跳至主要内容
临床试验/NCT03516942
NCT03516942
进行中(未招募)
不适用

Longitudinal Assessment of Financial Burden in Patients With Colon or Rectal Cancer Treated With Curative Intent

ECOG-ACRIN Cancer Research Group1278 个研究点 分布在 1 个国家目标入组 565 人2018年6月11日

概览

阶段
不适用
干预措施
Questionnaire Administration
疾病 / 适应症
Stage I Colon Cancer AJCC v8
发起方
ECOG-ACRIN Cancer Research Group
入组人数
565
试验地点
1278
主要终点
Comprehensive Score for Financial Toxicity (COST)
状态
进行中(未招募)
最后更新
11天前

概览

简要总结

This research trial studies the financial burden in patients with stage I-III colon or rectal cancer who are undergoing treatment. Collecting data from patients about their cost and quality of life may help doctors to better understand the impact of cancer treatment on a patient?s employment and finances.

详细描述

PRIMARY OBJECTIVES: I. Evaluate the change in level of self-reported financial burden from baseline (within 60 days of diagnosis) to 12 months after diagnosis of colon or rectal cancer treated with curative-intent. SECONDARY OBJECTVIES: I. Evaluate reported access and utilization of financial services (i.e. financial counselor, navigator, social workers) and its association to financial burden in the first 12 months after diagnosis of colon or rectal cancer treated with curative-intent. II. Evaluate the change in level of self-reported financial burden and employment limitations from baseline (within 60 days of diagnosis) to 3, 6, and 12 months after diagnosis of colon or rectal cancer treated with curative-intent. III. Evaluate long term outcomes at 24 months after diagnosis including financial burden, employment limitations and adherence to clinical follow-up guidelines. IV. Evaluate the change of quality-of-life outcome (QoL) from baseline to 12 months and its association with predictors. V. Evaluate the change in level of self-reported financial burden from baseline to 12 months using alternate measures of financial burden (i.e. impact of cost questions and single item from European Organization for Research and Treatment of Cancer \[EORTC\] questionnaire \[Q\]30). OUTLINE: Patients complete questionnaires over 20-60 minutes at baseline and at 3, 6, 12, and 24 months after cancer diagnosis.

注册库
clinicaltrials.gov
开始日期
2018年6月11日
结束日期
2028年9月1日
最后更新
11天前
研究类型
Observational
性别
All

研究者

发起方
ECOG-ACRIN Cancer Research Group
责任方
Sponsor

入排标准

入选标准

  • Patients must have a life expectancy of \>= 24 months
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-3
  • Patients must have a newly diagnosed colon or rectal cancer (initial diagnosis, either a biopsy or curative surgery, whichever is most recent) within 60 days of registration and have not yet received radiation or chemotherapy
  • Patients must have stage I, II, or III disease at the time of enrollment and will be treated with curative-intent; this can be defined either clinically or pathologically if they have already undergone surgery; for staging of both colon and rectal cancer, the definition of stage I-III is based on the seventh edition (2010) or an updated version of the tumor, node, metastasis (TNM) staging system
  • Patients are not eligible if they are already enrolled on a treatment clinical trial at the time of registration; they can remain on the study if they subsequently enroll on a treatment clinical trial during the study time period
  • Patients who choose to not receive radiation and/or chemotherapy after a curative-intent surgery are eligible to participate
  • Patients with a history of previous malignancy (except non-melanoma skin or cervical in-situ cancer) treated (with either surgery, chemotherapy, and/or radiation) within the last 3 years are not eligible
  • Patients must be able to complete questionnaires in English
  • Patients must sign and give written informed consent in accordance with institutional and federal guidelines

排除标准

  • 未提供

研究组 & 干预措施

Observational (questionnaire)

Patients complete questionnaires over 20-60 minutes at baseline and at 3, 6, 12, and 24 months after cancer diagnosis.

干预措施: Questionnaire Administration

Observational (questionnaire)

Patients complete questionnaires over 20-60 minutes at baseline and at 3, 6, 12, and 24 months after cancer diagnosis.

干预措施: Quality-of-Life Assessment

结局指标

主要结局

Comprehensive Score for Financial Toxicity (COST)

时间窗: Baseline and 12 months after cancer diagnosis

The Comprehensive Score for Financial Toxicity (COST) COST is an 11-item patient-reported outcome (PRO) of financial hardship that uses a 7-day time window and 5-point Likert response scale (ranging from 0, indicating not at all, to 4, very much). Higher COST scores (range, 0-44) represent better financial well-being. The primary objective is to evaluate the change in the level of self-reported financial burden from baseline (within 60 days of diagnosis) to 12 months from study registration. (12 mo - baseline)

次要结局

  • Reported Access and Utilization of Financial Services(Up to 12 months)
  • Change in Level of Self-reported Employment Limitations(Baseline, 6, 12, and 24 months after cancer diagnosis)
  • Level of Self-reported Employment Limitations (Dichotomized)(Baseline, 6, 12, and 24 months after cancer diagnosis)
  • Long Term Outcomes After Diagnosis for Adherence(At 24 months)
  • Long Term Outcomes After Diagnosis for Financial Burden(At 24 months)
  • Long Term Outcomes After Diagnosis for Employment Limitations(At 24 months)
  • Change of Quality-of-life (QoL) Outcome(Baseline up to 12 months)
  • Changes Self-reported Financial Burden Between Baseline and 12 Month [EORTC](Baseline and12 months)

研究点 (1278)

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