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Journal of Cancer Survivorship
Published in: Journal of Cancer Survivorship 3/2007

01-09-2007

Use of cancer support groups among Latina breast cancer survivors

Authors: Anna M. Nápoles-Springer, Carmen Ortíz, Helen O’Brien, Marynieves Díaz-Méndez, Eliseo J. Pérez-Stable

Published in: Journal of Cancer Survivorship | Issue 3/2007

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Abstract

Introduction

Although Latina women diagnosed with breast cancer may be at greater risk of psychosocial morbidity compared to white women, few utilize support services such as support groups. Reasons for this under-use among Latinas are unknown.

Methods

A cross-sectional telephone survey examined the association of predisposing, enabling, and need factors with use of cancer support groups among 330 Latina breast cancer survivors recruited from a population-based tumor registry in counties with Spanish language support groups.

Results

Thirty-two percent had ever used a support group. Among the 225 (68%) women who had never used one, major reasons for not using a support group included receiving enough support from other sources (20%), not needing one (18%), and being unaware of groups in their local area (17%). Women receiving quite a bit or a lot of encouragement from family members to attend a cancer support group were seven times more likely to have ever attended one than women receiving little or no encouragement (OR = 7.04, 95% CI 3.72, 13.30). Spiritual well-being was inversely associated with ever having attended a support group (OR = 0.93, 95% CI 0.89, 0.98).

Discussion

Results suggest that families play an important role in promoting use of support groups among Latina breast cancer survivors, and that spirituality may offer an alternative source of support.

Implications for Cancer Survivors

More effort should be directed toward providing culturally and linguistically appropriate support services to breast cancer survivors, and increasing awareness of these services among oncologists, patients and family members.
Literature
1.
Ashing-Giwa, K. T., Padilla, G., Tejero, J., Kraemer, J., Wright, K., Coscarelli, A., et al. (2004). Understanding the breast cancer experience of women: A qualitative study of African American, Asian American, Latina and Caucasian cancer survivors. Psychooncology, 13, 408–428.PubMedCrossRef
2.
Ashing-Giwa, K. T., Tejero, J. S., Kim, J., Padilla, G. V., & Hellemann, G. (2007). Examining predictive models of HRQOL in a population-based, multiethnic sample of women with breast carcinoma. Quality of Life Research, 16, 413–428.PubMedCrossRef
3.
American Cancer Society (2001). Cancer facts & figures for hispanics: 2000–2001. Atlanta, GA, pp 1–10.
4.
Aziz, N. M., & Rowland, J. H. (2002). Cancer survivorship research among ethnic minority and medically underserved groups. Oncology Nursing Forum, 29, 789–801.PubMedCrossRef
5.
Bauman, L. J., Gervey, R., & Spiegel, R. (1992). Factors associated with cancer patients’ participation in support groups. Journal of Psychosocial Oncology 10, 1–20.CrossRef
6.
7.
Brady, M. J., Peterman, A. H., Fitchett, G., Mo, M., & Cella, D. (1999). A case for including spirituality in quality of life measurement in oncology. Psychooncology, 8, 417–428.PubMedCrossRef
8.
Brislin, R. W. (1976). Translation: Applications and research. New York: Gardner.
9.
Brislin, R. W., Lonner, W. J., & Thorndike, E. M. (1973). Cross-cultural research methods. New York: Wiley.
10.
Bui, L. L., Last, L., Bradley, H., Law, C. H., Maier, B. A., & Smith, A. J. (2002). Interest and participation in support group programs among patients with colorectal cancer. Cancer Nursing, 25, 150–157.PubMedCrossRef
11.
Burgess, C., Cornelius, V., Love, S., Graham, J., Richards, M., & Ramirez, A. (2005). Depression and anxiety in women with early breast cancer: Five year observational cohort study. BMJ, 330, 702.PubMedCrossRef
12.
Classen, C., Butler, L. D., Koopman, C., Miller, E., DiMiceli, S., Giese-Davis, J., et al. (2001). Supportive–expressive group therapy and distress in patients with metastatic breast cancer: A randomized clinical intervention trial. Archives of General Psychiatry, 58, 494–501.PubMedCrossRef
13.
Cope, D. G. (1995). Functions of a breast cancer support group as perceived by the participants: An ethnographic study. Cancer Nursing, 18, 472–478.PubMedCrossRef
14.
Cunningham, A. J., & Edmonds, C. V. (1996). Group psychological therapy for cancer patients: A point of view, and discussion of the hierarchy of options. International Journal of Psychiatry In Medicine, 26, 51–82.PubMedCrossRef
15.
Culver, J. L., Arena, P. L., Antoni, M. H., & Carver, C. S. (2002). Coping and distress among women under treatment for early stage breast cancer: Comparing African Americans, Hispanics and non-Hispanic Whites. Psychooncology, 11, 495–504.PubMedCrossRef
16.
de Bocanegra, H. (1992). Cancer patients’ interest in group support programs. Cancer Nursing 15, 347–352.CrossRef
17.
Detmar, S. B., Aaronson, N. K., Wever, L. D., Muller, M., & Schornagel, J. H. (2000). How are you feeling? Who wants to know? Patients’ and oncologists’ preferences for discussing health-related quality-of-life issues. Journal of Clinical Oncology, 18, 3295–3301.PubMed
18.
Docherty, A. (2004). Experience, functions and benefits of a cancer support group. Patient Education and Counseling, 55, 87–93.PubMedCrossRef
19.
Eakin, E. G., & Strycker, L. A. (2001). Awareness and barriers to use of cancer support and information resources by HMO patients with breast, prostate, or colon cancer: Patient and provider perspectives. Psychooncology 10, 103–113.PubMedCrossRef
20.
Edelman, S., Bell, D. R., & Kidman, A. D. (1999). A group cognitive behaviour therapy programme with metastatic breast cancer patients. Psychooncology 8, 295–305.PubMedCrossRef
21.
Ell, K., Nishimoto, R., Morvay, T., Mantell, J., & Hamovitch, M. (1989). A longitudinal analysis of psychological adaptation among survivors of cancer. Cancer, 63, 406–413.PubMedCrossRef
22.
Ell, K., Sanchez, K., Vourlekis, B., Lee, P. J., Dwight-Johnson, M., Lagomasino, I., et al. (2005). Depression, correlates of depression, and receipt of depression care among low-income women with breast or gynecologic cancer. Journal of Clinical Oncology, 23, 3052–3060.PubMedCrossRef
23.
Gelberg, L., Andersen, R. M., & Leake, B. D. (2000). The behavioral model for vulnerable populations: Application to medical care use and outcomes for homeless people. Health Services Research, 34, 1273–1302.PubMed
24.
Gentry, C. (2002). Improving quality of care for Californians with breast cancer (pp. 1–36). Oakland, CA: California Healthcare Foundation.
25.
Gidron, B., Chesler, M. A., et al. (1991). Cross-cultural perspective on self-help groups: Comparison between participants and nonparticipants. American Journal of Community Psychology, 19, 667–681.CrossRef
26.
Giese-Davis, J., Koopman, C., Butler, L.D., Classen, C., Cordova, M., Fobair, P., et al. (2002). Change in emotion-regulation strategy for women with metastatic breast cancer following supportive–expressive group therapy. Journal of Consulting and Clinical Psychology, 70, 916–925.PubMedCrossRef
27.
Goodwin, P. J., Leszcz, M., Ennis, M., Koopmans, J., Vincent, L., Guther, H., et al. (2001). The effect of group psychosocial support on survival in metastatic breast cancer. New England Journal of Medicine, 345, 1719–1726.PubMedCrossRef
28.
Gottlieb, B. H., & Wachala, E. D. (2006). Cancer support groups: A critical review of empirical studies. Psychooncology, 16, 379–400.
29.
Gray, R., Fitch, M., Davis, C., & Phillips, C. (1997). A qualitative study of breast cancer self-help groups. Psychooncology, 6, 279–289.PubMedCrossRef
30.
Greater Bay Area Cancer Registry (2005). Northern California Cancer Center Greater Bay Area Cancer Registry, Northern California Cancer Center.
31.
Guidry, J. J., Aday, L. A., Zhang, D., & Winn, R. J. (1997). The role of informal and formal social support networks for patients with cancer. Cancer Practice, 5, 241–246.PubMed
32.
Guillemin, F., Bombardier, C., & Beaton, D. (1993). Cross-cultural adaptation of health-related quality of life measures: Literature review and proposed guidelines. Journal of Clinical Epidemiology, 46, 1417–1432.PubMedCrossRef
33.
Hays, R. D., & Hayashi, T. (1990). Beyond internal consistency reliability: Rationale and user’s guide for multitrait analysis program on the microcomputer. Santa Monica, CA: Rand.
34.
Helgeson, V. S., Cohen, S., Schulz, R., & Yasko, J. (1999). Education and peer discussion group interventions and adjustment to breast cancer. Archives of General Psychiatry, 56, 340–347.PubMedCrossRef
35.
Helgeson, V. S., Cohen, S., Schulz, R., & Yasko, J. (2000). Group support interventions for women with breast cancer: Who benefits from what? Health Psychology, 19, 107–114.PubMedCrossRef
36.
Hewitt, M., Breen, N., & Devesa, S. (1999). Cancer prevalence and survivorship issues: Analyses of the 1992 National Health Interview Survey. Journal of the National Cancer Institute, 91, 1480–1486.PubMedCrossRef
37.
Hewitt, M., Herdman, R., & Holland, J. (Eds.) (2004). Meeting psychosocial needs of women with breast cancer. Washington, D.C.: The National Academies.
38.
Hewitt, M., Greenfield, S., & Stovall, E. (Eds.) (2005). From cancer patient to cancer survivor: Lost in transition. Washington, D.C.: The National Academies.
39.
Juarez, G., Ferrell, B., & Borneman, T. (1998). Perceptions of quality of life in Hispanic patients with cancer. Cancer Practice, 6, 318–324.PubMedCrossRef
40.
Juarez, G., Ferrell, B., & Borneman, T. (1999). Cultural considerations in education for cancer pain management. Journal of Cancer Education, 14, 168–173.PubMed
41.
Kissane, D. W., Grabsch, B., Love, A., Clarke, D. M., Bloch, S., & Smith, G. C. (2004). Psychiatric disorder in women with early stage and advanced breast cancer: A comparative analysis. Australian and New Zealand Journal of Psychiatry, 38, 320–326.PubMedCrossRef
42.
Leedham, B., & Ganz, P. A. (1999). Psychosocial concerns and quality of life in breast cancer survivors. Cancer Investigation, 17, 342–348.PubMedCrossRef
43.
Lim, Y. W., Andersen, R., Leake, B., Cunningham, W., & Gelberg, L. (2002). How accessible is medical care for homeless women? Medical Care, 40, 510–520.PubMedCrossRef
44.
Markides, K. S., & Mindel, C. H. (1987). Aging & Ethnicity. Newbury Park: SAGE.
45.
Maunsell, E., Drolet, M., Ouhoummane, N., & Robert, J. (2005). Breast cancer survivors accurately reported key treatment and prognostic characteristics. Journal of Clinical Epidemiology, 58, 364–369.PubMedCrossRef
46.
Michalec, B., Van Willigen, M., Wilson, K., Schreier, A., & Williams, S. (2004). The race gap in support group participation by breast cancer survivors: Real or artifact? Evaluation Review, 28, 123–143.PubMedCrossRef
47.
Miller, B. A., Kolonel, K. L., Bernstein, L., Young, J. J. L., Swanson, G. M., West, D., et al. (Eds.) (1996). Racial/ethnic patterns of cancer in the United States, 1988–1992, Vol. NIH Pul. No. 96-4104. Bethesda, MD: National Cancer Institute.
48.
Moore, R. J., & Butow, P. (2004). Culture and oncology: Impact of context effects. In R. J. Moore & D. Spiegel (Eds.), Cancer, culture, and communication (pp. 15–54). New York, NY: Kluwer.CrossRef
49.
Meyerowitz, B. E., Formenti, S. C., Ell, K. O., & Leedham, B. (2000). Depression among Latina cervical cancer patients. Journal of Social and Clinical Psychology, 19, 352–371.
50.
Peterman, A. H., Fitchett, G., Brady, M. J., Hernandez, L., & Cella, D. (2002). Measuring spiritual well-being in people with cancer: The functional assessment of chronic illness therapy—Spiritual Well-being Scale (FACIT-Sp). Annals of Behavioral Medicine, 24, 49–58.PubMedCrossRef
51.
Petersson, L. M., Berglund, G., Brodin, O., Glimelius, B., & Sjoden, P. O. (2000). Group rehabilitation for cancer patients: Satisfaction and perceived benefits. Patient Education and Counseling, 40, 219–229.PubMedCrossRef
52.
Phillips, K. A., Milne, R. L., Buys, S., Friedlander, M. L., Ward, J. H., McCredie, M. R., et al. (2005). Agreement between self-reported breast cancer treatment and medical records in a population-based Breast Cancer Family Registry. Journal of Clinical Oncology, 23, 4679–4686.PubMedCrossRef
53.
Ries, L., Eisner, M. P., Kosary, C. L., Hankey, B. F., Miller, B. A., Clegg, L., et al. (2005). SEER cancer statistics review, 1975–2002. Bethesda, MD: National Cancer Institute.
54.
Rehse, B., & Pukrop, R. (2003). Effects of psychosocial interventions on quality of life in adult cancer patients: Meta analysis of 37 published controlled outcome studies. Patient Education and Counseling, 50, 179–186.PubMed
55.
Shapiro, S. L., Lopez, A. M., Schwartz, G. E., Bootzin, R., Figueredo, A. J., Braden, C. J., et al. (2001). Quality of life and breast cancer: Relationship to psychosocial variables. Journal of Clinical Psychology, 57, 501–519.PubMedCrossRef
56.
Simoni, J. M., & Perez, L. (1995). Latinos and mutual support group: A case for considering culture. American Journal of Orthopsychiatry, 65, 440–445.PubMedCrossRef
57.
Smiley, M. R., McMillan, S. C., Johnson, S., & Ojeda, M. (2000). Comparison of Florida hispanic and non-hispanic caucasian women in their health beliefs related to breast cancer and health locus of control. Oncology Nursing Forum, 27, 975–984.PubMed
58.
Spencer, S. M., Lehman, J. M., Wynings, C., Arena, P., Carver, C. S., Antoni, M. H., et al. (1999). Concerns about breast cancer and relations to psychosocial well-being in a multiethnic sample of early-stage patients. Health Psychology, 18, 159–168.PubMedCrossRef
59.
Stevenson, B. S., & Coles, P. M. (1993). A breast cancer support group: Activities and value to mastectomy patients. Journal of Cancer Education, 8, 239–242.PubMedCrossRef
60.
Squiers, L., Finney Rutten, L. J., Treiman, K., Bright, M. A., & Hesse, B. (2005). Cancer patients’ information needs across the cancer care continuum: Evidence from the cancer information service. Journal of Health Communication, 10(Suppl 1), 15–34.PubMedCrossRef
61.
Taylor, S. E., Lichtman, R. R., & Wood, J. V. (1984). Attributions, beliefs about control, and adjustment to breast cancer. Journal of Personality and Social Psychology, 46, 489–502.PubMedCrossRef
62.
US Census Bureau (1999). Current population reports, P25-1130 population projections of the United States by age, sex, Race, and hispanic origin: 1995 to 2050, vol. 2002.
63.
US Census Bureau (2006). Census Bureau Guideline: Language Translation of Data Collection Instruments and Supporting Materials (Census Advisory Committees, ed.).
64.
Wan, G. J., Counte, M. A., Cella, D. F., Hernandez, L., McGuire, D. B., Deasay, S., et al. (1999). The impact of socio-cultural and clinical factors on health-related quality of life reports among Hispanic and African-American cancer patients. Journal of Outcome Measurement, 3, 200–215.PubMed
65.
Ware, J. E., Harris, W. J., Gandek, B., Rogers, B. W., & Resse, P. R. (1997). MAP-R for windows: Multitrait/multi-item analysis program—revised user’s guide. Boston: Health Assessment Lab.
66.
Weidmer, B., Hurtado, M., Weech-Maldado, R., Ngo-Metzger, Q., & Bogen, K. (2006). Guidelines for Translating CAHPS Surveys, CHAPS.
67.
Werner, O. (1970). Translating, wording through interpreters, and the problem of decentering. In R. N. R. Cohen (ed.), A handbook of methods in cultural anthropology. New York: Museum of Natural History.
68.
Young, J. L. J., Roffers, S. D., Ries, L. A. G., Fritz, A. G., & Hurlbut, A. A. (2001). SEER summary staging manual—2000: Codes and coding instructions, vol. NIH Pub. No. 01-4969. Bethesda, MD: National Cancer Institute.
Metadata
Title
Use of cancer support groups among Latina breast cancer survivors
Authors
Anna M. Nápoles-Springer
Carmen Ortíz
Helen O’Brien
Marynieves Díaz-Méndez
Eliseo J. Pérez-Stable
Publication date
01-09-2007
Publisher
Springer US
Published in
Journal of Cancer Survivorship / Issue 3/2007
Print ISSN: 1932-2259
Electronic ISSN: 1932-2267
DOI
https://doi.org/10.1007/s11764-007-0029-7

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