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Published in: BMC Palliative Care 1/2021

Open Access 01-12-2021 | Care | Research article

Quality of online self-management resources for adults living with primary brain cancer, and their carers: a systematic environmental scan

Published in: BMC Palliative Care | Issue 1/2021

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Abstract

Background

A primary brain cancer diagnosis is a distressing, life changing event. It adversely affects the quality of life for the person living with brain cancer and their families (‘carers’). Timely access to evidence-based information is critical to enabling people living with brain cancer, and their carers, to self-manage the devastating impacts of this disease.

Method

A systematic environmental scan of web-based resources. A depersonalised search for online English-language resources published from 2009 to December 2019 and designed for adults (> 25 years of age), living with primary brain cancer, was undertaken using the Google search engine. The online information was classified according to: 1) the step on the cancer care continuum; 2) self-management domains (PRISMS taxonomy); 3) basic information disclosure (Silberg criteria); 4) independent quality verification (HonCode); 5) reliability of disease and treatment information (DISCERN Sections 1 and 2); and readability (Flesch-Kincaid reading grade).

Results

A total of 119 online resources were identified, most originating in England (n = 49); Australia (n = 27); or the USA (n = 27). The majority of resources related to active treatment (n = 76), without addressing recurrence (n = 3), survivorship (n = 1) or palliative care needs (n = 13). Few online resources directly provided self-management advice for adults living with brain cancer or their carers. Just over a fifth (n = 26, 22%) were underpinned by verifiable evidence. Only one quarter of organisations producing resources were HonCode certified (n = 9, 24%). The median resource reliability as measured by Section 1, DISCERN tool, was 56%. A median of 8.8 years of education was required to understand these online resources.

Conclusions

More targeted online information is needed to provide people affected by brain cancer with practical self-management advice. Resources need to better address patient and carer needs related to: rehabilitation, managing behavioural changes, survivorship and living with uncertainty; recurrence; and transition to palliative care. Developing online resources that don’t require a high level of literacy and/or cognition are also required.
Appendix
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Literature
1.
go back to reference Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.CrossRefPubMed Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.CrossRefPubMed
2.
go back to reference Allemani C, Matsuda T, Di Carlo V, Harewood R, Matz M, Nikšić M, Bonaventure A, Valkov M, Johnson CJ, Estève J. Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries. Lancet. 2018;391(10125):1023–75.PubMedPubMedCentralCrossRef Allemani C, Matsuda T, Di Carlo V, Harewood R, Matz M, Nikšić M, Bonaventure A, Valkov M, Johnson CJ, Estève J. Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries. Lancet. 2018;391(10125):1023–75.PubMedPubMedCentralCrossRef
3.
go back to reference Patel AP, Fisher JL, Nichols E, Abd-Allah F, Abdela J, Abdelalim A, Abraha HN, Agius D, Alahdab F, Alam T. Global, regional, and national burden of brain and other CNS cancer, 1990–2016: a systematic analysis for the global burden of disease study 2016. Lancet Neurol. 2019;18(4):376–93.CrossRef Patel AP, Fisher JL, Nichols E, Abd-Allah F, Abdela J, Abdelalim A, Abraha HN, Agius D, Alahdab F, Alam T. Global, regional, and national burden of brain and other CNS cancer, 1990–2016: a systematic analysis for the global burden of disease study 2016. Lancet Neurol. 2019;18(4):376–93.CrossRef
4.
go back to reference Kochovska S, Luckett T, Agar M, Phillips JL. Impacts on employment, finances, and lifestyle for working age people facing an expected premature death: a systematic review. Palliat Support Care. 2018;16(3):347–64.PubMedCrossRef Kochovska S, Luckett T, Agar M, Phillips JL. Impacts on employment, finances, and lifestyle for working age people facing an expected premature death: a systematic review. Palliat Support Care. 2018;16(3):347–64.PubMedCrossRef
5.
go back to reference Matsuyama RK, Kuhn LA, Molisani A, Wilson-Genderson MC. Cancer patients’ information needs the first nine months after diagnosis. Patient Educ Couns. 2013;90(1):96–102.PubMedCrossRef Matsuyama RK, Kuhn LA, Molisani A, Wilson-Genderson MC. Cancer patients’ information needs the first nine months after diagnosis. Patient Educ Couns. 2013;90(1):96–102.PubMedCrossRef
6.
go back to reference Halkett GKB, Lobb EA, Oldham L, Nowak AK. The information and support needs of patients diagnosed with high grade Glioma. Patient Educ Couns. 2010;79(1):112–9.PubMedCrossRef Halkett GKB, Lobb EA, Oldham L, Nowak AK. The information and support needs of patients diagnosed with high grade Glioma. Patient Educ Couns. 2010;79(1):112–9.PubMedCrossRef
7.
go back to reference National Health Priority Council. National Service Improvement Framework for Cancer. Canberra: Australian Government Department of Health and Ageing; 2006. National Health Priority Council. National Service Improvement Framework for Cancer. Canberra: Australian Government Department of Health and Ageing; 2006.
8.
go back to reference Ramsay I, Peters M, Corsini N, Eckert M. Consumer health information needs and preferences: a rapid evidence review, vol. 695. Sydney: Australian Commission on Safety and Quality in Health; 2017. Ramsay I, Peters M, Corsini N, Eckert M. Consumer health information needs and preferences: a rapid evidence review, vol. 695. Sydney: Australian Commission on Safety and Quality in Health; 2017.
9.
go back to reference Castleton K, Fong T, Wang-Gillam A, Waqar MA, Jeffe DB, Kehlenbrink L, Gao F, Govindan R. A survey of internet utilization among patients with cancer. Support Care Cancer. 2011;19(8):1183–90.PubMedCrossRef Castleton K, Fong T, Wang-Gillam A, Waqar MA, Jeffe DB, Kehlenbrink L, Gao F, Govindan R. A survey of internet utilization among patients with cancer. Support Care Cancer. 2011;19(8):1183–90.PubMedCrossRef
10.
go back to reference Germeni E, Schulz PJ. Information seeking and avoidance throughout the cancer patient journey: two sides of the same coin? A synthesis of qualitative studies. Psychooncology. 2014;23(12):1373–81.PubMedCrossRef Germeni E, Schulz PJ. Information seeking and avoidance throughout the cancer patient journey: two sides of the same coin? A synthesis of qualitative studies. Psychooncology. 2014;23(12):1373–81.PubMedCrossRef
11.
go back to reference Catt S, Chalmers A, Fallowfield L. Psychosocial and supportive-care needs in high-grade glioma. Lancet Oncol. 2008;9(9):884–91.PubMedCrossRef Catt S, Chalmers A, Fallowfield L. Psychosocial and supportive-care needs in high-grade glioma. Lancet Oncol. 2008;9(9):884–91.PubMedCrossRef
12.
go back to reference Moore G, Collins A, Brand C, Gold M, Lethborg C, Murphy M, Sundararajan V, Philip J. Palliative and supportive care needs of patients with high-grade glioma and their carers: a systematic review of qualitative literature. Patient Educ Couns. 2013;91(2):141–53.PubMedCrossRef Moore G, Collins A, Brand C, Gold M, Lethborg C, Murphy M, Sundararajan V, Philip J. Palliative and supportive care needs of patients with high-grade glioma and their carers: a systematic review of qualitative literature. Patient Educ Couns. 2013;91(2):141–53.PubMedCrossRef
13.
go back to reference Sizoo EM, Pasman HRW, Dirven L, Marosi C, Grisold W, Stockhammer G, Egeter J, Grant R, Chang S, Heimans JJ, Deliens L, Reijneveld JC, Taphoorn MJB. The end-of-life phase of high-grade glioma patients: a systematic review. Support Care Cancer. 2014;22(3):847–57.PubMedCrossRef Sizoo EM, Pasman HRW, Dirven L, Marosi C, Grisold W, Stockhammer G, Egeter J, Grant R, Chang S, Heimans JJ, Deliens L, Reijneveld JC, Taphoorn MJB. The end-of-life phase of high-grade glioma patients: a systematic review. Support Care Cancer. 2014;22(3):847–57.PubMedCrossRef
14.
go back to reference Garcia CR, Slone SA, Pittman T, St. Clair WH, Lightner DD, Villano JL. Comprehensive evaluation of treatment and outcomes of low-grade diffuse gliomas. PLoS One. 2018;13(9):e0203639.PubMedPubMedCentralCrossRef Garcia CR, Slone SA, Pittman T, St. Clair WH, Lightner DD, Villano JL. Comprehensive evaluation of treatment and outcomes of low-grade diffuse gliomas. PLoS One. 2018;13(9):e0203639.PubMedPubMedCentralCrossRef
15.
go back to reference Eheman CR, Berkowitz Z, Lee J, Mohile S, Purnell J, Marie Rodriguez E, Roscoe J, Johnson D, Kirshner J, Morrow G. Information-seeking styles among cancer patients before and after treatment by demographics and use of information sources. J Health Commun. 2009;14(5):487–502.PubMedPubMedCentralCrossRef Eheman CR, Berkowitz Z, Lee J, Mohile S, Purnell J, Marie Rodriguez E, Roscoe J, Johnson D, Kirshner J, Morrow G. Information-seeking styles among cancer patients before and after treatment by demographics and use of information sources. J Health Commun. 2009;14(5):487–502.PubMedPubMedCentralCrossRef
16.
go back to reference Kim H, Xie B. Health literacy in the eHealth era: a systematic review of the literature. Patient Educ Couns. 2017;100(6):1073–82.PubMedCrossRef Kim H, Xie B. Health literacy in the eHealth era: a systematic review of the literature. Patient Educ Couns. 2017;100(6):1073–82.PubMedCrossRef
17.
go back to reference Lee K, Hoti K, Hughes JD, Emmerton LM. Consumer use of “Dr Google”: a survey on health information-seeking behaviors and navigational needs. J Med Internet Res. 2015;17(12):e288.PubMedPubMedCentralCrossRef Lee K, Hoti K, Hughes JD, Emmerton LM. Consumer use of “Dr Google”: a survey on health information-seeking behaviors and navigational needs. J Med Internet Res. 2015;17(12):e288.PubMedPubMedCentralCrossRef
18.
go back to reference McCorkle R, Ercolano E, Lazenby M, Schulman-Green D, Schilling LS, Lorig K, Wagner EH. Self-management: enabling and empowering patients living with cancer as a chronic illness. CA Cancer J Clin. 2011;61(1):50–62.PubMedPubMedCentralCrossRef McCorkle R, Ercolano E, Lazenby M, Schulman-Green D, Schilling LS, Lorig K, Wagner EH. Self-management: enabling and empowering patients living with cancer as a chronic illness. CA Cancer J Clin. 2011;61(1):50–62.PubMedPubMedCentralCrossRef
19.
go back to reference Trappenburg J, Jonkman N, Jaarsma T, van Os-Medendorp H, Kort H, de Wit N, Hoes A, Schuurmans M. Self-management: one size does not fit all. Patient Educ Couns. 2013;92(1):134–7.PubMedCrossRef Trappenburg J, Jonkman N, Jaarsma T, van Os-Medendorp H, Kort H, de Wit N, Hoes A, Schuurmans M. Self-management: one size does not fit all. Patient Educ Couns. 2013;92(1):134–7.PubMedCrossRef
20.
go back to reference DeMarco J, Nystrom M, Salvatore K. The importance of patient education throughout the continuum of health care. J Cons Health Internet. 2011;15(1):22–31.CrossRef DeMarco J, Nystrom M, Salvatore K. The importance of patient education throughout the continuum of health care. J Cons Health Internet. 2011;15(1):22–31.CrossRef
21.
go back to reference Hibbard JH. Patient activation and the use of information to support informed health decisions. Patient Educ Couns. 2017;100(1):5–7.PubMedCrossRef Hibbard JH. Patient activation and the use of information to support informed health decisions. Patient Educ Couns. 2017;100(1):5–7.PubMedCrossRef
22.
go back to reference Kearney M, Jennrich MK, Lyons S, Robinson R, Berger B. Effects of preoperative education on patient outcomes after joint replacement surgery. Orthop Nurs. 2011;30(6):391–6.PubMedCrossRef Kearney M, Jennrich MK, Lyons S, Robinson R, Berger B. Effects of preoperative education on patient outcomes after joint replacement surgery. Orthop Nurs. 2011;30(6):391–6.PubMedCrossRef
23.
go back to reference Semchuk W. Empowering providers to meet patient information needs: reduce patient anxiety to support adherence. Can Pharm J (Ott). 2004;137(3):46–9.CrossRef Semchuk W. Empowering providers to meet patient information needs: reduce patient anxiety to support adherence. Can Pharm J (Ott). 2004;137(3):46–9.CrossRef
24.
go back to reference Guo P, East L, Arthur A. A preoperative education intervention to reduce anxiety and improve recovery among Chinese cardiac patients: a randomized controlled trial. Int J Nurs. 2012;49(2):129–37.CrossRef Guo P, East L, Arthur A. A preoperative education intervention to reduce anxiety and improve recovery among Chinese cardiac patients: a randomized controlled trial. Int J Nurs. 2012;49(2):129–37.CrossRef
26.
go back to reference Chen J, Mullins CD, Novak P, Thomas SB. Personalized strategies to activate and empower patients in health care and reduce health disparities. Health Educ Behav. 2016;43(1):25–34.PubMedCrossRef Chen J, Mullins CD, Novak P, Thomas SB. Personalized strategies to activate and empower patients in health care and reduce health disparities. Health Educ Behav. 2016;43(1):25–34.PubMedCrossRef
27.
go back to reference Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, Ioannidis JPA, Clarke M, Devereaux PJ, Kleijnen J, Moher D. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration, vol. 339; 2009. p. b2700. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, Ioannidis JPA, Clarke M, Devereaux PJ, Kleijnen J, Moher D. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration, vol. 339; 2009. p. b2700.
28.
go back to reference Pearce G, Parke HL, Pinnock H, Epiphaniou E, Bourne CL, Sheikh A, Taylor SJ. The PRISMS taxonomy of self-management support: derivation of a novel taxonomy and initial testing of its utility. J Health Serv Res Policy. 2016;21(2):73–82.PubMedCrossRef Pearce G, Parke HL, Pinnock H, Epiphaniou E, Bourne CL, Sheikh A, Taylor SJ. The PRISMS taxonomy of self-management support: derivation of a novel taxonomy and initial testing of its utility. J Health Serv Res Policy. 2016;21(2):73–82.PubMedCrossRef
29.
go back to reference Louis DN, Perry A, Reifenberger G, Von Deimling A, Figarella-Branger D, Cavenee WK, Ohgaki H, Wiestler OD, Kleihues P, Ellison DW. The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol. 2016;131(6):803–20.CrossRefPubMed Louis DN, Perry A, Reifenberger G, Von Deimling A, Figarella-Branger D, Cavenee WK, Ohgaki H, Wiestler OD, Kleihues P, Ellison DW. The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol. 2016;131(6):803–20.CrossRefPubMed
30.
go back to reference Hadfield R, Bates J. Overview of Current Knowledge in Brain Cancer Research with a Focus on Survival. Cure Brain Cancer Foundation; 2018. Hadfield R, Bates J. Overview of Current Knowledge in Brain Cancer Research with a Focus on Survival. Cure Brain Cancer Foundation; 2018.
31.
go back to reference Silberg WM, Lundberg GD, Musacchio RA. Assessing, controlling, and assuring the quality of medical information on the internet: Caveant lector et viewor—let the reader and viewer beware. JAMA. 1997;277(15):1244–5.PubMedCrossRef Silberg WM, Lundberg GD, Musacchio RA. Assessing, controlling, and assuring the quality of medical information on the internet: Caveant lector et viewor—let the reader and viewer beware. JAMA. 1997;277(15):1244–5.PubMedCrossRef
34.
go back to reference Charnock D, Shepperd S, Needham G, Gann R. DISCERN: an instrument for judging the quality of written consumer health information on treatment choices. J Epidemiol Commun H. 1999;53(2):105–11.CrossRef Charnock D, Shepperd S, Needham G, Gann R. DISCERN: an instrument for judging the quality of written consumer health information on treatment choices. J Epidemiol Commun H. 1999;53(2):105–11.CrossRef
35.
go back to reference Kincaid JP, Fishburne RP Jr, Rogers RL, Chissom BS. Derivation of new readability formulas (automated readability index, fog count and flesch reading ease formula) for navy enlisted personnel. (Branch Report No 8–75) Millington, TN: Chief of Naval Training 359 Actes de la 2ème Conférence Internationale Éducation, Économie et Société – Paris 2010; 1975.CrossRef Kincaid JP, Fishburne RP Jr, Rogers RL, Chissom BS. Derivation of new readability formulas (automated readability index, fog count and flesch reading ease formula) for navy enlisted personnel. (Branch Report No 8–75) Millington, TN: Chief of Naval Training 359 Actes de la 2ème Conférence Internationale Éducation, Économie et Société – Paris 2010; 1975.CrossRef
37.
go back to reference Cappiello M, Cunningham RS, Tish Knobf M, Erdos D. Breast cancer survivors: information and support after treatment. Clin Nurs Res. 2007;16(4):278–93.PubMedCrossRef Cappiello M, Cunningham RS, Tish Knobf M, Erdos D. Breast cancer survivors: information and support after treatment. Clin Nurs Res. 2007;16(4):278–93.PubMedCrossRef
39.
go back to reference Hours PS, Rusenas I, Simmonds MA, Hueford DL. Information needs of families of cancer patients: a literature review and recommendations. J Cancer Educ. 1991;6(4):255–61.CrossRef Hours PS, Rusenas I, Simmonds MA, Hueford DL. Information needs of families of cancer patients: a literature review and recommendations. J Cancer Educ. 1991;6(4):255–61.CrossRef
40.
go back to reference Lobb EA, Halkett GK, Nowak AK. Patient and caregiver perceptions of communication of prognosis in high grade glioma. J Neuro-Oncol. 2011;104(1):315–22.CrossRef Lobb EA, Halkett GK, Nowak AK. Patient and caregiver perceptions of communication of prognosis in high grade glioma. J Neuro-Oncol. 2011;104(1):315–22.CrossRef
51.
go back to reference Vierhout M, Daniels M, Mazzotta P, Vlahos J, Mason WP, Bernstein M. The views of patients with brain cancer about palliative care: a qualitative study. Curr Oncol Rep. 2017;24(6):374.CrossRef Vierhout M, Daniels M, Mazzotta P, Vlahos J, Mason WP, Bernstein M. The views of patients with brain cancer about palliative care: a qualitative study. Curr Oncol Rep. 2017;24(6):374.CrossRef
52.
go back to reference McCartney A, Butler C, Acreman S. Exploring access to rehabilitation services from allied health professionals for patients with primary high-grade brain tumours. J Palliat Med. 2011;25(8):788–96.CrossRef McCartney A, Butler C, Acreman S. Exploring access to rehabilitation services from allied health professionals for patients with primary high-grade brain tumours. J Palliat Med. 2011;25(8):788–96.CrossRef
53.
go back to reference Langbecker D, Janda M, Yates P. Health professionals' perspectives on information provision for patients with brain tumours and their families. Eur J Cancer Care. 2013;22(2):179–87.CrossRef Langbecker D, Janda M, Yates P. Health professionals' perspectives on information provision for patients with brain tumours and their families. Eur J Cancer Care. 2013;22(2):179–87.CrossRef
54.
go back to reference Cubis L, Ownsworth T, Pinkham MB, Chambers S. The social trajectory of brain tumor: a qualitative metasynthesis. Disabil Rehabil. 2018;40(16):1857–69.PubMedCrossRef Cubis L, Ownsworth T, Pinkham MB, Chambers S. The social trajectory of brain tumor: a qualitative metasynthesis. Disabil Rehabil. 2018;40(16):1857–69.PubMedCrossRef
55.
go back to reference Gehring K, Kloek CJJ, Aaronson NK, Janssen KW, Jones LW, Sitskoorn MM, Stuiver MM. Feasibility of a home-based exercise intervention with remote guidance for patients with stable grade II and III gliomas: a pilot randomized controlled trial. Clin Rehabil. 2018;32(3):352–66.PubMedCrossRef Gehring K, Kloek CJJ, Aaronson NK, Janssen KW, Jones LW, Sitskoorn MM, Stuiver MM. Feasibility of a home-based exercise intervention with remote guidance for patients with stable grade II and III gliomas: a pilot randomized controlled trial. Clin Rehabil. 2018;32(3):352–66.PubMedCrossRef
56.
go back to reference Biegler KA, Alejandro Chaoul M, Cohen L. Cancer, cognitive impairment, and meditation. Acta Oncol. 2009;48(1):18–26.PubMedCrossRef Biegler KA, Alejandro Chaoul M, Cohen L. Cancer, cognitive impairment, and meditation. Acta Oncol. 2009;48(1):18–26.PubMedCrossRef
57.
go back to reference Miaskowski C, Dodd M, West C, Schumacher K, Paul SM, Tripathy D, Koo P. Randomized clinical trial of the effectiveness of a self-care intervention to improve cancer pain management. J Clin Oncol. 2004;22(9):1713–20.PubMedCrossRef Miaskowski C, Dodd M, West C, Schumacher K, Paul SM, Tripathy D, Koo P. Randomized clinical trial of the effectiveness of a self-care intervention to improve cancer pain management. J Clin Oncol. 2004;22(9):1713–20.PubMedCrossRef
58.
go back to reference McConigley R, Halkett G, Lobb E, Nowak A. Caring for someone with high-grade glioma: a time of rapid change for caregivers. J Palliat Med. 2010;24(5):473–9.CrossRef McConigley R, Halkett G, Lobb E, Nowak A. Caring for someone with high-grade glioma: a time of rapid change for caregivers. J Palliat Med. 2010;24(5):473–9.CrossRef
59.
go back to reference Culos-Reed SN, Leach HJ, Capozzi LC, Easaw J, Eves N, Millet GY. Exercise preferences and associations between fitness parameters, physical activity, and quality of life in high-grade glioma patients. Support Care Cancer. 2017;25(4):1237–46.CrossRef Culos-Reed SN, Leach HJ, Capozzi LC, Easaw J, Eves N, Millet GY. Exercise preferences and associations between fitness parameters, physical activity, and quality of life in high-grade glioma patients. Support Care Cancer. 2017;25(4):1237–46.CrossRef
60.
go back to reference Lee V, Cohen SR, Edgar L, Laizner AM, Gagnon AJ. Meaning-making intervention during breast or colorectal cancer treatment improves self-esteem, optimism, and self-efficacy. Soc Sci Med. 2006;62(12):3133–45.PubMedCrossRef Lee V, Cohen SR, Edgar L, Laizner AM, Gagnon AJ. Meaning-making intervention during breast or colorectal cancer treatment improves self-esteem, optimism, and self-efficacy. Soc Sci Med. 2006;62(12):3133–45.PubMedCrossRef
61.
go back to reference Gehring K, Sitskoorn MM, Gundy CM, Sikkes SA, Klein M, Postma TJ, van den Bent MJ, Beute GN, Enting RH, Kappelle AC. Cognitive rehabilitation in patients with gliomas: a randomized, controlled trial. J Clin Oncol. 2009;27(22):3712–22.PubMedCrossRef Gehring K, Sitskoorn MM, Gundy CM, Sikkes SA, Klein M, Postma TJ, van den Bent MJ, Beute GN, Enting RH, Kappelle AC. Cognitive rehabilitation in patients with gliomas: a randomized, controlled trial. J Clin Oncol. 2009;27(22):3712–22.PubMedCrossRef
62.
go back to reference Poggi G, Liscio M, Pastore V, Adduci A, Galbiati S, Spreafico F, Gandola L, Massimino M. Psychological intervention in young brain tumor survivors: the efficacy of the cognitive behavioural approach. Disabil Rehabil. 2009;31(13):1066–73.PubMedCrossRef Poggi G, Liscio M, Pastore V, Adduci A, Galbiati S, Spreafico F, Gandola L, Massimino M. Psychological intervention in young brain tumor survivors: the efficacy of the cognitive behavioural approach. Disabil Rehabil. 2009;31(13):1066–73.PubMedCrossRef
63.
go back to reference Janssen S, Fahlbusch FB, Käsmann L, Rades D, Vordermark D. Radiotherapy for prostate cancer: DISCERN quality assessment of patient-oriented websites in 2018. BMC Urol. 2019;19(1):42.PubMedPubMedCentralCrossRef Janssen S, Fahlbusch FB, Käsmann L, Rades D, Vordermark D. Radiotherapy for prostate cancer: DISCERN quality assessment of patient-oriented websites in 2018. BMC Urol. 2019;19(1):42.PubMedPubMedCentralCrossRef
64.
go back to reference Diviani N, van den Putte B, Giani S, van Weert JC. Low health literacy and evaluation of online health information: a systematic review of the literature. J Med Internet Res. 2015;17(5):e112.PubMedPubMedCentralCrossRef Diviani N, van den Putte B, Giani S, van Weert JC. Low health literacy and evaluation of online health information: a systematic review of the literature. J Med Internet Res. 2015;17(5):e112.PubMedPubMedCentralCrossRef
65.
go back to reference Gaglio B, Glasgow RE, Bull SS. Do patient preferences for health information vary by health literacy or numeracy? A qualitative assessment. J Health Commun. 2012;17(sup3):109–21.PubMedCrossRef Gaglio B, Glasgow RE, Bull SS. Do patient preferences for health information vary by health literacy or numeracy? A qualitative assessment. J Health Commun. 2012;17(sup3):109–21.PubMedCrossRef
66.
go back to reference Ali FS, Hussain MR, Gutiérrez C, Demireva P, Ballester LY, Zhu J-J, Blanco A, Esquenazi Y. Cognitive disability in adult patients with brain tumors. Cancer Treat Rev. 2018;65:33–40.PubMedCrossRef Ali FS, Hussain MR, Gutiérrez C, Demireva P, Ballester LY, Zhu J-J, Blanco A, Esquenazi Y. Cognitive disability in adult patients with brain tumors. Cancer Treat Rev. 2018;65:33–40.PubMedCrossRef
Metadata
Title
Quality of online self-management resources for adults living with primary brain cancer, and their carers: a systematic environmental scan
Publication date
01-12-2021
Keyword
Care
Published in
BMC Palliative Care / Issue 1/2021
Electronic ISSN: 1472-684X
DOI
https://doi.org/10.1186/s12904-021-00715-4

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