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. 2010 May 13;10:122. doi: 10.1186/1472-6963-10-122

Table 2.

Objective and subjective clinical characteristics of the 20 caregiver and 20 care recipient participants.

Subjective and Objective measures of burden Statistics mean (range) ± SD
DRS2, mean [CI α = 0.05] 95 [83-107] (35-130) ± 25
BADLS Total, mean [CI α = 0.05] 7.6 [7-8] (4-10) ± 1.8
Care Recipient Age at Diagnosis, 74 (53-90) ± 9
Formal Diagnosis, Yes/No N (%) 18 (90)/2 (10)
Measures of Carer Burden
GHQ-30, mean [CI α = 0.05] scoring 5 or more 8 [5-12] (0-27) ± 7 N (%) 13 (65)
CCL-CR Behaviour where max possible = 52 19 (8-37) ± 8
CCL-Carer stress where max possible = 52 15 (3-32) ± 8
CCL-Overall burden 3 (2-5) ± 1
CCL-Physical burden 3 (1-5) ± 1
CCL-Emotional burden 4 (1-5) ± 1
CCL-Financial burden 2 (1-5) ± 1
CCL-Social burden 3 (1-5) ± 1
CCL-Carer rated stress by service needs 2 (0-8) ± 3
Services Provided
Total out of home respite hours over 3 months receiving ANY hrs 52 (0-294) ± 72 N (%) 14 (70)
Total in home respite over 3 months receiving ANY hrs 29 (0-119) ± 34 N (%) 11 (55)
Total practical help over 3 months receiving ANY hrs 22 (0-125) ± 32 N (%) 12 (60)
CCL-carer feels need more from services 3 (0-8) ± 2
Need more help from services than I am given - yes, N (%) 13 (65)
Need more information than I am given - yes, N (%) 8 (40)
Services should work together & communicate more - yes N (%) 10 (50)
Need better access to services - yes N (%) 11 (55)