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NCT05081778 Clinical Trial

Dissociative Disorders in Obesity (Dissobe)

Obesity Clinical Trial

— Dissobe  

Official title:
Dissociative Disorders in Obesity

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05081778
Other study ID # 2018-A02797-48
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 5, 2019
Est. completion date December 5, 2019

Study information
Verified date October 2021
Source Ramsay Générale de Santé
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

THe aim of this study is to determine the frequency of dissociative tendencies in the obese population treated at the CELIOBE (Liberal Center for Obesity Support) at Hôpital Privé La Louvière among patients consulting for the first time and looking for a medical or surgical course. The DES scale of Carlson and Putman will be used.

Recruitment information / eligibility
Status Completed
Enrollment 240
Est. completion date December 5, 2019
Est. primary completion date July 5, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age over 18 - Obesity defined by a Body Mass Index (BMI) = 30 kg / m2 - Patient seen in consultation at CELIOBE for the first time for the management of an overweight problem, wishing for surgical or medical care - Patient having been informed and not opposing to this research - Patient affiliated or beneficiary of a social security scheme Exclusion Criteria: - Psychotic antecedents: Schizophrenia, Schizoaffective disorders, Hallucinatory psychoses, Brief psychotic attacks - Addictive behaviors (alcohol, drug addiction) - Drug use - Taking antipsychotics and mood stabilizers - Dissociative identity disorders proven - Bipolar disorders or severe mental illness - Understanding troubles - Protected patient: Major under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision; Hospitalized without consent - Pregnant, breastfeeding or parturient woman

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Obese patient following a medical course
Questionnaires for the assessment of dissociative disorders in obese patients : DES scale of Carlson and Putman, SDQ-20 of Nijenhuis, comorbidities, Dutch Eating Behaviour Questionnaire (DEBQ), questionnaire of Rosenberg

Locations
Country Name City State
France Hôpital privé La Louvière Lille Haut De France

Sponsors (2)
Lead Sponsor Collaborator
Ramsay Générale de Santé European Clinical Trial Experts Network

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary The degree of dissociative tendencies The degree of dissociative tendencies measured by the Carlson and Putman DES scale. 1 day
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