Table 2 Unpublished training material subjects
Theme/Topic | Frequency |
|---|---|
Role of a PPI Contributor | 11 |
Explanation of what an oversight committee is | 8 |
Number of meetings to attend | 8 |
Who to contact for more information/support | 7 |
Background to the specific trial under review | 6 |
Key qualities of a PPI Contributor | 6 |
Description of the role of each committee | 5 |
Activity required between meetings | 5 |
Confidentiality | 5 |
Payment/expenses | 5 |
Explanation of what PPI is | 4 |
Non-attendance of meetings | 4 |
Who makes up the membership of the committee | 4 |
Evaluation of involvement (feedback/review) | 4 |
Examples of activity of Contributors may undertake | 3 |
Background to clinical trials | 3 |
What happens at a committee meeting | 3 |
Duration of the committee membership | 3 |
Terms of Reference for the committee | 3 |
Specific training to be completed | 3 |
Trial timeline (from idea conception to results published) | 2 |
Implications of involvement on studies (benefits/tax codes etc.) | 2 |
Location of committee meetings | 2 |
Training predominantly conducted as a face-to-face discussion | 2 |
Importance of Plain English | 1 |
Background to trial design | 1 |
Common challenges to research | 1 |
Developing a proposal | 1 |
Getting your voice heard at meetings | 1 |
Resignation from the committee | 1 |
Safety checks to be completed (e.g. DBS) | 1 |
Application process for committee membership | 1 |
Explanation of what a CTU is | 1 |
Glossary of terms | 1 |