跳至主要内容
临床试验/NCT03516799
NCT03516799已完成不适用

A Pilot Study of Acupuncture for Pain Management for AYA With Cancer

Children's Hospital of Philadelphia2 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2018年8月13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
55
试验地点
2
主要终点
Acceptability of use of Acupuncture for pain management of AYA and associates

研究概览

简要总结

The aim of the study is to innovatively extend acupuncture research in adult oncology to adolescents and young adults (AYA) by piloting a tailored acupuncture protocol for pain management in AYA in the Children's Hospital of Philadelphia (CHOP's) Center for Integrative Health.

详细描述

Acupuncture is an integrative medicine (IM) with a growing evidence base that is often incorporated into comprehensive pain management in adult oncology. However, it is under-utilized and under-researched in pediatric oncology, especially with adolescents and young adults (AYA). Acupuncture is a promising palliative therapy to manage pain and improve quality of life (QOL) of AYA. AYA are underserved and typically endure more morbidity and longer treatments than younger patients. More than half report at least three debilitating cancer-related symptoms and their QOL is significantly lower compared to norms, with symptoms being the greatest contributor to poor QOL. Not surprisingly, AYA identify pain management as an unmet need, leading a majority of AYA to want information on IM or seek it for treatment. Given the potential benefit of acupuncture for addressing unmet needs of AYA by reducing physical suffering, and the established difficulty with pain management using conventional methods, there is a critical need to establish the efficacy of acupuncture for pain management in AYA. The few studies that have evaluated acupuncture in pediatric oncology, demonstrating it to be safe, accepted, and associated with symptom relief are uncontrolled, retrospective, and/or unprotocolized, and none focus on AYA. To establish the evidence base for acupuncture in AYA oncology, research is needed to determine and test optimal acupuncture protocols.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
13 Years 至 24 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Report a pain severity score of ≥ 4 in last 7 days on an 11-point (0-10) numerical rating scale and reports a pain distress score of ≥ 2 on a 5-point numerical rating scale
  • Males or females age 13 to 24 years
  • On treatment for cancer for at least one month or within two years of completing treatment
  • Not expected to be terminal within the next 6 months
  • Absence of infection or bleeding disorder
  • Physically and medically able to get to the acupuncture clinic
  • Able to read and write English

排除标准

  • Absence of inclusion criteria above
  • Parents'guardians or subjects who, in the opinion of the investigator, may be non-compliant with the study schedules or procedures
  • Cognitive impairments that would limit AYA's ability to complete measures or to independently care for health as determined by medical team
  • Parent/Guardian Inclusion Criteria:
  • Be primary parent/guardian of the AYA participant
  • Be able to read and write English
  • Parent/Guardian Exclusion Criteria:
  • Cognitive impairments that would limit the parent/guardian's ability to complete measures
  • Absence of inclusion criteria above

结局指标

主要结局

Acceptability of use of Acupuncture for pain management of AYA and associates

时间窗: 15 weeks

Number of participants who report satisfaction and intention for future use through a qualitative semi-structured interview. ("How satisfied were you with the number of acupuncture sessions you received over the course of the study?"...."how likely would you be to continue to receive acupuncture in the future?")

Incidence of patient-reported adverse events of AYA who opt in to acupuncture relative to those who opt out

时间窗: 15 weeks

Limited report of acupuncture-related side effects which will be logged as patient reported outcomes ("did you experience any adverse events?") post-acupuncture sessions. Treatment-Related Adverse Events as Assessed by CTCAE v4.0, change from baseline in pain scores.

Number of acupuncture sessions completed

时间窗: 15 weeks

Number of sessions participants complete and time between sessions, which will be logged by research team for feasibility.

Number of participant-reported barriers to participating in acupuncture sessions for AYA who opt in

时间窗: 15 weeks

Number of participants who report barriers to participation during qualitative semi-structured interview for feasibility. ("How difficult or inconvenient did you find going to your acupuncture appointment over the course of these past 10 weeks to be?")

次要结局

  • Acupuncture as a pain management tool(15 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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