Clinical trials help to inform clinical practice and improve the survival and quality of life of cancer patients.
Clinical trials are carefully designed research studies that investigate a new medical test or treatment for people.
There are two main study types used in medical research – observational and interventional.
Cancer clinical trials are part of a broader drug development pathway, during which new drugs are identified, tested and approved for clinical use.
Consumers bring their experience as a person affected by cancer and also their skills and learnings from their cancer journey, their careers and their life experience.
Consumers can be involved in some aspects of communication clinical trial results.
Informed consent is an ethical and legal requirement for any human research.
When involved in cancer clinical trials as a consumer, most of the work involves meetings. These could be one-off meetings such as focus groups, or regular meetings as part of a group, committee or board.