Abstract
Objective
To assess the effect of a research prioritization partnership that aimed to influence the research agenda relating to urinary incontinence (UI).
Study Design and Setting
Research often neglects important gaps in existing evidence so that decisions must be made about treatments without reliable evidence of their effectiveness. In 2007–2009, a United Kingdom partnership of eight patient and 13 clinician organizations identified and prioritized gaps in the evidence that affect everyday decisions about treatment of UI. The top 10 prioritized research questions were published and reported to research funders in 2009. A year later, new research or funding applications relating to the prioritized topics were identified through reviews of research databases and consultation with funding organizations, elements of the research community, and organizations that participated in the partnership.
Results
Since dissemination of the prioritized topics, five studies are known to have been funded, three in development; five new systematic reviews are under way, one is being updated; five questions are under consideration by a national research commissioning body.
Conclusion
The partnership successfully developed and used a methodology for identification and prioritization of research needs through patient–clinician consensus. Prioritization through consensus can be effective in informing the development of clinically useful research.
To assess the effect of a research prioritization partnership that aimed to influence the research agenda relating to urinary incontinence (UI).
Study Design and Setting
Research often neglects important gaps in existing evidence so that decisions must be made about treatments without reliable evidence of their effectiveness. In 2007–2009, a United Kingdom partnership of eight patient and 13 clinician organizations identified and prioritized gaps in the evidence that affect everyday decisions about treatment of UI. The top 10 prioritized research questions were published and reported to research funders in 2009. A year later, new research or funding applications relating to the prioritized topics were identified through reviews of research databases and consultation with funding organizations, elements of the research community, and organizations that participated in the partnership.
Results
Since dissemination of the prioritized topics, five studies are known to have been funded, three in development; five new systematic reviews are under way, one is being updated; five questions are under consideration by a national research commissioning body.
Conclusion
The partnership successfully developed and used a methodology for identification and prioritization of research needs through patient–clinician consensus. Prioritization through consensus can be effective in informing the development of clinically useful research.
| Original language | English |
|---|---|
| Pages (from-to) | 483-489 |
| Number of pages | 7 |
| Journal | Journal of Clinical Epidemiology |
| Volume | 66 |
| Issue number | 5 |
| Early online date | 4 Aug 2011 |
| DOIs | |
| Publication status | Published - May 2013 |
Keywords
- cooperative behavior
- evidence-based medicine
- female
- Great Britain
- health services research
- humans
- male
- needs assessment
- physician's practice patterns
- physician-patient relations
- research design
- urinary incontinence