Palliative Care Intervention in Improving Symptom Control and Quality of Life in Patients With Stage II-IV Non-small Cell Lung Cancer and Their Family Caregivers
This clinical trial studies a palliative care intervention in improving symptom control and quality of life in patients with stage II-IV non-small cell lung cancer and their family caregivers. Palliative care programs can provide patients and their caregivers with information on how to manage their symptoms, maintain health and well-being, and access supportive care services. An interdisciplinary palliative care model may effectively link lung cancer patients to the appropriate supportive care services in a timely fashion.
Ask AI to explain this studyKey things to know
This describes the study’s primary purpose.
Plus 1 other study approaches.
These are broad labels—not an eligibility decision.
Checked against the public recordLast updated Oct 2, 2026 · Source: ClinicalTrials.gov
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Interventional
Locations may change over time.
Study sponsor
What this study is about
- Purpose
- Supportive Care
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- City of Hope Medical Center
- Interventions being studied
- Other: Palliative Therapy; Other: quality-of-life assessment; Other: questionnaire administration
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.
- Patient eligibility criteria for entry into the project include:
- Diagnosis of stages II-IV non-small cell lung cancer (NSCLC)
- Undergoing treatment with surgery, chemotherapy, radiation, or combined modalities
- In Phase 2, subjects are also required on accrual to be referred to Palliative Care FCG eligibility criteria include:
- Designated by the patient as a person closely involved in their care
- Age 18 years and older All subjects must have the ability to understand and the willingness to sign a written informed consent
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- City of Hope Medical CenterDuarte, California
- Southern California Permanente Medical GroupIrvine, California
- Kaiser Permanente-Ontario Vineyard Medical Offices and Ambulatory SurgiCenterOntario, California
- Kaiser Permanente Department of Research and EvaluationPasadena, California
- Kaiser Permanente Medical CenterRiverside, California
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 2, 2026. Always confirm current availability with the study team.