Literature DB >> 23076587

Using incentives in surveys of cancer patients: do "best practices" apply?

Jonathan B Vangeest1, Timothy P Johnson.   

Abstract

PURPOSE: Surveys of cancer patients are an important means of collecting data necessary to improve cancer prevention and control. However, health surveys generally are characterized by declining response rates, with incentives often employed to encourage participation. While successful, magnitude of effect is partially dependent upon situational characteristics of respondents, including health status. Given the health challenges experienced by cancer patients, it is unclear to what extent incentives can improve survey participation. In this study, we examine the effectiveness of monetary and non-monetary incentives in improving response to cancer patient surveys.
METHODS: We reviewed the available experimental literature regarding efforts to improve response rates among cancer patients/survivors via incentives. Relevant studies were identified through searches of the MEDLINE, PubMed, and PsychINFO databases from 1975 to 2012. Seed sources (e.g., Cancer Causes & Control, Cancer Epidemiology, Biomarkers & Prevention, and BMC Medical Research Methodology) were also referenced extensively in order to establish a comprehensive set of studies.
RESULTS: Although limited, evidence does suggest that token incentives may be less effective for improving survey participation among cancer patients, relative to other population groups. These results are contrary to well-established evidence regarding the efficacy of incentives in improving survey participation generally. Potential reasons why incentives may be less effective in this population are explored.
CONCLUSIONS: While more research is necessary, results suggest that survey research strategies targeting cancer patients be purposively designed in a manner that gives consideration to the distress associated with the condition, including selection of alternative strategies to improve response.

Entities:  

Mesh:

Year:  2012        PMID: 23076587     DOI: 10.1007/s10552-012-0082-z

Source DB:  PubMed          Journal:  Cancer Causes Control        ISSN: 0957-5243            Impact factor:   2.506


  5 in total

1.  Characterization of skin reactions and pain reported by patients receiving radiation therapy for cancer at different sites.

Authors:  Jennifer S Gewandter; Joanna Walker; Charles E Heckler; Gary R Morrow; Julie L Ryan
Journal:  J Support Oncol       Date:  2013-12

2.  How to implement routine electronic patient-reported outcome monitoring in oncology rehabilitation.

Authors:  Lisa M Wintner; Monika Sztankay; David Riedl; Gerhard Rumpold; Alain Nickels; Thomas Licht; Bernhard Holzner
Journal:  Int J Clin Pract       Date:  2020-10-02       Impact factor: 2.503

3.  Population-Based Survey Methods for Reaching Adolescent and Young Adult Survivors of Pediatric Cancer and Their Parents.

Authors:  Ann S Hamilton; Xueyan Zhuang; Denise Modjeski; Rhona Slaughter; Anamara Ritt-Olson; Joel Milam
Journal:  J Adolesc Young Adult Oncol       Date:  2018-09-15       Impact factor: 1.757

4.  Integrating patient reported outcomes with clinical cancer registry data: a feasibility study of the electronic Patient-Reported Outcomes From Cancer Survivors (ePOCS) system.

Authors:  Laura Ashley; Helen Jones; James Thomas; Alex Newsham; Amy Downing; Eva Morris; Julia Brown; Galina Velikova; David Forman; Penny Wright
Journal:  J Med Internet Res       Date:  2013-10-25       Impact factor: 5.428

5.  Electronic Patient Reporting of Adverse Events and Quality of Life: A Prospective Feasibility Study in General Oncology.

Authors:  Fiona Kennedy; Kate Absolom; Beverly Clayton; Zoe Rogers; Kathryn Gordon; Elaine O'Connell Francischetto; Jane M Blazeby; Julia Brown; Galina Velikova
Journal:  JCO Oncol Pract       Date:  2020-08-27
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.