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Effects of enhanced caregiver training program on cancer caregiver’s self-efficacy, preparedness, and psychological well-being

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Abstract

Purpose

We examined the effects of an enhanced informal caregiver training (Enhanced-CT) protocol in cancer symptom and caregiver stress management to caregivers of hospitalized cancer patients.

Methods

We recruited adult patients in oncology units and their informal caregivers. We utilized a two-armed, randomized controlled trial design with data collected at baseline, post-training, and at 2 and 4 weeks after hospital discharge. Primary outcomes were self-efficacy for managing patients’ cancer symptoms and caregiver stress and preparedness for caregiving. Secondary outcomes were caregiver depression, anxiety, and burden. The education comparison (EDUC) group received information about community resources. We used general linear models to test for differences in the Enhanced-CT relative to the EDUC group.

Results

We consented and randomized 138 dyads: Enhanced-CT = 68 and EDUC = 70. The Enhanced-CT group had a greater increase in caregiver self-efficacy for cancer symptom management and stress management and preparation for caregiving at the post-training assessment compared to the EDUC group but not at 2- and 4-week post-discharge assessments. There were no intervention group differences in depression, anxiety, and burden.

Conclusion

An Enhanced-CT protocol resulted in short-term improvements in self-efficacy for managing patients’ cancer symptoms and caregiver stress and preparedness for caregiving but not in caregivers’ psychological well-being. The lack of sustained effects may be related to the single-dose nature of our intervention and the changing needs of informal caregivers after hospital discharge.

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References

  1. Adler NE, Page AEK (2008) Cancer care for the whole patient: meeting psychosocial health needs. National Academies Press, Washington, DC

    Google Scholar 

  2. Smith BD, Smith GL, Hurria A et al (2009) Future of cancer incidence in the United States: burdens upon an aging, changing nation. J Clin Oncol 27:2758–65

    Article  PubMed  Google Scholar 

  3. American Cancer Society (2014) Cancer facts & figures 2014. Atlanta, American Cancer Society http://www.cancer.org/acs/groups/content/@research/documents/webcontent/acspc-042151.pdf

  4. Kim Y, Schulz R (2008) Family caregivers’ strains: comparative analysis of cancer caregiving with dementia, diabetes, and frail elderly caregiving. J Aging Health 20:483–503

    Article  PubMed  Google Scholar 

  5. Schumacher KL, Koresawa S, West C et al (2002) Putting cancer pain management regimens into practice at home. J Pain Symptom Manage 23:369–82

    Article  PubMed  Google Scholar 

  6. Sutton LM, Clipp EC, Winer EP (2000) Mangement of the terminally ill patient. In: Hunter CP, Johnson KA, Muss HB (eds) Cancer in the elderly. Dekker, New York, pp 543–572

    Google Scholar 

  7. Given B, Sherwood PR (2006) Family care for the older person with cancer. Semin Oncol Nurs 22:43–50

    Article  PubMed  Google Scholar 

  8. Scherbring M (2002) Effect of caregiver perception of preparedness on burden in an oncology population. Oncol Nurs Forum 29:E70–E76

    Article  PubMed  Google Scholar 

  9. Hodges LJ, Humphris GM, Macfarlane G (2005) A meta-analytic investigation of the relationship between the psychological distress of cancer patients and their carers. Soc Sci Med 60:1–12

    Article  CAS  PubMed  Google Scholar 

  10. Cornwell P, Dicks B, Fleming J et al (2012) Care and support needs of patients and carers early post-discharge following treatment for non-malignant brain tumour: establishing a new reality. Support Care Cancer 20:2595–2610

    Article  PubMed  Google Scholar 

  11. Shaw J, Harrison J, Young J et al (2013) Coping with newly diagnosed upper gastrointestinal cancer: a longitudinal qualitative study of family caregivers’ role perception and supportive care needs. Support Care Cancer 21:749–756

    Article  PubMed  Google Scholar 

  12. Foust JB, Vuckovic N, Henriquez E (2012) Hospital to home health care transition: patient, caregiver, and clinician perspectives. West J Nurs Res 34:194–212

    Article  PubMed  Google Scholar 

  13. Nosbusch JM, Weiss ME, Bobay KL (2011) An integrated review of the literature on challenges confronting the acute care staff nurse in discharge planning. J Clin Nurs 20:754–774

    Article  PubMed  Google Scholar 

  14. Plank A, Mazzoni V, Cavada L (2012) Becoming a caregiver: new family carers’ experience during the transition from hospital to home. J Clin Nurs 21:2072–2082

    Article  PubMed  Google Scholar 

  15. Hendrix C, Ray C (2006) Informal caregiver training on home care and cancer symptom management prior to hospital discharge: a feasibility study. Oncology nursing forum 33:793–798

    Article  PubMed  Google Scholar 

  16. Hendrix CC, Abernethy A, Sloane R et al (2009) A pilot study on the influence of an individualized and experiential training on cancer caregiver’s self-efficacy in home care and symptom management. Home Healthc Nurse 27:271–278

    Article  PubMed Central  PubMed  Google Scholar 

  17. Hendrix CC, Landerman R, Abernethy AP (2013) Effects of an individualized caregiver training intervention on self-efficacy of cancer caregivers. West J Nurs Res 35:590–610

    Article  PubMed  Google Scholar 

  18. Bandura A (1997) Self-efficacy: the exercise of control. Freeman, New York

    Google Scholar 

  19. Bailey DE Jr, Steinhauser K, Hendrix C et al (2011) Pairing self-management with palliative care: intervening in life-limiting illness. J Nurs Healthc Chronic Illn 3:1–3

    Article  PubMed Central  PubMed  Google Scholar 

  20. Varvogli L, Darviri C (2011) Stress management techniques: evidence-based procedures that reduce stress and promote health. Health Science Journal 5:74–89

    Google Scholar 

  21. Porter LS, Keefe FJ, Garst J et al (2008) Self-efficacy for managing pain, symptoms, and function in patients with lung cancer and their informal caregivers: associations with symptoms and distress. Pain 137:306–315

    Article  PubMed Central  PubMed  Google Scholar 

  22. Archbold PG, Stewart BJ, Greenlick MR et al (1990) Mutuality and preparedness as predictors of caregiver role strain. Res Nurs Health 13:375–384

    Article  CAS  PubMed  Google Scholar 

  23. Grant JS, Elliott TR, Weaver M et al (2002) Telephone intervention with family caregivers of stroke survivors after rehabilitation. Stroke 33:2060–2065

    Article  PubMed  Google Scholar 

  24. Hudson PL, Hayman-White K (2006) Measuring the psychosocial characteristics of family caregivers of palliative care patients: psychometric properties of nine self-report instruments. J Pain Symptom Manage 31:215–228

    Article  PubMed  Google Scholar 

  25. Curran SL (1995) Short form of the profile of mood states (POMS-SF): psychometric information. Psychological Assessment 7:80–83

    Article  Google Scholar 

  26. Shacham S (1983) A shortened version of the profile of mood states. J Pers Assess 47:305–306

    Article  CAS  PubMed  Google Scholar 

  27. Hall LA, Gurley DN, Sachs B et al (1991) Psychosocial predictors of maternal depressive symptoms, parenting attitudes, and child behavior in single-parent families. Nurs Res 40:214–220

    Article  CAS  PubMed  Google Scholar 

  28. Radloff LS (1977) The CES-D scale a self-report depression scale for research in the general population. Applied psychological measurement 1:385–401

    Article  Google Scholar 

  29. Given CW, Given B, Stommel M et al (1992) The caregiver reaction assessment (CRA) for caregivers to persons with chronic physical and mental impairments. Res Nurs Health 15:271–283

    Article  CAS  PubMed  Google Scholar 

  30. Bass PF, Wilson JF, Griffith CH (2003) A shortened instrument for literacy screening. J Gen Intern Med 18:1036–1038

    Article  PubMed Central  PubMed  Google Scholar 

  31. Fillenbaum GG, Smyer MA (1981) The development, validity, and reliability of the OARS multidimensional functional assessment questionnaire. J Gerontol 36:428–434

    Article  CAS  PubMed  Google Scholar 

  32. Cella DF, Tulsky DS (1993) Quality of life in cancer: definition, purpose, and method of measurement. Cancer Invest 11:327–336

    Article  CAS  PubMed  Google Scholar 

  33. Cella DF, Tulsky DS, Gray G et al (1993) The Functional Assessment of Cancer Therapy scale: development and validation of the general measure. J Clin Oncol 11:570–579

    CAS  PubMed  Google Scholar 

  34. Lent L, Hahn E, Eremenco S et al (1999) Using cross-cultural input to adapt the Functional Assessment of Chronic Illness Therapy (FACIT) scales. Acta Oncol 38:695–702

    Article  CAS  PubMed  Google Scholar 

  35. Borm GF, Fransen J, Lemmens WA (2007) A simple sample size formula for analysis of covariance in randomized clinical trials. J Clin Epidemiol 60:1234–1238

    Article  PubMed  Google Scholar 

  36. Raghunathan TE, Lepkowski JM, Van Hoewyk J et al (2001) A multivariate technique for multiply imputing missing values using a sequence of regression models. Survey Methodology 27:85–96

    Google Scholar 

  37. Olsen MK, Stechuchak KM, Edinger JD et al (2012) Move over LOCF: principled methods for handling missing data in sleep disorder trials. Sleep Med 13:123–132

    Article  PubMed  Google Scholar 

  38. van Buuren S (2007) Multiple imputation of discrete and continuous data by fully conditional specification. Stat Methods Med Res 16:219–242

    Article  PubMed  Google Scholar 

  39. Grant JS, Glandon GL, Elliott TR et al (2004) Caregiving problems and feelings experienced by family caregivers of stroke survivors the first month after discharge. International Journal of Rehabilitation Research 27:105–111

    Article  PubMed  Google Scholar 

  40. Zarit SH (2006) Assessment of family caregivers: a research perspective. Caregiver assessment: voices and views from the field, volume II. San Francisco, CA, National Center on Caregiving at Family Caregiver Alliance https://caregiver.org/sites/caregiver.org/files/pdfs/v2_consensus.pdf

  41. Centers for Medicare & Medicaid Services (2014) Readmissions Reduction Program. http://www.cms.gov/Medicare/Medicare-Fee-for-Service-Payment/AcuteInpatientPPS/Readmissions-Reduction-Program.html.

  42. U.S. News and World Report, Health (2014) Duke University Hospital. http://health.usnews.com/best-hospitals/area/nc/duke-university-medical-center-6360355/cancer

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Acknowledgments

The authors thank Iris Pounds, Margaret Falkovic, Melanie Paige, Sarah Garrigues, Sophia Duong, and Terry Ervin for their assistance. We also extend our gratitude to Duke oncology unit staff and to all study participants for their time and effort.

Funding support

This study was funded by the National Institute of Nursing Research (P01 NR010948; Clinical Trials identifier NCT00938769). Dr. Abby J. Schwartz receives support from the National Institutes of Health grant number T32 AG000029.

Conflict of interest

The authors declare that they have no conflict of interest. The authors have full control of all primary data and agree to allow the journal to review the data if requested.

Disclaimer

The views expressed in this article are those of the authors and do not necessarily represent the views of the Department of Veterans Affairs.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of Duke University Health System Institutional Review Board and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

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Correspondence to Abby J. Schwartz.

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Hendrix, C.C., Bailey, D.E., Steinhauser, K.E. et al. Effects of enhanced caregiver training program on cancer caregiver’s self-efficacy, preparedness, and psychological well-being. Support Care Cancer 24, 327–336 (2016). https://doi.org/10.1007/s00520-015-2797-3

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  • DOI: https://doi.org/10.1007/s00520-015-2797-3

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