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临床试验/NCT07232056
NCT07232056尚未招募不适用

Geriatric Oncology Assessment to Link With Support for Older Women Taking Adjuvant Aromatase Inhibitor Therapy

Duke University0 个研究点目标入组 452 人开始时间: 2026年10月15日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
452
主要终点
Change in pain severity and interference as measured by the Brief Pain Inventory - Short Form

研究概览

简要总结

Older women (≥65 years) with HR+ non-metastatic breast cancer experience high symptom burden and reduced quality of life during aromatase inhibitor (AI) therapy. This hierarchical 2×2 factorial randomized controlled trial will test two interventions: (1) a clinic-level geriatric oncology assessment and support program (GOAL-AI) and (2) a patient-level CBT-based coping skills training (CST-AI). The study aims to improve pain, symptom burden, and health-related quality of life compared to enhanced usual care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female, age ≥65 years
  • HR+ non-metastatic breast cancer
  • Within 12 months of starting AI therapy
  • English-speaking
  • Able to provide consent

排除标准

  • Age <65 years
  • Metastatic cancer
  • Cognitive impairment preventing consent
  • Receiving care at multiple participating sites

研究组 & 干预措施

GOAL-AI + CST-AI

Experimental

Combination of clinic-level geriatric assessment and CBT-based coping skills training.

干预措施: GOAL-AI (Behavioral)

GOAL-AI + CST-AI

Experimental

Combination of clinic-level geriatric assessment and CBT-based coping skills training.

干预措施: CST-AI (Behavioral)

GOAL-AI alone

Experimental

Clinic-level geriatric assessment and support only.

干预措施: GOAL-AI (Behavioral)

CST-AI alone

Experimental

CBT-based coping skills training only.

干预措施: CST-AI (Behavioral)

Enhanced Usual Care

No Intervention

Standard care with educational materials.

结局指标

主要结局

Change in pain severity and interference as measured by the Brief Pain Inventory - Short Form

时间窗: Baseline, 6 months, 12 months

The Brief Pain Inventory-Short Form (BPI-SF) will be used to assess pain severity and interference from pain across important life domains (e.g., general activity, work, relations with others). To calculate a pain severity score, the BPI-SF averages worst, least, average and current pain severity ratings on a 0 to 10 scale, with higher scores indicating more severe pain. To calculate a pain interference score, 7 items asking about interference from pain across different life domains will be averaged, with higher scores indicating higher pain interference.

次要结局

  • Change in emotional distress, as measured by the PROMIS® Anxiety and Depression 4-item Short Forms(Baseline, 6 months, 12 months)
  • Change in fatigue, as measured by the PROMIS® Fatigue 6-item Short Form(Baseline, 6 months, 12 months)
  • Change in physical function, as measured by the Five Times Sit to Stand Test (5xSST)(Baseline, 6 months, 12 months)

研究者

申办方类型
Other
责任方
Sponsor

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