NCT03485469 The Impact of the Hypnosis on the Loss of Weight at Patients in Failure of Bariatric Surgery
| NCT ID | NCT03485469 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University Hospital, Montpellier |
| Condition | Obesity |
| Study Type | INTERVENTIONAL |
| Enrollment | 70 participants |
| Start Date | 2019-03-29 |
| Primary Completion | 2026-10 |
Trial Parameters
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Brief Summary
The therapeutic problem of obesity is weight control, a major difficulty, involving a significant change in eating behavior. A number of studies show that there are many factors of resistance to weight loss whether they are physiological, genetic, environmental pressure related, or psychological and behavioral. For some patients, the surgical approach seems the best alternative. Indeed, bariatric surgery is an effective therapeutic weapon in patients with morbid obesity. However, it has been shown that approximately 25% of patients are failing at two years of this surgery (Reinhold's index). Some of the failed subjects may benefit from surgical revision. As for the others, no intervention is currently proposed to them. Studies have shown that the psychological profile of patients who are candidates for bariatric surgery is predominantly impulsive, very anxious with a tendency to depression. The stress level of these patients would be important, and they would have low self-esteem. This study hypothesize that, in these patients, the establishment of hypnotherapeutic management associated with the usual dietary monitoring could modify eating habits thus promoting weight loss and an improvement in self-esteem , stress and anxiety compared to dietary monitoring alone.
Eligibility Criteria
Inclusion criteria: * Obese patient (BMI = 30 kg / m ²) * 18 - 65 years ( inclusive borders) * Patient in failure of bariatric surgery and in which no surgical resumption can be proposed (in view of Reinhold's classification, the failure will be considered as a loss of overweight lower than 50 % in two years further to a bariatric surgery). * Informed consent * Patient in measure to realize all the visits and to follow the procedures of the study - Subject affiliated to a social security system Exclusion criteria: * Pregnancy current or planned during the duration of the study, pregnant or breast-feeding women * Craniopharyngioma or any other evolutionary malignant pathology, or chronic illness in decompensation phase * Strong probability of not compliance to the protocol or drop-out * Psychiatric pathology of dissociated type (schizophrenia; psychosis, bipolarity …) * Sensory (hearing, visual) or cognitive deficits susceptible to hinder the progress of the sessions. * Incapacity to un
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