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Updated: Sep 19, 2025

Visualization of Intensity Levels to Reduce the Gap Between Self-Reported and Directly Measured Physical Activity
Published on: March 7, 2019
Digital intervention for increasing physical activity and reducing sedentary behaviour in cancer survivors: a trial
Erika Rees-Punia1, Matt Masters2, Scott Whalen2
1Department of Population Science, American Cancer Society, Atlanta, Georgia, USA erika.rees-punia@cancer.org.
Objective:
The aims of this study, which uses a trial within a cohort design, were to determine the efficacy of a web-based intervention to increase moderate-to-vigorous intensity physical activity (MVPA) and decrease sedentary behaviour in cancer survivors.
Methods:
Participants (n=415) in this trial were randomised 2:1 to an interactive physical activity website or a static balance and flexibility control website. Participants provided accelerometer data at baseline and at 3 (M3), 6 (M6) and 12 months (M12). Linear mixed models were used to investigate changes in MVPA and sedentary time overall, stratified by website use, and among participants who were inactive at baseline (<150 min MVPA/week).
Results:
Participants were mostly women (n=391, 94%) with an average age of 63 (SD=12) years. In intent-to-treat models, there were no statistically significant between-group differences in MVPA or sedentary time at any time point. However, participants who frequently used the physical activity website (ie, once per week for ≥80% of the study period) were significantly more active at M3 (mean (95% CI); 44 (40 to 48) min/day intervention vs 35 (30 to 39) min/day control), though differences between groups were no longer meaningfully different at M6 or M12. Similarly, among participants who were inactive at baseline, the intervention resulted in an additional 50 min of MVPA per week compared with the control at M3.
Conclusion:
While the intervention was not effective in the overall cohort, it increased MVPA in the short term among cancer survivors who frequently used the website or were inactive at baseline.
Trial Registration Number:
NCT05356988.
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