
臨床試驗研究
進行中
YMHC 健康組兒童研究計畫
【研究招募】:9–12 歲健康男童(無 ADHD 或其他重大身心疾病)(提供車馬費)
【研究目的】:蒐集一般健康兒童的相關資料,作為未來 ADHD 研究的重要比較基準。
【報名截止日】:
【研究目的】:蒐集一般健康兒童的相關資料,作為未來 ADHD 研究的重要比較基準。
【報名截止日】:
以身體活動作為憂鬱症介入治療的有效性評估
【研究招募】:
年齡 18 – 55 歲之成人
近期感到心情鬱悶、快樂不起來(輕中度憂鬱情形)
若有服用藥物,需穩定維持 1 個月以上
無懷孕、無嚴重影響運動之生理疾病
目前無進行心理治療或規律瑜伽練習者(每週至少一次)
【研究目的】:透過以瑜伽動作為主的身體活動練習,探討其對情緒與壓力調節的作用,提供促進心理健康的自我照顧方式。
【執行期間】:115年7-9月 每週三13:30-14:30 或 每週三 15:30-16:30
年齡 18 – 55 歲之成人
近期感到心情鬱悶、快樂不起來(輕中度憂鬱情形)
若有服用藥物,需穩定維持 1 個月以上
無懷孕、無嚴重影響運動之生理疾病
目前無進行心理治療或規律瑜伽練習者(每週至少一次)
【研究目的】:透過以瑜伽動作為主的身體活動練習,探討其對情緒與壓力調節的作用,提供促進心理健康的自我照顧方式。
【執行期間】:115年7-9月 每週三13:30-14:30 或 每週三 15:30-16:30
「NUTRIBRAIN-POWER生活型態介入預防憂鬱症狀者之認知功能障礙:從機制到臨床實踐 」
【研究招募】:【研究招募】50-80 歲憂鬱症成人
【研究目的】:了解探討發炎、代謝物和營養素與認知及憂鬱症狀變化的影響,並進一步評估Omega-3 介入之療效,作為未來老年認知障礙及憂鬱症狀以及進而提升患者功能與生活品質研究的重要依據。
【報名截止日】:
【研究目的】:了解探討發炎、代謝物和營養素與認知及憂鬱症狀變化的影響,並進一步評估Omega-3 介入之療效,作為未來老年認知障礙及憂鬱症狀以及進而提升患者功能與生活品質研究的重要依據。
【報名截止日】:
OSIMYDep 兒童青少年憂鬱症 Omega-3 雙盲臨床研究
【研究招募】:12–17 歲憂鬱症兒童與青少年(提供車馬費)
【研究目的】:了解憂鬱症青少年在臨床表現與身體生物指標上的特徵,並進一步評估 Omega-3 與SPMs之療效,作為未來兒童青少年心理健康研究的重要依據。
【報名截止日】:2028/07/31
【研究目的】:了解憂鬱症青少年在臨床表現與身體生物指標上的特徵,並進一步評估 Omega-3 與SPMs之療效,作為未來兒童青少年心理健康研究的重要依據。
【報名截止日】:2028/07/31
OSIMYDep 兒童青少年憂鬱症 Omega-3 雙盲臨床研究
【研究招募】12–17 歲健康青少年(提供車馬費)
【研究目的】:蒐集一般健康發展青少年的相關資料,作為未來憂鬱症研究的重要比較基準。
【報名截止日】:
【研究目的】:蒐集一般健康發展青少年的相關資料,作為未來憂鬱症研究的重要比較基準。
【報名截止日】:
已完成
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]
