[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Centre Hospitalier Esquirol\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":158},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,48,77,103,127],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100616444","climate-anxiety-in-a-young-population-at-risk-of-suicide-100616444",false,"NCT07305688","Climate Anxiety in a Young Population at Risk of Suicide","Anx-RS","Inclusion Criteria:\n\n* Men and women, boys and girls ;\n* Aged between 16 and 24;\n* Participants seen in adult or pediatric emergency departments, hospitalised in adult psychiatry or in child and adolescent psychiatry, or seen in outpatient consultation at Esquirol Hospital Center ;\n* Affiliated with a social security scheme or entitled to coverage under one ;\n* Having received full information about the study and having co-signed, together with the investigator, an informed consent form to participate in the study.\n* For minor participants: the consent to participate in the study must be signed by the holder(s) of parental authority, and the minor's assent will also be required.\n\nExclusion Criteria:\n\n* Participants will not be included in the study if their health condition is incompatible with understanding or completing the questionnaires used. This includes, in particular ;\n* Any chronic somatic pathology or major sensory impairment (for example : deafness or blindness) preventing reading, comprehension or communication with healthcare professionals ;\n* Any severe psychiatric pathology that significantly impairs cognitive or communication abilities, such as acute psychotic disorders, pervasive developmental disorders or confusional states ;\n* Participants hospitalised in units specialising in severe psychiatric disorders with major impairment of cognitive functions.\n* Adults under legal protection, in accordance with article L 1121-8 of the Public Health Code ;\n* Insufficient command of the French language","ALL","16 Years","24 Years",{"count":20,"type":21},108,"ESTIMATED","OBSERVATIONAL","Climate change has become a major source of concern, particularly among younger generations who are facing the progressive degradation of ecosystems, loss of biodiversity, and alarming environmental information disseminated through the media. The direct perception of climate-related disruptions has been shown to engender a profound sense of helplessness and loss. This distress, termed eco-anxiety, is characterised by feelings of fear, sadness and guilt regarding the planet's future.\n\nIn a context where there has been a marked increase in suicidal thoughts and attempts among young people over the past decade, it is essential to explore the psychological manifestations of eco-anxiety within this vulnerable population. The paucity of studies investigating this association underscores the significance of the present research.\n\nThe aims of this study is to examine the relationship between climate anxiety and suicidal risk among young people aged 16 to 24 years.\n\nThe study will encompass 108 young participants aged between 16 and 24 years, who are either hospitalised or receiving outpatient psychiatric care.\n\nEach participant will be required to complete one clinician-administered assessment, namely the Columbia Suicide Severity Rating Scale (C-SSRS), and two self-report questionnaires: the Climate Change Anxiety Scale - French version (CCAS-FR) and the State-Trait Anxiety Inventory (STAI-Y).\n\nFurthermore, a sociodemographic questionnaire will be administered in order to collect information regarding the subjects' age, sex, education level, living conditions, and psychiatric history.\n\nIt is hypothesised that there is a positive association between climate anxiety and suicidal risk, with the most eco-anxious participants showing higher C-SSRS scores. It is further predicted that eco-anxiety will correlate with elevated levels of state and trait anxiety, with the potential for modulating this relationship by sociodemographic factors, including gender.\n\nThis study will contribute to a better understanding of the psychological impacts of climate change on young people and help identify the most vulnerable profiles.",[25,26,27,28],"Anxiety","Suicidal Ideation","Mental Health Issue","Environmental Exposure",[30,31,32,33,34],"Eco-anxiety","Anxiety disorders","Suicide risk","Mental health","Young adults","RECRUITING","2026-06-02",{"date":38,"type":39},"2026-06-04","ACTUAL",{"date":41,"type":39},"2025-12-15",{"date":43,"type":21},"2027-03-15",{"name":45,"class":46},"Centre Hospitalier Esquirol","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":16,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":47},"100598512","sensory-profile-of-people-with-high-intellectual-potential-hip-100598512","NCT07072455","Sensory Profile of People With High Intellectual Potential (HIP)","Sensory Profile of People With High Intellectual Potential","HPIsens","Inclusion Criteria:\n\n* High Intellectual Potential:\n* Participants with a High Intellectual Potential : Cognitive assessment using the WAIS or WISC-V scale by a psychologist; Intelligence Quotient (IQ) ≥ 130, in the case of a homogeneous cognitive profile, or General Aptitude Index (GAI) \\> 130 \\[124-134\\], in the case of a heterogeneous cognitive profile\n* Gender and Age: Male or female, aged 18 to 65\n* Consent: Free, informed, and written consent (e-CRF)\n* Control :\n* Gender and Age: Male or female, aged 18 to 65\n* Consent: Free, informed, and written consent (e-CRF)\n\nExclusion Criteria:\n\n* High Intellectual Potential:\n* History or declared psychiatric disorder (characterized depressive episode, personality disorder, addiction, eating disorder, bipolar disorder, obsessive-compulsive disorder)\n* Neurodevelopmental disorders (autism spectrum disorder, attention deficit and hyperactivity disorder , developmental coordination disorder)\n* Sensory disability\n* Subjects under guardianship or curatorship\n* Pregnant or breast-feeding women\n* Control :\n* Presence of High Intellectual Potential known\n* Presence of intellectual development disorder\n* History or declared psychiatric disorder (characterized depressive episode, personality disorder, addiction, eating disorder, bipolar disorder, obsessive-compulsive disorder)\n* Neurodevelopmental disorders (autism spectrum disorder, attention deficit and hyperactivity disorder , developmental coordination disorder)\n* Sensory disability\n* Subjects under guardianship or curatorship\n* Pregnant or breast-feeding women",true,"18 Years","65 Years",{"count":60,"type":21},160,"This is a prospective observational psychology study on a non-clinical population, involving the use of questionnaires (non-interventional research).\n\nThis study involves the collection of data associated with High Intellectual Potential characteristics, sensory profile, and includes clinical measures such as anxiety anxiety, autistic traits and coping in High Intellectual Potential and control participants.",[63],"High Intellectual Potential",[63,65,66,25,67,68],"Sensory Profile","Coping Strategies","Sensory Processing","Autistic traits","2025-07-21",{"date":71,"type":39},"2025-07-24",{"date":73,"type":39},"2025-04-01",{"date":75,"type":21},"2027-04",{"name":45,"class":46},{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":16,"minAge":57,"maxAge":58,"enrollmentInfo":84,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":86,"conditions":87,"keywords":92,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":47},"100595329","exploratory-study-of-sensory-profile-and-coping-strategies-in-eating-disorders-100595329","NCT07031037","Exploratory Study of Sensory Profile and Coping Strategies in Eating Disorders","SensoryCop","Inclusion Criteria:\n\n* Gender and Age: Male or female, aged 18 to 65\n* Confirmed diagnosis of anorexia nervosa (F50.01; F50.02), boulimia nervosa (F50.2), hyperphagic episodes (F50.8) or restriction or avoidance of food intake (F50.8) according to DSM-5 criteria\n* Hospitalization or consultation for Eating Disorder at Centre Hospitalier Esquirol\n* Consent: Free, informed, and written consent, signed by the participant and\u002For their legal representative (for participants under protection measures) and the investigator (at the latest on the day of inclusion and before any research-related examination).\n\nExclusion Criteria:\n\n* Psychiatric comorbidity (non-tobacco addiction, characterized depressive episode, bipolar disorder, obsessive-compulsive disorder, schizophrenia and related disorders, neurodevelopmental disorder)\n* History of Eating Disorder other than current disorder\n* Proven sensory or neurological disability\n* Inability to understand questionnaires and information related to the study\n* Persons under psychiatric care in accordance with articles L. 3212-1 and L. 3213-1\n* Pregnant, nursing or parturient women\n* Adults subject to legal protection or unable to express their consent to express their consent\n* Persons not affiliated to a social security scheme or not benefiting from one social security scheme\n* Persons deprived of their liberty by judicial or administrative decision",{"count":85,"type":21},150,"This descriptive study aims primarily to characterize the sensory profile of patients with eating disorders (divided into three diagnostic groups: anorexia nervosa, boulimia nervosa and hyperphagia), controlling for possible autistic traits in this population.\n\nThe study involves measuring characteristics associated with eating disorders (diagnosis, BMI, anxiety), assessing the sensory profile (AASP), and coping strategies in patients with eating disorders who are hospitalised or followed up in consultation.",[88,89,90,91],"Eating Disorders","Anorexia Nervosa","Boulimia Nervosa","Hyperphagia",[65,66,88,93],"sensory processing disorder","NOT_YET_RECRUITING","2025-06-12",{"date":97,"type":39},"2025-06-22",{"date":99,"type":21},"2025-07",{"date":101,"type":21},"2028-07",{"name":45,"class":46},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":107,"acronym":108,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":16,"minAge":57,"maxAge":58,"enrollmentInfo":110,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":112,"conditions":113,"keywords":117,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":47},"100580642","sensory-profile-and-early-clinical-signs-of-calm-room-users-100580642","NCT06839950","Sensory Profile and Early Clinical Signs of Calm Room Users","EVAL-APAISE","Inclusion Criteria:\n\n* Gender and Age: Male or female, aged 18 to 65\n* Hospitalization: Admitted to the closed hospitalization unit for less than 10 days\n* Social security: Affiliated or beneficiary of a social security system\n* Consent: Free, informed, and written consent, signed by the participant and\u002For their legal representative (for participants under protection measures) and the investigator (at the latest on the day of inclusion and before any research-related examination).\n\nExclusion Criteria:\n\n* Inability to understand information related to the study\n* Proven sensory disability\n* Dementia\n* Pregnancy\n* Lack of social protection\n* Previous Participation in this research protocol (in the case of a new hospitalization)\n* Expression abilities incompatible with completing the AASP Scale (e.g., french language comprehension issues, mute individuals, patients in restraint and\u002For therapeutic isolation)",{"count":111,"type":21},80,"This descriptive study aims primarily to characterize the sensory profile of patients in a closed psychiatric hospital unit who use a calming room.\n\nThe main questions it aims to answer are :\n\n* Could sensory information processing disorders be the cause of distress and tension in these patients?\n* Could users of the calming room present extreme sensory processing profiles, characterized by either hypersensitivity or hyposensitivity ?\n\nParticipants will answer a survey to determine their the sensory profile. Participants can already use the calming room as part of their regular medical care and they will answer surveys before and after each use.",[114,115,116],"Psychotic Disorders","Personality Disorders","Mood Disorders",[118,114,65,116,115],"Calm room","2025-02-17",{"date":121,"type":39},"2025-02-21",{"date":123,"type":39},"2023-12-19",{"date":125,"type":21},"2028-05-19",{"name":45,"class":46},{"id":128,"slug":129,"hasResults":11,"nctId":130,"briefTitle":131,"officialTitle":132,"acronym":133,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":16,"minAge":135,"maxAge":136,"enrollmentInfo":137,"targetDuration":4,"studyType":139,"phases":140,"briefSummary":142,"conditions":143,"keywords":145,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":47},"100534080","impact-of-psychomotor-therapy-on-the-quality-of-life-in-depression-100534080","NCT06234176","Impact of Psychomotor Therapy on the Quality of Life in Depression","Influence of Psychomotor Therapy on Quality of Life in Patients With a Major Depressive Disorder: a Randomized Controlled Trial","PsyMot-Dep","Inclusion Criteria:\n\n* Diagnosis of depressive episode according to DSM-5 criteria.\n* HDRS \\> 16\n* Hospitalized or followed-up in one of the participating centers.\n* Affiliated or beneficiary of a social security scheme.\n* Free, informed and written consent signed by the participant and the investigator (no later than the day of inclusion and before any examination required by the research).\n\nExclusion Criteria:\n\n* Psychiatric comorbidity (non-tobacco addiction, eating disorders, bipolar disorder, obsessive-compulsive disorder, schizophrenia and related disorders)\n* Sensory impairment or proven neurological pathology\n* History of neurological brain damage (including stroke, tumor, trauma resulting in loss of consciousness lasting more than 10 minutes)\n* Limited functional ability (difficulty in moving about, performing manual tasks or moving about)\n* Inability to understand questionnaires and study information\n* Inability to travel to the inclusion center (personal vehicle, public transport)\n* Pregnant or breast-feeding women, on declaration\n* Forced hospitalization, subjects under guardianship or trusteeship, lack of social protection","20 Years","60 Years",{"count":138,"type":21},128,"INTERVENTIONAL",[141],"NA","The effectiveness of psychomotor therapy in improving clinical outcomes or quality of life for individuals with depression is unclear.\n\nThe investigators will assess how the participants' quality of life and psychomotor profile change over time.\n\nThe study aims to compare the quality of life at 3 months between patients who received 3 months of personalised psychomotor therapy in addition to standard treatment and those who received standard treatment alone.\n\nThe study lasted for 6 months, and the investigators expects a total of 128 people to participate in this research across several hospital establishments. This study evaluates the effectiveness of two types of treatment, divided into two randomly selected groups.\n\nTo participate, individuals must have a medical diagnosis of major depressive disorder (MDD) and be between the ages of 20 and 60.\n\nThey must have depressive symptoms with an HDRS score greater than 16 and provide informed consent. They must be treated or hospitalised at the Centre Hospitalier Esquirol or the Centre Hospitalier Henri Laborit (France).\n\nAfter providing consent, they will undergo an initial clinical interview that evaluates anxiety, self-esteem, pleasure, and quality of life. The therapist assessed the participant's muscle tone, gross motor skills, praxis, manual dexterity, rhythm, processing of sensory information, and body image.\n\nFollowing the assessment, the participant was randomly assigned to either the experimental or control group.\n\nThe experimental group received the usual treatment for depression and underwent psychomotor therapy once a week for 12 weeks.\n\nThe control group received the standard treatment for depression and underwent weekly telephone interviews.\n\nAn assessment is scheduled at 1 month to evaluate the participant's health status, including any changes to treatment and assessment of anxiety and depressive symptoms.\n\nAnother interim check-up is scheduled at 3 months to assess the patient's health status. The interview will also assess any changes to treatment, anxiety and depressive symptoms, quality of life, and psychomotor function.\n\nA final visit will be scheduled at 6 months for an assessment of the participant's health. The interview will also assess any changes to treatment, anxiety and depressive symptoms, quality of life, and psychomotor function.",[144],"Major Depressive Disorder",[146,147,148,149,150],"psychomotor therapy","quality of life","major depressive disorder","psychomotor profile","sensory processing",{"date":152,"type":39},"2025-02-19",{"date":154,"type":39},"2024-04-01",{"date":156,"type":21},"2026-08",{"name":45,"class":46},""]