HRB TMRN
HRB TMRN
  • Видео 159
  • Просмотров 26 565
Lynn Laidlaw - Co Production Collective on research ethics and PPIE/Co Production
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight
May 2nd, 2024
Lynn lives with a rare disease and multiple long term conditions and is involved with multiple research teams, academic institutions and organisations across the UK as a public contributor to research. Increasingly she is co producing research as a part of the team, working as a patient researcher and navigating issues such as applying for ethical approval. She has a long standing association with the HRA as part of their Public Involvement Network. She is part of the Co Production Collective based at University College London (UCL) and discussed the findings from the joint project be...
Просмотров: 114

Видео

Dr Amy Rogers - Ethical considerations for Decentralised Clinical Trials
Просмотров 1363 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Dr Amy Rogers is a Clinical Lecturer with MEMO Research at the University of Dundee. Having previously worked as a General Practitioner, Amy now researches pragmatic clinical trial methods, focusing on decentralised and healthcare-embedded clinical trials. Recent projects have included th...
Dr Cory Goldstein - Framework for ethical design & conduct of pragmatic trials in health/social care
Просмотров 603 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Title: A framework for the ethical design and conduct of pragmatic trials in health and social care Dr. Cory Goldstein is a Postdoctoral Fellow with the Clinical Epidemiology Program at the Ottawa Hospital Research Institute and the School of Epidemiology and Public Health at the Universi...
Prof. Charles Weijer - Ethical issues in cluster randomised trials of health and social care
Просмотров 1233 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Dr. Charles Weijer is Professor of Medicine and Philosophy at Western University in London, Canada. He is a leading expert in the ethics of randomized controlled trials. From 2008 to 2013 Charles co-led a collaboration that produced the first international ethics guidelines for cluster ra...
Prof. Shaun Treweek & Dr Hanne Bruhn - Trial Forge Guidance 5: Ethical issues in SWATs
Просмотров 213 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Shaun is a health services researcher interested in efficient trial design, particularly around inclusive recruitment and retention and the effective presentation of research evidence. He led the development of the NIHR INCLUDE Ethnicity Framework, a tool to help trialists design inclusiv...
Dr Suman Prinjha & Tracy Cripps - Ethics in Action: Inclusive Trials
Просмотров 313 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Dr Suman Prinjha is Associate Professor / Senior Research Fellow at University of York where she works within York Trials Unit and NIHR Research Support Service (RSS). She has over 20 years’ postdoctoral experience in qualitative research, and is a practising BACP-registered psychotherapi...
Prof. Mary Donnelly - Intersection of Ethics and Law in Research Trials
Просмотров 953 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Mary Donnelly is Professor of Law at University College Cork, Ireland. She publishes widely in health and capacity law. She is Associate Editor of the International Journal of Law and Psychiatry and is a member of the Editorial Board of the Medical Law Review and Medical Law International...
Dr Laura MacKey - When it isn’t an ethical issue, what is it?
Просмотров 553 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Laura Mackey is Programme Officer for the National Office for Research Ethics Committees. Her main responsibility is managing applications submitted via the Clinical Trials Information System and liaising with national and European stakeholders involved in this process. Laura originally t...
Dr Daniël Lakens - Methodological Review Boards
Просмотров 423 месяца назад
UCC & HRB-TMRN event: Deliberating Ethics in Trials: Scope and necessity of ethical oversight May 2nd, 2024 Daniël Lakens, PhD., is an Associate Professor of Metascience and chair of the Ethical Review Board at the Human-Technology Interaction group at Eindhoven University of Technology in The Netherlands. Lakens’ work focuses on improving research methods and statistical inferences in the soci...
Development of a guideline for reporting the results of randomised Studies Within A Trial
Просмотров 1,1 тыс.3 месяца назад
Evidence to support decisions on trial processes is minimal. A Study Within A Trial (SWAT) can however be used to test trial processes or explore methodological uncertainties. The replication of SWATs is required to ensure sufficient power and broad applicability of findings. Prompt reporting is therefore essential; however, SWAT publications are often the first to be abandoned in the face of o...
The role of AI in clinical trials
Просмотров 1 тыс.5 месяцев назад
With rapid increase in the use of artificial intelligence in healthcare, the need for thoughtful, ethical, and impactful application to support clinical trials is imperative. This webinar explored the current and future applications of artificial intelligence for clinical trial design, conduct, and reporting, with a focus on the ethical considerations of these new technologies. Dr Danielle Bitt...
Studies Within A Trial to test recruitment and retention strategies: lessons learnt from PROMETHEUS
Просмотров 446 месяцев назад
Randomised controlled trials are susceptible to poor participant recruitment and retention. Studies Within A Trial (SWATs) are the strongest methods for testing the effectiveness of strategies to improve recruitment and retention. However, relatively few of these have been conducted. The PROMoting THE Use of Studies Within A Trial (PROMETHEUS) programme aimed facilitated 42 SWATs evaluating rec...
Technology Innovation as a Way of Building Site Partnerships
Просмотров 287 месяцев назад
Dr Ronan Fox Senior Vice President in IT R & D ICON plc 8th HRB-TMRN Symposium 20th October, 2023 Galway
From idea to completion, the role of partners in ensuring reporting guidelines are useful
Просмотров 77 месяцев назад
Dr David Moher Senior Scientist, Ottawa Hospital Research Institute Professor, School of Epidemiology and Public Health, uOttawa 8th HRB-TMRN Symposium 20th October, 2023 Galway
Co-designing ID Trials to make them more inclusive and representative
Просмотров 107 месяцев назад
Stephen O'Hare Executive Director, HIV Ireland Chairperson, ID-CTNI PPI Community Advisory Board 8th HRB-TMRN Symposium 20th October, 2023 Galway
The communication of retention strategies in clinical trials
Просмотров 147 месяцев назад
The communication of retention strategies in clinical trials
Recruiting for international online advisory group for children & parents: challenges & facilitators
Просмотров 147 месяцев назад
Recruiting for international online advisory group for children & parents: challenges & facilitators
Developing a model for conducting PPI activities in maternal and neonatal clinical trials
Просмотров 117 месяцев назад
Developing a model for conducting PPI activities in maternal and neonatal clinical trials
Prodigy ILD
Просмотров 487 месяцев назад
Prodigy ILD
Opportunities and Pitfalls for Decentralized Clinical Trials
Просмотров 1727 месяцев назад
Opportunities and Pitfalls for Decentralized Clinical Trials
The Trials Methodology Research Agenda: A Priority Setting Exercise
Просмотров 487 месяцев назад
The Trials Methodology Research Agenda: A Priority Setting Exercise
Working in partnership with patients and clinicians to set priorities for research
Просмотров 207 месяцев назад
Working in partnership with patients and clinicians to set priorities for research
When is the Stepped-Wedge Cluster Randomized Trial (SW-CRT) a good design choice?
Просмотров 3077 месяцев назад
When is the Stepped-Wedge Cluster Randomized Trial (SW-CRT) a good design choice?
CTU partnerships to improve the conduct of trials through knowledge exchange and innovation
Просмотров 317 месяцев назад
CTU partnerships to improve the conduct of trials through knowledge exchange and innovation
Madness, Magic or Mystery - a Patient and Trial Methodology
Просмотров 227 месяцев назад
Madness, Magic or Mystery - a Patient and Trial Methodology
Managing “participation changes” in trials: the PeRSEVERE principles and what might come next
Просмотров 638 месяцев назад
Managing “participation changes” in trials: the PeRSEVERE principles and what might come next
How to start a conversation with public partners about estimands: a practical tool
Просмотров 888 месяцев назад
How to start a conversation with public partners about estimands: a practical tool
Decentralised Clinical Trials - Lessons from the Trials@Home project
Просмотров 10910 месяцев назад
Decentralised Clinical Trials - Lessons from the Trials@Home project
Dr Lydia O Sullivan - Designing Effective PILs
Просмотров 46Год назад
Dr Lydia O Sullivan - Designing Effective PILs
Dr Jane Bryant - Ethics in Randomised Trials
Просмотров 68Год назад
Dr Jane Bryant - Ethics in Randomised Trials

Комментарии

  • @jovelnom
    @jovelnom 3 дня назад

    Thanks for such insightful webinar.

  • @Aldraz
    @Aldraz 5 месяцев назад

    YT randomly recommended me this video, probably because I am developing an AI platform myself, but it is very interesting we can already use an AI in clinical trials. I think the problems you have mentioned are mostly details that will be fixed with a small improvement, like biases, hallucinations, etc.. but what we really need is for AIs to have actual reasoning skills, planning, executing, long-term thinking, etc.. those are some of the last missing pieces. After that we can do something much closer to real digital-twins. And with a perfect digital-twins you could probably skip the whole clinical trials as such and release the drug, quite literally to the public without waiting for years. But that is still a sci-fi for now.. and still might take about 2-5 years until we get to that point unfortunately. And then probably another 10 years until it is gonna be approved by the slow regulatory system lol.

  • @tysonwong968
    @tysonwong968 6 месяцев назад

    Gordon gyatt

  • @BUY_YOUTUB_VIEWS_841
    @BUY_YOUTUB_VIEWS_841 7 месяцев назад

    wish it was longer :/

  • @charlysvictor9742
    @charlysvictor9742 11 месяцев назад

    Even now, there is trouble in coducting feseability trials, and tris presentation helped me a lot, thank you very very very much

  • @ChienXuan-ns1mq
    @ChienXuan-ns1mq Год назад

    hidemyacc

  • @daylensantana5333
    @daylensantana5333 2 года назад

    Hello, thank you for this. Very helpful. Are slides available anywhere?

  • @franktheson
    @franktheson 2 года назад

    Where does the Embedding comes in?

  • @seans4893
    @seans4893 4 года назад

    A living legend.

  • @vinnyvn
    @vinnyvn 4 года назад

    Very helpful presentation! Thanks so much for this.

  • @mswfamu
    @mswfamu 6 лет назад

    Very informative!

  • @sorchascolai8078
    @sorchascolai8078 6 лет назад

    Oh my god look at siomha

  • @1985amaramar
    @1985amaramar 7 лет назад

    one question..is there any vendor available who can give us access to see their RMB platform to see how their RMB platform works

  • @synexussatv3679
    @synexussatv3679 8 лет назад

    I think this is brilliant.

  • @bronaghblackwood699
    @bronaghblackwood699 9 лет назад

    Excellent to see the good work undertaken by these aspiring PhD students!