This clinical trial evaluates whether a shared response plan (SHAREDCare) improves follow-up care for lung cancer survivors. As the number of cancer survivors increases, there is a new need for high-quality chronic illness care. High-quality chronic illness care can be difficult to deliver and involves working with the patient to be certain they have what they need to be actively involved with their care to meet their needs. SHAREDCare allows the patient to work with a navigator to review identified distress and social needs. The patient and navigator discuss the needs and develop a shared response plan to address the needs in ways that consider the patient's current behaviors, beliefs, and motivation. The plan also establishes specific patient goals, anticipates barriers, and establishes how the navigator will follow-up on the needs and adjust care and assistance when needed. Using a shared response plan may improve follow-up care for lung cancer survivors.
Primary Objective: Pilot and qualitatively assess the acceptability of SHAREDCare through semi- structured interviews Secondary Objectives: * Describe quantitative assessments of intervention acceptability, appropriateness, and feasibility. * Describe survivor level of unmet needs13 using a validated measure to collect data before and/or after completion of the SHAREDCare intervention. * Track clinical referrals and other actions made as a result of patient responses on the Electronic Distress Screening (EDS) and the percentage of referrals that have been "completed" (i.e. those referrals where a patient completed the relevant medical or social needs-related visit). * Track recruitment, assessment completion, and any related adverse events. OUTLINE: Patients receive a SHAREDCare call with a navigator to discuss identified distress and social needs and develop/deploy a shared response plan to address identified needs on study. Patients also receive standard of care automated referrals on study. Two weeks following the initial call, patients receive a second SHAREDCare call with a navigator to follow-up on the shared response plan. After completion of study intervention, patients are followed up 4 weeks after initial call.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
5
Receive SHAREDCare navigator calls
Ancillary studies
Ancillary studies
Receive standard of care automated referrals
Atrium Health Wake Forest Baptist Comprehensive Cancer Center (AH-WFBCCC)
Winston-Salem, North Carolina, United States
SHAREDCare's Qualitative Acceptability
Will be assessed with semi-structured interviews. These methods will be guided by Grounded Theory, a process using inductive coding to develop theory from data (e.g., themes relating to components, timing, or delivery of the intervention).
Time frame: At 4 weeks post-initial call
SHAREDCare's Quantitative Acceptability
Will be measured with the Acceptability of Intervention Measure. Quantitative analyses will include descriptive statistics of quantitative data on level of clinical and demographic characteristics and acceptability. Distributions of continuous variables (acceptability) will be examined for estimation of standard deviations (SD) that will be used to inform power analysis for future studies.
Time frame: At 4 weeks post-initial call
SHAREDCare's Quantitative Appropriateness
Will be measured with the Intervention Appropriateness Measure. Quantitative analyses will include descriptive statistics of quantitative data on level of clinical and demographic characteristics and appropriateness. Distributions of continuous variables (acceptability) will be examined for estimation of SD that will be used to inform power analysis for future studies.
Time frame: At 4 weeks post-initial call
SHAREDCare's Quantitative Feasibility
Will be measured with the Feasibility Intervention Measure. Quantitative analyses will include descriptive statistics of quantitative data on level of clinical and demographic characteristics and feasibility. Distributions of continuous variables (acceptability) will be examined for estimation of SD that will be used to inform power analysis for future studies
Time frame: At 4 weeks post-initial call
Number of Survivors With Unmet Needs
Will be assessed before and/or after completion of the SHAREDCare intervention using a validated measure called the Survivor Unmet Needs Survey. This measure will be used to determine the prevalence and predictors of cancer survivors' unmet needs. Scores at baseline and follow-up will be summarized as median (interquartile range, range). Changes will be tested by Wilcoxon signed-rank test.
Time frame: At baseline and at 4 weeks post-initial call
Number of Clinical Referrals Made
Quantitative analyses will include descriptive statistics of quantitative data on level of clinical and demographic characteristics and referrals.
Time frame: At 4 weeks post-initial call
Percentage of Referrals Completed
Will be defined as those referrals where a patient self-reported completing the relevant visit documented in a format adapted from another study. Quantitative analyses will include descriptive statistics of quantitative data on level of clinical and demographic characteristics and referrals.
Time frame: At 4 weeks post-initial call
Number of Participants Enrolled/Eligible
The number of eligible participants will be tracked and for those not enrolled, reasons will be summarized. Will calculate the percent of participants who complete the follow-up visit to assess retention. Will also compare demographic characteristics and baseline scores of participants who complete the follow-up visit to those who do not via Fisher's exact tests or Wilcoxon rank sum tests as appropriate.
Time frame: At 4 weeks post-initial call
Percentage of Assessments Completed
The percent of participants who complete the follow-up visit to assess retention. Will also compare demographic characteristics and baseline scores of participants who complete the follow-up visit to those who do not via Fisher's exact tests or Wilcoxon rank sum tests as appropriate.
Time frame: At 4 weeks post-initial call
Number of Adverse Events Reported
The frequency of any adverse events will be reported.
Time frame: At baseline (initial call) up to 4 weeks post-initial call
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.