From: ‘Is it worth doing?’ Measuring the impact of patient and public involvement in research
Categories of impact identified through literature reviews |
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1. Impact on the research agenda—the topic, research question and funding decisions |
2. Impact on research design and delivery—influencing the research design, tools and choice of method, recruitment, data collection and analysis, writing-up and dissemination. |
3. Impact on research ethics—the consent process and developing ethically acceptable research |
4. Impact on the people involved |
5. Impact on the researchers |
6. Impact on participants |
7. Impact on the wider community |
8. Impact on community organisations |
9. Impact on implementation and change |