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Research to Publication
1. Research to Publication
eLearning from BMJ for early career researchers
In partnership with UCSF
Dr Trish Groves
Head of research, BMJ; Editor-in-chief BMJ Open
Editorial lead for Research to Publication
2. What are the main reasons for journal editors to reject
a research paper, even if well written and presented?
• the research question isn’t sufficiently new,
interesting, or important
• the question is answered with suboptimal design
• investigators often lack training on developing good
research questions, choosing study designs, and
reporting research effectively
What’s the problem?
3. What should we think about researchers who use the
wrong techniques (either wilfully or in ignorance), use the
right techniques wrongly, misinterpret their results, report
their results selectively, cite the literature selectively, and
draw unjustified conclusions?
We should be appalled. Yet numerous studies of the
medical literature, in both general and specialist journals,
have shown that all of the above phenomena are
common... This is surely a scandal.”
The scandal of poor medical research
Altman DG. The scandal of poor medical research. BMJ 1994; 308 :283
4. Stages of waste in the production and reporting of research evidence relevant to
clinicians and patients; from Chalmers and Glasziou, The Lancet 2009
REWARD Alliance http://researchwaste.net/about/
5. • nations need research evidence that’s reliable and relevant
enough to help them build UHC (SDG 3, target 8)
• Africa’s share of annual research publications on health rose
from 0.7% in 2000 to 1.3% in 2014, but only three countries –
South Africa, Nigeria, and Kenya – contributed over half [1]
• publications retracted for plagiarism are significantly more
likely to have 1st author from a low income country [2]
Relevance to global health
1. Uthman et al. BMJ Open 2015;5:3 e006340
2. Stretton S et al. Curr Med Res Opin. 2012;28(10):1575-83.
6. Research to Publication (RtoP) is an eLearning programme for
early career academics in healthcare research to guide them
right through from designing a study to seeing it published in
an international journal
RtoP offers a comprehensive and flexible set of stand-alone,
self-study modules that let learners choose what to study, and
at their own pace
RtoP draws on expertise of The BMJ's senior research editors
and senior academics at the UCSF Clinical and Translational
Science Institute
Research to Publication eLearning programme
http://rtop.bmj.com
7. • courses on medical writing lack scientific depth
• Publish or perish = universal problem
• research output is an essential measurement of
institutional success but output is inadequate
• governments want/need to build research capability
• author/institutional demand (doctors, nurses and other
allied health researchers, postgraduates,
undergraduates, research integrity departments)
• extends The BMJ’s role in research integrity
• inside track from decision-making editors
Why Research to Publication?
8. • uniquely, combines expertise of
international medical publisher
and world-leading university
• focused on clinical and public
health research
• supports research integrity and
drives high ethical standards
• builds research skills
• increases relevance and quality,
of research; reduces waste
• improves chances of publication
• provides practical advice in a
user-friendly multimedia format
Value for learners and their institutions
• helps institutions build
research capabilities,
improve reputation, attract
funding
• offers the option for
integration into a Masters
programme
• Certificate of Completion
from BMJ and UCSF for
every module
• 75% discount on APCs for
protocols published in BMJ
Open and other BMJJs
9. • takes the lecture out of the classroom and brings homework in
• puts students in charge of their own learning
• students needing more time to master a concept aren’t left behind
Ideal for blended learning with “flipped classroom”
10. Before the flip After the flip
Before
class
• students assigned reading
• instructor/teacher/tutor prepares
lecture
• students guided through learning module
that asks and collects questions
• instructor prepares learning opportunities
Beginning
of class
• students have limited information
about what to expect
• instructor makes general
assumption about what is helpful
• students have specific questions in mind to
guide their learning
• instructor can anticipate where students
need the most help
During
class
• students try to follow along
• instructor tries to get through all
the material
• students practise skills
• instructor guides the process with
feedback and mini-lectures
After class • students attempt homework,
usually with delayed feedback
• instructor grades past work
• students continue applying their
knowledge skills after clarification and
feedback
• instructor posts any additional
explanations and resources as necessary,
and grades higher quality work
14. The faculty
Professor Deborah Grady
Associate Dean of Clinical
and Translational Research,
UCSF School of Medicine
Professor Bernard Lo
Professor of Medicine
Emeritus, UCSF CTSI
Dr Trish Groves
Head of research, BMJ;
Editor-in-chief BMJ
Open & Editorial lead for
Research to Publication
15.
16.
17. Use best study design to answer research Q
Descriptive studies answer “what’s happening?”
Analytic observational studies answer “why or how is it happening?”
Analytic experimental studies answer “can it work?”
Adapted from:
Centre for
Evidence Based
Medicine,
Oxford, UK
www.cebm.net
18. Imagine you want to design and conduct a study to answer this research question about risk:
“In my country, where 1 in 200 births is a stillbirth, what proportion of the women who have a
stillbirth will go on to have another stillbirth in their next pregnancy?” What would be the
best study design to answer this question?
a) a randomised controlled trial where 100 women who have had one stillbirth are randomly
allocated to one of two groups: i) a group having regular follow up by a midwife over the next
three years or ii) a group having no active follow up.
b) a cross sectional study where 100 women who have had one stillbirth in the past year are
sent an online survey asking about their current health and lifestyle.
c) a retrospective cohort study where a database of routinely collected health data is used to
compare the incidence of stillbirth in two groups of women: all women who had a stillbirth in
their previous pregnancy, compared with all women whose previous pregnancy led to a live
birth.
d) a qualitative study where 25 women who have had stillbirths are interviewed in depth
about their fears about becoming pregnant and their needs for support and care.
e) a case series where all consecutive stillbirths in one area are documented and described,
along with information about the mothers’ health and lifestyles.
Sample MCQ
24. • the research question
• study design
• subjects and variables
• enhancing causal inference
• sample size and power
• data and safety monitoring
• questionnaires and qualitative research
• ethical considerations in research
Course: designing clinical research
25. • trial designs
• randomisation
• selection of participants
• blinding
• choosing interventions and controls
• recruitment
• adherence and follow up
• outcome measures
• adverse events
• regulatory issues
• ethical issues in clinical trials
Course: introduction to clinical trials
26. • overview of clinical research regulations
• informed consent and related issues
• conflicts of interest
• authorship and research misconduct
• ethics in big data and “precision medicine”
• research in resource-poor environments
Course: responsible conduct of research
27. • the introduction: presenting the research question
• the methods: matching study designs to research questions
• ethics aspects of study methods
• reporting statistical methods and analyses
• the results: reporting all findings succinctly
• the discussion: using structure and balance
• choosing and citing references
• optimising the abstract and title
Course: how to write a paper
28. • compliance with journal and ICMJE requirements
• navigating journal and peer review processes
• surviving peer review
• what to do with rejections and appeals
• pre-submission inquiries and cover letters
• good medical writing
Course: what editors and peer reviewers look for
29. • patients’ consent to publication
• journal rules on authorship
• reporting conflicts of interest
• how to write up industry-sponsored trials
• scientific transparency: the pitfalls of selective reporting
• how and why to avoid plagiarism
• how journals uncover scientific fraud
• how journals act on scientific misconduct
Course: publication ethics
Editor's Notes
At BMJ Open we are offering a £250 APC (75% discount) for authors who have successfully completed the R2P protocols module in the past 6 months
Other Gold OA titles that publish protocol articles and might offer this discount: Open Heart, BMJ Open Gastroenterology, BMJ Open Respiratory Research, RMD Open
Image from
https://teachmspost.wordpress.com/2014/07/23/instructional-design-and-the-micro-mooc/
Licensed under Creative Commons Attribution-Share Alike 4.0 International License
Correct answer = c) a cohort study is the best study design for estimating the population risk of an outcome that is infrequent. The study scenario above is about the risk of recurrent stillbirth in a developed country where the baseline rate of stillbirth is 1 in 200 births and it is, therefore, a relatively uncommon event.
If you are unsure about why this is the correct answer, and/or you would like to know more about the uses, advantages, and disadvantages of different clinical and epidemiological study designs, these are explained well at the website of the Centre for Evidence Based Medicine, Oxford, UK:
http://www.cebm.net/study-designs/
Here is the information from CEBM about cohort studies:
In a cohort study:
Data are obtained from groups who have been exposed, or not exposed, to the new technology or factor of interest (eg from databases). No allocation of exposure is made by the researcher. Best for study the effect of predictive risk factors on an outcome.
Advantages:
ethically safe;
subjects can be matched;
can establish timing and directionality of events;
eligibility criteria and outcome assessments can be standardised;
administratively easier and cheaper than RCT.
Disadvantages:
controls may be difficult to identify;
exposure may be linked to a hidden confounder;
blinding is difficult;
randomisation not present;
for rare disease, large sample sizes or long follow-up necessary.