Comparison of Positive Psychological Capital among Caregivers of Depressed Patients with Different Marital Status
Main Article Content
Abstract
Major Depressive Disorder (MDD) or Depression is a psychiatric disorder involving with a serious mood disturbance and mostly co-occurrence with physical symptoms; those symptoms raise a higher burden for their caregivers. Previous scholar pointed out that caregivers with positive psychological capital (PsyCap) were able to perform proper care to their depressed patient. Therefore, this study aimed to (1) identifying the levels of PsyCap in the caregivers of depressive patients and (2) comparing the levels of PsyCap as classified by caregiver's marital status. Samples were 192 caregivers of depressed patients (62 males, 130 females) who continuously received the hospital services at the HRH Princess Maha Chakri Sirindhorn Medical Center. They were asked to complete questionnaire on demographic information and Positive Psychological Capital scale. Descriptive statistics and One-Way ANOVA with Scheffe Test were employed for analyzing the data. The results revealed that (1) caregivers had an overall score and a domain score of PsyCap at a high level (mean ranged from 4.04 to 4.20), and at a very high level for a domain of hope (mean = 4.40). The analysis of One-way ANOVA and Scheffe showed significant differences for overall scores and domain scores of PsyCap according to the caregiver's marital status, especially the differences between single-divorced and single-married. These findings shed on the importance of a support from spouses effecting on a difference of PsyCap of caregivers; it provides useful information for planning intervention fitting with a characteristic of these caregivers.
Downloads
Article Details

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
ผู้ส่งบทความ (และคณะผู้วิจัยทุกคน) ตระหนักและปฎิบัติตามจริยธรรมการวิจัยอย่างเคร่งครัด ทั้งนี้บทความ เนื้อหา ข้อมูล ข้อความ ภาพ ตาราง แผนภาพ แผนผัง หรือข้อคิดเห็นใดๆ ที่ปรากฎในบทความ เป็นความคิดเห็นและความรับผิดชอบของผู้ส่งบทความ กองบรรณาธิการไม่จำเป็นต้องเห็นตามเสมอไป และไม่มีส่วนรับผิดชอบใดๆ โดยถือเป็นความรับผิดของของเจ้าของบทความเพียงผู้เดียว
References
Brand, C., Barry, L., & Gallagher, S. (2016). Social support mediates the association between benefit finding and quality of life in caregivers. Journal of Health Psychology, 21(6), 1126-1136.
Dauphinot, V., Delphin-Combe, F., Mouchoux, C., Doreya, A., Bathsavanis, A., Makaroff, Z., & et al. (2015). Risk factors of caregiver burden among patients with Alzheimer's disease or related disorders: A cross-sectional study. Journal of Alzheimer's disease, 44, 907-916.
Department of mental health, Ministry of public health. (2016). Annual Report 2016. Bangkok: BangkokBlog.
Ding, Y., Yang, Y, Yang, X., Zhang, T., Qiu, X., He, X., & et al. (2015). The mediating role of coping style in the relationship between psychological capital and burnout among Chinese nurses. PLOS ONE, 10(4), e0122128.
Herbert, M. (2011). An exploration of the relationships between psychological capital (hope, optimism, self-efficacy, resilience), occupational stress, burnout and employee engagement. Unpublished master's thesis, University of Stellenbosch, South Africa.
HRH Princess Maha Chakri Sirindhorn medical center, Srinakharinwirot university. (2018). The statistical data of depressed patients. Nakhon Nayok: Author.
Hsiao, C-Y., & Tsai, Y-F. (2015). Factors of caregiver burden and family functioning among Taiwanese family caregivers living with schizophrenia. Journal of Clinical Nursing, 24, 1546-1556.
Joling, K. J., Marwijk, H. W., Veldhuijzen, A. E., Horst, H. E., Scheltens, P., Smit, F., & et al. (2015). The two-year incidence of depression and anxiety disorders in spousal caregivers of persons with dementia: Who is at the greatest risk. The American Journal of Geriatric Psychiatry, 23(3), 293-303.
Kardorff, E. V., Soltaninejad, A., Kamali, M., & Shahrbabaki, M. E. (2016). Family caregiver burden in mental illnesses: The case of affective disorders and schizophrenia a qualitative exploratory study. Nordic Journal of Psychiatry, 70(4), 248-254.
Luthans, F., Avolio, A. J., Avey, J. B., & Norman, S. M. (2007). Positive psychological capital: Measurement and relationship with performance and satisfaction. Personnel Psychology, 60, 541-572.
Luthans, F., Luthans, K. W., & Luthans, B. C. (2004). Positive psychological capital: Beyond human and social capital. Business Horizons, 47(1), 45-50.
Moller-Leimkuhler, A. M., & Wiesheu, A. (2012). Caregiver burden in chronic mental illness: the role of patient and caregiver characteristics. European Archives of Psychiatry and Clinical Neuroscience, 262, 157-166.
Mthembu, T. G., Brown, Z., Cupido, A., Razack, G., & Wassung, D. (2016). Family caregivers' perceptions and experiences regarding caring for older adults with chronic diseases. South African Journal of Occupational Therapy, 46(1), 83-88.
Ogilvie, A. D., Morant, N., & Goodwin, G. M. (2005). The burden on informal caregivers of people with bipolar disorder. Bipolar Disorders, 7(Suppl. 1), 25-32.
Pakenham, K. I. (2011). Caregiving tasks in caring for an adult with mental illness and associations with adjustment outcomes. International Journal of Behavioral Medicine, 19, 186-198.
Reinares, M., Bonnin, C. M., Hidalgo-Mazzei, D., Colom, F., Solé, B., Jiménez, E., & et al. (2016). Family functioning in bipolar disorder: Characteristics, congruity between patients and relatives, and clinical correlates. Psychiatry Research, 245, 66-73.
Reinares, M., MarBonnin, C., Hidalgo-Mazzei, D., Colom, F., Solé, B., Jiménez, E., & et al. (2016). Family functioning in Bipolar Disorder: characteristics, congruity between patients and relatives, and clinical correlates. Psychiatry Research, 245, 66-73.
Reinhard, S. C., Given, B., Petlick, N. H., & Bemis, A. (2008). Supporting family caregivers in providing care. In R. G. Hughes (Ed.), Patient safety and quality: An evidence-based handbook for nurses (Vol. 1, pp. 341-404). Rockville, MD: AHRQ.
Shiba, K., Kondo, N., & Kondo, K. (2016). Informal and formal social support and caregiver burden: The AGES caregiver survey. Journal of Epidemiology, 26(12), 622-628.
Zivin, K., Wharton, T., & Rostant, O. (2013). The economic, public health, and caregiver burden of late-life depression. Psychiatric Clinics of North America, 36(4), 631-649.