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Table 3 Participant data

From: Development of a core outcome set for the evaluation of interventions to enhance trial participation decisions on behalf of adults who lack capacity to consent: a mixed methods study (COnSiDER Study)

   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
  1. aParticipants with missing data n = 1
  2. bParticipants with missing data n = 3