Effectiveness of nursing counseling in reducing the burden of caregivers of patients with dementia: a pre-post study
DOI:
https://doi.org/10.54103/dn/28014Keywords:
Caregivers, Dementia, Caregiver Burden, Nursing, Nurse, Nursing CounselingAbstract
BACKGROUND: Dementia is a condition that is increasingly prevalent worldwide, recognized by the World Health Organization as a public health priority. As the disease progresses, caregivers face increased responsibilities, exposing them to health risks. Identifying key sources of stress and developing nursing counseling pathways could represent an effective strategy to support caregivers, improving their well-being and facilitating the patient's ability to remain at home. Aim: The objective of the study was to assess the impact of a nursing counseling intervention on the perceived burden of caregivers of patients with dementia in the Northern area of ASL NO.
METHODS: A pre- and post-intervention study was conducted with a sample of caregivers enrolled at the CDCD outpatient clinic. The Zarit Burden Interview scale was used to assess levels of stress/burden at baseline and three months after the intervention.
RESULTS: Although no statistically significant differences were found between the two groups (Student’s t-test P-value 0.46; Wilcoxon test 0.31), signs of stress reduction were observed in the experimental group, particularly regarding the desire to entrust caregiving to someone else (mean from 1.21 to 0.85; P-value 0.044).
CONCLUSION: Some improvements in the perception of burden were noted, but the worsening of the perception of health requires further investigation. The results suggest that nursing interventions, although with limitations, may be useful in supporting caregivers, but further studies are needed to confirm these findings.
Downloads
References
1. Linee di indirizzo Nazionali sui Percorsi Diagnostico Terapeutici Assistenziali per le demenze- Tavolo per il monitoraggio del recepimento ed implementazione del Piano Nazionale Demenze 5/07/2017.
2. Gale SA, Acar D, Daffner KR. Dementia. Am J Med 2018; 131:1161-1169.
3. Alzheimer’s Disease International. Numbers of people with dementia worldwide.https://www.alzint.org/resource/numbers-of-people-with-dementiaworldwide/. Accessed November 30, 2020.
4. Shah H, Albanese E, Duggan C, et al. Research priorities to reduce the global burden of dementia by 2025. Lancet Neurol 2016;15: 1285-1294.
5. Ku LJE, Chang SM, Pai MC, et al. Predictors of caregiver burden and care costs for older persons with dementia in Taiwan. Int Psychogeriatr 2019;31: 885-894.
6. Chiao CY, Wu HS, Hsiao CY. Caregiver burden for informal caregivers of patients with dementia: A systematic review. Int Nurs Rev. 2015 Sep;62(3):340-50. doi: 10.1111/inr.12194. Epub 2015 Jun 8. PMID: 26058542.
7. Tu JY, Jin G, Chen JH, Chen YC. Caregiver Burden and Dementia: A Systematic Review of Self-Report Instruments. J Alzheimers Dis. 2022;86(4):1527-1543. doi: 10.3233/JAD-215082. PMID: 35253744.
8. Adelman RD, Tmanova LL, Delgado D, Dion S, Lachs MS. Caregiver burden: a clinical review. JAMA. 2014 Mar 12;311(10):1052-60. doi: 10.1001/jama.2014.304. PMID: 24618967.
9. Chattat R, Cortesi V, Izzicupo F, Del Re ML, Sgarbi C, Fabbo A, Bergonzini E. The Italian version of the Zarit Burden interview: a validation study. Int Psychogeriatr. 2011 Jun;23(5):797-805. doi: 10.1017/S1041610210002218. Epub 2010 Dec 16. PMID: 21205379.
10. Ankri J, Andrieu S, Beaufils B, Grand A, Henrard JC. Beyond the global score of the Zarit Burden Interview: useful dimensions for clinicians. Int J Geriatr Psychiatry. 2005 Mar;20(3):254-60. doi: 10.1002/gps.1275. PMID: 15717336.
11. Zarit SH, Reever KE, Bach-Peterson J. Relatives of the impaired elderly: correlates of feelings of burden. Gerontologist. 1980 Dec;20(6):649-55. doi: 10.1093/geront/20.6.649. PMID: 7203086.
12. Zarit SH, Todd PA, Zarit JM. Subjective burden of husbands and wives as caregivers: a longitudinal study. The Gerontologist. Giugno 1986;26(3):260–6.
13. Dossier n° 141 - Schede di lettura 25 febbraio 2021 - La figura del caregiver nell’ordinamento italiano [Internet]. Disponibile su: https://www.camera.it/temiap/2021/03/09/OCD177-4856.pdf.
14. Manuale per prendersi cura del Malato di Alzheimer. Alzheimer Europe. Edizione Italiana a cura di Federazione Alzheimer Italia, 1999.
15. JAMA. 2014 Mar 12;311(10):1052-60. doi: 10.1001/jama.2014.304. Caregiver burden: a clinical review. Adelman RD(1), Tmanova LL(2), Delgado D(2), Dion S(1), Lachs MS(1).
16. Int Nurs Rev. 2015 Sep;62(3):340-50. doi: 10.1111/inr.12194. Epub 2015 Jun 8. Caregiver burden for informal caregivers of patients with dementia: A systematic review. Chiao CY(1), Wu HS(2), Hsiao CY(1).
17. J Alzheimers Dis. 2022;86(4):1527-1543. doi: 10.3233/JAD-215082. Caregiver Burden and Dementia: A Systematic Review of Self-Report Instruments.Tu JY(1), Jin G(2), Chen JH(3)(4), Chen YC(5)(6)(7).
18. Kawano Y, Terada S, Takenoshita S, Hayashi S, Oshima Y, Miki T, Yokota O, Yamada N. Patient affect and caregiver burden in dementia. Psychogeriatrics. 2020 Mar;20(2):189-195. doi: 10.1111/psyg.12487. Epub 2019 Nov 7. PMID: 31698515.
19. Liu S, Li C, Shi Z, Wang X, Zhou Y, Liu S, Liu J, Yu T, Ji Y. Caregiver burden and prevalence of depression, anxiety and sleep disturbances in Alzheimer’s disease caregivers in China. J Clin Nurs. 2017 May;26(9-10):1291-1300. doi: 10.1111/jocn.13601. Epub 2016 Nov 23. PMID: 27681477.
20. Abreu, W., Tolson, D., & Jackson, G. A. (2018). A cross-sectional study of family caregiver burden and psychological distress linked to frailty and functional dependency of a relative with advanced dementia, Dementia London, May 2.
21. Cheng ST., Lam LC., Kwok T., (2013), Neuropsychiatric symptom clusters of Alzheimer disease in Hong Kong Chinese: correlates with caregiver burden and depression, in The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry, 21(10), 1029–1037.
22. Truzzi A., Valente L., Ulstein I., Engelhardt E., Laks J., Engedal K., (2012), Burnout in familial caregivers of patients with dementia, in Revista Brasileira de Psiquiatria (Sao Paulo, Brazil : 1999), Dec; 34(4), 405–412.
23. Corvol A., Dreier A., Prudhomm J., Thyrian J. R., Hoffmann W., Somme D., Thyrian, J. R., (2017), Consequences of clinical case management for caregivers: a systematic review, in International Journal of Geriatric Psychiatry, 32(5), 473–483.
24. Scholzel-Dorenbos CJ., Draskovic I., Vernooij-Dasse MJ., Rikkert O. , (2009), Quality of life and burden of spouses of Alzheimer disease patients, in Alzheimer Disease and Associated Disorders, Apr-Jun; 23(2), 171–177.
25. Yilmaz A, Turan E, Gundogar D. Predictors of burnout in the family caregivers of Alzheimer’s disease: evidence from Turkey. Australas J Ageing. 2009 Mar;28(1):16-21. doi: 10.1111/j.1741-6612.2008.00319.x. PMID: 19243371.
26. Svendsboe E., Terum T., Testad I., Aarsland D., Ulstein I., Corbett A., Rongve A., (2016), Caregiver burden in family carers of people with dementia with Lewy bodies and Alzheimer’s disease, in International Journal of Geriatric Psychiatry, Sep 31(9), 1075–1083.
27. Dow J., Robinson J., Robalino S., Finch T., McColl E., Robinson L., (2018), How best to assess quality of life in informal carers of people with dementia; A systematic review of existing outcome measures, in PLoS One, Mar 14;13(3).
28. Landeiro F., Walsh K., Ghinai I., Mughal S., Nye E., Wace H., Roberts N., Lecomte P., Wittenberg R., Wolstenholme J., Handels R., Roncancio-Diaz E., Potashman MH., Tockhorn-Heidenreich A., Gray AM., (2018), Measuring quality of life of people with predementia and dementia and their caregivers: a systematic review protocol, BMJ Open. Mar 30;8(3):e019082.
29. Shikimoto R., Sado M., Ninomiya A., Yoshimura K., Ikeda B., Baba T., Mimura M., (2017), Predictive factors associated with psychological distress of caregivers of people with dementia in Japan : a cross-sectional, in International Psychogeriatrics, 2018 Aug; 30(8):1089-1098.
30. Wang J, Xiao LD, He GP, De Bellis A. Family caregiver challenges in dementia care in a country with undeveloped dementia services. J Adv Nurs. 2014 Jun;70(6):1369-80. doi: 10.1111/jan.12299. Epub 2013 Nov 6. PMID: 24192338.
31. Linee Guida: Diagnosi e trattamento di demenza e mild cognitive impairment. Istituto superiore della sanità.
32. Bleijlevens MH, Stolt M, Stephan A, Zabalegui A, Saks K, Sutcliffe C, Lethin C, Soto ME, Zwakhalen SM; RightTimePlaceCare Consortium. Changes in caregiver burden and health-related quality of life of informal caregivers of older people with Dementia: evidence from the European RightTimePlaceCare prospective cohort study. J Adv Nurs. 2015 Jun;71(6):1378-91. doi: 10.1111/jan.12561. Epub 2014 Nov 17. PMID: 25403434.
33. Daga E, Corvo E, Marucci AR, Sansoni J. L’esperienza dei caregiver primari che assistono a domicilio le persone affette dalla Malattia di Alzheimer [Alzheimer’s disease and caregivers experience in home care]. Prof Inferm. 2014 Jan-Mar;67(1):5-14. Italian. doi: 10.7429/pi.2014.671005. PMID: 24762767.
34. Etters L, Goodall D, Harrison BE. Caregiver burden among dementia patient caregivers: a review of the literature. J Am Acad Nurse Pract. 2008 Aug;20(8):423-8. doi: 10.1111/j.1745-7599.2008.00342.x. PMID: 18786017.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Romina Matella, Gaetano Auletta, Doriana Montani, Maria Teresa Fanni, Maria Patrizia Caruso, Linda Lazzaro

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Accepted 2025-10-09
Published 2026-01-31





