N/A
Completed N=17,033
PrOVE QUERI Project #1
Prevention and Control
Source: ClinicalTrials.gov NCT02765412 ↗
Enrolled (actual)
17,033
Serious AEs
0.0%
Results posted
Dec 2024
Primary outcomePrimary: Odds Ratio of the Interaction Between Lung Cancer Risk and Implementation Arm — 1.03; 1.53 odds ratio — p=0.081
Summary
The overall goal of this project is to test two strategies for implementing a shared decision making tool to be used by providers while talking to patients about lung cancer screening. Eight participating sites will be randomized to compare standard implementation with intensive implementation. Additionally, the investigators will determine the factors that were most important for successful implementation of the shared decision making tool. Finally, the investigators will survey patients to evaluate the effects of Decision Precision on patient's knowledge of the risks and benefits of lung cancer screening, the quality of their decision making, and their satisfaction with care.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Odds Ratio of the Interaction Between Lung Cancer Risk and Implementation Arm |
1.03; 1.53 | 0.081 |
| PRIMARY Patient Satisfaction With Decision and Process |
7; 7 | 0.35 |
| SECONDARY Number of Tool Assessments Where Patient Decision Aid Was Printed |
— | — |
| SECONDARY Number of Times Dynamic Pictograph Depicting Personalized Benefit and Harm Was Opened for Display |
— | — |
| SECONDARY Formative Evaluation to Determine the Factors Most Important for Successful Implementation of Decision Precision Tool |
25; 13 | — |
Eligibility Criteria
Inclusion Criteria
- Patients at participating sites without documented exclusions for lung cancer screening who have had initial lung cancer screening clinical reminders resolved during the recruitment period
Exclusion Criteria
Exclusions for initial lung cancer screening clinical reminders:
- history of lung, pancreatic, liver or esophageal cancer
- a health factor on file indicating they have a life expectancy of less than 6 months or who already had a chest CT in the past 12 months
Data sourced from ClinicalTrials.gov (NCT02765412). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.