","Quantitative Evaluation of Attention to Faces After Orthognathic Surgery With Eye-tracking","Pilot Study of Quantitative Evaluation of Attention to Faces of Patients With Orthognathic Surgery Using Eye-tracking","OCHIRO","Inclusion Criteria:\n\n* Naïve subject with regard to dentofacial deformities and their management\n* Subject with no known facial pathology\n* Subject having provided an informed consent\n* Subject \\> 18 years old\n\nExclusion Criteria:\n\n* Subject familiar with dentofacial deformities and their management (e.g., health professionals in the relevant specialties)\n* Subject with known facial pathology (dentofacial deformity or other)\n* Subject under guardianship, curators or justice protection",{"count":61,"type":22},[25],"Dentofacial deformities refer to morphological anomalies of the jaws. Their development during growth determines the shape of the lower third of the face and the type of dental occlusion. A maxillo-mandibular dysmorphosis associates morphological modification of the face and anomaly of the occlusion. If these anomalies are most often hereditary, they also depend on acquired factors such as swallowing, breathing, sucking or phonation disorders. Angle's classification defines three classes of dental occlusion: class I, when the ratio between the maxillary and mandibular first molars is normal, class II when the upper molar is too far forward, and class III when it is too far back. Class II and III dysmorphoses can result in an alteration of the masticatory function, pain (TMJ, headaches) or sleep apnea. At the same time, they cause patients to experience a decrease in self-esteem, anxiety and social discomfort. Class II and II usually require orthodontic treatment and orthognathic surgery to correctly align the jaws. This surgery has a positive impact on the dental occlusion and the functions concerned, but also on the facial morphology, all of which often leads to an improvement in the patient's quality of life.\n\nStandardized photographs presenting control subjects (class I) and patients (class II and class III) before and after surgery will be included in an approximately 10 min video sequence. Naive participants will look at this sequence during which the faces of the controls and the patients - before and after surgery - will alternate, with the instruction being free visual exploration of the images. The total fixation durations in defined areas of interest (eyes, nose, mouth, chin) will be recorded with an eye tracking device and the results will be processed using a dedicated software.",[250,251,252,29],"Dentofacial Deformities","Orthognathic Surgery","Social Perception",[250,254,255,148],"orthognathic surgery","social perception","2024-07-10",{"date":258,"type":45},"2024-07-11",{"date":260,"type":45},"2024-07-02",{"date":262,"type":22},"2026-08",{"name":79,"class":52}]