Ignite Creation Date:
2024-05-06 @ 8:18 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06338592
Status:
RECRUITING
Last Update Posted:
2024-06-06
First Post:
2024-03-18
Brief Title:
The MyLungHealth Study Protocol Engaging Patients to Enable Interoperable Lung Cancer Decision Support at Scale
Sponsor:
University of Utah
Organization:
University of Utah
Study Overview
Official Title:
The MyLungHealth Study Protocol A Pragmatic Patient-Randomized Controlled Trial to Evaluate a Patient-Centered Electronic Health Record-Integrated Intervention to Enhance Lung Cancer Screening in Primary Care
Status:
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:
MyLungHealth
Brief Summary:
Early lung cancer screening LCS through low-dose computed tomography LDCT is crucial but underused due to various barriers including incomplete or inaccurate patient smoking data in the electronic health record and limited time for shared decision-making The objective of this trial is to investigate a patient-centered intervention MyLungHealth delivered through the patient portal The intervention is designed to improve LCS rates through increased identification of eligible patients and informed decision making
Detailed Description:
MyLungHealth is a multi-site pragmatic trial involving University of Utah Health and New York University Langone Health primary care clinics The MyLungHealth intervention was developed using a user-centered design process informed by patient and provider focus groups and interviews The interventions effectiveness will be evaluated through a patient-randomized trial comparing the combined use of MyLungHealth and DecisionPrecision a provider-focused clinical decision support and shared decision-making intervention against DecisionPrecision alone
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