Ignite Creation Date:
2024-07-17 @ 11:55 AM
Last Modification Date:
2024-10-26 @ 3:33 PM
Study NCT ID:
NCT06474611
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-06-25
First Post:
2024-06-20
Brief Title:
Evaluation of a Patient Nudge on Engagement in Lung Cancer Screening
Sponsor:
Kaiser Permanente
Organization:
Kaiser Permanente
Study Overview
Official Title:
Evaluation of a Patient Nudge on Engagement in Lung Cancer Screening
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this quality improvement project is to conduct and evaluate the effect of sending an electronic reminder message to patients who qualify for lung cancer screening havent had a screening previously and who have an upcoming scheduled appointment with their doctor
Detailed Description:
United States Preventive Services Task Force USPSTF lung cancer screening LCS guidelines recommend LCS for those aged 50-80 with at least 20 pack-years smoking history who currently smoke or quit within the last 15 years In 2023 our study team found that there are approximately 6000 - 8000 Kaiser Permanente Colorado KPCO members who are unscreened and eligible for lung cancer screening LCS In support of KPs Population Health priority initiative to expand lung cancer screening participation for those who are eligible our study team was selected to move this work forward in 2024 with feasible implementation opportunities for the KPCO LCS OperationalInstitute for Health Research partnership at its core The primary objective of this project is to conduct and evaluate a randomized quality improvement pragmatic intervention of a 2-arm electronic message outreach to unscreened LCS members who are eligible for LCS and who have an upcoming scheduled Primary Care Provider PCP visit
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None