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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.