Evaluating Centralizing Interventions to Address Low Adherence to Lung Cancer Screening Follow-Up in Decentralized Settings (The ACCELL Interventional Trial)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Lung Carcinoma
- Sponsor
- Fred Hutchinson Cancer Center
- Enrollment
- 6772
- Locations
- 1
- Primary Endpoint
- Adherence to appropriate follow-up
- Status
- Enrolling By Invitation
- Last Updated
- 5 months ago
Overview
Brief Summary
This clinical trial tests the impact of lung cancer screening care coordination interventions implemented at the system-level on lung cancer screening adherence in community settings. Lung cancer remains the leading cause of cancer death in the United States. Although lung cancer screening (LCS) with yearly low-dose chest computed tomography has the potential to decrease lung deaths, the use of this screening technique remains low. In addition, studies have shown that adherence to lung cancer screening in clinical settings is far lower that those found in clinical trials. Improved care coordination services that include comprehensive, system-wide tracking of screening outcomes for all LCS participants, results reporting with direct-to-patient information, direct patient and physician communication, and active reviews of non-adherent patients and stepped support interventions may increase patient adherence to LCS. Coordination services at the system-level may decrease barriers and improve adherence to lung cancer screening in community settings.
Detailed Description
OUTLINE: Patients receive lung cancer screening follow-up care coordination services, delivered by a lung cancer screening care coordinator at their care site.
Investigators
Eligibility Criteria
Inclusion Criteria
- •AIM II: Age 50-80
- •AIM II: Current or former (within 15 years) smoker
- •AIM II: 20+ pack-years of cigarette use
- •AIM II: Undergone at least one lung cancer screening low-dose chest computed tomography (CT) at partnering sites within the study period
- •AIM III (PROVIDER INTERVIEWS): Age minimum of 18
- •AIM III (PROVIDER INTERVIEWS): Affiliation with Skagit Regional Health System, Confluence Health or Kadlec Regional Medical Center
- •AIM III (PROVIDER INTERVIEWS): Identifies as providing primary care or specialty care to LCS patients (medical doctor \[MD\], registered nurse \[RN\], physician assistant \[PA\], advanced registered nurse practitioner \[ARNP\])
- •AIM III (LCS PATIENT INTERVIEWS): Aged 50-80 years
- •AIM III (LCS PATIENT INTERVIEWS): Received lung cancer screening at Skagit Regional Health System, Confluence Health or Kadlec Regional Medical Center within the intervention period
- •AIM III (LCS PATIENT INTERVIEWS): Was eligible for LCS at time of performance by United States Preventative Services Taskforce (USPSTF) criteria
Exclusion Criteria
- •AIM II: No longer eligible for lung cancer screening chest CT during follow-up period (no longer meeting inclusion criteria during follow-up period)
- •AIM II: Request to not participate in the trial
- •AIM III (PROVIDER INTERVIEWS): Less than age 18
- •AIM III (PROVIDER INTERVIEWS): Do not have an affiliation with Skagit Regional Health System, Confluence Health or Kadlec Regional Medical Center
- •AIM III (PROVIDER INTERVIEWS): Does not identify as providing primary care or specialty care to LCS patients (MD, RN, PA, ARNP)
- •AIM III (LCS PATIENT INTERVIEWS): Less than age 50 or older than age 80
- •AIM III (LCS PATIENT INTERVIEWS): Did not receive lung cancer screening at Skagit Regional Health System, Confluence Health or Kadlec Regional Medical Center within the intervention period
- •AIM III (LCS PATIENT INTERVIEWS): Was not eligible for LCS at time of performance by USPSTF criteria
- •AIM III (LCS-SPECIFIC CARE COORDINATORS): Less than of 18
- •AIM III (LCS-SPECIFIC CARE COORDINATORS): Does not have an affiliation with Skagit Regional Health System, Confluence Health or Kadlec Regional Medical Center
Outcomes
Primary Outcomes
Adherence to appropriate follow-up
Time Frame: Up to 48 months
The time and covariate adjusted difference in adherence to appropriate follow-up will be assessed between the pre- and post-intervention period, separately for negative and positive exams. Follow-up will be considered on-time if occurring by the recommended follow up window + 30 days. The impact of the interventions on follow-up will be measured a using generalized estimating equations (GEE)-based approach. The modeling will be done using logistic regression. The Bonferroni correction will be used to account for testing two intervention coefficients.
Secondary Outcomes
- Characteristics associated with adherence to follow up(Up to 48 months)