Literature DB >> 29808504

Preferences for models of peer support in the digital era: A cross-sectional survey of people with cancer.

Allison Boyes1,2, Heidi Turon1,2, Alix Hall1,2, Rochelle Watson1,2, Anthony Proietto3, Robert Sanson-Fisher1,2.   

Abstract

OBJECTIVE: Many people with cancer report an unmet need for peer support, yet participation rates are low. This study examined cancer patients' preferences for participating in peer support, and the characteristics associated with having or wanting to participate in peer support.
METHODS: Adult cancer patients were recruited from outpatient oncology clinics at 5 hospitals in Australia. Participants were invited to self-complete 2 questionnaires: one at recruitment assessing their demographic and cancer characteristics, and another 4 weeks later assessing their preferences for participating in cancer-related peer support.
RESULTS: The peer support questionnaire was completed by 177/273 (65%) of participants. Most (59%, n = 104) had or wanted to participate in peer support. More than half reported that it was important the people they connected with had the same cancer treatment (56%, n = 99) or type of cancer (53%, n = 94) as themselves. Half had or wanted to participate in 1-to-1 peer support (52%, n = 92). Half had or wanted to connect with peers face-to-face (53%, n = 93). Only 13% (n = 23) were receptive to connecting with peers over the internet. Being aged ≤65 years was significantly associated (OR = 2.3; 95% CI: 1.1-5.1) with reporting a preference for participating in peer support.
CONCLUSIONS: Cancer patients are interested in participating in peer support, particularly those who are younger. Despite the digital era, traditional forms of peer support continue to be important in supporting people with cancer. Greater understanding of the barriers to cancer patients' involvement in potentially low cost and high reach web-based models of peer support is required.
© 2018 John Wiley & Sons, Ltd.

Entities:  

Keywords:  cancer; internet; neoplasm; oncology; patient participation; patient preference; peer group; self-help groups; social support; surveys and questionnaires

Mesh:

Year:  2018        PMID: 29808504     DOI: 10.1002/pon.4781

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  3 in total

1.  Examining management and research priorities in patients with polymyalgia rheumatica: a primary care questionnaire survey.

Authors:  Chris Morton; Sara Muller; Milica Bucknall; Kate Gilbert; Christian D Mallen; Samantha L Hider
Journal:  Clin Rheumatol       Date:  2019-01-07       Impact factor: 2.980

2.  Isolated already, how COVID-19 has exacerbated anxiety for Australian cancer patients.

Authors:  Danielle Spence
Journal:  Psychooncology       Date:  2020-08-07       Impact factor: 3.955

3.  Peer Mentors for People with Advanced Cancer: Lessons Learnt from Recruiting and Training Peer Mentors for a Feasibility Randomized Controlled Trial.

Authors:  Catherine Walshe; Diane Roberts; Lynn Calman; Lynda Appleton; Robert Croft; Guillermo Perez Algorta; Suzanne Skevington; Mari Lloyd-Williams; Gunn Grande
Journal:  J Cancer Educ       Date:  2021-08       Impact factor: 2.037

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.