Exploratory Study of Sensory Profile and Coping Strategies in Eating Disorders
NCT ID: NCT07031037
Last Updated: 2025-06-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
150 participants
OBSERVATIONAL
2025-07-31
2028-07-31
Brief Summary
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The 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.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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Scales
Five questionnaires were administered at inclusion, socio-demographic and clinical data were collected during an interview (anxiety-depression, treatments).
The following questionnaires were used: The Revised Ritvo Autism and Asperger Diagnostic Scale (RAADS-R-Fr), the Eating Disorder Examination Self-Report Questionnaire (EDE-Q), the Adolescent/Adult Sensory Profile (AASP), the Coping Inventory for Stressful Situations (CISS), the Hospital anxiety and depression scale (HAD) and the Multidimensional Assessment of Interoceptive Awareness Version 2 (MAIA-2).
Eligibility Criteria
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Inclusion Criteria
* 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
* Hospitalization or consultation for Eating Disorder at Centre Hospitalier Esquirol
* Consent: Free, informed, and written consent, signed by the participant and/or 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).
Exclusion Criteria
* History of Eating Disorder other than current disorder
* Proven sensory or neurological disability
* Inability to understand questionnaires and information related to the study
* Persons under psychiatric care in accordance with articles L. 3212-1 and L. 3213-1
* Pregnant, nursing or parturient women
* Adults subject to legal protection or unable to express their consent to express their consent
* Persons not affiliated to a social security scheme or not benefiting from one social security scheme
* Persons deprived of their liberty by judicial or administrative decision
18 Years
65 Years
ALL
No
Sponsors
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Centre Hospitalier Esquirol
OTHER
Responsible Party
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Aude Paquet
Psychomotor Therapist, Doctor in Psychology
Locations
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Esquirol Hospital Center
Limoges, Nouvelle-Aquitaine, France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2024-A01154-43
Identifier Type: -
Identifier Source: org_study_id
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