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. 2020 Jun 25;15(7):937–948. doi: 10.2215/CJN.00900120

Table 1.

Characteristics of the participants (N=67)

Characteristics n (%)
Role
 Patient 54 (81)
 Caregiver 13 (19)
Sex
 Male 24 (36)
 Female 43 (64)
Country
 United States (3 groups) 21 (31)
 Australia (4 groups) 28 (42)
 United Kingdom (3 groups) 18 (27)
Ethnicitya
 White 42 (63)
 Black (American) 11 (16)
 Black (British) 4 (6)
 Asian 4 (6)
 Othera 6 (9)
Age, yr
 18–30 4 (6)
 31–50 20 (30)
 51–70 38 (57)
 >70 5 (7)
Marital status
 Single 16 (24)
 Married/partnered 39 (58)
 Divorced/separated 10 (15)
 Widowed 2 (3)
Number of children
 0 18 (27)
 1–2 32 (48)
 ≥3 17 (25)
Employment
 Full time 24 (36)
 Part time/casual 11 (16)
 Student 3 (4)
 Not employed/disabled 13 (19)
 Retired 16 (24)
Education
 Before 10th grade (before age 16 yr) 4 (6)
 Completed 10th grade (age 16 yr) 5 (7)
 Completed 12th grade (ages 17–18 yr) 7 (10)
 Professional certificate 11 (16)
 Undergraduate degree 22 (33)
 Postgraduate degree 18 (27)
Age at time of diagnosisb
 <18 5 (7)
 18–30 11 (16)
 31–50 23 (34)
 51–70 14 (21)
Cause of kidney diseaseb
 Diabetes 9 (13)
 Hypertension 19 (28)
 PKD 7 (10)
 GN 19 (28)
 Infection 2 (3)
 Immune/autoimmune 7 (10)
 Reflux nephropathy 1 (1)
 Unknown/do not know 3 (4)
 Other 6 (9)
Type of KRT (current)b
 None 16 (24)
 Hemodialysis 14 (21)
 Peritoneal dialysis 4 (6)
 Kidney transplant 20 (30)
Duration of KRT (current)b
 <6 mo 1 (1)
 6–12 mo 3 (4)
 1–3 yr 13 (19)
 4–6 yr 7 (10)
 >6 yr 15 (22)

Numbers may not total 67 if not reported or participants could select multiple options. Approximately n=37 refused to participate or did not attend the focus groups because of other commitments, illness, or did not want to participate. PKD, polycystic kidney disease.

a

Included Hispanic Latino (n=1), Aboriginal Australian (n=1), Pakistani (n=2), Middle Eastern (n=1), and Indian (n=1).

b

Not applicable to caregivers.