Characteristics of Intensity and Dependence to Physical Activity in Anorexia Nervosa (HAP-AM)

September 12, 2016 updated by: Institut Mutualiste Montsouris

Intensity and Dependence to Physical Activity and Its Links With Clinical and Emotional Statuses in Comparison With Healthy Controls.

Etude d'épidémiologie clinique multicentrique (IMM), naturalistique, comparant un échantillon clinique à un échantillon de témoins issus de la population générale.

Cette recherche se fixe pour objectif principal de déterminer, sur un large échantillon de patients pris en charge pour anorexie mentale dans des unités de soins spécialisées, les caractéristiques de l'activité physique et la dépendance à l'exercice physique en comparaison avec des sujets issus de la population générale appariés pour l'âge et le sexe.

Nous faisons l'hypothèse que les patients anorexiques mentaux sont plus actifs et plus dépendants à l'exercice physique que des sujets de la population générale de même âge et de même sexe.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

300

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

  • France
      • Paris, France, 75014
        • Institut Mutualiste Montsouris

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

13 years to 23 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Pour l'échantillon clinique (patients témoins et contrôles) : prise en charge pour Anorexie Mentale (selon les critères DSM-IV) dans le département de psychiatrie de l'enfant et de l'adolescent de l'Institut Mutualiste Montsouris.

Pour l'échantillon individus sains témoins : Sujets issus de la population générale (collégiens lycéens étudiants).

Description

Inclusion Criteria:

  • Sujets de sexe masculin et féminin, âgés entre 13 et 23 ans.
  • Donnant leur consentement éclairé (et celui des parents pour les mineurs)
  • Pour l'échantillon clinique : prise en charge pour Anorexie Mentale (selon les critères DSM-IV) dans le département de psychiatrie de l'enfant et de l'adolescent de l'Institut Mutualiste Montsouris.
  • Pour l'échantillon témoin : Sujets issus de la population générale (collégiens lycéens étudiants).

Exclusion Criteria:

  • Personnes refusant la recherche
  • Personnes souffrant d'une condition médicale majeure ou d'une invalidité.

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

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Patients controles
Inpatients suffering from anorexia nervosa at Institut Mutualiste Montsouris
Individus sains témoins
Healthy controls selected from the general population

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
GPAQ-OMS
Time Frame: At initial assessment and 6 weeks later
Questionnaire de l'OMS sur la pratique d'activités physiques
At initial assessment and 6 weeks later
GLTEQ
Time Frame: At initial assessment and 6 weeks later
Godin Leisure-Time Exercise Questionnaire
At initial assessment and 6 weeks later
EDS-R
Time Frame: At initial assessment and 6 weeks later
Exercise-Dependence Scale-Revised
At initial assessment and 6 weeks later
EDQ
Time Frame: At initial assessment and 6 weeks later
Exercise-Dependence Questionnaire ; sélection des questions sur les motivations à pratiquer
At initial assessment and 6 weeks later
EDE-Q
Time Frame: At initial assessment and 6 weeks later
Eating Disorder Examination Questionnaire
At initial assessment and 6 weeks later
CIDI
Time Frame: At initial assessment
Composite International Diagnostic Interview
At initial assessment
MOCI
Time Frame: At initial assessment and 6 weeks later
Maudsley Obsessive Compulsive Inventory
At initial assessment and 6 weeks later

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
HAD
Time Frame: At initial assessment and 6 weeks later
Hospital Anxiety & Depression Scale
At initial assessment and 6 weeks later
EMPF
Time Frame: At initial assessment and 6 weeks later
Echelle Multidimensionnelle de Perfectionnisme de Frost
At initial assessment and 6 weeks later
TMMS
Time Frame: At initial assessment and 6 weeks later
(Trait Meta Mood Scale)
At initial assessment and 6 weeks later
RES
Time Frame: At initial assessment and 6 weeks later
(Rosenberg Self-Esteem Scale)
At initial assessment and 6 weeks later
BSQ
Time Frame: At initial assessment and 6 weeks later
(Body Shape Questionnaire)
At initial assessment and 6 weeks later
BIA
Time Frame: At initial assessment and 6 weeks later
Impedancemétrie Bioélectrique
At initial assessment and 6 weeks later

Collaborators and Investigators

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

Sponsor

Institut Mutualiste Montsouris

Investigators

  • Principal Investigator: Nathalie GODART, Institut Mutualiste Montsouris

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

February 1, 2014

Primary Completion (Actual)

May 1, 2015

Study Completion (Actual)

September 1, 2015

Study Registration Dates

First Submitted

May 2, 2014

First Submitted That Met QC Criteria

June 12, 2014

First Posted (Estimate)

June 18, 2014

Study Record Updates

Last Update Posted (Estimate)

September 13, 2016

Last Update Submitted That Met QC Criteria

September 12, 2016

Last Verified

September 1, 2016

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2014-02

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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