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Table 2 Participant demographics

From: Making a decision about trial participation: the feasibility of measuring deliberation during the informed consent process for clinical trials

Demographic characteristics

n(%)

Number of participants by trial

 

1

81 (60)

2

27 (20)

3

28 (20)

Number of participants by site (recruiting to trial 1, 2 or 3)

 

1 (trial 1, 2 and 3)

46 (34)

2 (trial 2 and 3)

14 (10)

3 (trial 3)

8 (6)

4 (trial 2)

6 (4)

5 (trial 1)

18 (13)

6 (trial 1 and 2)

25 (18)

7 (trial 1 and 2)

19 (14)

Median age, yr (IQR)

55 (43 to 65)

Males

34 (25)

Educational attainmenta

 

No formal education

38 (28)

Secondary

59 (44)

Higher

38 (28)

Previous trial participation (number of trials)

 

0

120 (88)

1

13 (10)

2

2 (2)

3

1 (1)

Person providing patient info leaflet

 

Research nurse

111 (82)

Consultant

8 (6)

Specialist Registrar

1 (1)

Other

16 (12)

Person taking consent

 

Research nurse

109 (81)

Consultant

7 (5)

Specialist registrar

2 (1)

Other

17 (13)

Consented to trial

128 (94)

Median time to make decision, days (IQR)

1 (0.04 to 14)

  1. aData for one respondent are missing.