Table 3 Participant data
| Participants recruited (n = 28) |
Completed Round 1 (n = 26)a | Completed Round 2 (n = 22)b | ||
|---|---|---|---|---|
| Age | ||||
| 18–24 | 0 | 0 | 0 | |
| 25–34 | 6 | 5 | 5 | |
| 35–49 | 14 | 13 | 10 | |
| 50–65 | 3 | 3 | 3 | |
| 65+ | 5 | 5 | 4 | |
| Gender | ||||
| Male | 10 | 9 | 8 | |
| Female | 18 | 17 | 14 | |
| Other (please specify) | 0 | 0 | 0 | |
| Country | ||||
| England | 20 | 19 | 15 | |
| Northern Ireland | 1 | 1 | 1 | |
| Scotland | 1 | 1 | 1 | |
| Wales | 6 | 5 | 5 | |
| Principal stakeholder group | ||||
| A family member/friend of someone affected by impaired capacity | 3 | 3 | 3 | |
| A researcher interested in aspects of trial design and conduct (e.g. ethicist, sociologist) | 5 | 5 | 4 | |
| A trial authoriser or advisor (e.g. research ethics committee member, PPI partner) | 3 | 3 | 3 | |
| A trial designer (e.g. trialist, methodologist, lead clinician) | 10 | 9 | 7 | |
| A trial recruiter (e.g. research nurse) | 7 | 6 | 5 |