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. 2009 Oct 7;18(3):303–308. doi: 10.1038/ejhg.2009.173

Table 1. Participants.

      Additional information  
Method Type of participant N Focus group participants no. (range) F M Cited as
Focus groups            
   All 12 66 (3–8) 59 7 Parent FG
   New parents – multi-ethnica 7 41 (3–8) 38 3  
   New parents – Afro-Caribbeanb 2 10 (5) 7 3  
   SCD lay consumersc 3 15 (4–7) 14 1 SCD FG
             
Interviews Health care providers          
   All 42 F M   Provider
   Pediatricians 5 3 2    
   Midwives 6 6 0    
   Nurses (maternal/newborn) 7 7 0    
   Nurses (hematological) 2 7 0    
   Obstetricians 3 0 3    
   Hematologists 3 0 3    
   Genetics professionals 9 4 5    
   Family physicians 7 3 4    
  Community advocates: SCD 8 7 1   Advocate
             
  Parents of SCD-carrier infants          
   Alld 6 Mothers Fathers   SCD-infant
      5 1    
a

New parents (infants 6–18 months) recruited through diverse community and primary care organizations in Hamilton, Toronto, and Peterborough, Ontario.

b

New parents (infants 6–18 months) recruited in neighborhoods and through community associations and newspapers serving the Afro-Caribbean community in Toronto, Ontario.

c

Parents of, and persons with, SCD recruited through patient advocacy and parent support groups serving the SCD community in Toronto and Ottawa, Ontario.

d

New parents (infants 6 months to 2 years) recruited through a Toronto hospital with an in-house NBS for SCD screening program that reported carriers.