Dissociative Disorders in Obesity (Dissobe) (NCT05081778) | Clinical Trial Compass
CompletedNot Applicable
Dissociative Disorders in Obesity (Dissobe)
France240 participantsStarted 2019-05-05
Plain-language 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.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The degree of dissociative tendencies
Timeframe: 1 day
Trial details
NCT IDNCT05081778
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche