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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03799497
Other study ID # 2009_48
Secondary ID 2010-A00545-34
Status Completed
Phase
First received
Last updated
Start date June 7, 2013
Est. completion date June 7, 2020

Study information

Verified date September 2020
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Body Image distortion is a key diagnostic feature for Anorexia Nervosa. Patients suffering from Anorexia Nervosa tend to perceive themselves as fatter than they are. This bias might be at the origin of a reinforcement of anorectic behavior which might alter medical care. The objective of this study is to identify neural correlates of self-recognition in Anorexia Nervosa. Patients are hypothesized to activate the self-recognition network when seeing images of a fatter body shape than their own.


Description:

Patients suffering from Anorexia Nervosa and control subjects (matched by age and study level) are recruited in medical care facilities in Lille's Metropolis. They are asked to identify their body shape when being presented with 3 different stimuli, i.e.real (RBS), estimated (EBS) and neutral body shape (NBS), in a functional magnetic resonance imaging or functional MRI (fMRI) machine. While answering to this identification paradigm, we hoped to identify modifications in the self body-recognition network.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date June 7, 2020
Est. primary completion date June 7, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 45 Years
Eligibility Inclusion Criteria:

- Providing informed, dated and signed consent (for minors, consent must be signed by both parents)

- With medical insurance

- With normal vision

- Only for the AN Group : Diagnosis of Anorexia Nervosa (AN) restrictive for at least one year and with a Body Masse index (BMI) between 14 and 18

- Only for the control Group : BMI between 18 and 25 and without any psychiatric disorder

Exclusion Criteria:

- Pregnant or breast-feeding women

- With antecedent or current neurologic disease

- With antecedent or current ophthalmologic disease

- Contraindication for IRMf

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHRU,Hôpital Fontan 2 Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure of the activation brain areas in self body-recognition network Level of activation areas in the self body-recognition network measured during fMRI 15 days
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