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临床试验/NCT03902119
NCT03902119已完成不适用

Effectiveness of a New Tool (INYBI) in Individuals With Chronic Non-specific Neck Pain.

University of Seville2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2019年4月24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
入组人数
58
试验地点
2
主要终点
Pressure pain threshold (PPT) in the evaluated muscles. The PPT levels will be evaluated in Kilograms / cm2

研究概览

简要总结

Objectives: To evaluate the clinical efficacy of using a manual inhibition technique for the suboccipital muscles compared with the use of the so-called INYBI tool in individuals with chronic non-specific neck pain, and the compare the results of using both approaches on pain relief, cervical range of motion neck and vertical maximum mouth opening.

Design: Quantitative, experimental, longitudinal, prospective, and double blinded study.

Subjects: Patients between 18 and 40 years, with chronic non-specific neck pain of at least 3 months of evolution.

Methods: The experimental group will undergo a 5 minutes intervention for the suboccipital muscles using the INYBI tool. The control group will receive a 5 minutes of treatment involving the suboccipital muscles manual inhibition technique.

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 (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical diagnosis of non-specific mechanical neck pain.
  • Pain of more than 3 months of duration.
  • Pain between the occiput and the third dorsal vertebra.
  • Willingness to participate in the treatment and in the follow-up measurements
  • Neck pain reproduced by neck movements or palpation

排除标准

  • Cognitive impairment or inability to communicate.
  • Having received manual therapy in the last two months before recruitment.
  • Having received anti-inflammatory treatment, antidepressants or muscle relaxants in the last 72 hours.
  • Any contraindication to treatment or evaluation procedures.
  • Diagnosis of systemic diseases
  • Diagnosis of fibromyalgia
  • Pregnancy
  • Signs of spinal nerve root compression
  • Previous whiplash
  • Any diagnosed possible cause for their neck pain (infection, cancer, spinal stenosis)

研究组 & 干预措施

INIBY tool

Experimental

Patients will undergo a single treatment session consisting of applying a suboccipital muscle inhibition technique using the so-called INYBI tool. The treatment session will last approximately 5 minutes

干预措施: INYBI tool (Device)

Manual suboccipital inhibition

Active Comparator

Patients will receive a single treatment session consisting of the use of the manual suboccipital muscles inhibition technique.The treatment session will last approximately 5 minutes

干预措施: Manual suboccipital inhibition (Other)

结局指标

主要结局

Pressure pain threshold (PPT) in the evaluated muscles. The PPT levels will be evaluated in Kilograms / cm2

时间窗: From baseline to immediately after treatment.

PPT levels, defined as the minimum necessary pressure to evoke pain will be evaluated using a handheld electronic pressure algometer.

Active cervical range of movement (ROM). The range of movement will be assessed in degrees

时间窗: From baseline to immediately after treatment.

Flexion, extension, left and right side flexion, and left and right rotation will be assessed using a digital inclinometer.

Pain free vertical mouth opening. This outcome will be evaluated in centimeters.

时间窗: From baseline to immediately after treatment.

Maximum pain free vertical mouth opening will be assessed using a digital caliper that will place between the incisors 11, 21, 31 y 41.

Atlas rotation ROM, assessed in degrees

时间窗: From baseline to immediately after treatment.

The atlas bone left and right rotation ROM will be assessed using the flexion-rotation test. For this test, with the participant in supine position, the maximum mobility in head rotation while keeping maximum passive neck flexion will be assessed

Self-reported pain intensity

时间窗: From baseline to immediately after treatment.

Self-perceived pain intensity will be evaluated during all active cervical movements by a 0 to 10 Visual Analogue Scale (VAS), where 0 denotes no pain at all, and 10 denotes the maximum possible pain

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

Alberto Marcos Heredia-Rizo

Assistant Proffesor

University of Seville

研究点 (2)

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