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. 2017 Sep 21;8:178. doi: 10.3389/fpsyt.2017.00178

Table 2.

Participants’ sociodemographic characteristics (N = 21).

Age, mean (SD) 47.52 (14.98)
Sex, N (%)
 Female 15 (71.4)
 Male 6 (28.6)
Relationship type, N (%)
 Mother/father 14 (66.7)
 Sister/brother 3 (14.3)
 Wife/husband 2 (9.5)
 Daughter/son 2 (9.5)
Completed education level, N (%)
 Compulsory education 4 (19.0)
 Apprenticeship 4 (19.0)
 High school graduate 2 (9.5)
 School profession, trade, normal, technical 3 (14.3)
 University 8 (38.1)
Professional activity, N (%)
 Salaried or own employer 15 (71.4)
 Pensioner 2 (9.5)
 Unemployed 3 (14.3)
 Student 1 (4.8)
Living under the same roof as patient, N (%)
 Yes 11 (52.4)
 No 10 (47.6)
Frequency of close contacts, N (%)
 Daily 13 (61.9)
 Weekly 7 (33.3)
 Monthly 1 (4.8)
Previously requested help, N (%)
 Yes 13 (61.9)
 No 8 (38.1)
Obtained first individual help as a caregiver
 Yes 21 (100)
 No
Reason for requesting help, N (%)
 Participate in research 7 (33.3)
 Manage the caregiving role 6 (28.6)
 Better understand the disease 5 (23.8)
 Gain professional support 2 (9.5)
 Support patient 1 (6.7)
Number of reasons for the request, N (%)
 One reason 7 (33.3)
 Several reasons 14 (66.7)
Patient’s diagnosis according to the caregiver, N (%)
 Schizophrenia 13 (61.9)
 Depression 4 (19.0)
 Bipolar disorder 2 (9.5)
 Anxious disorder 2 (9.5)
Duration of illness, N (%)
 Less than a year 7 (33.3)
 Between 1 and 2 years 2 (9.5)
 Between 3 and 10 years 9 (42.9)
 More than 10 years 3 (14.3)