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临床试验/NCT02835937
NCT02835937已完成不适用

Red Blood Cell Transfusion in the Ambulatory Setting: Impact on Home Functional Status

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2016年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
20
试验地点
1
主要终点
Percent Change in Average Daily Physical Activity

研究概览

简要总结

Do ambulatory RBC transfusions improve home functional status?

详细描述

Background: Red blood cell (RBC) transfusion is frequently employed in both ambulatory and hospital environments with the aim of improving patient functional status. The efficacy of this 10.5 billion dollar per year practice however has been increasingly called into question. The Investigators propose to directly measure the impact of outpatient RBC transfusions on at-home functional status by recording several physiological parameters and quantifiable physical activity metrics, e.g. daily energy expenditure and daily total step count, using the ActiGraph wGT3X-BT. This device is an accelerometer-based wearable similar in size to a small watch and is worn at the waist. Study participants will wear the device during the course of their daily activities giving the investigators quantifiable insight into activity levels in the home environment.

Methods/Design: This will be a randomized crossover pilot clinical trial with participant study duration of 28 days. The crossover nature allows each patient to serve as his/her own control. Details of the study design are provided in the text. Briefly, patients presenting at Mayo Clinic Scottsdale's Ambulatory Infusion Center (AIC) will be randomized to one of two arms: 1) receive an RBC transfusion as scheduled (transfuse), or 2) abstain from the scheduled transfusion (no-transfuse). After an appropriate washout period, patients will cross from the transfuse arm to the no-transfuse arm or vice-versa. Activity levels will be recorded continuously throughout the study with no need for intervention by the patient. In addition to device data, survey data will be collected via a weekly telephone interview. The primary outcome measures will include both technical performance metrics such as daily energy expenditure as well as practical performance metrics such as changes in step count. A variety of secondary outcome measures include daily sedentary time and PROMIS Global 10 scores.

Discussion: This trial will directly assess the impact of red blood cell transfusion on patient functional status in the location most important - the home. Patient recruitment will begin in August 2016 and is due to be completed in August 2017.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

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

  • •Age > 18 years
  • •At least on prior encounter in the AIC
  • •Planned RBC transfusion

排除标准

  • •Refusal to provide informed consent
  • •Refusal by the health care team
  • •Acute ischemia (e.g. MI, CVA)
  • •Hemoglobin < 7.0 g/dL
  • •Active bleeding
  • •Symptomatic anemia (hypotension, tachycardia, angina, syncope/pre-syncope believed related to anemia
  • •Non-ambulatory functional status
  • •Established or Uncertain Pregnancy Status

研究组 & 干预措施

Transfuse

No Intervention

Patients will receive a transfusion under standard care

No-Transfuse

Experimental

Patients will not receive a transfusion

干预措施: No-Transfuse (Other)

结局指标

主要结局

Percent Change in Average Daily Physical Activity

时间窗: Baseline to 7 Days

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Daryl J. Kor, M.D.

Prinicipal Investigator

Mayo Clinic

研究点 (1)

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