Validation of the transactional eHealth literacy instrument with cancer caregivers

[1]  Samantha R. Paige,et al.  Comparing Transactional eHealth Literacy of Individuals With Cancer and Surrogate Information Seekers: Mixed Methods Study , 2022, JMIR formative research.

[2]  Simon Dunne,et al.  Health literacy in cancer caregivers: a systematic review , 2021, Journal of Cancer Survivorship.

[3]  Carla L. Fisher,et al.  “Home wasn’t really home anymore”: Understanding caregivers’ perspectives of the impact of blood cancer caregiving on the family system , 2020, Supportive Care in Cancer.

[4]  A. Rosenberg,et al.  Supporting Family Caregivers of Adult and Pediatric Persons with Leukemia. , 2019, Seminars in oncology nursing.

[5]  Janice L. Krieger,et al.  Transactional eHealth Literacy: Developing and Testing a Multi-Dimensional Instrument , 2019, Journal of health communication.

[6]  A. Charalambous,et al.  Adapting the eHealth Literacy Scale for Carers of People With Chronic Diseases (eHeals-Carer) in a Sample of Greek and Cypriot Carers of People With Dementia: Reliability and Validation Study , 2018, Journal of medical Internet research.

[7]  Janice L. Krieger,et al.  Proposing a Transactional Model of eHealth Literacy: Concept Analysis , 2018, Journal of medical Internet research.

[8]  Janice L. Krieger,et al.  Electronic Health Literacy Across the Lifespan: Measurement Invariance Study , 2018, Journal of medical Internet research.

[9]  L. Ricciardelli,et al.  Health literacy of caregivers of adult care recipients: A systematic scoping review , 2018, Health & social care in the community.

[10]  Ronald C. Chen,et al.  eHealth Literacy and Partner Involvement in Treatment Decision Making for Men With Newly Diagnosed Localized Prostate Cancer , 2017, Oncology nursing forum.

[11]  D. Roth,et al.  Examining the context and helpfulness of family companion contributions to older adults' primary care visits. , 2017, Patient education and counseling.

[12]  K. Attwood,et al.  Adjustment to Acute Leukemia: The Impact of Social Support and Marital Satisfaction on Distress and Quality of Life Among Newly Diagnosed Patients and Their Caregivers , 2016, Journal of Clinical Psychology in Medical Settings.

[13]  P. Butow,et al.  Attitudes and experiences of family involvement in cancer consultations: a qualitative exploration of patient and family member perspectives , 2016, Supportive Care in Cancer.

[14]  W. Wood,et al.  Use of ED and hospital services for patients with acute leukemia after induction therapy: one year follow-up. , 2015, Leukemia research.

[15]  Samantha R. Paige,et al.  eHealth Literacy and Web 2.0 Health Information Seeking Behaviors Among Baby Boomers and Older Adults , 2015, Journal of medical Internet research.

[16]  Shih-chuan Chen,et al.  Information needs and information sources of family caregivers of cancer patients , 2014, Aslib J. Inf. Manag..

[17]  D. Iżycki,et al.  Cancer: a family at risk , 2014, Przeglad menopauzalny = Menopause review.

[18]  T. Luger,et al.  Health Information-Seeking on Behalf of Others: Characteristics of “Surrogate Seekers” , 2014, Journal of Cancer Education.

[19]  S. Lipsitz,et al.  Physicians' needs in coping with emotional stressors: the case for peer support. , 2012, Archives of surgery.

[20]  Cameron D. Norman.  eHealth Literacy 2.0: Problems and Opportunities With an Evolving Concept , 2011, Journal of medical Internet research.

[21]  C. Maddock,et al.  3643 POSTER European Patient Online Information Needs , 2011 .

[22]  Y. Chiu,et al.  Probing, Impelling, But Not Offending Doctors , 2011, Qualitative health research.

[23]  Carma L. Bylund,et al.  Cancer patients' decisions about discussing Internet information with their doctors , 2009, Psycho-oncology.

[24]  P. Piselli,et al.  Communicating cancer diagnosis and prognosis: when the target is the elderly patient-a GIOGer study. , 2009, European journal of cancer.

[25]  Amy Aldridge Sanford,et al.  Patients' Reasons for Refraining from Discussing Internet Health Information with Their Healthcare Providers , 2008, Health communication.

[26]  Peter R. Harris,et al.  How do patients evaluate and make use of online health information? , 2007, Social science & medicine.

[27]  Cameron D. Norman,et al.  eHealth Literacy: Essential Skills for Consumer Health in a Networked World , 2006, Journal of medical Internet research.

[28]  M. Glajchen.  The emerging role and needs of family caregivers in cancer care. , 2004, The journal of supportive oncology.

[29]  B. Given,et al.  Family Support in Advanced Cancer , 2001, CA: a cancer journal for clinicians.

[30]  R. Kravitz,et al.  Health information on the Internet: accessibility, quality, and readability in English and Spanish. , 2001, JAMA.

[31]  A. Ek,et al.  Explaining different profiles in quality of life experiences in acute and chronic leukemia. , 1997, Cancer nursing.

[32]  A. Ek,et al.  A substantive theory of quality of life of adults with chronic leukaemia. , 1997, International journal of nursing studies.

[33]  June Williamson,et al.  Context for Change , 2013 .

[34]  Michael R Hamblin,et al.  CA : A Cancer Journal for Clinicians , 2011 .