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Table 1 Number of informants in the different data collections, across study sites.

From: Mass screening for celiac disease from the perspective of newly diagnosed adolescents and their parents: A mixed-method study

Study site

CD-cases

Focus group discussion

Written narrative

Questionnaire

  

Invitedb

Participated

Invitedb

Participated

Invitedc

Participated

   

Adolescents

Parents

 

Adolescents

Parents

 

Parents

 

n

n

n

n

n

n

n

n

n

Umeå

16

16

8

9

16

7

10

16

10

Norrtälje

18

18

3

8

18

10

13

18

14

Norrköping

17

17

8

12

17

10

13

17

14

Lund

65

65

12

14

65

45

48

65

55

Växjö

29

0

0

0

29

19

21

29

21

Total

145 a

116

31

43

145

91

105

145

114

% females

52

54

45

60

52

53

85

52

84

% of invited

--

 

21

--d

 

63

72

 

79

  1. a All screening-detected CD cases found in the multicenter CD screening, forming the recruitment basis for this study.
  2. b Adolescents with their parent(s) were invited.
  3. c Only parents invited.
  4. d Not possible to calculate since we do not know the total number of parents living with the adolescents.