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临床试验/NCT05331430
NCT05331430已完成不适用

Effectiveness of Dry Needling and Stretching on Joint Range and Myofascial Pain at the Cervical Level in People With Fibromyalgia.

Universidad de Murcia2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年5月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Goniometer measurement

研究概览

简要总结

Effectiveness of dry needling and stretching on joint range and myofascial pain at the cervical level in people with fibromyalgia

详细描述

A randomised clinical trial will be conducted in which there will be 3 groups. One control group and 2 experimental groups; one of them will undergo dry needling of the upper trapezius fibres and the other will undergo passive stretching of the upper trapezius fibres. Both groups will have the joint range of cervical lateral tilt, pain measurement by algometer and visual analogue scale (VAS) measured. All these measurements will be taken before and after treatment. The participants of the study will be people who have been diagnosed with fibromyalgia at least 6 months before the start of the study, who are members of the FIBROFAMUR association. Association of Fibromyalgia, Chronic Fatigue, Rheumatic and Musculoskeletal Diseases of Murcia. The data collected will be: socio-demographic data, age, sex, measurement of cervical joint range using a goniometer and measurement of pain using an algometer and visual analogue scale (VAS). As undesirable effects, in exceptional cases, the dry needling technique may produce residual discomfort in the puncture area that may last between 1 and 3 days.

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, Outcomes Assessor)

盲法说明

Masked participants. Masked data analyst

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have a diagnosis of fibromyalgia at least six months before the start of the study.
  • Be of legal age.
  • Report at least one episode of neck pain in the last six months.

排除标准

  • Surgical interventions or scars at cervical level.
  • Dizziness or vertigo.
  • Dermatological problems.
  • Severe psychiatric disorders.

结局指标

主要结局

Goniometer measurement

时间窗: One month

Measurement of the joint range of the contralateral cervical tilt using a goniometer. Measurement of the lateral tilt range in degrees.Values may vary from zero to 45 degrees.

Measurement of pain with an algometer.

时间窗: One month

Measurement of cervical myofascial trigger point pain with an algometer. Measurement of pain in kilograms per square centimetre. Values may vary from zero to 10 kilograms.

Visual analogue scale (VAS)

时间窗: One month

Measurement of the degree of pain using the visual analogue scale. Measured from zero to ten, zero corresponds to no pain and ten corresponds to worst pain imaginable.

次要结局

未报告次要终点

研究者

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

Angel Martínez Carrasco

Clinical Professor PhP

Universidad de Murcia

研究点 (2)

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