Perception and Representation of Internal Body in Anorexia Nervosa (PERCEPCOR)

July 19, 2021 updated by: Aude Paquet, Centre Hospitalier Esquirol
This study focuses on representations of the interior of the body and interoceptive awareness in women with anorexia nervosa in comparison with women without eating disorders.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Limoges, France, 87000
        • Centre Hospitalier Esquirol

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

10 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Anorexia Nervosa according to DSM-5
  • aged above than 14
  • BMI between 14 and 18.5 for adults or less than the reference age by age for minors

Exclusion Criteria:

  • Unable to understand the tests, poor understanding of the French language
  • Mental retardation
  • Severe psychiatric comorbidity (bipolar disorder, schizophrenia)
  • Lesion or pathology of the upper limbs
  • Pregnancy
  • Absence of social protection
  • Hospitalization under duress

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Anorexia
Subjects with anorexia nervosa
many tests are realized: a drawing of the interior of the body a heartbeat detection test an ischemia induction test many scales: Eating Attitude Test; Body Awareness Questionnaire; Body Shape Questionnaire; Hospital Anxiety and Depression; Questionnaire de Satisfaction Corporelle et de Perception Globale de Soi
Other Names:
  • scales
Active Comparator: Control
Subjects without eating disorders
many tests are realized: a drawing of the interior of the body a heartbeat detection test an ischemia induction test many scales: Eating Attitude Test; Body Awareness Questionnaire; Body Shape Questionnaire; Hospital Anxiety and Depression; Questionnaire de Satisfaction Corporelle et de Perception Globale de Soi
Other Names:
  • scales

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
drawing
Time Frame: At inclusion
Number and nature of organs drawn
At inclusion

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
IAI
Time Frame: At inclusion
interoceptive awareness index
At inclusion
Time
Time Frame: At inclusion
time to obtain a score of 3 on the analogue visual scale at the ischemia induction test
At inclusion

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 11, 2018

Primary Completion (Actual)

March 25, 2019

Study Completion (Actual)

July 7, 2021

Study Registration Dates

First Submitted

June 13, 2019

First Submitted That Met QC Criteria

June 13, 2019

First Posted (Actual)

June 17, 2019

Study Record Updates

Last Update Posted (Actual)

July 20, 2021

Last Update Submitted That Met QC Criteria

July 19, 2021

Last Verified

July 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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