Literature DB >> 26507369

Development and usability testing of a web-based self-management intervention for oral cancer survivors and their family caregivers.

H Badr1, D Lipnick1, M A Diefenbach2, M Posner3,4, T Kotz3, B Miles3, E Genden3.   

Abstract

Oral cancer (OC) survivors experience debilitating side effects that affect their quality of life (QOL) and that of their caregivers. This study aimed to develop and evaluate a dyadic, web-based intervention to improve survivor self-management and survivor/caregiver QOL. A qualitative needs assessment (semi-structured interviews) with 13 OC survivors and 12 caregivers was conducted to discern information and support needs as well as preferences regarding website features and tools. Results using Grounded Theory analysis showed that OC survivors and caregivers: (1) want and need practical advice about managing side effects; (2) want to reach out to other survivors/caregivers for information and support; and (3) have both overlapping and unique needs and preferences regarding website features. Usability testing (N = 6 survivors; 5 caregivers) uncovered problems with the intuitiveness, navigation and design of the website that were subsequently addressed. Users rated the website favourably on the dimensions of attractiveness, controllability, efficiency, intuitiveness and learnability, and gave it a total usability score of 80/100. Overall, this study demonstrates that OC survivors and caregivers are interested in using an online programme to improve QOL, and that providing tailored website content and features based on the person's role as survivor or caregiver is important in this population.
© 2015 John Wiley & Sons Ltd.

Entities:  

Keywords:  head and neck cancer; patient education

Mesh:

Year:  2015        PMID: 26507369      PMCID: PMC4848171          DOI: 10.1111/ecc.12396

Source DB:  PubMed          Journal:  Eur J Cancer Care (Engl)        ISSN: 0961-5423            Impact factor:   2.520


  36 in total

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  16 in total

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Review 3.  Interventions to improve quality of life (QOL) and/or mood in patients with head and neck cancer (HNC): a review of the evidence.

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5.  A study protocol for a multicenter randomized pilot trial of a dyadic, tailored, web-based, psychosocial, and physical activity self-management program (TEMPO) for men with prostate cancer and their caregivers.

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6.  Development of a Web-Based Supportive Care Program for Patients With Head and Neck Cancer.

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Review 7.  Availability and use of web-based interventions for patients with head and neck cancer: a scoping review.

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9.  Health information technology to support cancer survivorship care planning: A systematic review.

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10.  Informational and Support Needs of Patients with Head and Neck Cancer: Current Status and Emerging Issues.

Authors:  Carolyn Y Fang; Carolyn J Heckman
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