跳至主要内容
临床试验/NCT04122118
NCT04122118已完成不适用

Pharmacist-led Transitions of Care in the Outpatient Oncology Infusion Center

Thomas Jefferson University2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2019年9月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
26
试验地点
2
主要终点
Number of medical related problem (MRP)s identified by the pharmacist through retrospective chart reviews (Phase I)

研究概览

简要总结

This trial studies how well pharmacist-led transitions of care works in the outpatient oncology infusion center for patients with solid tumor. Having a pharmacist in the outpatient oncology infusion center may help to identify and correct medical related problems and improve overall patient and staff satisfaction. Patients receiving education may benefit from gaining a better understanding of their antineoplastic therapy. Understanding the side effects associated with the therapy may also help patients better be prepared to manage any adverse effects they may experience.

详细描述

PRIMARY OBJECTIVE:

I. To demonstrate the effectiveness of a clinical oncology pharmacist in the outpatient infusion center through education, and the identification and correction of medication related problem (MRP)s.

SECONDARY OBJECTIVE:

I. To evaluate overall patient and staff satisfaction with the added clinical oncology pharmacy education.

EXPLORATORY OBJECTIVE:

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Solid tumor diagnosis
  • Starting day 1 of new antineoplastic infusion
  • English speaking (and/or English-speaking primary caregiver/proxy)

排除标准

  • Metastasis to the brain and/or central nervous system (CNS) with evidence of impaired cognition
  • Severe cognitive impairment including dementia with inability to consent to the study

结局指标

主要结局

Number of medical related problem (MRP)s identified by the pharmacist through retrospective chart reviews (Phase I)

时间窗: Up to 1 year

MRPs will be assigned to a specific category and the total number of MRPs in each category will be recorded. Categories include but are not limited to: incorrect dose, therapeutic duplication, drug not indicated, drug interaction, monitoring recommendation, drug allergy, or potential for adverse event.

Percent of MRPs corrected as a result of the clinical oncology pharmacist services (Phase II)

时间窗: Up to 1 year

In phase 2 (prospective) MRPs will also be recorded and categorized, but in addition the outcomes relating to each MRP pharmacist intervention will be recorded. MRPs found by the pharmacist will be communicated to the patient's oncologist or primary care provider, and the pharmacist will follow-up to see if changes were made.

次要结局

  • Patient and provider satisfaction with the pharmacist-led education(Up to 1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验