DeADT - Living Well With Prostate Cancer
Completed · Not applicable
Conditions studied: Prostate Cancer
In brief
The goal of this randomized de-implementation trial is to compare two strategies to reduce low-value androgen deprivation therapy (ADT) use for prostate cancer care. The aim of the study is to compare implementation of the two strategies: use of a clinical reminder order check intervention versus a provider script/patient education approach, and their impacts on low-value ADT use after six months. The main goal of both interventions will be to decrease ADT overuse for patients with prostate cancer, but to do this in a way that is acceptable to the clinicians who treat these patients. The interventions will be initiated for providers only across 4 participating facilities. Provider participants will engage with one of the interventions triggered in the electronic health record when their patients are deemed likely to be receiving low-value ADT. Each provider participant receives only one of the interventions. The intervention is triggered for every clinic visit involving a patient deemed to be receiving low-value ADT, so provider participants may receive their assigned intervention multiple times. Researchers will compare provider use of both strategies to determine implementation outcomes and whether one was more effective in reducing low-value ADT use.
Key facts
- Study ID
- NCT06199986
- Run by
- University of Michigan
- People needed
- 50
- Starts
- 2022-10-04
- Expected to finish
- 2024-04-16
- Last updated by the study team
- 2025-06-26
Who can join
Age: any. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Any provider at participating sites who prescribes ADT for prostate cancer patients
You may not qualify if…
- Providers opting out of study
Where it is running
- VA Ann Arbor Healthcare System — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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