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