跳至主要内容
临床试验/NCT06322615
NCT06322615已完成不适用

Acupressure for Anxiety: A Pilot Study of a Nurse-Led Acupressure Intervention for Patients Receiving Chemotherapy

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年8月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
30
试验地点
2
主要终点
Time taken for each nurse-led acupressure intervention in the chemotherapy unit (Feasibility)

研究概览

简要总结

This clinical trial evaluates whether acupressure is helpful to reduce anxiety related to chemotherapy. Anxiety is experienced by many patients with cancer. Anxiety can be related to chemotherapy and may contribute to other symptoms, such as nausea and poor quality of life. Some patients diagnosed with cancer express interest in non-medicinal ways to manage symptoms. Acupressure is a noninvasive intervention that can be used for many different symptoms. Acupressure is well tolerated with minimal reports of adverse reactions, making it a good choice for patients with cancer. This study may help researchers learn whether acupressure is useful for managing anxiety in patients undergoing chemotherapy.

详细描述

PRIMARY OBJECTIVES:

I. Evaluate the feasibility of a nurse- and patient-applied acupressure intervention for patients with anxiety associated with active cancer-directed therapy.

II. Patient-reported changes in acute anxiety associated with both the nurse and self-led acupressure interventions will be ascertained.

OUTLINE:

Patients undergo acupressure over 15-120 seconds at a time for up to 15 minutes. After completion of the session, patients may optionally receive an education session on using acupressure at home.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

入选标准

  • Be over 18 years of age
  • Be actively undergoing chemotherapy in the Mayo Clinic chemotherapy unit
  • Report anxiety as a 1 or higher, on a scale from 0 (no anxiety) to 4 (severe anxiety)
  • Be willing to undergo a short acupressure session

排除标准

  • Does not meet the inclusion criteria

结局指标

主要结局

Time taken for each nurse-led acupressure intervention in the chemotherapy unit (Feasibility)

时间窗: Up to 1 year

Assess by the time recorded for ach nurse-led acupressure intervention in the chemotherapy unit.

Number of patients approached about undergoing acupressure intervention (Feasibility)

时间窗: Up to 1 year

Assessed by the number of patients approached about undergoing acupressure intervention.

Patient-reported changes in acute anxiety

时间窗: At baseline, after a one-time nurse-administered acupressure session, and after one week of self-administered acupressure sessions

Assessed with a brief anxiety questionnaire that inquires about the three different domains of anxiety: cognitive symptoms, emotional symptoms, and physical symptoms. Seven questions are answered using 11-point (0-10) scales with different values assigned to the scale per question (e.g. 0=no anxiety/10=worst possible anxiety or 0=strongly disagree/10=strongly agree).

Number of patients interested in the initial acupressure intervention in the chemotherapy unit (Feasibility)

时间窗: Up to 1 year

Assessed by the number of patients who express interest in the initial acupressure intervention in the chemotherapy unit.

Number of patients interested in the home acupressure intervention (Feasibility)

时间窗: Up to 1 year

Assessed by the number of patients who express interest in the home acupressure intervention.

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
Sponsor

研究点 (2)

Loading locations...

相似试验