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临床试验/NCT05965206
NCT05965206已完成不适用

Implementation of a Pharmacist-Based, Post-Chemotherapy Follow-up Clinic

Cedars-Sinai Medical Center1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年7月20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
40
试验地点
1
主要终点
Hospital admission related to chemotherapy within 30-day post treatment

研究概览

简要总结

The purpose of this study is to determine the impact of pharmacists on reducing chemotherapy-related side effects by providing education before and after patients receive intravenous chemotherapy at one of Cedars-Sinai outpatient infusion centers.

Participants will be interviewed via telephone within 7 business days after receiving intravenous chemotherapy from the outpatient cancer center infusion clinic.

详细描述

The study involves participation at a single timepoint only.

Participants who consented to participate and are considered eligible will be interviewed by a pharmacist via phone at approximately 7 business days after receiving intravenous chemotherapy infusion. Phone call will be made between the hours of 9am - 6pm on Monday - Saturday. Calls are anticipated to last between 15 to 20 minutes. Participants will be asked if they have experienced any adverse events since the infusion, whether or not they have had any barriers taking supportive care medications, and if the patient understands how to manage potential adverse events. If applicable, participants will be provided further education on optimizing adverse events, guided on proper medication administration times, and will be provided with non-pharmacological clinical pearls to minimize chemotherapy-related side effects and optimize supportive care management.

If unable to reach the participant or caregiver after three attempts, the participant will be considered ineligible. Participants can decline participation at any time during the phone call.

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

入选标准

  • At least 18 years old
  • Diagnosed with cancer and is receiving treatment with intravenous chemotherapy
  • Treatment initiated at Cedars-Sinai Cancer Samuel Oschin Cancer Center (SOCC) or Cedars-Sinai Cancer Beverly Hills (CSCBH)
  • English-speaking or lives with English-speaking person
  • Access to a working phone

排除标准

  • Received follow-up calls through other specialty pharmacy program
  • History of infusion related reactions
  • Declined participation on follow-up interview
  • Age less than 18 years old
  • Non-English speaking
  • Electronic health record flagged for research opt out

结局指标

主要结局

Hospital admission related to chemotherapy within 30-day post treatment

时间窗: 30 days after receiving the first intravenous chemotherapy

Number of hospital admission related to chemotherapy

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Suwicha Limvorasak

PharmD

Cedars-Sinai Medical Center

研究点 (1)

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