Abstract
This study evaluates the amount and change of information cancer patients report receiving related to disease, diagnostic tests, treatments, physical care, and psychosocial resources over 9 months of treatment. Information received by newly diagnosed, stages II–IV cancer patients receiving treatment (N = 139) at baseline, 4, and 9 months is examined through a two-stage latent growth model. Each information-received category was modeled with latent variables of intercept and slope. Random intercept and slope factors are then regressed on multiple sociodemographic covariates. The mean amount of information received does not change over time, but significant inter-individual variability was observed. Age (younger) and marital status (married) are significantly associated with a higher total amount of information received while education (less) and race (African-American) are significantly associated with slower declines of information received over time. While the mean amount of information cancer patients receive is relatively constant over the course of treatment for the first 9 months, the level and rate of information received is somewhat varied based on patient characteristics. Healthcare professionals need to be aware of the varying amounts of information received by patients and ensure that the amount is consistent with the patient’s individual needs.
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Feldman-Stewart D, Capirci C, Brennenstuhl S, Tong C, Abacioglu U, Gawkowska-Suwinska M et al (2010) Information needs of early-stage prostate cancer patients: A comparison of nine countries. Radiother Oncol 94(3):328–333
Halkett GK, Kristjanson LJ, Lobb E, Little J, Shaw T, Taylor M et al (2012) Information needs and preferences of women as they proceed through radiotherapy for breast cancer. Patient Educ Couns 86(3):396–404
Husson O, Mols F, van de Poll-Franse LV (2011) The relation between information provision and health-related quality of life, anxiety and depression among cancer survivors: a systematic review. Ann Oncol 22(4):761–772
Mistry A, Wilson S, Priestman T, Damery S, Haque M (2010) How do the information needs of cancer patients differ at different stages of the cancer journey? A cross-sectional survey. JRSM Short Rep 1(4):30
Muusses LD, Weert JC, Dulmen S, Jansen J (2012) Chemotherapy and information-seeking behaviour: characteristics of patients using mass-media information sources. Psychooncology 21(9):993–1002
Dieng M, Trevena L, Turner RM, Wadolowski M, McCaffery K (2013) What Australian women want and when they want it: cervical screening testing preferences, decision-making styles and information needs. Health Expect 16(2):177–188
Eheman CR, Berkowitz Z, Lee J, Mohile S, Purnell J, Rodriguez EM et al (2009) Information-seeking styles among cancer patients before and after treatment by demographics and use of information sources. J Health Commun 14(5):487–502
Flocke SA, Stange KC, Cooper GS, Wunderlich TL, Oja-Tebbe N, Divine G et al (2011) Patient-rated importance and receipt of information for colorectal cancer screening. Cancer Epidemiol Biomarkers Prev 20(10):2168–2173
Halkett GK, Short M, Kristjanson LJ (2009) How do radiation oncology health professionals inform breast cancer patients about the medical and technical aspects of their treatment? Radiother Oncol 90(1):153–159
Kinnane NA (2012) Evaluation of a hospital-based cancer information and support centre. Support Care Cancer 20(2):287–300
McCarthy B (2011) Family members of patients with cancer: What they know, how they know and what they want to know. Eur J Oncol Nurs 15(5):428–441
Neumann M, Wirtz M, Ernstmann N, Ommen O, Langler A, Edelhauser F et al (2011) Identifying and predicting subgroups of information needs among cancer patients: an initial study using latent class analysis. Support Care Cancer 19(8):1197–1209
Walsh MC, Trentham-Dietz A, Schroepfer TA, Reding DJ, Campbell B, Foote ML et al (2010) Cancer information sources used by patients to inform and influence treatment decisions. J Health Commun 15(4):445–463
Wittmann E, Beaton C, Lewis WG, Hopper AN, Zamawi F, Jackson C et al (2011) Comparison of patients’ needs and doctors’ perceptions of information requirements related to a diagnosis of oesophageal or gastric cancer. Eur J Cancer Care (Engl) 20(2):187–195
Jean-Pierre P, Fiscella K, Griggs J, Joseph JV, Morrow G, Carroll J et al (2010) Race/ethnicity-based concerns over understanding cancer diagnosis and treatment plan. J Natl Med Assoc 102(3):184–189
Jacobs-Lawson JM, Schumacher MM, Hughes T, Arnold S (2009) The relationship between lung cancer patients’ educational level and evaluation of their treatment information needs. J Cancer Educ 24(4):346–350
Matsuyama RK, Wilson-Genderson M, Kuhn L, Moghanaki D, Vachhani H, Paasche-Orlow M (2011) Education level, not health literacy, associated with information needs for patients with cancer. Patient Educ Couns 85(3):e229–e236
Halkett GK, Kristjanson LJ, Lobb E, O’Driscoll C, Taylor M, Spry N (2010) Meeting breast cancer patients’ information needs during radiotherapy: what can we do to improve the information and support that is currently provided? Eur J Cancer Care (Engl) 19(4):538–547
Russell BJ, Ward AM (2011) Deciding what information is necessary: Do patients with advanced cancer want to know all the details? Cancer Manag Res 3:191–199
Zeguers M, de Haes HC, Zandbelt LC, Ter Hoeven CL, Franssen SJ, Geijsen DD et al (2012) The information needs of new radiotherapy patients: how to measure? Do they want to know everything? And if not, why? Int J Radiat Oncol Biol Phys 82(1):418–424
Chen SC, Lai YH, Liao CT, Chang JT, Lin CC (2009) Unmet information needs and preferences in newly diagnosed and surgically treated oral cavity cancer patients. Oral Oncol 45(11):946–952
Guleser GN, Tasci S, Kaplan B (2012) The experience of symptoms and information needs of cancer patients undergoing radiotherapy. J Cancer Educ 27(1):46–53
Matsuyama RK, Kuhn LA, Molisani A, Wilson-Genderson MC (2013) Cancer patients’ information needs the first nine months after diagnosis. Patient Educ Couns 90(1):96–102
Arraras JI, Greimel E, Sezer O, Chie WC, Bergenmar M, Costantini A et al (2010) An international validation study of the EORTC QLQ-INFO25 questionnaire: An instrument to assess the information given to cancer patients. Eur J Cancer 46(15):2726–2738
Adler J, Paelecke-Habermann Y, Jahn P, Landenberger M, Leplow B, Vordermark D (2009) Patient information in radiation oncology: a cross-sectional pilot study using the EORTC QLQ-INFO26 module. Radiat Oncol 4:40
Protière C, Moumjid N, Bouhnik A, Soriano, Anne Gaëlle Le C, Moatti JP (2012) Heterogeneity of cancer patient information-seeking behaviors. Med Decis Mak 32(2):362–375
Galloway S, Graydon J, Harrison D, Evans–Boyden B, Palmer–Wickham S, Burlein–Hall S et al (1997) Informational needs of women with a recent diagnosis of breast cancer: Development and initial testing of a tool. J Adv Nurs 25(6):1175–1183
Muthén, L.K., & Muthén, B.O. Mplus user’s guide. 1998–2012, Los Angeles, CA.
Almyroudi A, Degner LF, Paika V, Pavlidis N, Hyphantis T (2011) Decision-making preferences and information needs among Greek breast cancer patients. Psychooncology 20(8):871–879
Glycopantis D, Stavropoulou C (2011) The supply of information in an emotional setting. CESifo Econ Stud 57(4):740–762
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This project was funded by the American Cancer Society (MRSGT-08-143-01-CPPB).
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Molisani, A., Dumenci, L. & Matsuyama, R.K. Influences of Patient Sociodemographics on Cancer Information Received Through the First 9 Months of Treatment. J Canc Educ 29, 158–166 (2014). https://doi.org/10.1007/s13187-013-0564-z
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DOI: https://doi.org/10.1007/s13187-013-0564-z