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Program for Screening and Prevention of Eating Disorders in Obese Young People in Vulnerable Neighborhoods of Marseille: an Action Research

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ClinicalTrials.gov Identifier: NCT03357354
Recruitment Status : Not yet recruiting
First Posted : November 29, 2017
Last Update Posted : November 29, 2017
Sponsor:
Information provided by (Responsible Party):
Assistance Publique Hopitaux De Marseille

Brief Summary:

Action research has been developed in this direction in order to use a tool to identify food disorder behavior among obese youths in their neighborhoods and social centers in vulnerable neighborhoods of Marseille, with the aim of a multi-professional therapeutic management (psychosocial support, theater) and a specialized orientation.

This program consists of the participation of each patient recruited in collective workshops. A total of 60 patients considered. Our hypothesis lies in the fact that for young people to participate in an adapted device, taking into account the global needs of young people and their entourage, would limit the deleterious effects of obesity and promote the young person's autonomy and allow him to be a actor in the request for care.

The project's objective is to provide support in the form of workshops with patients identified by the Marseille Hospitals Public Assistance Health Center as obese children and adolescents, in a precarious situation; to identify the presence of binge eating disorders and evaluate the impact of participation in these workshops on subsequent management by highly specialized professionals in food disorder behavior.


Condition or disease Intervention/treatment Phase
Obesity Behavioral: collective workshop Not Applicable

Detailed Description:
The mobile team (EM) of the Marseille Hospitals Public Assistance Health Center has the mission to inform, screen, support and guide the access to care of people in targeted neighborhoods, said to be vulnerable, by the city's policy of Marseille. The health space, a place of welcome and care, is located at a distance from any hospital structure within the most vulnerable neighborhoods of the city.

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 60 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Program for Screening and Prevention of Eating Disorders in Obese Young People in Vulnerable Neighborhoods of Marseille: an Action Research
Estimated Study Start Date : February 1, 2018
Estimated Primary Completion Date : February 1, 2020
Estimated Study Completion Date : December 1, 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Eating Disorders

Arm Intervention/treatment
Experimental: Obese Children in precarious situations Behavioral: collective workshop
diet, sports games, food budget, feeling of satiety and hunger, self-image




Primary Outcome Measures :
  1. Number of subjects included in the three months following the end of the workshops in a device specialized in the management of behavioral disorders. [ Time Frame: 6 MONTHS ]
    Tracking interview after the end of workshops


Secondary Outcome Measures :
  1. Evaluation of with the ADO-BEDS [ Time Frame: 6 MONTHS ]
    children and teenagers will be asked to answer some items



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Ages Eligible for Study:   11 Years to 17 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria :

  • Boys or girls aged 11 to 17
  • Reside in the territory of intervention of the mobile team, i.e the 3rd, 14th, 15th and 16th arrondissement of Marseille, districts said to be vulnerable by the city's policy.
  • Body mass index greater than or equal to IOTF-30 (HAS, 2011)
  • Social precariousness score EPICES greater than or equal to 30riteria:
  • Diagnosed Eating Disorder without medical and/or multi-professional care

Exclusion Criteria:

  • Child with major difficulty of behavior
  • Patient with medical care

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03357354


Contacts
Contact: ANNE GALINIER 04.91.96.66.61 anne.galinier@ap-hm.fr
Contact: claire morando 04.91.38.21.83 claire.morando@ap-hm.fr

Locations
France
Assistance Publique Hopitaux de Marseille Not yet recruiting
Marseille, France, 13354
Contact: ANNE GALINIER    04.91.96.66.61    anne.galinier@ap-hm.fr   
Contact: CLAIRE MORANDO    04.91.38.21.83    claire.morando@ap-hm.fr   
Sponsors and Collaborators
Assistance Publique Hopitaux De Marseille
Investigators
Study Director: Urielle DESALBRES Assistance Publique Hopitaux De Marseille

Responsible Party: Assistance Publique Hopitaux De Marseille
ClinicalTrials.gov Identifier: NCT03357354     History of Changes
Other Study ID Numbers: 2017-31
First Posted: November 29, 2017    Key Record Dates
Last Update Posted: November 29, 2017
Last Verified: November 2017

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Feeding and Eating Disorders
Mental Disorders