Precision Lung Cancer Survivorship Care Intervention

NCT05857995 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2026-02-23

No results posted yet for this study

Summary

The overarching goal of the Kentucky LEADS Collaborative Lung Cancer Survivorship Care program is to reduce the burden of lung cancer by offering an innovative survivorship care approach that improves lung cancer quality of life, overcomes lung cancer stigma, and helps survivors engage with care. The project involves a two-group parallel randomized clinical trial comparing the impact of the Kentucky LEADS Collaborative Lung Cancer Survivorship Care program (KLCLCSC) among lung cancer survivors (N=300) against an enhanced usual care condition (bibliotherapy+assessment) on quality of life outcomes.

Conditions

  • Lung Cancer
  • Pulmonary Neoplasm
  • Neoplasms, Lung
  • Neoplasms, Pulmonary
  • Neoplasm, Pulmonary
  • Cancer, Lung
  • Cancers, Lung
  • Pulmonary Cancer
  • Cancer, Pulmonary
  • Cancers, Pulmonary
  • Pulmonary Cancers
  • Cancer of the Lung
  • Cancer of Lung
  • Pulmonary Neoplasms
  • Lung Cancers

Interventions

BEHAVIORAL

Kentucky LEADS Collaborative Lung Cancer Survivorship Care Program

KLCLCSC is a survivor or survivor plus caregiver-focused psychosocial and behavioral intervention designed to engage lung cancer survivors and improve lung cancer outcomes.

BEHAVIORAL

Enhanced Usual Care

EUC involves a combination of the standard of care plus a bibliotherapy intervention and assessment.

Sponsors & Collaborators

  • University of Louisville

    collaborator OTHER
  • G02 for Lung Cancer

    collaborator UNKNOWN
  • National Cancer Institute (NCI)

    collaborator NIH
  • Jerod L Stapleton, PhD

    lead OTHER

Principal Investigators

  • Jamie L Studts, PhD · University of Colorado School of Medicine

  • Jerod L Stapleton, PhD · University of Kentucky

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-08-16
Primary Completion
2027-07-01
Completion
2028-03-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05857995 on ClinicalTrials.gov