Eating disorders are multifactorial disorders currently conceptualized in a biopsychosocial model, but pathophysiology remains relatively unknown, and robust etiological models to guide treatment are therefore lacking. Different endophenotypes and neurocognitive vulnerability factors have been found in eating disorders including decision making abnormalities. The investigators hypothesize that decision making abnormalities are associated with a lower level of functioning and quality of life which could lead to social and interpersonal difficulties. The investigators also hypothesize that these anomalies are associated with a particular clinical profile (more restrictive profile, more hyperactivity, less insight on the disease and desire for care ...).
The investigators will recruit a total of 340 patients with an eating disorder in the university hospital of Montpellier. * Participation consists of a one-day visit with a multidisciplinary assessment. No action is specific to research. This is the usual management of patients with eating disorders addressed to our department. * An ancillary study will be proposed, if the patient is addressed by his general practitioner for an annual evaluation. This second visit will be exactly the same as the initial visit.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
340
All patients assessed in the day-hospital will performed the same evaluation : * Blood sampling * Calorimetry * Osteodensitometry * Psychiatric assessment * Endocrinologic assessment * Dietetic assessment * Neuropsychological assessment * Self-questionnaires With the patient agreement, a biological collection will be constituted. The objective is the subsequent study of biological factors involved in eating disorders (in particular genetic factors)
Hôpital Lapeyronie
Montpellier, France
Level of functional impairment assessed by the Work and Social Adjustment Scale (WSAS)
We aim to investigate the link between decision-making and daily functioning of patients with eating disorder.
Time frame: Baseline
Quality of life assessed by the Eating disorder quality of life (EDQOL) scale.
We aim to investigate the link between quality of life and alteration of cognitive flexibility of patients with eating disorder.
Time frame: Baseline
Level of functional impairment assessed by the clinician with the Functional Assessment Staging Test (FAST) scale
We aim to investigate the link between global functioning and alteration of cognitive flexibility of patients with eating disorder.
Time frame: Baseline
Quality of life assessed by the Eating disorder quality of life (EDQOL) scale.
We aim to investigate the link between quality of life and alteration central coherence of patients with eating disorder.
Time frame: Baseline
Level of functional impairment assessed by the clinician with the FAST scale
We aim to investigate the link between global functioning and alteration central coherence of patients with eating disorder.
Time frame: Baseline
Score to decision making test (Iowa gambling task)
We aim to investigate the prognostic value of decision making abnormalities on the rates of recovery
Time frame: At 12 months if patient is included in the ancillary study
Score to decision making test (Iowa gambling task)
We aim to investigate the prognostic value of decision making abnormalities on weight recovery (for anorexic patients)
Time frame: At 12 months if patient is included in the ancillary study
Score to decision making test (Iowa gambling task)
We aim to investigate the prognostic value of decision making abnormalities on daily functioning
Time frame: At 12 months if patient is included in the ancillary study
Score to decision making test (Iowa gambling task)
We aim to investigate the prognostic value of decision making abnormalities on switch to another subtype of eating disorder
Time frame: At 12 months if patient is included in the ancillary study
Score to decision making test (Iowa gambling task)
We aim to investigate the impact of weight recovery on decision making abilities
Time frame: At 12 months if patient is included in the ancillary study
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