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Table 3 Meta consent preferences

From: Eliciting meta consent for future secondary research use of health data using a smartphone application - a proof of concept study in the Danish population

Type of data

Blanket refusal (Never allowed)

Specific consent (Ask always)

Broad consent (Ask rarely)

Blanket consent (Always allowed)

Electronic patient record

1 (0.5)a

90 (40.7)

39 (17.6)

91 (41.2)

Health data in registries

2 (0.9)

74 (33.5)

43 (19.5)

102 (46.2)

Data from samples

1 (0.5)

83 (37.6)

40 (18.1)

97 (43.9)

Other data in registries

2 (0.9)

97 (43.9)

47 (21.3)

75 (33.9)

Type of research

 Public research

3 (1.4)

66 (29.9)

52 (23.5)

100 (45.2)

 Private commercial research

9 (4.1)

137 (62.0)

41 (18.6)

34 (15.4))

 Private non-commercial research

4 (1.8)

113 (51.1)

52 (23.5)

52 (23.5)

 Danish research

4 (1.8)

79 (35.7)

54 (24.4)

84 (38.0)

 International research

7 (3.2)

121 (54.8)

46 (20.8)

47 (21.3)

  1. N = 221 a n (%)