Recruiting studies
Obesity
Study
Participate in our clinical trial to evaluate the effectiveness of a therapeutic approach for weight management in adults living with excess weight and an associated health condition.
The situation: Living with excess weight presents daily challenges, and the presence of other risk factors such as prediabetes, hypertension, dyslipidemia, sleep apnea, or cardiovascular disease can increase the workload placed on your body.
Finding a suitable solution to promote weight loss while safely and rigorously managing these related health conditions is a priority for current medical research.
The objective of the study: We are preparing a clinical trial to evaluate the effectiveness of an investigational treatment for weight management.
This protocol aims to analyze the effects of weight loss and support for overall health in participants with excess weight and at least one associated medical comorbidity.
What participating in this study means:
- Free access to treatment: Eligible participants will have free access to the study weight-loss treatment for the duration of their participation.
- Specialized medical supervision: You will benefit from regular follow-ups and examinations related to the clinical study, fully supervised by our healthcare professionals.
- Contribution to science: Your participation helps advance medical knowledge about the interactions between weight management and other metabolic or cardiovascular disorders.
- Compensation: Financial compensation is provided to cover your time and travel expenses.
Eligibility and Voluntary Participation
Participation in this research is entirely voluntary. You may withdraw from the study at any time, without providing a reason, and this will not affect the quality of your future care.
Each medical profile is rigorously reviewed by our team of professionals.
To be eligible, you must:
- Be 18 years of age or older.
- Have a body mass index (BMI) between 27.0 and 29.9 kg/m².
- Have received a formal diagnosis for at least one of the following weight-related conditions: prediabetes, hypertension, dyslipidemia (including stable lipid-lowering therapy for at least 4 weeks, or abnormal LDL, HDL, or triglyceride levels), obstructive sleep apnea, or a weight-related cardiovascular condition (such as ischemic cardiovascular disease or heart failure).
Would you like more information?
Our recruitment team is available to explain the study process, answer your questions, and confirm your eligibility.
I want to apply to this clinical study
Participate in the study of Trois-Rivières
For more information, contact us at 819 801-9797 (Trois-Rivières) or at 1-844-739-3439 (toll free), or fill the online form.
The study process in pictures
Explanation
Step 1 | Before starting the study, we will take time to fully explain the selection process and the conduct of the study by phone.
Meeting
Step 2 | After the initial phone interview, if you are still interested in taking part in a study, we schedule a preliminary meeting with you during which you may ask all the questions you wish and take the time you require to read over the consent form. This form explains, in detail, the different stages of each study.
Decision
Step 3 | You may make a decision at that time to move forward with or terminate the selection process. However, you are under no obligation to make an immediate decision. Based on briefing content, you may take the time necessary to come to a decision and consult with your personal physician or loved ones.
Tests
Step 4 | Depending on the nature of the study, some tests or medical examinations may be required. In the majority of cases, these tests or examinations are conducted on Diex Research premises based on your individual availability.
Departure
Step 5 | If you are eligible, you may then begin a clinical study with us.
