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临床试验/NCT02528539
NCT02528539已完成不适用

Prevention of Secondary Lymphedema by Utilizing Self-management Education in Conjunction With Acupuncture Among Breast Cancer Patients Who Are at High Risk of Developing Lymphedema

Huntington Memorial Hospital2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2013年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
2
主要终点
Arm circumference measurements of the upper limbs using at 4 cm interval

研究概览

简要总结

Introduction: Breast cancer women who are treated with axillary node dissection are at increased risk for lymphedema - the lifetime risk in these women is estimated at 15-50% and the risk can significantly increase with chemotherapy and radiation therapy

Objectives:

  1. To evaluate the feasibility and effectiveness of implementing the integrative therapy program (ITP) intervention. ITP consists of self-management education in conjunction with acupuncture.
  2. To determine if ITP affects quality of life, self-efficacy, lymphedema knowledge, pain, and early detection and management of lymphedema.

Design: the exploratory study aims to evaluate the feasibility and benefits of the integrative therapy program (ITP) intervention post-operatively for 18 months.

Subjects: Women with breast cancer treated with axillary node dissection with normal baseline pre-operative bioimpedance (L-dex U400) score.

Sample size: 30 subjects

详细描述

Recruitment and Intervention:

The study participants are recruited by their breast surgeon after they undergo axillary node dissection surgery. 4-6 weeks following surgery, the participants will receive a combination of acupuncture and self management education .

Contents of self-management education include:

  1. Lymphedema knowledge: functions of the lymphatic system, anatomy of the lymph nodes and direction of the lymphatic drainage, risk factors that could precipitate lymphedema, the signs and symptoms of lymphedema and infection, and lymphedema resources.
  2. Selfcare techniques:healthy diet (eating whole food encouraged), neck, shoulder and chest wall stretching exercises, walk daily, self-manual lymphatic drainage with deep breathing techniques, and self-acupressure over eighteen months following their surgery.

Outcome measurements include: L-Dex U400 measurement, arm circumference, pain scale, self-efficacy, and lymphedema knowledge, and Functional Assessment of Cancer Therapy-Breast FACT-B.

研究设计

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

入排标准

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

入选标准

  • Subjects must be able to read and understand the informed consent form and have the capacity to give consent.
  • Adults age 18 and older
  • Subject with a newly diagnosed stage I-III breast cancer with a documented pre-operative baseline L-Dex U400 who underwent axillary lymph node dissection within 4-6 weeks prior to enrollment.
  • Subjects must be able to return to the study site for the duration of the study (18 months).

排除标准

  • Subjects who do not read or understand the informed consent are ineligible.
  • Subjects who have any contraindications to the affected upper-limb exercises, which include congestive heart failure, cardiac arrhythmia, deep vein thrombosis, infectious disease complications such as cellulitis and lymphangitis.
  • Women with double mastectomy with axillary node dissection bilaterally.
  • Women with a prior history of axillary surgeries in the ipsilateral side and/or primary lymphedema
  • Women with metal implants (e.g. shoulder replacement) or cardiac implants (e.g. automated implanted cardiac defibrillator (AICD) or pacemaker).
  • All subjects with objective or subjective signs and symptoms of lymphedema.
  • Women of childbearing age who are pregnant.

结局指标

主要结局

Arm circumference measurements of the upper limbs using at 4 cm interval

时间窗: 18 months

measure the circumference in centimeters

Bioimpedance (L-dex U400)

时间窗: 18 months

use L-dex machine

次要结局

  • Quality of Life (Functional Assessment of Cancer Therapy-Breast)(18 months)
  • Self-Efficacy Scale(18 months)
  • Lymphedema Knowledge Scale(18 months)
  • Wong-Baker FACES Pain Scale(18 months)

研究者

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

Suzie Kline

PhD, NP, LAc

Huntington Memorial Hospital

研究点 (2)

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