Establish what is known and which trials are already being done
ISRCTN Current Controlled Trials Register (ISRCTN)
Clinicaltrials.gov US Government Clinical Trials Register
CENTRAL Cochrane Central Register of Controlled Trials
PubMed searches and regular email updates of the selected topics
Cochrane Database of Systematic Reviews
Is my project audit or research?
Develop a research protocol
NIHR Study Support Service Check this out early in the study planning stage
How to do a systematic review
Five steps to conducting a systematic review read this first for key principles
PROPSPERO Register your systematic review once protocol finalized
PRISMA checklist and guidance for systematic reviews and meta-analysis
GRADE Cochrane risk of Bias tool, Jadad, and JBI are tools for assessing risk of bias
Doing a systematic review. A concise guidebook for Masters students by Rumona Dickson.
Evidence appraisal and grading of recommendations
Oxford centre for evidence based medicine levels of evidence and grade of recommendation
NIHR Grant Finder (Program Grant, HTA, EME, i4i, Health Service Research, Fellowships)
British Heart Foundation
Dunhill Medical Trust
The Stroke Association
The Leverhulme Trust Early Career Fellowship
Dunhill Medical Trust
Francis Crick Institute
Writing a grant application
10 key sentences for grant applications by Parker Derrington
Getting started Writing a research paper: advice for beginners
ICJME International Committee for Medical Journal Editors Recommendations for writing articles (The Uniform Requirement).
ICH GCP guidance on structure and content of clinical study reports (E3). Consult this on detailed guidance on how to write up research reports (MSc, thesis, research paper).
Clinical Trials: The CONSORT statement is an important research tool that takes an evidence-based approach to improve the quality of reports of randomized trials. The CONSORT flow chart shows how recruitment and study drop outs should be reported. This document must be consulted before recruitment starts and at write-up stage. The CONSORT check list gives prompts to all the information to be included in a research report. More information on each item in the list can be gained by clicking on underlined terms. Recent extensions guide reporting of pragmatic trials.
Observational Studies: The STROBE statement is provides guidance for the reporting of observational studies. This includes case series, cohort studies and cross sectional studies.
Case Reports: Guidance on writing case reports
Most simple statistics (mean, median, SD, t-test) can be done using the Excel functions. Links to common tests not found in Excel are below.
Figures and tables
Most medical journals use Vancouver (example below)
Name AA, Name BB…… . Title. Journal (abbreviated). Year month day;volume(issue)page-page.
Optionally, the article’s unique identifier (DOI or PMID) may be added to the citation.
Resources for PhD/ DM students
Keele Research Support Links to resources from project development to completion
Guidance and documents for DM/PhD – click link for access to:
Code of Practice on Postgraduate Research Degrees Please check your submission for doctoral progression against the requirements listed in Annex C4 and and the submission of your thesis against Annex D4 “Preparation and presentation of a thesis”.
Research Governance ensures the delivery of high quality research. Every student should read this before embarking on research.
Resources for Medical Students
Keele guidance for medical students interested in research. Best to get started in y3. Research Opportunities for Keele Medical students