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Engagement with a Social Networking Intervention for Cancer-Related Distress

  • Original Article
  • Published:
Annals of Behavioral Medicine

Abstract

Background

Understanding patterns and predictors of engagement could improve the efficacy of Internet interventions.

Purpose

The purpose of the study was to characterize engagement in a multi-component Internet intervention for cancer survivors with distress.

Methods

Data were derived from 296 cancer survivors provided with access to the Internet intervention and included self-report measures and directly-measured engagement with each component of the intervention.

Results

Over 12 weeks, average total engagement was 7.3 h (sd = 11.7), and 42 % of participants spent >3 h on the website. Participants spent more time using social networking components than structured intervention content. Greater early and total engagement was associated with previous chemotherapy, being female, and being recruited via the Internet. Early engagement was associated with greater fatigue and more social constraints.

Conclusions

For many users, engagement with an Internet intervention was quite high. Reducing attrition and tailoring content to better meet the needs of those who do not engage should be a focus of future efforts.

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Conflicts of Interest

Jason Owen, Annette Stanton, Amanda Gorlick, and Erin Bantum declare that they have no conflict of interest. All procedures, including the informed consent process, were conducted in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000.

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Correspondence to Jason E. Owen PhD, MPH.

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Owen, J.E., Bantum, E.O., Gorlick, A. et al. Engagement with a Social Networking Intervention for Cancer-Related Distress. ann. behav. med. 49, 154–164 (2015). https://doi.org/10.1007/s12160-014-9643-6

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  • DOI: https://doi.org/10.1007/s12160-014-9643-6

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