Improving the informed consent process for clinical trials
Sustainable Solutions to Translating Best Practices for Informed Consent
This study is working to make the consent process for clinical trials clearer and easier to understand, especially for people from different backgrounds, including older adults and those living in rural areas, so that everyone can feel comfortable and informed when deciding whether to participate.
Quick facts
| Grant type | R01 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | Washington University NIH-funded |
| Lab location | 1 site (Saint Louis, United States) |
| Project ID | NIH-10917307 on NIH RePORTER |
What this research studies
This research aims to enhance the informed consent process used in clinical trials, which often confuses potential participants due to complex language and repetitive information. By engaging with stakeholders, the team will develop and test a new consent template that is easier to understand and implement. The project will utilize mixed-methods to ensure that the new process is feasible and meets the needs of diverse populations, including racially minoritized groups, rural residents, and older adults. A community advisory board will be involved throughout the project to ensure alignment with community needs.
Who could benefit from this research
Good fit: Ideal candidates for this research are individuals from racially minoritized populations, rural areas, and older adults who may face challenges in understanding traditional informed consent forms.
Not a fit: Patients who are already well-versed in clinical trial processes or those who do not require informed consent for participation may not benefit from this research.
Why it matters
Potential benefit: If successful, this research could lead to a more accessible and understandable informed consent process, increasing participation in clinical trials among underrepresented populations.
How similar studies have performed: Previous research has shown that simplifying informed consent processes can improve understanding and participation, indicating that this approach has potential for success.
Where this research is happening
Saint Louis, United States
- Washington University — Saint Louis, United States (Active)
Researchers
- Principal investigator: Politi, Mary C — Washington University
- Study coordinator: Politi, Mary C
About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page below.