Last reviewed · How we verify
NCT05214937
A Intervention for Reducing Sedentary Behaviour Among Prostate Cancer Survivors
NA trial testing Intervention in Sedentary Behavior in 120 participants. Currently enrolling.
1 December 2025
Quick facts
| Lead sponsor | University of Toronto |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 120 |
| Start date | 15 February 2022 |
| Primary completion | 1 December 2025 |
| Estimated completion | 1 December 2026 |
| Sites | 1 location across Canada |
Drugs / interventions tested
- Intervention
- FitBit Only
Conditions studied
- Sedentary Behavior — all drugs for Sedentary Behavior →
- Cancer of Prostate — all drugs for Cancer of Prostate →
Sponsor
University of Toronto
Who can join
18 and older, male only, with Sedentary Behavior or Cancer of Prostate. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
A distance-based, randomized controlled trial for reducing sedentary behavior among prostate cancer survivors: a study protocol.
Trinh L, Sabiston CM, Alibhai SMH, Jones JM, et al · · 2022 · cited 2× · PMID 35484523 · DOI 10.1186/s12889-022-13218-5
Verify or expand the search:
- PubMed search for NCT05214937
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05214937 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Toronto
- Last refreshed: 4 December 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05214937.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing