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The Impact of the Hypnosis on the Loss of Weight at Patients in Failure of Bariatric Surgery (BARIATHYPNOSE)

Primary Purpose

Obesity, Bariatric Surgery

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Hypnosis
Standard Care
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Obesity, bariatric surgery, Hypnosis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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 understand the nature and the purpose of the study and\or communication difficulties with the investigator
  • Patient having already benefited from a coverage by hypnotherapy for loss of weight
  • Taken by treatment having an impact on the loss of weight (corticoid, antithyroid …)
  • Major protected by the law or considered vulnerable (under guardianship)

Sites / Locations

  • CHR Saint Pierre - maladies métaboliquesRecruiting
  • Cécile GODELRecruiting
  • Orléans University HospitalRecruiting
  • Reims University HospitalRecruiting
  • Toulouse University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Usual Care

Hypnosis

Arm Description

The control group will benefit from a standard care dietary consultation in the service and 9 dietary consultations by phone every 15 days.

The experimental group will benefit from a dietary consultation in the service, 9 dietary consultations by telephone every 15 days to which will be associated 7 individual sessions of hypnosis and 3 individual sessions of learning to autohypnosis. A recording containing the induction of a self-hypnosis session will be given to the subject at the end of the 10 sessions, in order to promote the continuation of home-made autohypnosis.

Outcomes

Primary Outcome Measures

Change in weight in 5 months
Patient weight (in kg) measurement will be performed on the same scale by staff who are unaware of the patient's randomization group.

Secondary Outcome Measures

Change in weight in 12 months
Patient weight (in kg) measurement will be performed on the same scale by staff who are unaware of the patient's randomization group.
Self-esteem
It will be evaluated by the scale of "Rosenberg's Self Esteem Scale" (1965) validated in French. It represents an assessment of the overall self-esteem that the person can have of herself. The scale includes 10 statements measured on a scale of 1 to 4.
Evolution of Quality of life
it will be evaluated by the variation of the scores obtained in the self-questionnaire EQVOD (Echelle de Qualité de Vie, Obésité et Diététique) of O. Ziegler et al (2005). It's a specific quality of life questionnaire for obese people.
Anxiety and depressive state
It will be evaluated by the Hospital Anxiety and Depression Scale - HAD (Sigmond et al, 1983). It is a self-administered 14-item questionnaire that assesses the current level of depressive and anxious symptomatology by eliminating somatic depressions that may skew assessments.
Feeding behavior
It will be evaluated by the TFEQ-R21 (Three-Factor Eating Questionnaire) self-questionnaire (Cappelleri et al, 2009). TFEQ has been validated in the general population and has been used in many studies. It explores three components of eating behavior: cognitive restriction, uncontrolled eating, and emotional eating.
Patients' satisfaction with their care
It will be evaluated the Likert scales of the self-satisfaction questionnaire. It is composed of 5 Likert scales coded from 1 to 5 which will be analyzed separately

Full Information

First Posted
March 26, 2018
Last Updated
May 11, 2023
Sponsor
University Hospital, Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT03485469
Brief Title
The Impact of the Hypnosis on the Loss of Weight at Patients in Failure of Bariatric Surgery
Acronym
BARIATHYPNOSE
Official Title
A Prospective Randomized Clinical Trial, in Open-label, Multicenter, Estimating the Impact of the Hypnosis on the Loss of Weight at Patients in Failure of Bariatric Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 29, 2019 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
October 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.
Detailed Description
he 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. There are still no studies assessing the impact of hypnotherapeutic management and self-hypnosis on the weight curve, self-esteem, stress, anxiety, or the quality of life of patients Obese in failure of bariatric surgery. It is an Interventional, prospective, multi-center, controlled, randomized, open-label study with 2 parallel arms, evaluating the efficacy of hypnotherapeutic management in patients with bariatric surgery failure, compared to dietary monitoring alone. Number of visits: 13 visits are planned: 1 visit of inclusion, a visit ensuring the first dietary follow-up, 9 hypnosis sessions (for the experimental group), two visits dedicated to the collection of the judgment criteria. Each patient is followed for 12 months. The estimated duration of recruitment is 18 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Bariatric Surgery
Keywords
Obesity, bariatric surgery, Hypnosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
Other
Arm Description
The control group will benefit from a standard care dietary consultation in the service and 9 dietary consultations by phone every 15 days.
Arm Title
Hypnosis
Arm Type
Other
Arm Description
The experimental group will benefit from a dietary consultation in the service, 9 dietary consultations by telephone every 15 days to which will be associated 7 individual sessions of hypnosis and 3 individual sessions of learning to autohypnosis. A recording containing the induction of a self-hypnosis session will be given to the subject at the end of the 10 sessions, in order to promote the continuation of home-made autohypnosis.
Intervention Type
Behavioral
Intervention Name(s)
Hypnosis
Intervention Description
There ar 10 hypnosis sessions : 1st session of hypnosis : relaxation and orientation towards "emotional cleansing". 2nd session of hypnosis: oriented towards digestion, physical and psychological 3rd session of hypnosis: oriented towards the feeling of security. 4th session of hypnosis: self-esteem oriented. 5th hypnosis session: oriented towards emotional management. 6th hypnosis session: oriented towards self-confidence. 7th hypnosis session: oriented towards the completion of the projects. 8th, 9th and 10th sessions: concern the learning of self-hypnosis and autonomy. A USB key containing the induction of a session of autohypnosis will be given to the subject to promote the continuation of home-made auto-hypnosis.
Intervention Type
Behavioral
Intervention Name(s)
Standard Care
Intervention Description
The dietary advice given during these dietary consultations is part of the standard care adapted to patients who have undergone bariatric surgery while increasing the frequency of consultations (Fractionation of meals, Volume of meals, Taking meals, Drinks, Food diversity)
Primary Outcome Measure Information:
Title
Change in weight in 5 months
Description
Patient weight (in kg) measurement will be performed on the same scale by staff who are unaware of the patient's randomization group.
Time Frame
5 months
Secondary Outcome Measure Information:
Title
Change in weight in 12 months
Description
Patient weight (in kg) measurement will be performed on the same scale by staff who are unaware of the patient's randomization group.
Time Frame
12 months
Title
Self-esteem
Description
It will be evaluated by the scale of "Rosenberg's Self Esteem Scale" (1965) validated in French. It represents an assessment of the overall self-esteem that the person can have of herself. The scale includes 10 statements measured on a scale of 1 to 4.
Time Frame
12 months
Title
Evolution of Quality of life
Description
it will be evaluated by the variation of the scores obtained in the self-questionnaire EQVOD (Echelle de Qualité de Vie, Obésité et Diététique) of O. Ziegler et al (2005). It's a specific quality of life questionnaire for obese people.
Time Frame
12 months
Title
Anxiety and depressive state
Description
It will be evaluated by the Hospital Anxiety and Depression Scale - HAD (Sigmond et al, 1983). It is a self-administered 14-item questionnaire that assesses the current level of depressive and anxious symptomatology by eliminating somatic depressions that may skew assessments.
Time Frame
12 months
Title
Feeding behavior
Description
It will be evaluated by the TFEQ-R21 (Three-Factor Eating Questionnaire) self-questionnaire (Cappelleri et al, 2009). TFEQ has been validated in the general population and has been used in many studies. It explores three components of eating behavior: cognitive restriction, uncontrolled eating, and emotional eating.
Time Frame
12 months
Title
Patients' satisfaction with their care
Description
It will be evaluated the Likert scales of the self-satisfaction questionnaire. It is composed of 5 Likert scales coded from 1 to 5 which will be analyzed separately
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
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 understand the nature and the purpose of the study and\or communication difficulties with the investigator Patient having already benefited from a coverage by hypnotherapy for loss of weight Taken by treatment having an impact on the loss of weight (corticoid, antithyroid …) Major protected by the law or considered vulnerable (under guardianship)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cécile GODEL, Dietetician
Phone
04.67.33.79.52
Ext
+33
Email
c-godel@chu-montpellier.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Mélanie DELOZE, CRA
Email
m-deloze@chu-montpellier.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David NOCCA, PU-PH
Organizational Affiliation
University Hospital, Montpellier
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHR Saint Pierre - maladies métaboliques
City
La Réunion
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nathalie LEMOULEC
Facility Name
Cécile GODEL
City
Montpellier
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cécile GODEL, Dietetician
Phone
04.67.33.79.52
Email
c-godel@chu-montpellier.fr
First Name & Middle Initial & Last Name & Degree
Mélanie DELOZE, CRA
Email
m-deloze@chu-montpellier.fr
Facility Name
Orléans University Hospital
City
Orléans
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elise MONGEOIS
Facility Name
Reims University Hospital
City
Reims
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eric BERTIN
Facility Name
Toulouse University Hospital
City
Toulouse
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrick RITZ

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Impact of the Hypnosis on the Loss of Weight at Patients in Failure of Bariatric Surgery

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