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临床试验/NCT03299985
NCT03299985已完成不适用

Effects of Diaphragmatic Myofascial Release in Gastroesophageal Reflux Disease

Cardenal Herrera University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年10月5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
发起方
入组人数
30
试验地点
2
主要终点
GERD symptoms

研究概览

简要总结

This study is a double blinded randomized clinical trial with two arms which aims to study the effects of diaphragmatic myofascial release in patients with gastroesophageal reflux disease (GERD).

GERD has become in the last decades a common disease at the occidental world affecting between 10 to 15% of this population. That implies a high socio-health cost and the decline of the quality of life of those patients.

The diaphragm muscle surrounds the lower esophageal sphincter, and helps to prevent gastroesophageal reflux. If one or both structures become incompetent, it may appear GERD. Until the moment, the treatment for GERD begins by lifestyle modification, and if it fails, the treatment becomes medical and, in selected cases, surgical.

It exists some studies that have demonstrate that diaphragmatic breathing training can have a positive effect in GERD and the need of drug usage. But until the moment, the effects of a myofascial release of the diaphragm haven't been explored on these patients.

Thirty patients with GERD referred from different hospitals of Valencia will be randomized into two groups:

  • Intervention with myofascial release for the diaphragm
  • Sham treatment group which is going to receive the same number of session treatments with the same manual techniques, but without the myofascial stimulus The protocol that will be applied consists of 4 identical sessions of myofascial release techniques aimed to normalize the myofascial tension of the diaphragmatic muscle. These sessions will be distributed in two weeks.

The study focuses on the analysis of the following variables:

  • Frequency and intensity of the symptoms of GERD: Reflux Disease Questionnaire (RDQ)
  • Specific quality of life for gastrointestinal disease: Gastrointestinal Quality of life Index (GIQLI)
  • Drug usage: weekly milligrams usage of proton pomp inhibitors (PPI) The results of these pre-intervention and post-intervention variables will be compared between the two groups at baseline (first session), at week 3 and at week 6.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with the diagnostic of GERD

排除标准

  • hiatal hernia >2 cm
  • previous operation at the LES
  • actual erosive esophagitis
  • Congenital or acquired immune disorders.
  • Allergic status of any kind.
  • Systemic diseases (rheumatic, infectious conditions, febrile state, vascular alterations, endocrine including diabetes, metabolic and neoplastic).
  • Leukemia.
  • Severe psychiatric disorders.
  • Neuromuscular or neurological injuries.
  • Aneurysms.
  • Abdominal or spine surgery.
  • Vertebral fractures.
  • Osteoporosis (advanced stage).
  • Acute lesions of soft tissues or in an inflammatory state.
  • Open wounds.
  • Pregnancy.
  • Intrauterine device.
  • Patients with corticosteroid therapy.
  • Hemophilia or treatment with anticoagulant therapy.
  • Hypersensitivity of the skin or dermatological diseases in the trunk that impossibilities the application of the techniques.
  • Rejection of manual contact.
  • Non-Spanish speaking patients.
  • Patients who have previously received some treatment of myofascial release.

研究组 & 干预措施

Diaphragmatic myofascial release

Experimental

Subjects in this arm will receive different myofascial release techniques aimed to normalize the myofascial tension of the diaphragmatic muscle

干预措施: Diaphragmatic myofascial release (Other)

Sham myofascial release

Sham Comparator

Subjects in this arm will receive the same manual techniques of the diaphragmatic myofascial release group, but without the myofascial stimulus

干预措施: Sham myofascial release (Other)

结局指标

主要结局

GERD symptoms

时间窗: 6 weeks

Frequency and intensity of GERD symptoms measured by the Reflux Disease questionnaire (RDQ)

次要结局

  • Drug Usage(6 weeks)
  • Specific quality of life for gastrointestinal disease(6 weeks)

研究者

发起方
Cardenal Herrera University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Juan F. Lisón Párraga, Dr

Head of medicine department

Cardenal Herrera University

研究点 (2)

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