跳至主要内容
临床试验/NCT04678947
NCT04678947终止不适用

The BARF Project: A Pilot Study Using the BARF Scale to Assess CINV in Children

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2021年3月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
6
试验地点
1
主要终点
Doses of anti-emetic medication administered during inpatient chemotherapy admissions

研究概览

简要总结

In this pilot study, the Baxter Retching Faces (BARF) Scale will be used to assess chemotherapy induced nausea and vomiting (CINV) in the pediatric cancer population during chemotherapy admissions, and the corresponding administration of anti-emetic medications will be reviewed.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
4 Years 至 12 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Patients diagnosed with cancer of any kind.
  • •Patients receiving inpatient chemotherapy at SLCH on the general pediatric oncology service
  • •Patients admitted for a course of inpatient chemotherapy scheduled to last at least 24 hours and but no more than 7 days.
  • •Patients who have received any prior cancer treatment, including radiation therapy, and/or surgery.
  • •Patients ages 4 to 12 years of age.
  • •Patient with a guardian who has the ability to understand English and the willingness to sign an IRB approved written informed consent document.

排除标准

  • •Any patient who is not undergoing inpatient chemotherapy on the general pediatric oncology service, including patients undergoing chemotherapy as conditioning for hematopoietic stem cell transplantation or other cellular therapy.
  • •Any patient who is receiving their first cycle of inpatient chemotherapy (however, they can be included during a future cycle).
  • •Any patient who is blind or unable to communicate by speaking or pointing.

研究组 & 干预措施

BARF scale

Experimental
  • Nursing staff (which may include patient technicians and nursing assistants) will use the scale to assess the patient's nausea for the entire duration of the admission. These assessments will take place in conjunction with vital sign monitoring, every 4 hours. The associated script will be read while the laminated scale is shown to the patient.
  • The nurse will then log the patient's response in the patient's electronic medical record

干预措施: Baxter Retching Faces (BARF) scale (Behavioral)

No intervention

No Intervention

-Patients in the control group will proceed with their inpatient chemotherapy admissions without any interventions. These admissions will take place prior to the admissions of the experimental group, so as not to bias providers.

结局指标

主要结局

Doses of anti-emetic medication administered during inpatient chemotherapy admissions

时间窗: 24 hours - 7 days (estimated)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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