Literature DB >> 10977266

The use and selection of sources in information seeking: the Cancer Information Service experience. Part 8.

C Muha1, K S Smith, S Baum, J Ter Maat, J A Ward.   

Abstract

The Cancer Information Service (CIS), the voice of the National Cancer Institute (NCI) for more than 20 years, disseminates information through two channels: a toll-free telephone service (1-800-4-CANCER) and an outreach program which develops partnerships with organizations that reach underserved populations. In 1996, the telephone service handled approximately 500,000 calls on a range of topics, including cancer treatment, clinical trials, coping issues, referrals to services, prevention, causes, and symptoms of cancer. As part of a national telephone service user survey, conducted in 1996, that examined the impact of the CIS program, callers were asked what additional sources they went to for the same information that they requested from the CIS. The survey revealed that the CIS plays a critical role for information seekers. Almost 59% of surveyed callers contacted no other sources to address the topic they discussed with the CIS. Almost half of the callers who contacted other sources made all of those contacts before calling the CIS. Younger callers (under 40), those with a higher level of education, and those seeking information about treatment and causes of cancer were more likely to contact other sources for the same information. Health professionals, libraries, and bookstores were the most commonly used non-CIS sources. This variety in information seeking highlights the need for services, like the CIS, that can meet the diverse information needs of callers.

Entities:  

Mesh:

Year:  1998        PMID: 10977266     DOI: 10.1080/108107398127292

Source DB:  PubMed          Journal:  J Health Commun        ISSN: 1081-0730


  11 in total

1.  Differences in information seeking among breast, prostate, and colorectal cancer patients: results from a population-based survey.

Authors:  Rebekah H Nagler; Stacy W Gray; Anca Romantan; Bridget J Kelly; Angela DeMichele; Katrina Armstrong; J Sanford Schwartz; Robert C Hornik
Journal:  Patient Educ Couns       Date:  2010-10-08

2.  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

3.  Examining cross-source engagement with cancer-related information and its impact on doctor-patient relations.

Authors:  Nehama Lewis; Stacy W Gray; Derek R Freres; Robert C Hornik
Journal:  Health Commun       Date:  2009-12

4.  Cancer information scanning and seeking in the general population.

Authors:  Bridget Kelly; Robert Hornik; Anca Romantan; J Sanford Schwartz; Katrina Armstrong; Angela DeMichele; Martin Fishbein; Stacy Gray; Shawnika Hull; Annice Kim; Rebekah Nagler; Jeff Niederdeppe; A Susana Ramírez; Aaron Smith-McLallen; Norman Wong
Journal:  J Health Commun       Date:  2010-10

5.  Are rural Ohio Appalachia cancer survivors needs different than urban cancer survivors?

Authors:  Mira L Katz; Paul L Reiter; Sandy Corbin; Janet S de Moor; Electra D Paskett; Charles L Shapiro
Journal:  J Cancer Surviv       Date:  2010-01-23       Impact factor: 4.442

6.  Effects of scanning (routine health information exposure) on cancer screening and prevention behaviors in the general population.

Authors:  Robert Hornik; Sarah Parvanta; Susan Mello; Derek Freres; Bridget Kelly; J Sanford Schwartz
Journal:  J Health Commun       Date:  2013-10-01

7.  Patient expectations of benefit from phase I clinical trials: linguistic considerations in diagnosing a therapeutic misconception.

Authors:  K P Weinfurt; D P Sulmasy; K A Schulman; N J Meropol
Journal:  Theor Med Bioeth       Date:  2003

8.  Cancer-related information sought by the general public: evidence from the National Cancer Institute's Cancer Information Service, 2002-2003.

Authors:  Lila J Finney Rutten; Linda Squiers; Bradford Hesse
Journal:  J Cancer Educ       Date:  2007       Impact factor: 2.037

9.  Acceptability of delivering and accessing health information through text messaging among community health advisors.

Authors:  Yu-Mei Schoenberger; Janice Phillips; Mohammed Omar Mohiuddin; Patrick McNees; Isabel Scarinci
Journal:  JMIR Mhealth Uhealth       Date:  2013-09-09       Impact factor: 4.773

10.  Optimistic bias, information seeking and intention to undergo prostate cancer screening: A Taiwan study on male adults.

Authors:  Hung-Yi Lu; James E Andrews; Hsin-Ya Hou
Journal:  J Mens Health       Date:  2009-08-11       Impact factor: 0.537

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