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Table 1 Participant characteristics

From: Development and evaluation of a quality of life measurement scale in English and Chinese for family caregivers of patients with advanced cancers

Characteristics

Mean (SD) or N (%)a

All (n = 612)

English (n = 304)

Chinese (n = 308)

Age (years)

48 (14)

45 (14)

51 (13)

Gender

 Female

373 (61.0%)

181 (59.5%)

192 (62.3%)

 Male

239 (39.0%)

123 (40.5%)

116 (37.7%)

Ethnicity

 Chinese

521 (85.1%)

214 (70.4%)

307 (99.7%)

 Malay

53 (8.7%)

53 (17.4%)

0 (0.0%)

 Indian

19 (3.1%)

19 (6.3%)

0 (0.0%)

 Others

19 (3.1%)

18 (5.9%)

1 (0.3%)

Education

 Primary or below

93 (15.2%)

11 (3.6%)

82 (26.6%)

 Secondary

204 (33.3%)

93 (30.6%)

111 (36.0%)

 Post-secondary

315 (51.5%)

200 (65.8%)

115 (37.3%)

Relationship with patient

 Spouse

237 (38.7%)

97 (31.9%)

140 (45.5%)

 Son or daughter

283 (46.2%)

168 (55.3%)

115 (37.3%)

 Others relatives

92 (15.0%)

39 (12.8%)

53 (17.2%)

Hours caregiving per week

44 (38)

41 (36)

47 (40)

BASC scoreb

1.98 (0.57)

1.95 (0.58)

2.01 (0.56)

Patient’s performance status

 0 (Best)

71 (11.6%)

44 (14.5%)

27 (8.8%)

 1

205 (33.5%)

106 (34.9%)

99 (32.1%)

 2

81 (13.2%)

39 (12.8%)

42 (13.6%)

 3

170 (27.8%)

76 (25.0%)

94 (30.5%)

 4 (Worst)

85 (13.9%)

39 (12.8%)

46 (14.9%)

Recruitment setting

 Outpatient

394 (64.4%)

181 (59.5%)

213 (69.2%)

 Inpatient

218 (35.6%)

123 (40.5%)

95 (30.8%)

  1. aMean and standard deviation (SD) for continuous variables; frequency (N) and percent for categorical variables
  2. bBrief Assessment Scale for Caregivers (range 0-3)