Improving Well-being for Older Adults With Lung Cancer

This study is developing a new behavioral intervention called LuCA Behavioral Intervention for older adults (60 years and up) with lung cancer. It aims to help you manage concerns related to aging and lung cancer by teaching skills from Cognitive Behavioral Therapy and Acceptance and Commitment Therapy. The study will first create a way to assess your needs and then test this new intervention. Success for this study means seeing how many people join and complete the study activities, and how satisfied they are with the intervention. This study is currently unclear about its recruitment status.

Study design
This is an interventional study with a planned enrollment of 46 participants. It is not specified if it is randomized or blinded.
What's involved
In the first phase, you would participate in two individual interviews, each 30-45 minutes long, via teleconference. The behavioral intervention involves 5 sessions delivered individually.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoints for feasibility and acceptability are measured at 5 weeks.

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NCT06636721

Lung Cancer and Aging: Improving Well-being for Older Adults With Lung Cancer

Not Yet Recruiting
NAAges 60+InterventionalSupportive care
Duke University
~16 participants
Updated 2026-08-28 on ClinicalTrials.gov
What's tested:LuCA Behavioral Intervention

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility as measured by number of recruited participants who enrolled
Measured over 5 weeks
+2 more outcomes measured
Lung Cancer
1 sites across 1 states
North Carolina1
  • Rebecca A Shelby, PhD · PRINCIPAL_INVESTIGATOR · Duke Psychiatry & Behavioral Sciences

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Lung cancer diagnosis
60 years of age or older
Receiving active treatment at Duke University Health System
Able to speak/read English and provide informed consent

Exclusion

Visual or hearing impairment, cognitive impairment, or severe mental illness interfering with participation
  • Feasibility as measured by number of recruited participants who enrolled5 weeks

    Study feasibility will be measured by number of recruited participants who enroll.

  • Feasibility as measured by number of participants who completed all study activities5 weeks

    Feasibility of the study will be measured by number of participants who complete all study activities.

  • Acceptability as measured by Study Satisfaction Questionnaire5 weeks

    Acceptability of the study will be measured by the Study Satisfaction Questionnaire. This is a 15-item measure using a 5-point Likert scale (from "strongly disagree" to "strongly agree") in which a higher score indicates greater satisfaction.