Table 1 Stakeholder groups per year
From: Lessons learned in measuring patient engagement in a Canada-wide childhood disability network
Stakeholder group | Year 1 2018 | Year 2 2019 | Year 3 2020 |
|---|---|---|---|
n (%) | n (%) | n (%) | |
Researchers/investigators | 99 (36.4) | 101 (33.1) | 111 (25.5) |
Research staff | 42 (15.4) | 48 (15.7) | 80 (18.3) |
Committee members | 44 (16.2) | 41 (13.4) | 54 (12.4) |
Patient-partners (parents/caregivers) | 44 (16.2) | 60 (19.7) | 87 (20.0) |
Youth advisors | 2 (0.7) | 2 (0.7) | 10 (2.3) |
Trainees | 16 (5.9) | 26 (8.5) | 49 (11.2) |
Education/health professionals | 9 (3.3) | 8 (2.6) | 20 (4.6) |
Support services/consultants | 14 (5.1) | 15 (4.9) | 14 (3.2) |
Policy makers | 2 (0.7) | 4 (1.3) | 8 (1.8) |
Industry partners | – | – | 3 (0.7) |
Total n (%) | 272 (100) | 305 (100) | 436 (100) |