Situation and Evolution of the Misuse of Alcohol and Other Addictive Behaviors in Obese Patients Being Managed at Nîmes University Hospital (ADOB)

Obesity is a multifactorial pathology in which external (lifestyle, environment) and internal (psychological or biological, especially genetic) factors are involved. These are responsible for a positive energy balance. One of the external factors that can intervene in the genesis of obesity is the existence of eating disorders: bulimic hyperphagia. Some teams consider bulimic hyperphagia as a form of addiction. After bariatric surgery, the appearance of new addictions has been observed.

In connection with Pr Perney's addictology department, the investigators have observed that some patients under treatment for obesity at the endocrinology department subsequently developed other addictions, in particular misuse of alcohol.

The hypotheses of this research are :

There appears to be a transfer from eating disorders to substance misuse addiction in post-treatment of obesity, particularly in patients who have undergone bariatric surgery.

The misuse of addictive substances most concerned by this transfer of addiction in the post-treatment of obesity, particularly after bariatric surgery, seems to be the misuse of alcohol.

This will be the first French cohort study on addictive behaviors in patients undergoing bariatric surgery and the first international study including non-operated obese patients benefiting from medical care alone. This study will improve the multidisciplinary management of these patients by integrating addictologists.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

800

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Nîmes, France
        • Recruiting
        • CHU de Nîmes
        • Principal Investigator:
          • Emma LUCQUIAUD, Dr.
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

The target population for this study corresponds to all patients being managed for obesity (Body Mass Index ≥ 30 kg.m-²).

The source population for this study corresponds to all patients being managed by the obesity clinic at Nîmes University Hospital for obesity with a BMI ≥ 30 kg.m-² at the time of their first visit (complete hospitalization outpatients or consultation) for initiation to management (incident subjects).

Description

  • Patient being managed for the first time at Nîmes University Hospital Obesity Clinic ( complete hospitalization, outpatients' or consultation).
  • Patient being managed for obesity defined by a body mass index (BMI) of 30 kg.m-² or over
  • Patient affiliated to or covered by a health insurance scheme.
  • Adult patient (≥ 18 years).

Exclusion Criteria:

  • Patient with psychiatric disorder reducing capacity for comprehension.
  • Patient in an exclusion period determined by another study.
  • Patient under legal guardianship, tutorship or curatorship.
  • Patient to whom it is impossible to give clear information
  • Patient who is pregnant, about to give birth or breastfeeding.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Presence of alcohol abuse evaluated at the first clinical consultation according to the AUDIT(Alcohol Use Disorders Identification Test) questionnaire.
Time Frame: Day 0
The Alcohol Use Disorders Identification Test (AUDIT) self-questionnaire consists of 10 questions covering consumption (the first 3 questions), behaviors that may evoke dependency (not being able to stop drinking, inability to carry out one's plans, needing a drink in the morning) and problems related to alcohol consumption (guilt or remorse, memory loss, injuries, concerns from family and friends). Each question can be scored from 0 (low) - 4 (high) points, leading to a possible total score of 40 points. This questionnaire therefore makes it possible to cover all aspects of alcohol misuse in a very short space of time. It has been validated with good diagnostic performance: sensitivity at 92% and specificity at 94% for a threshold ≥ 8 (Saunders et al. 1993; Coulton et al. 2006). Moreover, this questionnaire is very widely used and recognized in scientific articles on addictology.
Day 0
Presence of alcohol abuse evaluated at the first clinical consultation according to the AUDIT(Alcohol Use Disorders Identification Test) questionnaire.
Time Frame: Month 12
The Alcohol Use Disorders Identification Test (AUDIT) self-questionnaire consists of 10 questions covering consumption (the first 3 questions), behaviors that may evoke dependency (not being able to stop drinking, inability to carry out one's plans, needing a drink in the morning) and problems related to alcohol consumption (guilt or remorse, memory loss, injuries, concerns from family and friends).Each question can be scored from 0 (low) - 4 (high) points, leading to a possible total score of 40 points. This questionnaire therefore makes it possible to cover all aspects of alcohol misuse in a very short space of time. It has been validated with good diagnostic performance: sensitivity at 92% and specificity at 94% for a threshold ≥ 8 (Saunders et al. 1993; Coulton et al. 2006). Moreover, this questionnaire is very widely used and recognized in scientific articles on addictology.
Month 12
Presence of alcohol abuse evaluated at the first clinical consultation according to the AUDIT(Alcohol Use Disorders Identification Test) questionnaire.
Time Frame: Month 24
The Alcohol Use Disorders Identification Test (AUDIT) self-questionnaire consists of 10 questions covering consumption (the first 3 questions), behaviors that may evoke dependency (not being able to stop drinking, inability to carry out one's plans, needing a drink in the morning) and problems related to alcohol consumption (guilt or remorse, memory loss, injuries, concerns from family and friends). Each question can be scored from 0 (low) - 4 (high) points, leading to a possible total score of 40 points.This questionnaire therefore makes it possible to cover all aspects of alcohol misuse in a very short space of time. It has been validated with good diagnostic performance: sensitivity at 92% and specificity at 94% for a threshold ≥ 8 (Saunders et al. 1993; Coulton et al. 2006). Moreover, this questionnaire is very widely used and recognized in scientific articles on addictology.
Month 24
Presence of alcohol abuse evaluated at the first clinical consultation according to the DSM-5 questionnaire
Time Frame: Day 0
The DSM-5 criteria are used to identify depression in all patients with high alcohol consumption (over14 glasses a week for women, 21 for men, or more than 4 glasses on one occasion). The DSM-5 outlines the following criterion to make a diagnosis of depression. The individual must be experiencing five or more symptoms during the same 2-week period and at least one of the symptoms should be either (1) depressed mood or (2) loss of interest or pleasure.
Day 0
Presence of alcohol abuse evaluated at the first clinical consultation according to the DSM-5 questionnaire
Time Frame: Month 12
The DSM-5 criteria are used to identify depression in all patients with high alcohol consumption (over14 glasses a week for women, 21 for men, or more than 4 glasses on one occasion). The DSM-5 outlines the following criterion to make a diagnosis of depression. The individual must be experiencing five or more symptoms during the same 2-week period and at least one of the symptoms should be either (1) depressed mood or (2) loss of interest or pleasure.
Month 12
Presence of alcohol abuse evaluated at the first clinical consultation according to the DSM-5 questionnaire
Time Frame: Month 24
The DSM-5 criteria are used to identify depression in all patients with high alcohol consumption (over14 glasses a week for women, 21 for men, or more than 4 glasses on one occasion). The DSM-5 outlines the following criterion to make a diagnosis of depression. The individual must be experiencing five or more symptoms during the same 2-week period and at least one of the symptoms should be either (1) depressed mood or (2) loss of interest or pleasure.
Month 24

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Smoking (tobacco addiction) according to the Fagerström test
Time Frame: Day 0
The Fagerström test consists of six questions. A score of 0 - 10 is obtained depending on the answers given. A score of 0 - 2 = zero addiction, 3 - 4 = slight addiction, 5 - 6 = moderate addiction, 7 ou 8 heavy addiction and 9 - 10 = very heavy addiction.
Day 0
Smoking (tobacco addiction) according to the Fagerström test
Time Frame: Month 12
The Fagerström test consists of six questions. A score of 0 - 10 is obtained depending on the answers given. A score of 0 - 2 = zero addiction, 3 - 4 = slight addiction, 5 - 6 = moderate addiction, 7 ou 8 heavy addiction and 9 - 10 = very heavy addiction.
Month 12
Smoking (tobacco addiction) according to the Fagerström test
Time Frame: Month 24
The Fagerström test consists of six questions. A score of 0 - 10 is obtained depending on the answers given. A score of 0 - 2 = zero addiction, 3 - 4 = slight addiction, 5 - 6 = moderate addiction, 7 ou 8 heavy addiction and 9 - 10 = very heavy addiction.
Month 24
Cannabis addiction
Time Frame: Day 0
The Cannabis Abuse Screening Test (CAST) questionnaire has 6 questions to which the answer YES (=1) or NO (=0) is given. A score ≥ 3 on the CAST indicates addiction to Cannabis.
Day 0
Cannabis addiction
Time Frame: Month 12
The Cannabis Abuse Screening Test (CAST) questionnaire has 6 questions to which the answer YES (=1) or NO (=0) is given. A score ≥ 3 on the CAST indicates addiction to Cannabis.
Month 12
Cannabis addiction
Time Frame: Month 24
The Cannabis Abuse Screening Test (CAST) questionnaire has 6 questions to which the answer YES (=1) or NO (=0) is given. A score ≥ 3 on the CAST indicates addiction to Cannabis.
Month 24
Use of cocaine
Time Frame: Day 0
The patient will be interviewed to find out whether he/she uses cocaine. This will be noted as Yes/No
Day 0
Use of cocaine
Time Frame: Month 12
The patient will be interviewed to find out whether he/she uses cocaine. This will be noted as Yes/No
Month 12
Use of cocaine
Time Frame: Month 24
The patient will be interviewed to find out whether he/she uses cocaine. This will be noted as Yes/No
Month 24
Use of amphetamines
Time Frame: Day 0
The patient will be interviewed to find out whether he/she uses amphetamines. This will be noted as Yes/No
Day 0
Use of amphetamines
Time Frame: Month 12
The patient will be interviewed to find out whether he/she uses amphetamines. This will be noted as Yes/No
Month 12
Use of amphetamines
Time Frame: Month 24
The patient will be interviewed to find out whether he/she uses amphetamines. This will be noted as Yes/No
Month 24
Use of opioids
Time Frame: Day 0
The patient will be interviewed to find out whether he/she uses opioids. This will be noted as Yes/No
Day 0
Use of opioids
Time Frame: Month 12
The patient will be interviewed to find out whether he/she uses opioids. This will be noted as Yes/No
Month 12
Use of opioids
Time Frame: Month 24
The patient will be interviewed to find out whether he/she uses opioids. This will be noted as Yes/No
Month 24
Use of hallucinogenic drugs and/or new synthetic drugs
Time Frame: Day 0
The patient will be interviewed to find out whether he/she uses hallucinogenic drugs and/or new synthetic drugs. This will be noted as Yes/No
Day 0
Use of hallucinogenic drugs and/or new synthetic drugs
Time Frame: Month 12
The patient will be interviewed to find out whether he/she uses hallucinogenic drugs and/or new synthetic drugs. This will be noted as Yes/No
Month 12
Use of hallucinogenic drugs and/or new synthetic drugs
Time Frame: Month 24
The patient will be interviewed to find out whether he/she uses hallucinogenic drugs and/or new synthetic drugs. This will be noted as Yes/No
Month 24
Eating disorders
Time Frame: Day 0
A score ≥ 17 on the BES (Binge Eating Scale) questionnaire indicates presence of an eating disorder.
Day 0
Eating disorders
Time Frame: Month 12
A score ≥ 17 on the BES (Binge Eating Scale) questionnaire indicates presence of an eating disorder.
Month 12
Eating disorders
Time Frame: Month 24
A score ≥ 17 on the BES (Binge Eating Scale) questionnaire indicates presence of an eating disorder.
Month 24
Comorbidities
Time Frame: Day 0
Presence of comorbidities for obesity (High blood pressure / Glucose intolerance or Diabetes / Sleep apnea syndrome / Dyslipidemia / Hepatic Steatosis / Cardiovascular diseases) will be noted from data in the patient file.
Day 0
Comorbidities
Time Frame: Month 12
Presence of comorbidities for obesity (High blood pressure / Glucose intolerance or Diabetes / Sleep apnea syndrome / Dyslipidemia / Hepatic Steatosis / Cardiovascular diseases) will be noted from data in the patient file.
Month 12
Comorbidities
Time Frame: Month 24
Presence of comorbidities for obesity (High blood pressure / Glucose intolerance or Diabetes / Sleep apnea syndrome / Dyslipidemia / Hepatic Steatosis / Cardiovascular diseases) will be noted from data in the patient file.
Month 24
Quality of Life according to the EQVOD scale
Time Frame: Day 0
The "Echelle de Qualité de Vie, Obésité et Diététique - EQVOD" (Quality of Life, Obesity and Dietetics Scale ) is a self-questionnaire validated in French which is adapted to the socio-cultural factors of obesity in France, making it possible to take into account the effects of dietary treatments on the quality of life of obese subjects (see Appendix 17.5) (Ziegler et al. 2005). It consists of 36 items, rated from 1 (always/highly) to 5 (never/not at all). It explores five dimensions (physical impact - Q1-Q11, psychosocial impact - Q12-Q22, impact on sexual life - Q23-Q26, food well-being - Q27-Q31 and diet experience - Q32-Q36). The rating for each dimension is reported as 100. The closer the score is to 100, the better the quality of life related to that dimension.
Day 0
Quality of Life according to the EQVOD scale
Time Frame: Month 12
The "Echelle de Qualité de Vie, Obésité et Diététique - EQVOD" (Quality of Life, Obesity and Dietetics Scale ) is a self-questionnaire validated in French which is adapted to the socio-cultural factors of obesity in France, making it possible to take into account the effects of dietary treatments on the quality of life of obese subjects (see Appendix 17.5) (Ziegler et al. 2005). It consists of 36 items, rated from 1 (always/highly) to 5 (never/not at all). It explores five dimensions (physical impact - Q1-Q11, psychosocial impact - Q12-Q22, impact on sexual life - Q23-Q26, food well-being - Q27-Q31 and diet experience - Q32-Q36). The rating for each dimension is reported as 100. The closer the score is to 100, the better the quality of life related to that dimension.
Month 12
Quality of Life according to the EQVOD scale
Time Frame: Month 24
The "Echelle de Qualité de Vie, Obésité et Diététique - EQVOD" (Quality of Life, Obesity and Dietetics Scale ) is a self-questionnaire validated in French which is adapted to the socio-cultural factors of obesity in France, making it possible to take into account the effects of dietary treatments on the quality of life of obese subjects (see Appendix 17.5) (Ziegler et al. 2005). It consists of 36 items, rated from 1 (always/highly) to 5 (never/not at all). It explores five dimensions (physical impact - Q1-Q11, psychosocial impact - Q12-Q22, impact on sexual life - Q23-Q26, food well-being - Q27-Q31 and diet experience - Q32-Q36). The rating for each dimension is reported as 100. The closer the score is to 100, the better the quality of life related to that dimension.
Month 24
Anxiety and Depression
Time Frame: Day 0

The Hospital Anxiety and Depression Scale (HADS) is a self-report questionnaire that assesses depressive and anxiety symptomatology (excluding somatic symptoms) and measures severity in patients between 16 and 65 years of age from a hospital environment (Zigmong & Snaith 1983, Snaith et al. 2003). The HADS consists of two parts: (a) 7 questions for screening for depression, and (b) 7 questions for screening for anxiety disorders. Each question receives a score between 0 and 3. The score for each part is obtained by adding the items that make up the part. The higher the score, the greater the severity of the corresponding symptoms.

The French version was validated by Razavi et al. 1989 and Friedman et al. 2001.

Day 0
Anxiety and Depression
Time Frame: Month 12

The Hospital Anxiety and Depression Scale (HADS) is a self-report questionnaire that assesses depressive and anxiety symptomatology (excluding somatic symptoms) and measures severity in patients between 16 and 65 years of age from a hospital environment (Zigmong & Snaith 1983, Snaith et al. 2003). The HADS consists of two parts: (a) 7 questions for screening for depression, and (b) 7 questions for screening for anxiety disorders. Each question receives a score between 0 and 3. The score for each part is obtained by adding the items that make up the part. The higher the score, the greater the severity of the corresponding symptoms.

The French version was validated by Razavi et al. 1989 and Friedman et al. 2001.

Month 12
Anxiety and Depression
Time Frame: Month 24

The Hospital Anxiety and Depression Scale (HADS) is a self-report questionnaire that assesses depressive and anxiety symptomatology (excluding somatic symptoms) and measures severity in patients between 16 and 65 years of age from a hospital environment (Zigmong & Snaith 1983, Snaith et al. 2003). The HADS consists of two parts: (a) 7 questions for screening for depression, and (b) 7 questions for screening for anxiety disorders. Each question receives a score between 0 and 3. The score for each part is obtained by adding the items that make up the part. The higher the score, the greater the severity of the corresponding symptoms.

The French version was validated by Razavi et al. 1989 and Friedman et al. 2001.

Month 24
Binge eating
Time Frame: Day 0
The Binge Eating Scale (BES) is a self-administered questionnaire that diagnoses Binge Eating Disorder (BED) and assesses the behavioural, emotional and cognitive symptoms associated with Binge Eating Disorder in obese individuals (Gormally et al. 1982). It is composed of 16 items corresponding to groups of sentences including one to be selected from 3 to 4 propositions, which best describe how one feels. For each item, the subject has to choose the formulation that best corresponds to his current situation, which results in a score varying between 0 and 3 or between 0 and 2 for each item. Half of the items measure eating behaviours and the other half assess feelings or cognitions occurring during compulsive episodes. It gives a total score (from 0 to 46) that reflects the severity of the BED. A score greater than or equal to 18 indicates significant bulimic hyperphagia. The French version of this questionnaire was translated and validated by Brunault et al (2016).
Day 0
Binge eating
Time Frame: Month 12
The Binge Eating Scale (BES) is a self-administered questionnaire that diagnoses Binge Eating Disorder (BED) and assesses the behavioural, emotional and cognitive symptoms associated with Binge Eating Disorder in obese individuals (Gormally et al. 1982). It is composed of 16 items corresponding to groups of sentences including one to be selected from 3 to 4 propositions, which best describe how one feels. For each item, the subject has to choose the formulation that best corresponds to his current situation, which results in a score varying between 0 and 3 or between 0 and 2 for each item. Half of the items measure eating behaviours and the other half assess feelings or cognitions occurring during compulsive episodes. It gives a total score (from 0 to 46) that reflects the severity of the BED. A score greater than or equal to 18 indicates significant bulimic hyperphagia. The French version of this questionnaire was translated and validated by Brunault et al (2016).
Month 12
Binge eating
Time Frame: Month 24
The Binge Eating Scale (BES) is a self-administered questionnaire that diagnoses Binge Eating Disorder (BED) and assesses the behavioural, emotional and cognitive symptoms associated with Binge Eating Disorder in obese individuals (Gormally et al. 1982). It is composed of 16 items corresponding to groups of sentences including one to be selected from 3 to 4 propositions, which best describe how one feels. For each item, the subject has to choose the formulation that best corresponds to his current situation, which results in a score varying between 0 and 3 or between 0 and 2 for each item. Half of the items measure eating behaviours and the other half assess feelings or cognitions occurring during compulsive episodes. It gives a total score (from 0 to 46) that reflects the severity of the BED. A score greater than or equal to 18 indicates significant bulimic hyperphagia. The French version of this questionnaire was translated and validated by Brunault et al (2016).
Month 24

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Age
Time Frame: Day 0
Age will be recorded in years
Day 0
Age
Time Frame: Month 12
Age will be recorded in years
Month 12
Age
Time Frame: Month 24
Age will be recorded in years
Month 24
Weight
Time Frame: Day 0
Weight will be recorded in kg.
Day 0
Weight
Time Frame: Month 12
Weight will be recorded in kg.
Month 12
Weight
Time Frame: Month 24
Weight will be recorded in kg.
Month 24
Height
Time Frame: Day 0
Height will be recorded in cm
Day 0
Height
Time Frame: Month 12
Height will be recorded in cm
Month 12
Height
Time Frame: Month 24
Height will be recorded in cm
Month 24
Sex
Time Frame: Day 0
Male/Female
Day 0
Sex
Time Frame: Month 12
Male/Female
Month 12
Sex
Time Frame: Month 24
Male/Female
Month 24
Other relevant items
Time Frame: Day 0
All items (X-rays, biological tests, medicinal treatment…) relevant to the patient's care will be noted
Day 0
Other relevant items
Time Frame: Month 12
All items (X-rays, biological tests, medicinal treatment…) relevant to the patient's care will be noted
Month 12
Other relevant items
Time Frame: Month 24
All items (X-rays, biological tests, medicinal treatment…) relevant to the patient's care will be noted
Month 24
Insulinemia only in the immun-Adob subpopulation
Time Frame: Day 0 and Month 12
Method of determining insulin levels
Day 0 and Month 12
Homa index in the Immun-Adob subpopulation
Time Frame: Day 0 and Month 12
Blood glucose measurement that is routine test
Day 0 and Month 12
Presence of waist circumference criterion ≥ 94 cm in men, ≥ 80 cm in women or BMI > 30 kg/m²
Time Frame: Day 0
clinically determined visceral obesity
Day 0
Triglyceride levels ≥ 1.5 G/L or treatment
Time Frame: Day 0
Triglyceride measurements that are routine tests
Day 0
Low HDL levels < 0.40g/L in men and < 0.50 in women or treatment
Time Frame: Day 0
HDL measurement which is a routine biological analysis.
Day 0
High blood pressure SBP ≥ 130 mmHg or DBP ≥ 85 mmHg or treatment.
Time Frame: Day 0
Hypertension is determined clinically
Day 0
Fasting blood glucose ≥ 1g/L
Time Frame: Day 0
Glucose intolerance measurement which is a routine biological test.
Day 0
Therelationship between membership in the immune activation profile of hyperinsulinism and the evolution of insulin levels
Time Frame: Between Day 0 and Month 12
The percentages of CD57+, PD-1+, CD38+, HLA-DR+, naive or memory T4 or T8 cells will be determined by flow cytometry
Between Day 0 and Month 12
The link between belonging to the immune activation profile of hyperinsulinism and the evolution of the HOMA index
Time Frame: Between Day 0 and Month 12
The percentages of CD57+, PD-1+, CD38+, HLA-DR+, naive or memory T4 or T8 cells will be determined by flow cytometry
Between Day 0 and Month 12
The link between the membership to the immune activation profile of hyperinsulinism and the evolution of the metabolic syndrome
Time Frame: Between Day 0 and Month 12
Between Day 0 and Month 12

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 16, 2021

Primary Completion (Estimated)

December 15, 2026

Study Completion (Estimated)

December 15, 2026

Study Registration Dates

First Submitted

October 28, 2020

First Submitted That Met QC Criteria

October 28, 2020

First Posted (Actual)

November 3, 2020

Study Record Updates

Last Update Posted (Actual)

June 16, 2026

Last Update Submitted That Met QC Criteria

June 15, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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