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Table 2 Views of the study population on informing and informed consent

From: Population attitudes towards research use of health care registries: a population-based survey in Finland

Would you like to be informed if your information would be used for research purposes?

Women %

Men %

<=30 %

31-40 %

41-50 %

51-60 %

61-70 %

>70 %

Total %

I would like to be informed every time

47.5

48.1

31.8

48.9

56.1

48.3

56.0

29.2

47.8

In some cases there is no need to inform

35.3

30.0

36.4

36.2

24.6

36.8

28.0

43.8

33.1

No need to inform at all

17.3

21.9

31.8

14.9

19.3

14.9

16.0

27.1

19.1

   

p = 0.028

  

Should an informed consent be obtained from every study participant in a register-based study?

Women %

Men %

<=30 %

31-40 %

41-50 %

51-60 %

61-70 %

>70 %

Total %

No need for obtaining informed consent

26.5

37.1

29.5

23.4

33.3

23.9

35.2

33.3

30.3

In some cases informed consent should be obtained

44.4

31.4

50.0

44.7

36.8

43.2

35.2

33.3

39.6

Informed consent should always be obtained

29.2

31.4

20.5

31.9

29.8

33.0

29.6

33.3

30.1

 

p = 0.019

       

What kind of practice would be best, if informed consent was required for register-based studies?

Women %

Men %

<=30 %

31-40 %

41-50 %

51-60 %

61-70 %

>70 %

Total %

Informed consent should be obtained for every study

12.9

13.5

9.1

13.3

14.3

8.1

17.2

15.9

13.4

One informed consent for one field of research (for example cancer research)

43.3

47.1

50.0

44.4

41.4

46.5

45.9

36.4

44.6

One informed consent for research use of a certain register

43.4

38.1

40.9

42.2

41.4

45.9

36.9

45.5

41.3

Other

0.4

1.3

0.0

0.0

3.6

0.0

0.0

2.3

0.8