NIHR Oxford Biomedical Research Centre

Enabling translational research through partnership

MENUMENU
  • About
    • About the NIHR Oxford Biomedical Research Centre
    • NIHR Oxford BRC impact
    • Steering Committee
    • Promoting equality, diversity and inclusion in research
    • Current Vacancies
    • Stay in Touch
    • Contact Us
  • Research

        • Research Overview
        • Clinical Research Facility
        • Health Economics
        • Ethics in the NIHR Oxford BRC
        • Medical Statistics
        • Infections in Oxfordshire Database (IORD)
        • 15 Research Themes

        • Cancer
        • Cardiovascular Medicine
        • Digital Health from Hospital to Home
        • Gene and Cell Therapy
        • Genomic Medicine
        • Imaging
        • Inflammation across Tissues
        • Life-saving Vaccines
        • Metabolic Experimental Medicine
        • Modernising Medical Microbiology and Big Infection Diagnostics
        • Musculoskeletal
        • Preventive Neurology
        • Respiratory Medicine
        • Surgical Innovation, Technology and Evaluation
        • Translational Data Science
  • Patient and Public Involvement
    • For patients and the public
    • For researchers
    • More information
  • Training Hub
    • Training Hub Overview
    • Clinical Academic Pathway
    • Internships
    • Pre-doctoral Research Fellowships
    • Senior Research Fellowships
    • Research Training Bursaries
    • Doctoral Awards
    • Post-Doctoral Awards
    • PARC Programme
    • Other funding
    • Leadership Training
    • Useful Links
    • Training and Education Resources
    • Upcoming Training Events & Courses
  • Industry
    • Collaborate with Oxford BRC
    • Who Do We Work With?
    • Events
    • Further Information and Additional Resources
    • Contacts for Industry
  • Videos
  • News
  • Events

** HEALTH RESEARCH SHOWCASE THURSDAY 29 MAY 2025 **

Patient and Public Involvement

You are here: Home > PPIE > A Delphi survey to identify a core set of items for sharing the results of randomised trials with patients and the public

INVOLVEMENT CATEGORIES

Ageing | Brain | Cancer | COVID-19 | Dementia | Heart | Joints | Liver | Mental Health | Neurological Conditions | Other | Stroke | Women's Health | ALL

A Delphi survey to identify a core set of items for sharing the results of randomised trials with patients and the public

Posted 9 May 2025 · Listed under Other

Patients and public motif, healthcare, medicines

Delphi survey

Follow this link to access the survey. The deadline for completion is 9 June 2025.

Why this matters

Randomised trials help us understand which treatments work and which don’t. But too often, the results aren’t shared clearly—or at all—with the very people who could benefit most: patients and the public. We believe everyone should have access to information that can help them make informed decisions about their health. Following our initial study in 2024, we are asking for people to be involved in the next stage of the research.

What’s this about?

We’re creating a reporting guideline to help researchers share trial results in clear, simple, and meaningful ways. To do this, we need your input! This online survey will ask for your thoughts on what kinds of information should be shared.
You will be asked to rate each item (a piece of information) on a scale from 1 to 5, based on how important and meaningful you think it is to share with patients and the public when sharing the results of randomised trials.

Who can take part?

We’re looking for people with different perspectives and experiences, including:

  • Patients, carers, and members of the public
  • Researchers involved in clinical trials
  • People who review or approve trials (e.g., ethics or regulatory reviewers)
  • Funders and commissioners of research
  • People who use trial findings (e.g., journal editors, peer reviewers, guideline developers)
If that sounds like you—or someone you know—we’d love to hear from you!
Participants should be over 18 years old. The aim is to be as inclusive and diverse as possible. Preference will be given to participants who are from ethnic minority communities or any other minority groups as I want to reflect the viewpoints of the under-represented and ensure their voices are heard.
 

What to expect

There will be 2-3 rounds of survey. The survey is quick (just 15–20 minutes per round), and your views will directly shape how trial results are shared in the future. You’ll also find a Participant Information Sheet here for full details.

Date required

Ongoing

Organisation

University of Oxford, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences

Contact

Sanjana Choudhury: sanjana.choudhury@wolfson.ox.ac.uk

Phone: +44 7574279163

https://www.ndorms.ox.ac.uk/team/sanjana-choudhury

This listing will expire Sunday 31st August 2025 11:33am

For Patients and the Public

  • Welcome
  • Opportunities for patients and the public
  • Training for patients and the public
  • Public events
Register for the involvement email bulletin
Follow @OxfordPPI
RESEARCHER GUIDANCE →

More Information

  • Patient and public groups
    • Patient and Public Advisory Group
    • Diversity in Research Group
  • Meet the team
  • Case Studies
  • Strategy
  • Videos
  • News

Subscribe to the Oxford BRC Newsletter

Keep informed about the work of the Oxford BRC by subscribing to our Mailchimp e-newsletter. It is produced several times a year and delivers news and information about upcoming events straight to your inbox.

Subscribe Now

Feedback

We’d love to hear your feedback. Please contact us at obrcenquiries@ouh.nhs.uk

Oxford BRC on Social Media

  • Bluesky
  • Facebook
  • LinkedIn
  • Threads
  • Twitter
  • YouTube
  • Data Control and Privacy
  • Accessibility
  • Our Partners
  • Disclaimer
  • Contact

Copyright © 2025 NIHR Oxford Biomedical Research Centre