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Набор скоро начнётся NCT07031037

Exploratory Study of Sensory Profile and Coping Strategies in Eating Disorders

— Наблюдательное Eating Disorders Anorexia Nervosa Boulimia Nervosa Hyperphagia

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Scales.
Кому может быть актуально
Состояния в реестре: Eating Disorders, Anorexia Nervosa, Boulimia Nervosa, Hyperphagia. Базовые параметры: 18 лет — 65 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Франция
Следующий шаг
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Обзор

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. 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.

Вмешательства

  • Другое 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 Multidimens

Первичные конечные точки

  • Sensory profile from the Adolescent and Adult Sensory Profile (Brown and Dunn, 2002) according to each diagnostic group. [Срок оценки: At enrollment]
  • Scores for task coping drawn from the Coping Inventory for Stressful Situations (Endler & Parker, adapted by JP Rolland) according to each diagnostic group [Срок оценки: at enrollment]
Вторичные конечные точки (4)
  • Description of the frequency of autistic traits for each diagnostic group [Срок оценки: At enrollment]
  • Description of the frequency of eating disorders for each diagnostic group. [Срок оценки: At enrollment]
  • Anxiety according to each diagnostic group. [Срок оценки: At enrollment]
  • Body awareness from the multidimensional assessment of interoceptive awareness for each diagnostic group. [Срок оценки: At enrollment]

Критерии участия

Критерии включения

  • Gender and Age: Male or female, aged 18 to 65
  • 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).

Критерии исключения

  • Psychiatric comorbidity (non-tobacco addiction, characterized depressive episode, bipolar disorder, obsessive-compulsive disorder, schizophrenia and related disorders, neurodevelopmental disorder)
  • 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

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Только случаи

Центры проведения

Франция · 1 центр
  • Esquirol Hospital Center — Limoges

Идентификаторы

NCT: NCT07031037 · 2024-A01154-43

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗