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临床试验/NCT05379140
NCT05379140Unknown不适用

Using Therapeutic Chinese Massage to Treat Peripheral Neuropathy in People With Human Immunodeficiency Virus: A Randomized Control Trial Pilot Study.

University of Houston Downtown2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2021年9月10日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
24
试验地点
2
主要终点
Feasibility of this study design

研究概览

简要总结

Background: Peripheral neuropathy (PN) occurs in half of the people with human immunodeficiency virus (PHIV). Currently, there is no Food and Drug Administration-approved treatment for HIV-related PN. Only half of PHIV who take medications report a significant reduction in pain. Therapeutic Chinese Massage, structured palpations or movements of soft tissues of the body, is a promising non-harmful, and non-costly intervention that can potentially alleviate or even treat PN but relevant research is limited.

Method: Investigators conducted a single centered, two-arm, single-blinded randomized controlled trial pilot study to examine if a series of three weekly 25-minute therapeutic Chinese massage sessions by a therapist of therapeutic Chinese massage, compared with placebo massage, could reduce PN-related pain and improve lower extremity functioning in PHIV. Twenty PHIV were recruited from the AIDS Foundation Houston, Inc in Texas. Pain, lower extremity functioning, and health-related quality of life were assessed for both groups prior to and post-massage.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

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

  • Clinical diagnosis of HIV and peripheral neuropathy have self-reported PN-related pain in lower extremity are not taking any kind of medications to alleviate PN symptoms age at least 18 years old not pregnant or lactating

排除标准

  • have received any kind of massage in the past three months Can not give informed consent

结局指标

主要结局

Feasibility of this study design

时间窗: through study completion, an average of one year

recruitment and completion rates, patient safety, and treatment adherence and compliance

次要结局

  • Change in Peripheral neuropathy related pain at the third visit(Through study completion, an average of one year)
  • Change in health related quality of life at the third visit(Through study completion, an average of one year)
  • Change in lower extremity functioning at the third visit(Through study completion, an average of one year)

研究者

发起方
University of Houston Downtown
申办方类型
Other
责任方
Principal Investigator
主要研究者

Song Ge

Assistant Professor

University of Houston Downtown

研究点 (2)

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