Literature DB >> 18792791

Health-related information needs in a large and diverse sample of adult cancer survivors: implications for cancer care.

Ellen Burke Beckjord1, Neeraj K Arora, Wendy McLaughlin, Ingrid Oakley-Girvan, Ann S Hamilton, Bradford W Hesse.   

Abstract

BACKGROUND: This study describes the information needs of adult cancer survivors, identifies sociodemographic, health, and healthcare-related factors associated with information needs, and examines the relationship between information needs and survivors' perceived mental and physical health.
METHODS: One thousand forty survivors 2-5 years post-diagnosis who were identified via two cancer registries were included in the present analysis. Self-report questionnaires assessed six categories of information needs, sociodemographic, health, and healthcare-related variables, and perceived mental and physical health.
RESULTS: Information needs were prevalent and varied; most survivors need more information about tests and treatments, health promotion, side effects and symptoms, and interpersonal and emotional issues. Multivariate analyses suggested that survivors who were younger, who reported non-White race/ethnicity, who reported less than excellent quality of follow-up cancer care, and who had more comorbid health conditions had more information needs. After adjustment for sociodemographic and health-related variables, more information needs were associated with worse perceived mental and physical health.
CONCLUSIONS: Most cancer survivors needed more information about maintaining good health outcomes during survivorship. Health communication interventions, such as Survivorship Care Plans, have excellent potential to address survivors' information needs while improving quality of follow-up cancer care and health-related quality of life.

Entities:  

Mesh:

Year:  2008        PMID: 18792791     DOI: 10.1007/s11764-008-0055-0

Source DB:  PubMed          Journal:  J Cancer Surviv        ISSN: 1932-2259            Impact factor:   4.442


  43 in total

1.  Communicating health risk to ethnic groups: reaching Hispanics as a case study.

Authors:  E E Huerta; E Macario
Journal:  J Natl Cancer Inst Monogr       Date:  1999

2.  Quality improvement in chronic illness care: a collaborative approach.

Authors:  E H Wagner; R E Glasgow; C Davis; A E Bonomi; L Provost; D McCulloch; P Carver; C Sixta
Journal:  Jt Comm J Qual Improv       Date:  2001-02

3.  Achieving cultural appropriateness in health promotion programs: targeted and tailored approaches.

Authors:  Matthew W Kreuter; Susan N Lukwago; R D Dawn C Bucholtz; Eddie M Clark; Vetta Sanders-Thompson
Journal:  Health Educ Behav       Date:  2003-04

Review 4.  Information needs and sources of information among cancer patients: a systematic review of research (1980-2003).

Authors:  Lila J Finney Rutten; Neeraj K Arora; Alexis D Bakos; Noreen Aziz; Julia Rowland
Journal:  Patient Educ Couns       Date:  2005-06

Review 5.  The communication goals and needs of cancer patients: a review.

Authors:  Thomas F Hack; Lesley F Degner; Patricia A Parker
Journal:  Psychooncology       Date:  2005-10       Impact factor: 3.894

Review 6.  Identifying and screening patients at risk of second cancers.

Authors:  Victor G Vogel
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2006-10-20       Impact factor: 4.254

7.  Relating information-needs to the cancer experience. 1. Jenny's story: a cancer narrative.

Authors:  B van der Molen
Journal:  Eur J Cancer Care (Engl)       Date:  2000-03       Impact factor: 2.520

Review 8.  Lifestyle interventions in cancer survivors: designing programs that meet the needs of this vulnerable and growing population.

Authors:  Valeda B Stull; Denise C Snyder; Wendy Demark-Wahnefried
Journal:  J Nutr       Date:  2007-01       Impact factor: 4.798

9.  Decision-making role preferences of patients receiving adjuvant cancer treatment: a university of Rochester cancer center community clinical oncology program.

Authors:  Cleveland G Shields; Gary R Morrow; Jennifer Griggs; Julie Mallinger; Joseph Roscoe; James L Wade; Shaker R Dakhil; Tom R Fitch
Journal:  Support Cancer Ther       Date:  2004-01-01

10.  Population-based survivorship research using cancer registries: a study of non-Hodgkin's lymphoma survivors.

Authors:  Neeraj K Arora; Ann S Hamilton; Arnold L Potosky; Julia H Rowland; Noreen M Aziz; Keith M Bellizzi; Carrie N Klabunde; Wendy McLaughlin; Jennifer Stevens
Journal:  J Cancer Surviv       Date:  2007-03       Impact factor: 4.442

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  70 in total

1.  The use of cancer treatment summaries and care plans among Massachusetts physicians.

Authors:  Anna Merport; Stephenie C Lemon; Joshua Nyambose; Marianne N Prout
Journal:  Support Care Cancer       Date:  2012-04-14       Impact factor: 3.603

2.  Perception and Assessment of Verbal and Written Information on Sex and Relationships after Hematopoietic Stem Cell Transplantation.

Authors:  Christel Wendt
Journal:  J Cancer Educ       Date:  2017-12       Impact factor: 2.037

3.  Needs of low-income african american cancer survivors: multifaceted and practical.

Authors:  Maghboeba Mosavel; Kimberley Sanders
Journal:  J Cancer Educ       Date:  2011-12       Impact factor: 2.037

4.  Health-related Internet use among cancer survivors: data from the Health Information National Trends Survey, 2003-2008.

Authors:  Wen-Ying Sylvia Chou; Benmei Liu; Samantha Post; Bradford Hesse
Journal:  J Cancer Surviv       Date:  2011-04-20       Impact factor: 4.442

5.  How do cancer patients navigate the public information environment? Understanding patterns and motivations for movement among information sources.

Authors:  Rebekah H Nagler; Anca Romantan; Bridget J Kelly; Robin S Stevens; Stacy W Gray; Shawnika J Hull; A Susana Ramirez; Robert C Hornik
Journal:  J Cancer Educ       Date:  2010-03-05       Impact factor: 2.037

6.  Cancer Survivorship for Primary Care Annotated Bibliography.

Authors:  Matthew Y Westfall; Linda Overholser; Linda Zittleman; John M Westfall
Journal:  J Cancer Policy       Date:  2015-06-01

7.  Achieving value in mobile health applications for cancer survivors.

Authors:  Sharon Watkins Davis; Ingrid Oakley-Girvan
Journal:  J Cancer Surviv       Date:  2017-03-24       Impact factor: 4.442

8.  A feasibility study to evaluate breast cancer patients' knowledge of their diagnosis and treatment.

Authors:  Stephanie M Smith; Raymond R Balise; Catherine Norton; Mary M Chen; Alissa N Flesher; Alice E Guardino
Journal:  Patient Educ Couns       Date:  2012-09-30

9.  Meeting the information needs of lower income cancer survivors: results of a randomized control trial evaluating the american cancer society's "I can cope".

Authors:  Michelle Y Martin; Mary B Evans; Polly Kratt; Lori A Pollack; Judith Lee Smith; Robert Oster; Mark Dignan; Heather Prayor-Patterson; Christopher Watson; Peter Houston; Shiquina Andrews; Amandiy Liwo; Tung Sung Tseng; Sandral Hullett; Joann Oliver; Maria Pisu
Journal:  J Health Commun       Date:  2014-01-16

10.  Receipt of psychosocial care among cancer survivors in the United States.

Authors:  Laura P Forsythe; Erin E Kent; Kathryn E Weaver; Natasha Buchanan; Nikki A Hawkins; Juan L Rodriguez; A Blythe Ryerson; Julia H Rowland
Journal:  J Clin Oncol       Date:  2013-04-22       Impact factor: 44.544

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