0

Shopping cart

Close

No products in the cart.

Reading and Interpreting Diabetes Research Publications (RIDRP)

Description

Reading and Interpreting Diabetes Research Publications (RIDRP) is a specialized online course offered by the Chellaram Diabetes Institute E-Learning Academy, tailored for healthcare professionals, researchers, and students involved in diabetes care and research. This self-paced course provides an in-depth understanding of how to critically read, analyze, and apply diabetes-related scientific research to real-world clinical practice.

The course covers a wide spectrum of research methodologies including cross-sectional, case-control, cohort studies, and randomized controlled trials (RCTs), as well as systematic reviews and meta-analyses. Participants will learn how to assess the credibility of a research paper, understand the hierarchy of evidence, and extract key findings that influence clinical decision-making.

Whether you are a medical student, clinician, diabetes educator, or healthcare researcher, RIDRP equips you with the skills to transform academic research into actionable clinical insights, ensuring your practice remains aligned with the latest scientific evidence in diabetes care.

Course Description

In an era where evidence-based medicine shapes the future of healthcare, the ability to accurately interpret research is a crucial skill for anyone involved in diabetes prevention, management, and treatment. The RIDRP online course is designed to bridge the gap between complex scientific publications and practical clinical application.

Through comprehensive modules, you will:

  • Understand the importance of staying up-to-date with diabetes research.
  • Learn the structure and key components of scientific research papers.
  • Explore different types of study designs, including cross-sectional studies, case-control studies, cohort studies, and RCTs.
  • Gain insights into systematic reviews and meta-analyses, and how they contribute to treatment guidelines.
  • Master the hierarchy of evidence and develop a critical eye for assessing the quality of research.
  • Learn how to extract and present the salient aspects of research to colleagues and stakeholders.
  • Translate research findings into clinical practice, improving patient outcomes and promoting better care decisions.

This course is ideal for:

  • Endocrinologists, diabetologists, and general physicians
  • Healthcare practitioners involved in diabetes care
  • Nutritionists, clinical pharmacists, and diabetes educators
  • Postgraduate students and researchers in medical sciences
  • Public health professionals and evidence-based policy makers

Participants will receive a certificate of completion from Chellaram Diabetes Institute, a leader in diabetes education and research in India. With practical examples, expert-led guidance, and user-friendly content, RIDRP helps you become a more informed, evidence-based healthcare provider.

 

Course Highlights

Eligibility Criteria

MBBS / Allopathy Doctors

FAQs

What will I learn from this course?
In the Reading and Interpreting Diabetes Research Publications (RIDRP) course, you will learn how to critically read, evaluate, and apply diabetes-related scientific research to clinical practice. The course covers key topics such as the structure of research papers, study designs (including cross-sectional, case-control, cohort studies, and randomized controlled trials), systematic reviews, meta-analyses, and the hierarchy of evidence. You’ll also gain skills in assessing the quality of research, presenting key findings, and using research insights to make evidence-based clinical decisions.
The Reading and Interpreting Diabetes Research Publications (RIDRP) course is ideal for healthcare professionals, medical students, diabetes educators, clinical researchers, and public health practitioners who want to enhance their ability to understand and apply scientific research in diabetes care. Whether you’re a physician, nurse, dietitian, pharmacist, or academic, this course will help you build essential research literacy skills and strengthen your evidence-based practice.

The Course has a maximum allowed duration of 6 months, providing flexibility for learners to complete the program within this timeframe.

The course is delivered entirely online through a user-friendly e-learning platform. It includes video lectures, interactive modules, case studies, and readings. Learners can access the materials anytime, and there are live webinars and discussions to support learning.

You will be assessed through a combination of pre-tests and post-tests to gauge your progress, along with multiple-choice quizzes after each module. The course concludes with a comprehensive exit exam to evaluate your overall understanding and skills.

Upon successful completion of the course, you will receive a Certificate from Chellaram Diabetes Institute, recognizing your expertise in the specific area of the course.

For any support, you can contact our dedicated support team via WhatsApp, Email, or Phone. Details for each contact method are provided on the platform. Our team is available to assist you with any questions or issues you may encounter during the course.

Instructor

Dr A G Unnikrishnan
CEO & Chief Endocrinologist
Dr Ragini Bhake
Endocrinologist
Dr Shailesh Deshpande
Head - Education

Course Preview

* 72. END

END (RIDRP)


* 71. Summary of the Study-Format 3

Summary of the Study-Format 3 (RIDRP)


* 01. Introduction to RIDRP

Introduction (RIDRP)


* 02. Components of a Research Paper

Components of a Research Paper (RIDRP)


* 03. Components of a Research Paper - 2

Components of a Research Paper - 2 (RIDRP)


* 04. Introduction to Cross-Sectional Studies

Introduction to Cross-Sectional Studies (RIDRP)


* 05. Example of a Cross-Sectional Study-Slide1

Example of a Cross-Sectional Study-Slide1 (RIDRP)


* 06. Example of a Cross-Sectional Study-Slide2

Example of a Cross-Sectional Study-Slide2 (RIDRP)


* 07. Example of a Cross-Sectional Study-Slide3

Example of a Cross-Sectional Study-Slide3 (RIDRP)


* 08. Example of a Cross-Sectional Study-Slide4

Example of a Cross-Sectional Study-Slide4 (RIDRP)


* 09. Advantages and Disadvantages of a Cross-Sectional Study

Advantages and Disadvantages of a Cross-Sectional Study (RIDRP)


* 10. Introduction to Case-Control Studies

Introduction to Case-Control Studies (RIDRP)


* 11. Introduction to Case-Control Studies-2

Introduction to Case-Control Studies-2 (RIDRP)


* 12. Example of a Case-Control Study

Example of a Case-Control Study (RIDRP)


* 13. Example of a Case-Control Study-2

Example of a Case-Control Study (RIDRP)


* 14. Framework for Analysis

Framework for Analysis (RIDRP)


* 15. Results from the Example of Case-Control Study

Results from the Example of Case-Control Study (RIDRP)


* 16. Results from the Example of Case-Control Study-2

Results from the Example of Case-Control Study-2 (RIDRP)


* 17. The P-Value

The P-Value (RIDRP)


* 18. Steps in a Case-Control Study

Steps in a Case-Control Study (RIDRP)


* 19. Confounding Factor Slide1

Confounding Factor Slide1 (RIDRP)


* 20. Confounding Factor Slide2

Confounding Factor Slide2 (RIDRP)


* 21. Bias in Case-Control Study Slide1

Bias in Case-Control Study Slide1(RIDRP)


* 22. Bias in Case-Control Study Slide2

Bias in Case-Control Study Slide2 (RIDRP)


* 23. Bias in Case-Control Study Slide3

Bias in Case-Control Study Slide2 (RIDRP)


* 24. Bias in Case-Control Study Slide4

Bias in Case-Control Study Slide4 (RIDRP)


* 25. Bias in Case-Control Study Slide5

Bias in Case-Control Study Slide5 (RIDRP)


* 26. Bias in Case-Control Study Slide6

Bias in Case-Control Study Slide6 (RIDRP)


* 27. Bias in Case-Control Study Slide7

Bias in Case-Control Study Slide7  (RIDRP)


* 28. Bias in Case-Control Study Slide8

Bias in Case-Control Study Slide8 (RIDRP)


* 29. Advantages and Disadvantages of a Case-Control Study

Advantages and Disadvantages of a Case-Control Study (RIDRP)


* 30(B). Introduction to Cohort Studies-2

Introduction to Cohort Studies-2 (RIDRP)


* 31. Types of Cohort Studies

Types of Cohort Studies (RIDRP)


* 32. Cohort Study Design

Cohort Study Design (RIDRP)


* 33. Steps in a Cohort Study (A)

Steps in a Cohort Study (A) (RIDRP)


* 34. The EPIC-Norfolk Study Slide1

The EPIC-Norfolk Study Slide1 (RIDRP)


* 35. The EPIC-Norfolk Study Slide2

The EPIC-Norfolk Study Slide2 (RIDRP)


* 36. The EPIC-Norfolk Study Slide3

The EPIC-Norfolk Study Slide3 (RIDRP)


* 37. The EPIC-Norfolk Study Slide4

The EPIC-Norfolk Study Slide (RIDRP)


* 38. Framework for Analysis (A)

Framework for Analysis (RIDRP)


* 39. EPIC-Norfolk Study Results Slide1

EPIC-Norfolk Study Results Slide1 (RIDRP)


* 40. EPIC-Norfolk Study Results Slide2

EPIC-Norfolk Study Results Slide2 (RIDRP)


* 41. Bias in Cohort Study Slide1

Bias in Cohort Study Slide1 (RIDRP)


* 42. Bias in Cohort Study Slide2

Bias in Cohort Study Slide2 (RIDRP)


* 43. Advantages and Disadvantages of a Cohort Study

Advantages and Disadvantages of a Cohort Study (RIDRP)


* 44. Introduction to Clinical Trials (A)

Introduction to Clinical Trials (A) (RIDRP)


* 45. Introduction to Clinical Trials 2

Introduction to Clinical Trials 2 (RIDRP)


* 46. The DCCT Trial Introduction Slide 1

The DCCT Trial Introduction Slide 1 (RIDRP)


* 47. The DCCT Trial Introduction Slide 2

The DCCT Trial Introduction Slide 2 (RIDRP)


* 48. The DCCT Trial Introduction Slide 3

The DCCT Trial Introduction Slide 3 (RIDRP)


* 49. The DCCT Trial Introduction Slide 4

The DCCT Trial Introduction Slide 4 (RIDRP)


* 50. The DCCT Trial Introduction Slide 5

The DCCT Trial Introduction Slide 5 (RIDRP)


* 51. The DCCT Trial Introduction Slide 6

The DCCT Trial Introduction Slide 6 (RIDRP)


* 52. The DCCT Trial Introduction Slide 7

The DCCT Trial Introduction Slide 7 (RIDRP)


* 53. The DCCT Trial Introduction Slide 8

The DCCT Trial Introduction Slide 8 (RIDRP)


* 54. The DCCT Trial Results

The DCCT Trial Results (RIDRP)


* 55. The DCCT Trial Results Slide 2

The DCCT Trial Results Slide 2 (RIDRP)


* 56. The DCCT Trial Results Slide 3

The DCCT Trial Results Slide 3 (RIDRP)


* 57. The DCCT Trial Results Slide 4

The DCCT Trial Results Slide 4  (RIDRP)


* 58. The DCCT Trial Results Slide 5

The DCCT Trial Results Slide 5 (RIDRP)


* 59. The DCCT Trial Results - 2

The DCCT Trial Results - 2 (RIDRP)


* 60. The DCCT Trial Results - 2 - Slide 2

The DCCT Trial Results - 2 - Slide 2 (RIDRP)


* 61. The DCCT Trial Final Points (A)

The DCCT Trial Final Points (A) (RIDRP)


* 62. Randomized Controlled Trials Summing up

Randomized Controlled Trials Summing up (RIDRP)


* 63. Randomized Controlled Trials Summing up - Slide 2

Randomized Controlled Trials Summing up - Slide 2 (RIDRP)


* 64. Systematic Review and Meta-Analysis

Systematic Review and Meta-Analysis (RIDRP)


* 65. Forest Plot

Forest Plot (RIDRP)


* 66. Forest Plot-Example-1

Forest Plot-Example-1 (RIDRP)


* 67. Forest Plot-Example-2

Forest Plot-Example-2 (RIDRP)


* 68. Hierarchy of Evidence

Hierarchy of Evidence (RIDRP)


* 69. How to Assess a Research Paper

How to Assess a Research Paper (RIDRP)


* 70. Presentation of the Salient Aspects of the Published Research

Presentation of the Salient Aspects of  the Published Research (RIDRP)


* 04(B) - Introduction to Cross-Sectional Studies

04(B) - Introduction to Cross-Sectional Studies (RIDRP)


* 04(A) - Introduction to the various types of Studies

04(A) - Introduction to the various types of Studies (RIDRP)


* 30(A) - Introduction to Cohort Studies-1

30(A) - Introduction to Cohort Studies-1 (RIDRP)


* 61. The DCCT Trial Final Points (B)

The DCCT Trial Final Points (B) (RIDRP)


* 44. Introduction to Clinical Trials (B)

Introduction to Clinical Trials (B) (RIDRP)


* 38. Framework for Analysis (B)

Framework for Analysis (B)


* 33. Steps in a Cohort Study (B)

Steps in a Cohort Study (B) (RIDRP)


* RIDRP - EXIT EXAM

RIDRP -  EXIT EXAM


-
+

3,500.00

Eligibility: MBBS / Allopathy Doctors

Duration: 6 Months

Mode: Online

Sample Certificate

    Want to Know More Before You Enroll?
    Contact Us!

    Popular Courses

    × How can I help you?