Epilepsy (Canada) Engagement Summary

  • Published: 15 September 2021
  • Version: V1
  • 1 min read

Gathering uncertainties

Methods used (eg, survey, focus groups, interviews)

Survey

Number %
Total respondents (across all methods) 500 100
Total people with Epilepsy 254 50.8
Total Caregivers of Someone with Epilepsy 71 14.2
Total Friends and Family Members of Someone with Epilepsy 110 22
Total Health Care Professionals 45 9
Total Representatives of Community Epilepsy Agencies 8 1.6
Total Respondents with Unreported Role 12 2.4
Total number of original uncertainties submitted 2126 100
Original uncertainties in scope 1707 80.3
Original uncertainties out of scope 419 19.7

Interim prioritisation

Methods used (eg, survey, focus groups, interviews):

Survey.

Number %
Total number of indicative questions (answered & unanswered) 161 100
Number of verified answered questions 66 41
Number of verified unanswered questions 95 59
Number of verified unanswered questions included in the interim prioritisation 43
Total respondents (across all methods) 590 100
Total patients and carers 484 82
Total health and care professionals 106 18
Number of questions taken to final workshop 16

Final priority setting workshop

Number %
Total participants 22 100
Total patients and carers 11 50
Total health and care professionals 11 50