Table 3

Percentage of participants having no understanding of clinical trial concepts: pretest versus post-test

ChildrenParents
TFIPTFIP
Clinical trial
 Pre46 (66.7)44 (67.7)22 (29.3)22 (30.1)
 Post19 (27.5)14 (21.2)11 (14.7) 5 (6.8)
 Δ Pre-post39.246.514.623.3
Randomisation
 Pre38 (55.1)27 (41.5)44 (58.7)33 (45.2)
 Post23 (33.3)12 (18.2)*19 (25.3)11 (15.1)
 Δ Pre-post21.823.333.430.1
Placebo
 Pre61 (88.4)58 (89.2)24 (32.0)25 (34.2)
 Post38 (55.1) 6 (9.1)*10 (13.3) 6 (8.2)
 Δ Pre-post33.380.118.726.0
Single blinding
 Pre67 (98.6)64 (98.5)49 (65.3)44 (61.1)
 Post32 (46.4)12 (18.2)*11 (14.7) 6 (8.2)
 Δ Pre-post52.280.350.652.9
Double blinding
 Pre67 (98.6)64 (98.5)56 (74.7)55 (75.3)
 Post33 (47.8) 9 (13.6)*11 (14.7)10 (13.7)
 Δ Pre-post50.884.960.061.6
Informed consent
 Pre27 (39.1)35 (53.8) 9 (12.0) 8 (11.0)
 Post21 (30.4)28 (42.4) 5 (6.7) 3 (4.1)
 Δ Pre-post 8.711.4 5.3 6.9
  • Data are presented as n (%).

  • Δ=Pre-post change in understanding, *p<0.05 versus TF.

  • IP, interactive digital program; TF, traditional paper format.