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Clinical Research Documents

  1. Research Protocol / Proposal
    1.1 Template – Basic Protocol For Investigator – Initiatied Research
    1.2 Proposal Template – Clinical Trial
    1.3 Proposal Template – Observational Study
    1.4 Checklist For Clinical Trial Protocols Involving Human Subjects And Generating Data Intended To Be Submitted To Regulatory Authorities Patient Information Sheet And Informed Consent Form
  2. Patient Information Sheet And Informed Consent Form
    2.1 Template for Participant Information Sheet (BM Version)
    2.2 Template for Participant Information Sheet (ENG Version)
  3. Informed Consent
    3.1 WHO Ethics Review Committee : Informed Consent Form Template for Clinical Studies
  4. Guide To Medical Writing
    4.1 Exploring New Frontiers Of Electronic 4.18 Writing A Case Report
    4.2 Why Write? 4.19 Writing A Review Article
    4.3 Basic Structure & Types of Scientific Papers 4.20 Writing A Systematic Review
    4.4 Preparing TheTitle And Title Page 4.21 Writing An Invited Commentary
    4.5 Preparing The Abstract And Keywords 4.22 Writing Qualitative Paper
    4.6 Writing The Introduction 4.23 Letter To The Editor
    4.7 Writing The Materials And Methods 4.24 How A Submitted Manuscript Is Processed
    4.8 Writing The Results 4.25 Role Of The Manuscript Reviewer
    4.9 Writing The Discussion 4.26 Dealing With Editors’And Reviewers’
    4.10 Preparing The References 4.27 Electronic Publishing
    4.11 Presenting The Statistical Results 4.28 Language & Multilingualism In Scientific Com
    4.12 Preparing Effective Tables 4.29 Publishing And Academic Promotion
    4.13 Preparing Effective Illustrations.Part 1 4.30 Practical Exercise 1
    4.14 Preparing Effective Illustrations.Part 2 4.31 Practical Exercise 2
    4.15 Preparing A Manuscript For Submission 4.32 Practical Exercise 3
    4.16 Why The Body Matters 4.33 Practical Exercise 4
    4.17 Authorship And Acknowledgements
  5. Reference Materials For Good Practice In Medical Writing
    5.1 The Consolidated Standards of Reporting Trials CONSORT Checklist of Items To Include When Reporting Randomised Trials
    5.2 The Standards for The Reporting of Diagnostic Accuracy Studies STARD Checklist of Items for Reporting Studies On Diagnostic Accuracy
    5.3 The Preferred Reporting Items for Systematic Reviews and Meta-Analyses PRISMA Checklist For Systematic Reviews And Meta Analyses
    5.4 Writing a Scientic Paper: From Clutter to Clarit
    5.5 Elements of Stylefor Writing Scientific Journal Articles
  6. Validated questionnaire
    6.1 Irritable Bowel Syndrome
    6.2 Functional Dyspepsia
    6.3 Urogenital Distress Inventory (UDI-6)
    6.4 Berlin Questionnaire As A Screening Tool To Identify Patients With Obstructive Sleep Apnoea
    6.5 Diabetes Quality of Life (DQOL) Questionnaire (Children | Adults)
    6.6 EDEQ Questionnaire
    6.7 The 5-Item Version of the International Index of Erectile Function (IIEF-5) : BM | ENG
  7. Others
    7.1 Research Grants Managed By MOSTI – That Fund Clinical Trial