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临床试验/NCT06472856
NCT06472856已完成不适用

Vasomotor Symptom Alleviation Through Acupuncture in Patients With Prostate Cancer

University College Cork1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2024年8月30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
入组人数
12
试验地点
1
主要终点
Feasibility of the intervention

研究概览

简要总结

A pilot study to assess the acceptability and efficacy of acupuncture in alleviating vasomotor symptoms (hot flushes and night sweats) in Irish patients with prostate cancer receiving androgen deprivation therapy.

研究设计

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

入排标准

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

入选标准

  • All participants must have a histologically confirmed diagnosis of prostate cancer and currently be treated with androgen deprivation therapy with or without additional prostate cancer therapies.
  • Patients under the care of a Medical Oncologist in either Bons Secours Hospital or Cork University Hospital
  • All participants must be experiencing moderate to severe vasomotor symptoms as defined by a score of 4 or more on the Hot Flash Index.

排除标准

  • Patients under
  • Patients with HFI scores below
  • Patients not currently being treated with androgen deprivation therapy.
  • Patients with contraindications to acupuncture.
  • Patients already receiving acupuncture for vasomotor symptoms.
  • Patients unwilling to participate in the study.

研究组 & 干预措施

Acupuncture

Experimental

干预措施: Acupuncture (Procedure)

结局指标

主要结局

Feasibility of the intervention

时间窗: Completed after 6 weeks of acupuncture sessions and repeated 3 months after acupuncture has finished

Specially designed questionnaire

次要结局

  • Changes in symptom interference scores(Completed after 6 weeks of acupuncture sessions and repeated 3 months after acupuncture has finished)
  • Changes in sleep quality(Completed after 6 weeks of acupuncture sessions and repeated 3 months after acupuncture has finished)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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