Ainamani, H. E., Alele, P. E., Rukundo, G. Z., Maling, S., Wakida, E. K., Obua, C., & Tsai, A. C. (2020). Caring for people with dementia in rural Uganda: Qualitative study of caregiving burden experienced by informal and formal caregivers. Journal of Global Health Reports, 4. https://dx.doi.org/10.29392%2F001c.12848

Bekhet, A. K., & Garnier-Villarreal, M. (2020). Effects of p[ositive thinking on dementia caregivers’ burden and care-recipients’ behavioral problems. Western Journal of Nursing Research, 42(5), 365-372. https://doi.org/10.1177%2F0193945919861970

Bell, J. F., Whitney, R. L., & Young, H. M. (2019). Family caregiving in serious illness in the United States: Recommendations to support an invisible workforce. Journal of the American Geriatrics Society, 67(S2), S451-S456. https://doi.org/10.1111/jgs.15820

Camak, D. J. (2015). Addressing the burden of stroke caregivers: A literature review. Journal of Clinical Nursing, 24(17-18), 2376-2382. https://doi.org/10.1111/jocn.12884

Committee on Family Caregiving for Older Adults; Board on Health Care Services; Health and Medicine Division; National Academies of Sciences, E., and Medicine. (2016). In R. Schulz & J. Eden (Eds.), Families caring for an aging America. National Academies Press (US). https://doi.org/10.17226/23606

Donovan, R., Williams, A., Stajduhar, K., Brazil, K., & Marshall, D. (2011). The influence of culture on home-based family caregiving at end-of-life: A case study of Dutch reformed family care givers in Ontario, Canada. Social Science & Medicine, 72(3), 338-346. https://doi.org/10.1016/j.socscimed.2010.10.010

Gaugler, J. E., Pestka, D. L., Davila, H., Sales, R., Owen, G., Baumgartner, S. A., Shook, R., Cunningham, J., & Kenney, M. (2018). The complexities of family caregiving at work: A mixed-methods study. The International Journal of Aging and Human Development, 87(4), 347-376. https://doi.org/10.1177%2F0091415017752936

Gilbert, S. M., Nemeth, L., Amella, E., Edlund, B., & Burggraf, V. (2018). Adult children and the transition of aging parents. Issues in Mental Health Nursing, 39(5), 374-381. https://doi.org/10.1080/01612840.2018.1434842

Gitlin, L. N. (2019). Whose responsibility is it? balancing individual, family, and societal needs for supporting seriously ill older adults. Journal of the American Geriatrics Society, 67(Suppl 2), S457-S460. https://dx.doi.org/10.1111%2Fjgs.15819

Han, A., Yuen, H. K., & Jenkins, J. (2021). Acceptance and commitment therapy for family caregivers: A systematic review and meta-analysis. Journal of Health Psychology, 26(1), 82-102. https://doi.org/10.1177%2F1359105320941217

Harvath, T. A., Mongoven, J. M., Bidwell, J. T., Cothran, F. A., Sexson, K. E., Mason, D. J., & Buckwalter, K. (2020). Research priorities in family caregiving: process and outcomes of a conference on family-centered care across the trajectory of serious illness. The Gerontologist, 60(Supplement_1), S5-S13. https://doi.org/10.1093/geront/gnz138

Hashemi-Ghasemabadi, M., Taleghani, F., Yousefy, A., & Kohan, S. (2016). Transition to the new role of caregiving for families of patients with breast cancer: A qualitative descriptive exploratory study. Supportive Care in Cancer, 24(3), 1269-1276. https://doi.org/10.1007/s00520-015-2906-3

Hickman, R., Zdrodowska, M. A., Kellner, S., Cersonsky, T. E. K., Trujillo Diaz, D., Louis, E. D., & Monin, J. K. (2020). The “Caring Giver”: Emotional caregiving in the setting of essential tremor. Research on Aging, 42(2), 83-91. https://doi.org/10.1177%2F0164027519890132

Jehangir, A., Collier, A., Shakhatreh, M., Malik, Z., & Parkman, H. P. (2019). Caregiver burden in gastroparesis and GERD: Correlation with disease severity, healthcare utilization and work productivity. Digestive Diseases and Sciences, 64(12), 3451-3462. https://doi.org/10.1007/s10620-019-05723-2

Kaplan, D. B., & Berkman, B. J. (2021). Family caregiving for older adults. https://www.msdmanuals.com/professional/geriatrics/social-issues-in-older-adults/family-caregiving-for-older-adults

Kellner, S., Morgan, S., Gutierrez, J., Collins, K., Rohl, B., Migliore, F., Cosentino, S., Huey, E. D., Louis, E. D., & Monin, J. K. (2017). Perceived embarrassment and caregiver burden in essential tremor caregivers. Journal of the Neurological Sciences, 383, 205-210. https://doi.org/10.1016/j.jns.2017.11.020

Kivunja, C. (2018). Distinguishing between theory, theoretical framework, and conceptual framework: A systematic review of lessons from the field. International Journal of Higher Education, 7(6), 44-53. https://doi.org/10.5430/ijhe.v7n6p44

Kristanti, M. S., Kusmaryanto, K., & Effendy, C. (2021). Common ethical dilemmas of family caregivers of palliative patients in Indonesia. Belitung Nursing Journal, 7(3), 246-250. https://doi.org/10.33546/bnj.1457

Levy, S. G. (2017). An axiomatic approach to human behavior. Universal Journal of Psychology, 5(2), 88-94. http://dx.doi.org/10.13189/ujp.2017.050205

Liu, S., Liu, J., Wang, X.-D., Shi, Z., Zhou, Y., Li, J., Yu, T., & Ji, Y. (2018). Caregiver burden, sleep quality, depression, and anxiety in dementia caregivers: A comparison of frontotemporal lobar degeneration, dementia with Lewy bodies, and Alzheimer's disease. International Psychogeriatrics, 30(8), 1131-1138. https://doi.org/10.1017/S1041610217002630

Lou, Q., Liu, S., Huo, Y. R., Liu, M., Liu, S., & Ji, Y. (2015). Comprehensive analysis of patient and caregiver predictors for caregiver burden, anxiety and depression in Alzheimer's disease. Journal of Clinical Nursing, 24(17-18), 2668-2678. https://doi.org/10.1111/jocn.12870

Luichies, I., Goossensen, A., & der Meide, H. v. (2021). Caregiving for ageing parents: A literature review on the experience of adult children. Nursing Ethics, 28(6), 844-863. https://doi.org/10.1177%2F0969733019881713

Nguyen, H., Nguyen, T., Tran, D., & Hinton, L. (2021). “It’s extremely hard but it’s not a burden”: A qualitative study of family caregiving for people living with dementia in Vietnam. PloS One, 16(11), e0259788. https://doi.org/10.1371/journal.pone.0259788

Nguyen, T., & Levkoff, S. (2020). “What Will Come Will Come”: The Journey of adjustment and acceptance on the path of dementia care among Vietnamese family caregivers. Qualitative Health Research, 30(10), 1529-1545. https://doi.org/10.1177/1049732320919390

OMalley, K. A., & Qualls, S. H. (2020). Validation of a comprehensive measure of the family caregiver experience: The Caregiver Reaction Scale. Clinical Gerontologist, 1-11. https://doi.org/10.1080/07317115.2020.1774455

Paguirigan, M. R. B. (2019). Services for the older persons. In G. T. Cruz, C. J. P. Cruz, & Y. Saito (Eds.), Ageing and health in the Philippines (pp. 149-160). Economic Research Institute for ASEAN and East Asia.

Paré, G., & Kitsiou, S. (2017). Methods for literature reviews. In F. Lau & C. Kuziemsky (Eds.), Handbook of eHealth evaluation: An evidence-based approach [Internet]. University of Victoria.

Pinto, C., Geraghty, A. W. A., Yardley, L., & Dennison, L. (2021). Emotional distress and well-being among people with motor neurone disease (MND) and their family caregivers: A qualitative interview study. BMJ Open, 11(8), e044724. http://dx.doi.org/10.1136/bmjopen-2020-044724

Potter, E. C., Roberto, K. A., Brossoie, N., & Blieszner, R. (2017). Decisions, decisions: African American families’ responses to mild cognitive impairment. Research on Aging, 39(4), 476-500. https://doi.org/10.1177/0164027516655581

Reinhard, S. C., Feinberg, L., & Choula, R. (2011). The challenges of family caregiving: What experts say needs to be done. Washington, District of Columbia: AARP Public Policy Institute.

Revenson, T., Griva, K., Luszczynska, A., Morrison, V., Panagopoulou, E., Vilchinsky, N., & Hagedoorn, M. (2016). Caregiving in the illness context. UK: Palgrave Macmillan.

Robinson, C. A., Bottorff, J. L., Pesut, B., & Zerr, J. (2020). Development and implementation of the family caregiver decision guide. Qualitative Health Research, 30(2), 303-313. https://doi.org/10.1177%2F1049732319887166

Sakakibara, K., Kabayama, M., & Ito, M. (2015). Experiences of “endless” caregiving of impaired elderly at home by family caregivers: A qualitative study. BMC Research Notes, 8(1), 1-11. https://doi.org/10.1186/s13104-015-1829-x

Scheibl, F., Farquhar, M., Buck, J., Barclay, S., Brayne, C., & Fleming, J. (2019). When frail older people relocate in very old age, who makes the decision? Innovation in Aging, 3(4), igz030. https://doi.org/10.1093/geroni/igz030

Schulz, R., Beach, S. R., Czaja, S. J., Martire, L. M., & Monin, J. K. (2020). Family caregiving for older adults. Annual Review of Psychology, 71, 635-659. https://doi.org/10.1146/annurev-psych-010419-050754

Solomon, D. N., Hansen, L., & Baggs, J. G. (2018). It’s all about the relationship: Cognitively intact mother–daughter care dyads in hospice at home. The Gerontologist, 58(4), 625-634. https://doi.org/10.1093/geront/gnw263

Thomas, P. A., Liu, H., & Umberson, D. (2017). Family relationships and well-being. Innovation in Aging, 1(3), igx025. https://doi.org/10.1093/geroni/igx025

Ursavas, F. E., Karayurt, Ö., & İşeri, Ö. (2014). Nursing approach based on Roy Adaptation Model in a patient undergoing breast conserving surgery for breast cancer. The Journal of Breast Health, 10(3), 134-140. https://dx.doi.org/10.5152%2Ftjbh.2014.1910

Utley, R., Kristina Henry, D. N. P., & Smith, L. (2017). Frameworks for advanced nursing practice and research: Philosophies, theories, models, and taxonomies. New York: Springer Publishing Company.