
How does the modern world understand the mechanisms of depression and other mental health disorders? How do we verify which care approaches are effective? Through research, collaboration between professionals and individuals with mental health conditions allows us to build evidence-based scientific knowledge. This transforms mental health care from an area of uncertainty into one of clarity, making treatments more effective, safer, and more personalized.
By participating in research, you will receive a professional evaluation from researchers while also complying with the required interventions and assuming associated risks (such as time commitment for assessments or blood tests). Your participation will contribute to advancements in mental health treatment.
By participating in research, you will receive a professional evaluation from researchers while also complying with the required interventions and assuming associated risks (such as time commitment for assessments or blood tests). Your participation will contribute to advancements in mental health treatment.
1. Why Join a Clinical Trial?
Scientific research plays a critical role in understanding mental health disorders and developing effective treatment solutions. Through collaborative studies between researchers and individuals with lived experience, clinical trials generate data-driven insights that enhance mental health care.
2. Participant Benefits:
Access to professional evaluations from trained researchers.
Participation in evidence-based intervention programs.
Contribution to advancing mental health research.
For information on currently available clinical treatments, please [click here].
Participation in evidence-based intervention programs.
Contribution to advancing mental health research.
For information on currently available clinical treatments, please [click here].
3. Understanding Clinical Trials
A clinical trial is a structured research study designed to:
Evaluate the safety and efficacy of medical or psychological treatments.
Determine whether a new intervention should be approved for broader clinical use.
Evaluate the safety and efficacy of medical or psychological treatments.
Determine whether a new intervention should be approved for broader clinical use.
Some trials involve randomized treatment assignments to compare the effectiveness of different therapies under strict ethical and scientific standards.
At MBI Lab & Care, our trials focus on:
Investigating biological and psychological mechanisms underlying mental health conditions.
Developing non-pharmacological adjunct therapies that offer safe and effective treatment options.
Ensuring Participant Safety
Our priority is participant safety, which is protected through strict regulatory protocols:
Regulatory Oversight:
All studies comply with Ministry of Health and Welfare regulations.
Each trial undergoes Institutional Review Board (IRB) approval before commencement.
The IRB ensures ethical standards and participant protection.
Medical Monitoring:
Participants receive regular assessments by a study physician.
Medical oversight includes:
Routine health check-ups
Laboratory evaluations
Comprehensive mental and physical monitoring
If necessary, additional medical interventions are provided outside the study.
Confidentiality & Data Security:
All personal and health information remains strictly confidential.
Research findings are anonymized to protect participant privacy.
How to Enroll in a Clinical Trial
To learn more about participation opportunities, contact us through:
[Contact Us]
[Our Locations]
At MBI Lab & Care, our trials focus on:
Investigating biological and psychological mechanisms underlying mental health conditions.
Developing non-pharmacological adjunct therapies that offer safe and effective treatment options.
Ensuring Participant Safety
Our priority is participant safety, which is protected through strict regulatory protocols:
Regulatory Oversight:
All studies comply with Ministry of Health and Welfare regulations.
Each trial undergoes Institutional Review Board (IRB) approval before commencement.
The IRB ensures ethical standards and participant protection.
Medical Monitoring:
Participants receive regular assessments by a study physician.
Medical oversight includes:
Routine health check-ups
Laboratory evaluations
Comprehensive mental and physical monitoring
If necessary, additional medical interventions are provided outside the study.
Confidentiality & Data Security:
All personal and health information remains strictly confidential.
Research findings are anonymized to protect participant privacy.
How to Enroll in a Clinical Trial
To learn more about participation opportunities, contact us through:
[Contact Us]
[Our Locations]