How the internet affects patients' experience of cancer: a qualitative study. - Wikidata - awgldk - TriplyDB

How the internet affects patients' experience of cancer: a qualitative study.

How the internet affects patients' experience of cancer: a qualitative study.

http://www.wikidata.org/entity/Q37261359

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Information from the Internet and the doctor-patient relationship: the patient perspective--a qualitative study Creating a framework for online cancer services research to facilitate timely and interdisciplinary applications How new subscribers use cancer-related online mailing lists How cancer survivors provide support on cancer-related Internet mailing lists Online cancer communities as informatics intervention for social support: conceptualization, characterization, and impact Health and illness in a connected world: how might sharing experiences on the internet affect people's health?High-quality Health Information Provision for Stroke Patients Does sustained participation in an online health community affect sentiment?Developing a web-based information resource for palliative care: an action-research inspired approach.Decisions to use complementary and alternative medicine (CAM) by male cancer patients: information-seeking roles and types of evidence used.Health information seeking on the Internet: a double divide? Results from a representative survey in the Paris metropolitan area, France, 2005-2006 Linguistic processing and classification of semi structured bibliographic data on complementary medicine.Patterns of computer and Internet usage among urology patients in two rural Northern Ontario communities How breast cancer patients want to search for and retrieve information from stories of other patients on the internet: an online randomized controlled experiment The Role of Web-Based Health Information in Help-Seeking Behavior Prior to a Diagnosis of Lung Cancer: A Mixed-Methods Study Health information on the web and consumers' perspectives on health professionals' responses to information exchange.Informed citizen and empowered citizen in health: results from an European survey.Piloting the role of a pharmacist in a community palliative care multidisciplinary team: an Australian experience.Medical paternalism and expensive unsubsidised drugs.Navigating the "liberation procedure": a qualitative study of motivating and hesitating factors among people with multiple sclerosis Exploring older and younger adults' preferences for health information and participation in decision making using the Health Information Wants Questionnaire (HIWQ).Communication and cybercoping: coping with chronic illness through communicative action in online support networks.General practitioners' views on quality markers for children in UK primary care: a qualitative study Health information on the Internet: gold mine or minefield?Design and process evaluation of an informative website tailored to breast cancer survivors' and intimate partners' post-treatment care needs Self-reported use of internet by cervical cancer clients in two National Referral Hospitals in Kenya.Internet health resources and the cancer patient.Web-based cancer communication and decision making systems: connecting patients, caregivers, and clinicians for improved health outcomes.Cancer patients' self-reported attitudes about the Internet.On-line health companion contact among chronically ill in the Netherlands Torrenting values, feelings, and thoughts-Cyber nursing and virtual self-care in a breast augmentation forum Men's experience of their partners' postpartum psychiatric disorders: narratives from the internet When do older adults turn to the internet for health information? Findings from the Wisconsin Longitudinal Study.Cancer patients' experiences of using an Interactive Health Communication Application (IHCA)Longitudinal qualitative exploration of cancer information-seeking experiences across the disease trajectory: the INFO-SEEK protocol Evaluation of Health on the Net seal label and DISCERN as content quality indicators for patients seeking information about thumb sucking habit The tidal waves of connected health devices with healthcare applications: consequences on privacy and care management in European healthcare systems.Health literacy: more choice, but do cancer patients have the skills to decide?Breast cancer: patient information needs reflected in English and German web sites.Antecedent characteristics of online cancer information seeking among rural breast cancer patients: an application of the Cognitive-Social Health Information Processing (C-SHIP) model.

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How the internet affects patients' experience of cancer: a qualitative study.

http://www.wikidata.org/entity/Q37261359

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bilimsel makale

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scientific article published on March 2004

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vedecký článok

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vetenskaplig artikel

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vědecký článek

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name

How the internet affects patients' experience of cancer: a qualitative study.

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How the internet affects patients' experience of cancer: a qualitative study.

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How the internet affects patients' experience of cancer: a qualitative study.

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How the internet affects patients' experience of cancer: a qualitative study.

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How the internet affects patients' experience of cancer: a qualitative study.

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How the internet affects patients' experience of cancer: a qualitative study.

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How the internet affects patients' experience of cancer: a qualitative study.

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Alison Chapple

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Carol Dumelow

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Julie Evans

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Linda Rozmovits

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Sue Ziebland

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Suman Prinjha

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