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Study identifier: NCT05214937 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Intervention for Reducing Sedentary Behaviour Among Prostate Cancer Survivors

Condition: Sedentary Behavior · Cancer of Prostate  ·  Sponsor: University of Toronto

PhaseNA
Planned participants120
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This randomized controlled trial (RCT) will aim to examine the effect of a 12-week behavioural intervention on changing the sedentary behaviours (SB) of prostate cancer survivors (PCS) compared to a control group (FitBit-only group). PCS in the intervention group will receive a FitBit and 6 behavioural support sessions with a movement specialist guided by behavioural theory (i.e., the Multi-Process Action Control \[M-PAC\]). The FitBit-only group will only receive a FitBit and access to public health resources on physical activity (PA). The primary purpose of this study is to determine the efficacy of the intervention on changing SB of PCS immediately following the 12-week intervention and 6-months later. It is hypothesized that that the intervention will decrease their SB compared to the FitBit-only control condition at both timepoints. This trial will also examine the effect of the intervention on changing PA, motivational outcomes from the M-PAC framework, sleep quality, social support, physical function, quality of life, fatigue, disability and mental health compared to the active control condition.

This description comes directly from the study's public registry record.

Talk to the study team

Linda Trinh, PhD  ·  416-946-3624  ·  linda.trinh@utoronto.ca

Always discuss trial participation with your own doctor first.

Locations (1)

University of TorontoToronto, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT05214937