跳至主要内容
临床试验/NCT06567704
NCT06567704招募中不适用

Cancer-related Fatigue During Maintenance Immunotherapy for Non-small Cell Lung Cancer (NSCLC): a Qualitative Study

Wake Forest University Health Sciences4 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年3月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
4
主要终点
Themes from qualitative interviews with patients

研究概览

简要总结

The purpose of this research is to understand cancer related fatigue in patients with non-small cell lung cancer (NSCLC), who are being treated with an immune checkpoint inhibitor.

详细描述

This is an observational pilot study. The target population includes adult patients diagnosed with NSCLC receiving an immune checkpoint inhibitor and reporting concerns of fatigue to their provider. This study will be conducted at Levine Cancer Institute (LCI) and Atrium Health Wake Forest Baptist Comprehensive Cancer Center (AHWFBCCC). This study consists of qualitative interviews at two-time points, the primary, and the follow-up. During the primary interview, patients with NSCLC will be asked to complete the PROMIS® Fatigue-Short Form 7a consisting of seven items. During the follow-up interviews, participants will be asked about any change in their fatigue and views on physical activity.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •≥ 18 years of age at the time of consent.
  • •Must be able to speak, read, and understand English.
  • •Participants diagnosed with NSCLC, and:
  • •have advanced/metastatic disease who are currently receiving immunotherapy monotherapy, or
  • •have locally advanced disease who are currently receiving immunotherapy monotherapy after completing thoracic radiation therapy, or
  • •who underwent resection and are currently receiving immunotherapy monotherapy after completing all other perioperative treatment
  • •Immunotherapy planned to continue for at least three months after the time of study enrollment (to ensure participant remains on IO long enough to obtain study assessments)
  • •Have completed at least two cycles of immunotherapy.
  • •Self-reported cancer-related fatigued that impacts daily function.

排除标准

  • •Participants who have received a dose of chemotherapy (including maintenance pemetrexed) within the past 3 months
  • •Participants who have received radiation therapy within the past 3 months. Note: a short course of palliative radiation therapy within up to 20 Gy and up to 5 fractions is permissible.
  • •Diagnosis of dementia.
  • •Anemia Hgb <10 g/dL.
  • •Sarcopenia which is being pharmacologically treated with a prescribed appetite stimulant (e.g., megestrol).
  • •Untreated hypothyroidism.
  • •Symptomatic heart failure.
  • •Oxygen dependent lung disease.
  • •Cognitively unable to complete interviews per investigator.

研究组 & 干预措施

Non-small cell lung cancer (NSCLC)

Non-small cell lung cancer (NSCLC) patients treated with with immune checkpoint inhibitor.

干预措施: Interviews (Behavioral)

结局指标

主要结局

Themes from qualitative interviews with patients

时间窗: At 3 months

Two semi-structured qualitative interviews will be conducted with 20 patients. Themes will be determined through inductive analysis and will focus on key aspects of symptomatic fatigue, including but not limited to the frequency, duration, and severity of CRF and resulting functional impairments. In addition, history of physical activity before diagnosis, preferences for physical activity to treat CRF, and support needed to adhere to physical activity regimens will be considered. Themes from the first and second interviews will be synthesized to capture changes in fatigue and views on physical activity.

次要结局

  • Severity and impact of cancer-related fatigue (CRF)(At 3 months)
  • Severity and impact of cancer-related fatigue (CRF)(At 3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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