- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05602805
BariaPSY: the Data Bank
Mental Health, Eating Disorders and Obesity Databank
Multimorbidity, the co-occurrence of several chronic conditions, is a growing phenomenon that poses new challenges for clinicians and researchers. The association between a mental health disorder and a physical health disorder represents a particularly frequent subtype of multimorbidity and is associated with greater severity and higher consumption of care. It is essential and urgent to explore the specific pathophysiology of this subtype of multimorbidity in order to develop adapted therapeutic strategies.
Psychiatric disorders, such as mood disorders, anxiety disorders, attention deficit disorder and binge eating disorder, are common in people with obesity. For example, although most of these disorders may improve after bariatric surgery, some components of these disorders, such as emotional dysregulation and impulsivity, need to be addressed as they appear to be involved in the development of addiction and suicidality after bariatric surgery. Therefore, screening and vigilance of these risks appear increasingly necessary.
To address this challenge, the BariaPsy databank aims to explore the screening of certain mental health disorders frequently observed in adults with obesity through an innovative approach that explores behaviors in the form of dimensions. It will help clinicians to quickly identify markers of certain disorders, thus helping them to further investigate the problem and provide personalized resources to their patient.
Study Overview
Status
Conditions
Detailed Description
The specific research objectives pursued by BariaPsy are as follows:
- To develop a comprehensive screening tool to support the health professionals (surgeon, physician, specialized practice nurse) in their consultation regarding the mental health of the candidate for overweight or obesity management, helping them to delve deeper into the problem and to give personalized resources to their patient so that they can be well supported.
- To evaluate the interest of such an evaluation device on the effectiveness and tolerance of the management proposed to the participants.
- To better characterize patients with physical-mental multimorbidity and the impact of this phenotype on management, in order to issue appropriate recommendations.
- To identify the prevalence of psychiatric disorders, including mood disorders, anxiety disorders, attention deficit disorder, and binge eating disorder, in the hospital setting, in the overweight/obese population.
- To identify potential pathophysiological mechanisms to explain the links between mental health and obesity by relating the affected psychological dimensions to the anthropometric, metabolic and sociodemographic parameters of the participants (through information contained in the medical records).
- Identify potential pathophysiological mechanisms to explain the links between mental health and obesity by relating the affected psychological dimensions to the parameters of current biology available in the medical record (liver, inflammatory, carbohydrate and lipid balance, etc.), but also biological and histological parameters (e.g., adipose tissue samples) in relation to the biobank or management frameworks that are already in place (e.g., in the bariatric surgery service).
Also, the participant's authorization will be requested in the Information and Consent Form to have access to their IUCPQ medical record, which contains a collection of sociodemographic, anthropometric and biological information as well as information related to their obesity management (data collection by the bariatric surgery program nurse and/or data collection carried out when the questionnaire is sent to the bariatric medicine or psychiatry programs).
The BariaPsy databank will improve the screening of certain mental health disorders frequently observed in the context of overweight or obesity in adults. The data collected will be used for several research studies with the objective of better characterizing patients with physical-mental multimorbidity and the impact of this phenotype on management, in order to issue appropriate recommendations.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Sylvain Iceta, Md, PhD
- Phone Number: 4565 +1 (418) 656-8711
- Email: equipe.iceta@criucpq.ulaval.ca
Study Locations
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Quebec
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Québec, Quebec, Canada, G1V4G5
- Recruiting
- IUCPQ
-
Contact:
- Sylvain Iceta, MD, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Be a patient referred to the IUCPQ for management of overweight or obesity
- Have a body mass index (BMI) ≥25 kg/m2
- Be 18 years old or older
Exclusion Criteria:
- Be an incapacitated or protected adult as defined by law
- Not registered or eligible for RAMQ
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Binge Eating Disorder (BEDS-7)
Time Frame: Baseline
|
A screening tool that has been designed to screen adults who may have binge eating disorder. The results indicate whether or not the test screens for binge eating behaviors (yes or no). |
Baseline
|
|
Binge Eating Scale (BES)
Time Frame: Baseline
|
To assess the presence of certain binge eating behaviors that may be indicative of an eating disorder. The higher the score, the more binge eating behaviors is observed. The minimum score is 0 while the maximum score is 46. The final result allows to say if the person has an absent (less than 17), moderate (between 18 and 26) or severe (more than 27) binging level. |
Baseline
|
|
Generalized Anxiety Disorder (GAD-7)
Time Frame: Baseline
|
A screening tool and severity measure for generalised anxiety disorder. The higher the score, the higher the level of anxiety. The minimum score is 0 and the maximum score is 21. The clinically significant score is 15. |
Baseline
|
|
Patient Health Questionnaire (PHQ-9)
Time Frame: Baseline
|
The PHQ-9 is a multipurpose instrument for screening, monitoring and measuring the severity of depression. The higher the score, the more depressive symptoms are present. The minimum score is 0 and the maximum score is 27. It allows to evaluate if there is no depression (9 and less), a major depression (between 10 and 19) or a severe major depression (20 and more). |
Baseline
|
|
Adult ADHD Self-Report Scale (ASRS-5)
Time Frame: Baseline
|
To evaluate the manifestations and behaviors of attention deficit and hyperactivity disorder in adults. The higher the final score, the more evidence of ADHD is present. The minimum score is 6 and the maximum score is 30. |
Baseline
|
|
Modified Yale Food Addiction Scale 2.0 (mYFAS 2.0)
Time Frame: Baseline
|
The mYFAS 2.0 was designed to assess food addiction using a shorter version than the YFAS 2.0.It assesses the symptoms of food addiction and the resulting distress and impaired functioning. The higher the level of symptoms, the more severe the food addiction. Impaired functioning and distress are scored from 0 to 2. Symptoms are scored from 0 to 11. If the functioning and distress score is 1 and above, the food addiction may be mild (2-3 symptoms), moderate (4-5 symptoms), or severe (6+ symptoms). |
Baseline
|
|
Impulsive Behavior Scale Short Form (UPPS-P)
Time Frame: Baseline
|
Measurement of factors that can lead to impulsive behavior. There are five subscales: Positive Urgency, Negative Urgency, Lack of Premeditation, Lack of Perseverance, and Sensation Seeking. A higher score on the scale or subscale corresponds to a higher level of impulsivity. The minimum total score is 1 and the maximum total score is 4. |
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gender identity
Time Frame: Baseline (Sociodemographic Questionnaire)
|
Choose from: Cisgender, Transgender, non-binary, Queer, I refuse to answer, Other
|
Baseline (Sociodemographic Questionnaire)
|
|
Ethnic origin
Time Frame: Baseline (Sociodemographic Questionnaire)
|
Choose from: Black, East Asian, Latino, Middle Eastern, South Asian, Southeast Asian, South Asian descent, White, I refuse to answer, Other
|
Baseline (Sociodemographic Questionnaire)
|
|
Marital status
Time Frame: Baseline (Sociodemographic Questionnaire)
|
Choose from: Single, Common-law, Married, Divorced, Widowed, I refuse to answer, Other
|
Baseline (Sociodemographic Questionnaire)
|
|
Highest level of education
Time Frame: Baseline (Sociodemographic Questionnaire)
|
Choose from: None, High School, Cegep, Diploma of Vocational Studies, Vocational Technical, Undergraduate University, Graduate University, Postgraduate University or Other
|
Baseline (Sociodemographic Questionnaire)
|
|
Average annual income
Time Frame: Baseline (Sociodemographic Questionnaire)
|
In dollars.
|
Baseline (Sociodemographic Questionnaire)
|
|
Living space for most of the year
Time Frame: Baseline (Sociodemographic Questionnaire)
|
Choose from: House/apartment/condominium, apartment or condominium for seniors, home of a relative or friend, retirement home, adult foster home, CHSLD, other
|
Baseline (Sociodemographic Questionnaire)
|
|
Current employment status
Time Frame: Baseline (Sociodemographic Questionnaire)
|
Choose from: working full time, working part time, unemployed or laid off looking for work, unemployed not looking for work, homemaker, student, retired, disable
|
Baseline (Sociodemographic Questionnaire)
|
|
Number of person living at your place of residence
Time Frame: Baseline (Sociodemographic Questionnaire)
|
Choose from: living alone, 1 person, 2 persons, 3 persons, 4 persons, 5 persons or more
|
Baseline (Sociodemographic Questionnaire)
|
|
Weight
Time Frame: Baseline (Sociodemographic Questionnaire)
|
In kilograms (kg).
|
Baseline (Sociodemographic Questionnaire)
|
|
Height
Time Frame: Baseline (Sociodemographic Questionnaire)
|
In meters (m).
|
Baseline (Sociodemographic Questionnaire)
|
|
Food allergies or intolerances
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open answer
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Lifestyle habits
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Choice: tobacco products, electronic cigarettes (with or without nicotine), alcohol and/or drugs. Quantity, frequency and cessation date, if applicable, are requested. |
Baseline (Bariatric Surgery Initial Assessment)
|
|
Health history and conditions
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Choice: Type 1 or 2 diabetes, hypothyroidism, hyperthyroidism, thyroid nodules, cirrhosis, inflammatory bowel disease, recent prior digestive investigation (less than 5 years), colonoscopy, abdominal surgery, bariatric surgery, other surgery, asthma, COPD, home oxygen, sleep apnea, menstruation (hysterectomy, hormone therapy, pills or IUD), coronary angioplasty (with or without stent), myocardial infarction, cardiac surgery, thrombophlebitis, coagulopathy, pulmonary embolism, renal lithiasis, CKD, psychiatric hospitalization, suicide attempt, mental health diagnosis, eating disorders, neoplasia, chronic pain, other health conditions If applicable, since when and followed by whom. |
Baseline (Bariatric Surgery Initial Assessment)
|
|
Family history of bariatric surgery
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open-ended questions about obesity and bariatric surgeries in the applicant's family.
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Weight and diet history
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open-ended questions about current and past weight and dieting to get a sense of the person's history over time in relation to their weight.
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Food history
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open-ended questions related to meal intake, meal frequency, food consumed and food-related behaviors.
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Physical activity History
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open-ended questions about physical activity, which ones are practiced, how often and what barriers are encountered.
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Perception of body image
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open-ended questions about body image and motivation to treat obesity.
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Expectations of health care professionals
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open-ended response to know the expectations towards health professionals in the management of their obesity.
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Motivation to have surgery
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Since when does he want to have surgery and for what reasons?
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Nutritional recommendations
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Three recommendations personally issued by a nutritionist are requested.
|
Baseline (Bariatric Surgery Initial Assessment)
|
|
Knowledge of bariatric surgery
Time Frame: Baseline (Bariatric Surgery Initial Assessment)
|
Open-ended questions about the different resources that should have been consulted as well as the knowledge required (side effects, recommendations, complication and percentage of failure) are asked.
|
Baseline (Bariatric Surgery Initial Assessment)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023-3886, 22254
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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