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临床试验/NCT03202056
NCT03202056Unknown不适用

Effects of Dry Needling Technique in Hip Muscles in Subjects With Grade I-III Hip Osteoarthritis

Universidad de Zaragoza1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2018年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
45
试验地点
1
主要终点
Intensity symptoms

研究概览

简要总结

Dry needling is a new treatment technique, addressed to mechanical pain of the neuromusculoskeletal system. Recent investigations has developed new hypothesis about the etiology of the osteoarthritis and could be in relation to musculoskeletal disorders, but there is no published studies evaluating the results of this technique in hip osteoarthritis patients.

The objective of this trial is to evaluate if dry needling is more effective in symptoms, function, range of motion, strength, muscular length, pain threshold and compared to sham dry needling and control.

For this purpose the investigators conduct a randomized controlled trial double-blind (patient and examiner). The investigators included patients diagnosed of hip osteoarthritis Grade I-III by Scale of Kellgren and Lawrence.

Patients included are randomized into 3 groups one receive Dry needling, other sham dry needling and the other is a control. Groups receive 3 treatment sessions.

The variables are measured at the beginning and end of treatment. And also some variables are measured before and after each session. Patients who participated in sham dry needling or control group, when the intervention finish the investigators will be given the opportunity to receive the actual 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 (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • •Diagnosed medically with a X-Ray test
  • •American College of Rheumatology Criteria

排除标准

  • •Secondary osteoarthritis by a traumatism, Paget disease, inflammatory or metabolic disease, congenital diseases etc.
  • •Vascular or neurological disease.
  • •Musculoskeletal pathologies in lumbar spine, pelvis or lower limbs
  • •Grade IV in Kellgren and Laurence Scale
  • •Fear of needles

研究组 & 干预措施

Sham Dry needling

Sham Comparator

Sham Dry needling technique in each active myofascial trigger point once per week for 3 weeks.

干预措施: Sham Dry needling (Other)

Control

No Intervention

Control group. No intervention.

Dry needling

Experimental

Dry needling technique in each active myofascial trigger point once per week for 3 weeks.

干预措施: Dry needling (Other)

结局指标

主要结局

Intensity symptoms

时间窗: through study completion, an average 21 days

The investigators measure the intensity of with a visual analogic scale at the end of the intervention (3 weeks after baseline the investigators measure the intensity of symptoms through study completion, an average 21 days)

Functional Capacity with functional tests

时间窗: through study completion, an average 21 days

The investigator measure the functional capacity with functional test: "Test Up and Go" (TUG test), "20 and 40 meters self-placed" and "30 seconds-chair and stand" at the end of the intervention (through study completion, an average 21 days).

Functional Capacity with functional tests

时间窗: Baseline

The investigators measure the functional capacity with functional test: "test Up and Go" (TUG), "20 and 40 meters self-placed" and "30 seconds-chair stand" at baseline

Intensity symptoms

时间窗: Baseline

The investigators measure the intensity of with a visual analogic scale pre-intervention at baseline

次要结局

  • Hip Range of motion(through study completion, an average 21 days)
  • Anxiety and depression with a validated questionnaire (HADS)(through study completion, an average 21 days)
  • Gait in treadmill(through study completion)
  • Muscular strength(through study completion, an average 21 days)
  • Muscular length(through study completion, an average 21 days)
  • Pain threshold(through study completion, an average 21 days)
  • Functional capacity with a validated questionnaire (WOMAC)(through study completion, an average 21 days)
  • Hip Range of motion(Baseline)
  • Muscular strength(Baseline)
  • Muscular length(Baseline)
  • Pain threshold(Baseline)
  • Anxiety and depression with a validated questionnaire (HADS)(Baseline)
  • Functional capacity with a validated questionnaire (WOMAC)(Baseline)
  • Gait in treadmill(Baseline)

研究者

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

Luis Ceballos Laita

Principal Investigator

Universidad de Zaragoza

研究点 (1)

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