The Clinical Trials Charter: for researchers
The Clinical Trials Charter aims to set a standard of practice for those involved in clinical trials for Parkinson’s.
As researchers, you are responsible for designing and delivering ethical studies that are of relevance to patients; you aim to ensure participants’ safety and to protect their rights and dignity.
The Clinical Trials Charter
Before the trial
As researchers you should strive to:
- Communicate effectively with all participants and wider stakeholders which will involve:
- Identifying individuals to be responsible for communication.
- Producing information about the trial which is accessible and easy to understand.
- Providing ample opportunity to address participants’ concerns or questions about the study.
- Involving patient advocates and prospective participants in all aspects of study design and conduct as appropriate.
- Be transparent and clear in what we hope to achieve from the study, its potential, the risks and benefits.
- Ensure all appropriate approvals and safeguards are in place prior to the start of the study.
During the trial
- Listen carefully to participants’ concerns and address unforeseen issues rapidly as they arise.
- Employ and continuously re-evaluate the practices used in this trial, to ensure the optimum care of participants.
- Communicate effectively and keep trial participants informed, motivated and supported.
- Use data collected during the trial to re-assess the design and validity of the study and its potential value in future research.
After the trial
- Create a project debrief for all participants using a range of media and collect feedback from patients on their trial experience (good and bad).
- Disseminate lessons learnt to the wider Parkinson’s community – best practice should evolve.
- Communicate the results of the trial to the Parkinson’s and wider communities – if possible publish results as open access.
- Use information collected from above to improve future trials.