Writing Your First Clinical Research Protocol

Writing Your First Clinical Research Protocol

Author: Colleen Aldous

Publisher: Juta

Published: 2011-09-01

Total Pages: 96

ISBN-13: 9780702188947

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Students embarking on their first clinical research protocol are often daunted by the task at hand, particularly by the statistical terminology, concepts and the choice of appropriate statistical tests. The authors understand the difficulties and pitfalls students might encounter and have written an introductory text that will make writing that first protocol 'a breeze'. Beginning with a section entitled 'Whats in it for me', which outlines the benefits of research, the text provides ideas and advice on topics such as finding the research focus, writing the proposal, considering ethical requirements, compiling a budget and writing the executive summary.


Book Synopsis Writing Your First Clinical Research Protocol by : Colleen Aldous

Download or read book Writing Your First Clinical Research Protocol written by Colleen Aldous and published by Juta. This book was released on 2011-09-01 with total page 96 pages. Available in PDF, EPUB and Kindle. Book excerpt: Students embarking on their first clinical research protocol are often daunted by the task at hand, particularly by the statistical terminology, concepts and the choice of appropriate statistical tests. The authors understand the difficulties and pitfalls students might encounter and have written an introductory text that will make writing that first protocol 'a breeze'. Beginning with a section entitled 'Whats in it for me', which outlines the benefits of research, the text provides ideas and advice on topics such as finding the research focus, writing the proposal, considering ethical requirements, compiling a budget and writing the executive summary.

9 Steps Guide on How to Write a Clinical Trial Protocol?

9 Steps Guide on How to Write a Clinical Trial Protocol?

Author: K. Ashish

Publisher: O2 Publications

Published: 2014-06-01

Total Pages: 174

ISBN-13: 9788192853741

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This book "9 Steps Guide On How To Write A Clinical Trial Protocol" is specially designed for the Clinical Trial investigators, Physicians, Sponsors, healthcare students and other clinical research professionals, who are involved or keen to explore clinical research in future to develop skills to write protocol for clinical studies. The books covers the topics Essential Clinical Trial Documents, Protocol Structure, Type of Research Studies, Trial Design Consideration, Ethical Consideration, Elementary Statistics, Randomization and its type, Blinding, Sample Sizing etc.The book is designed and written in a manner so that a reader can understand overall protocol writing and the essential element involved in it. We hope that the book would guide the readers to understand the overall process of protocol writing and impart essential skills involved in it.


Book Synopsis 9 Steps Guide on How to Write a Clinical Trial Protocol? by : K. Ashish

Download or read book 9 Steps Guide on How to Write a Clinical Trial Protocol? written by K. Ashish and published by O2 Publications. This book was released on 2014-06-01 with total page 174 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book "9 Steps Guide On How To Write A Clinical Trial Protocol" is specially designed for the Clinical Trial investigators, Physicians, Sponsors, healthcare students and other clinical research professionals, who are involved or keen to explore clinical research in future to develop skills to write protocol for clinical studies. The books covers the topics Essential Clinical Trial Documents, Protocol Structure, Type of Research Studies, Trial Design Consideration, Ethical Consideration, Elementary Statistics, Randomization and its type, Blinding, Sample Sizing etc.The book is designed and written in a manner so that a reader can understand overall protocol writing and the essential element involved in it. We hope that the book would guide the readers to understand the overall process of protocol writing and impart essential skills involved in it.

Writing Clinical Research Protocols

Writing Clinical Research Protocols

Author: Evan DeRenzo

Publisher: Elsevier

Published: 2005-09-08

Total Pages: 320

ISBN-13: 0080454208

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This highly engaging guide for clinical researchers provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. Writing Clinical Research Protocols includes practical information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents, getting protocols approved, special populations, confidentiality issues, and the reporting of adverse events. A valuable appendix includes a listing of web resources about research ethics as well as a glossary. This is an invaluable resource for basic scientists collaborating in clinical trials, physician investigators, clinical research fellows, research nurse coordinators, residents, and anyone who wants a better understanding of the clinical trials process. Walks investigators and trainees through identification of the ethical aspects of each section of a clinical research protocol Includes a chapter containing Case Histories Contains information on conducting clinical research within the pharmaceutical industry An appendix includes internet resources and world wide web addresses for important research ethics documents and regulations Chapter on 'Study Design and Methodology' purposely expanded to explicitly address biostatistical considerations


Book Synopsis Writing Clinical Research Protocols by : Evan DeRenzo

Download or read book Writing Clinical Research Protocols written by Evan DeRenzo and published by Elsevier. This book was released on 2005-09-08 with total page 320 pages. Available in PDF, EPUB and Kindle. Book excerpt: This highly engaging guide for clinical researchers provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. Writing Clinical Research Protocols includes practical information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents, getting protocols approved, special populations, confidentiality issues, and the reporting of adverse events. A valuable appendix includes a listing of web resources about research ethics as well as a glossary. This is an invaluable resource for basic scientists collaborating in clinical trials, physician investigators, clinical research fellows, research nurse coordinators, residents, and anyone who wants a better understanding of the clinical trials process. Walks investigators and trainees through identification of the ethical aspects of each section of a clinical research protocol Includes a chapter containing Case Histories Contains information on conducting clinical research within the pharmaceutical industry An appendix includes internet resources and world wide web addresses for important research ethics documents and regulations Chapter on 'Study Design and Methodology' purposely expanded to explicitly address biostatistical considerations

Clinical Research

Clinical Research

Author: Robert D. Toto

Publisher: Lippincott Williams & Wilkins

Published: 2012-03-28

Total Pages: 272

ISBN-13: 145115335X

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This book will serve as a road map for students and junior researchers seeking to successfully design, implement, and publish clinical research. It covers the basic elements of research proposals and implementation including regulatory approvals, continuing regulatory oversight, investigational new drug and device applications, monitoring patient safety, recruitment, clinical assessments, laboratory assessments, provision of treatment, and on-going quality control. The authors provide instruction on how to integrate research resources to successfully conduct a clinical research project, and offer guidelines on collection, quality control, and analysis of data. A companion website will include the fully searchable text and links to Journal of Investigative Medicine's "Research Tools and Issues" feature.


Book Synopsis Clinical Research by : Robert D. Toto

Download or read book Clinical Research written by Robert D. Toto and published by Lippincott Williams & Wilkins. This book was released on 2012-03-28 with total page 272 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book will serve as a road map for students and junior researchers seeking to successfully design, implement, and publish clinical research. It covers the basic elements of research proposals and implementation including regulatory approvals, continuing regulatory oversight, investigational new drug and device applications, monitoring patient safety, recruitment, clinical assessments, laboratory assessments, provision of treatment, and on-going quality control. The authors provide instruction on how to integrate research resources to successfully conduct a clinical research project, and offer guidelines on collection, quality control, and analysis of data. A companion website will include the fully searchable text and links to Journal of Investigative Medicine's "Research Tools and Issues" feature.

A Practical Guide for Health Researchers

A Practical Guide for Health Researchers

Author: M. F. Fathalla

Publisher: WHOROEM

Published: 2004

Total Pages: 234

ISBN-13: 9789290213635

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Health researchers, the intended audience of this book, are not limited to scientists pursuing a research career. They include health professionals, administrators, policymakers and non-governmental organizations, among others, who can and should use the scientific method to guide their work for improving the health of individuals and communities. Even if they do not pursue much research themselves, they need to grasp the principles of the scientific method, to understand the value and also the limitations of science, and to be able to assess and evaluate results of research before applying them. This book includes the following chapters: Introduction and overview; ethics in health research; what research to do; planning the research; writing the research protocol; submitting a research proposal; implementing the research project; describing and analysing the research results; communicating research; guidelines on writing a scientific paper; publishing a scientific paper; guidelines on making a scientific presentation; assessing and evaluating research.


Book Synopsis A Practical Guide for Health Researchers by : M. F. Fathalla

Download or read book A Practical Guide for Health Researchers written by M. F. Fathalla and published by WHOROEM. This book was released on 2004 with total page 234 pages. Available in PDF, EPUB and Kindle. Book excerpt: Health researchers, the intended audience of this book, are not limited to scientists pursuing a research career. They include health professionals, administrators, policymakers and non-governmental organizations, among others, who can and should use the scientific method to guide their work for improving the health of individuals and communities. Even if they do not pursue much research themselves, they need to grasp the principles of the scientific method, to understand the value and also the limitations of science, and to be able to assess and evaluate results of research before applying them. This book includes the following chapters: Introduction and overview; ethics in health research; what research to do; planning the research; writing the research protocol; submitting a research proposal; implementing the research project; describing and analysing the research results; communicating research; guidelines on writing a scientific paper; publishing a scientific paper; guidelines on making a scientific presentation; assessing and evaluating research.

The Lancet Handbook of Essential Concepts in Clinical Research

The Lancet Handbook of Essential Concepts in Clinical Research

Author: Kenneth F. Schulz

Publisher: Elsevier Health Sciences TW

Published: 2006

Total Pages: 248

ISBN-13: 9789868379268

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"The Lancet Handbook of Essential Concepts in Clinical Research speaks to two audiences: those who read and those who conduct research. Clinicians are medical detectives by training. For each patient, they assemble clinical clues to establish causes (e.g. diagnoses) of signs and symptoms. The task involves both clinical acumen and knowledge of medical research. This book helps guide clinicians through this detective work, by enabling them to make sense of research and to review medical literature critically. It will also be invaluable to researchers who conduct clinical research, particularly randomized controlled trials. Building on previously published, peer-reviewed articles from The Lancet, this handbook is essential for busy clinicians and active researchers interested in research methods."--BOOK JACKET.


Book Synopsis The Lancet Handbook of Essential Concepts in Clinical Research by : Kenneth F. Schulz

Download or read book The Lancet Handbook of Essential Concepts in Clinical Research written by Kenneth F. Schulz and published by Elsevier Health Sciences TW. This book was released on 2006 with total page 248 pages. Available in PDF, EPUB and Kindle. Book excerpt: "The Lancet Handbook of Essential Concepts in Clinical Research speaks to two audiences: those who read and those who conduct research. Clinicians are medical detectives by training. For each patient, they assemble clinical clues to establish causes (e.g. diagnoses) of signs and symptoms. The task involves both clinical acumen and knowledge of medical research. This book helps guide clinicians through this detective work, by enabling them to make sense of research and to review medical literature critically. It will also be invaluable to researchers who conduct clinical research, particularly randomized controlled trials. Building on previously published, peer-reviewed articles from The Lancet, this handbook is essential for busy clinicians and active researchers interested in research methods."--BOOK JACKET.

Medical Writing

Medical Writing

Author: Robert B. Taylor

Publisher: Springer Science & Business Media

Published: 2011-08-17

Total Pages: 376

ISBN-13: 1441982345

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The first edition of this book (titled “The Clinician’s Guide to Medical Writing”) has become a standard in its field and remains an indispensible reference for any clinician, academic physician, or health professional who wishes to hone their writing skills. However, since its publication in 2004, significant changes have taken place in the way medical professionals communicate with each other and the world. Medical Writing: A Guide for Clinicians and Academicians, 2e retains all of the fundamental writing advice of the first edition and has been expanded to include two brand new chapters: How to Write a Research Protocol (including why a research project needs a written protocol, elements of the research protocol and common problems) How to Write a Grant Proposal (including sections on government and private grant funding sources, what you need to know about grant writing, and elements of a successful grant proposal) New information is also included throughout the book on becoming a successful writer, medical tables and figures, conflict of interest and disclosures, how to review a scientific article, statistical analysis, “pay-to-publish” journal publishing, electronic submission of manuscripts, issues in medical publishing and the future of medical writing and publication. New appendices address commonly encountered research and statistical terms and memorable aphorisms regarding writing, medical and otherwise.


Book Synopsis Medical Writing by : Robert B. Taylor

Download or read book Medical Writing written by Robert B. Taylor and published by Springer Science & Business Media. This book was released on 2011-08-17 with total page 376 pages. Available in PDF, EPUB and Kindle. Book excerpt: The first edition of this book (titled “The Clinician’s Guide to Medical Writing”) has become a standard in its field and remains an indispensible reference for any clinician, academic physician, or health professional who wishes to hone their writing skills. However, since its publication in 2004, significant changes have taken place in the way medical professionals communicate with each other and the world. Medical Writing: A Guide for Clinicians and Academicians, 2e retains all of the fundamental writing advice of the first edition and has been expanded to include two brand new chapters: How to Write a Research Protocol (including why a research project needs a written protocol, elements of the research protocol and common problems) How to Write a Grant Proposal (including sections on government and private grant funding sources, what you need to know about grant writing, and elements of a successful grant proposal) New information is also included throughout the book on becoming a successful writer, medical tables and figures, conflict of interest and disclosures, how to review a scientific article, statistical analysis, “pay-to-publish” journal publishing, electronic submission of manuscripts, issues in medical publishing and the future of medical writing and publication. New appendices address commonly encountered research and statistical terms and memorable aphorisms regarding writing, medical and otherwise.

How to Write Clinical Research Documents

How to Write Clinical Research Documents

Author: Kanosia

Publisher: CreateSpace

Published: 2015-07-10

Total Pages: 84

ISBN-13: 9781515015505

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This book on "How to write Clinical Research Documents (Protocol, IB, & Study Report Writing) "Clinical Research Documentation Preparation is a humble treatise on the requirement of Clinical Research Documentation in the arena of stricter regulations and statutory compliances. This is a basic textbook on the subject matter and covers the general topic on the writing of Study Protocol, Investigator's Brochure (IB) & Clinical Research Study Report (CSR). The book is a continuous effort of the author to provide the knowledge and guidance involved in the field of Clinical Research and regulatory documentations. The book summarizes how to write these documents with ease and every step is explained in detail. There is also glossary of terms and Abbreviations given- in which detailed supporting reading material has been provided.


Book Synopsis How to Write Clinical Research Documents by : Kanosia

Download or read book How to Write Clinical Research Documents written by Kanosia and published by CreateSpace. This book was released on 2015-07-10 with total page 84 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book on "How to write Clinical Research Documents (Protocol, IB, & Study Report Writing) "Clinical Research Documentation Preparation is a humble treatise on the requirement of Clinical Research Documentation in the arena of stricter regulations and statutory compliances. This is a basic textbook on the subject matter and covers the general topic on the writing of Study Protocol, Investigator's Brochure (IB) & Clinical Research Study Report (CSR). The book is a continuous effort of the author to provide the knowledge and guidance involved in the field of Clinical Research and regulatory documentations. The book summarizes how to write these documents with ease and every step is explained in detail. There is also glossary of terms and Abbreviations given- in which detailed supporting reading material has been provided.

Principles and Practice of Clinical Research

Principles and Practice of Clinical Research

Author: John I. Gallin

Publisher: Elsevier

Published: 2011-04-28

Total Pages: 447

ISBN-13: 0080489567

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The second edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research. Molecular medicine, genomics, and proteomics have opened vast opportunities for translation of basic science observations to the bedside through clinical research. As an introductory reference it gives clinical investigators in all fields an awareness of the tools required to ensure research protocols are well designed and comply with the rigorous regulatory requirements necessary to maximize the safety of research subjects. Complete with sections on the history of clinical research and ethics, copious figures and charts, and sample documents it serves as an excellent companion text for any course on clinical research and as a must-have reference for seasoned researchers. *Incorporates new chapters on Managing Conflicts of Interest in Human Subjects Research, Clinical Research from the Patient's Perspective, The Clinical Researcher and the Media, Data Management in Clinical Research, Evaluation of a Protocol Budget, Clinical Research from the Industry Perspective, and Genetics in Clinical Research *Addresses the vast opportunities for translation of basic science observations to the bedside through clinical research*Delves into data management and addresses how to collect data and use it for discovery*Contains valuable, up-to-date information on how to obtain funding from the federal government


Book Synopsis Principles and Practice of Clinical Research by : John I. Gallin

Download or read book Principles and Practice of Clinical Research written by John I. Gallin and published by Elsevier. This book was released on 2011-04-28 with total page 447 pages. Available in PDF, EPUB and Kindle. Book excerpt: The second edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research. Molecular medicine, genomics, and proteomics have opened vast opportunities for translation of basic science observations to the bedside through clinical research. As an introductory reference it gives clinical investigators in all fields an awareness of the tools required to ensure research protocols are well designed and comply with the rigorous regulatory requirements necessary to maximize the safety of research subjects. Complete with sections on the history of clinical research and ethics, copious figures and charts, and sample documents it serves as an excellent companion text for any course on clinical research and as a must-have reference for seasoned researchers. *Incorporates new chapters on Managing Conflicts of Interest in Human Subjects Research, Clinical Research from the Patient's Perspective, The Clinical Researcher and the Media, Data Management in Clinical Research, Evaluation of a Protocol Budget, Clinical Research from the Industry Perspective, and Genetics in Clinical Research *Addresses the vast opportunities for translation of basic science observations to the bedside through clinical research*Delves into data management and addresses how to collect data and use it for discovery*Contains valuable, up-to-date information on how to obtain funding from the federal government

Introducing, Designing and Conducting Research for Paramedics

Introducing, Designing and Conducting Research for Paramedics

Author: Alexander Olaussen

Publisher: Elsevier Health Sciences

Published: 2022-09-15

Total Pages: 218

ISBN-13: 0729589730

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The profession of paramedicine is rapidly expanding and primary research relating to prehospital interventions is exploding worldwide. This new book provides, for the first time, a meaningful and easy to understand guide to research specifically tailored for paramedics. Written by experts in research, medicine and paramedicine, Introducing, Designing and Conducting Research for Paramedics introduces the reader to the concepts of research through real-life examples. The structure follows a logical sequence from an overview of the research process to how to generate, consume and implement evidence. This book will be a valuable resource for paramedics and prehospital clinicians at any level, worldwide, who wish to contribute to the rapidly emerging body of evidence on paramedicine and understand how they can make use of this in their practice. Important concepts described in terms of their relevance to paramedicine, making the text meaningful and easy to understand Written and edited by key academics and clinicians in the field of paramedic research Paramedicine examples used throughout to explain aspects of research methodology (e.g. qualitative, quantitative, mixed methods and literature reviews) Key objectives, relevant terms, reference lists, further suggested readings and useful resources support the reader to engage further with research Discussion/review questions and reflective exercises in each chapter to reinforce learning An eBook included with print purchase


Book Synopsis Introducing, Designing and Conducting Research for Paramedics by : Alexander Olaussen

Download or read book Introducing, Designing and Conducting Research for Paramedics written by Alexander Olaussen and published by Elsevier Health Sciences. This book was released on 2022-09-15 with total page 218 pages. Available in PDF, EPUB and Kindle. Book excerpt: The profession of paramedicine is rapidly expanding and primary research relating to prehospital interventions is exploding worldwide. This new book provides, for the first time, a meaningful and easy to understand guide to research specifically tailored for paramedics. Written by experts in research, medicine and paramedicine, Introducing, Designing and Conducting Research for Paramedics introduces the reader to the concepts of research through real-life examples. The structure follows a logical sequence from an overview of the research process to how to generate, consume and implement evidence. This book will be a valuable resource for paramedics and prehospital clinicians at any level, worldwide, who wish to contribute to the rapidly emerging body of evidence on paramedicine and understand how they can make use of this in their practice. Important concepts described in terms of their relevance to paramedicine, making the text meaningful and easy to understand Written and edited by key academics and clinicians in the field of paramedic research Paramedicine examples used throughout to explain aspects of research methodology (e.g. qualitative, quantitative, mixed methods and literature reviews) Key objectives, relevant terms, reference lists, further suggested readings and useful resources support the reader to engage further with research Discussion/review questions and reflective exercises in each chapter to reinforce learning An eBook included with print purchase