A Pilot Study to Assess Feasibility and Explore Variability in Biomarkers and Patient Reported Outcome Measures in Patients Undergoing Induction Chemotherapy for Acute Myeloid Leukemia
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- Completion rate
研究概览
简要总结
This research study is being conducted to help understand how the symptoms during treatment for acute myeloid leukemia (AML) may be affected by metabolism and how best to study this association. Symptoms include experiences like fatigue, sleep disturbance, pain, and depression.
详细描述
This is a prospective, longitudinal, observational exploratory study. Ten participants will be enrolled and will complete baseline and week 4 blood sample collections. Symptom questionnaires will be completed at baseline, 1-, 2-, 3- and 4-weeks.
This research study is a Pilot Study, which means it is the first time that researchers are studying the associations between symptoms and metabolism in this way.
The National Institute of Nursing Research is supporting this research study by providing funding for the research study.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 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
- •The Cantor Center CRC will attend weekly protocol meetings in the DFCI adult leukemia center to identify eligible patients and will confirm eligibility by reviewing the electronic health record and, if needed, contacting the treating physician. Subjects enrolled in clinical trials or other studies requiring extra blood samples and/or completion of questionnaires will be discussed with their oncology care team and/or investigators of the other study teams to ensure avoidance of excess subject burden. Only subjects deemed appropriate for enrollment without adding excess burden will be approached about this study.
- •Inclusion Criteria:
- •Adult (18+ years old)
- •New diagnosis of acute myeloid leukemia (AML)
- •Admitted to the DFCI Inpatient Hospital in the BWH for intensive induction chemotherapy (e.g., 7+3 regimen)
- •Eastern Cooperative Oncology Group Scale of Performance Status (ECOG PS) ≤ 3 OR Karnofsky Performance Status (KPS) ≥ 50
- •Ability to comprehend and speak English
- •Ability to provide informed consent
排除标准
- •Cognitive or psychiatric conditions prohibiting study consent or participation
- •Multiple primary cancers
- •A treating clinician reports that the subject is inappropriate for the study or that the study presents excess subject burden
结局指标
主要结局
Completion rate
时间窗: 30 Days
Evaluate the feasibility of conducting this type of study on an in-patient oncology unit (i.e., \>70% of enrolled participants will complete 30-day outcome assessments). Using descriptive statistics, feasibility will be calculated as the percent of eligible participants who enroll in the study and among those who enroll, the percent who complete the study. Using a 90%-exact binomial confidence interval estimate, 8 out of 10 participants completing the 30-day study will be considered acceptable for feasibility
次要结局
- Enrollment rate(30 Days)
研究者
Marilyn Hammer, PhD
Principal Investigator
Dana-Farber Cancer Institute