跳至主要内容
临床试验/NCT02333617
NCT02333617终止不适用

Manual Therapy to Treat Gluteus Medius Trigger Points to Improve Hip Abduction Strength in Patients With Anterior Knee Pain.

Mitchell Selhorst2 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2015年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
3
试验地点
2
主要终点
Change in Hip Abduction Dynamometer test

研究概览

简要总结

This is a blinded randomized controlled trial to assess the effectiveness of manual therapy to improve hip abduction strength in patients with acute anterior knee pain.

The primary objective of this study is to see if manual therapy to the gluteus medius can significantly alter within-session measurements of hip abductor strength in patients with anterior knee pain.

The secondary objective of this study is to see if manual therapy to the gluteus medius can significantly alter within session pain in patients with anterior knee pain.

详细描述

People with anterior knee pain have significant hip abductor muscle weakness compared to healthy people (Prins, 2009). Hip abductor weakness has a strong correlation with impaired lower extremity mechanics and increased pain with functional activity (Stickler et al. 2014). A study by Roach et al in 2013 found that 97% of patients with anterior knee pain had a trigger point in their gluteus medius muscle, while only 23% of healthy controls had trigger points. Trigger points alter normal muscle activity and increase pain in patients (Lucas, 2010, Ibarra et al 2011). Hip abduction strengthening has been found to significantly decrease pain and improve function in patients with anterior knee pain (Earl, 2011). By decreasing trigger points in the gluteus medius the investigators may be able to increase hip abduction strength reducing pain and dysfunction in patients with anterior knee pain.

Both Dry Needling (DN) and Soft Tissue Mobilization (STM) are manual therapy interventions commonly used by physical therapist to decrease trigger points in muscles. Currently, no research has examined the effectiveness of manual therapy to treat trigger points and improve hip abductor strength in patients with anterior knee pain. Clinically, the investigators have noted that after a patient has been treated with STM or DN that the investigators see immediate improvements in hip abduction strength. The investigators do not know if noted improvements result from repeated strength testing practice or actual improved firing strength of muscles.

The primary objective of this study is to see if manual therapy to the gluteus medius can significantly alter within-session measurements of hip abductor strength in patients with anterior knee pain.

The secondary objective of this study is to see if manual therapy to the gluteus medius can significantly alter within session pain in patients with anterior knee pain.

Patients referred to our physical therapy clinic for anterior knee pain will be considered for this study. After explaining the study and answering any patient or parent questions, informed consent will be obtained for those individuals wishing to participate. The participants will be screened to see if they meet the inclusion criteria, and will be randomly to a treatment group (Dry Needling, Soft Tissue Mobilization, Placebo control). This will be a single blinded research study with the assessor being blinded to the intervention. The therapist who performs the hip abductor strength measurements will not be the same therapist who performs the experimental interventions. The patient cannot be blinded to the treatment that they receive. The therapist performing the intervention will open a sealed envelope that allocates patient to Dry Needling, Soft Tissue Mobilization, or Sham Needling group. Following the experimental intervention all patients will perform the same hip and core exercise protocol.

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 (Outcomes Assessor)

入排标准

年龄范围
13 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Acute anterior knee pain of <90days
  • Ipsilateral hip abductor weakness of >15%
  • 2/10 pain with single leg squat

排除标准

  • Contraindication to dry needling or soft tissue mobilization
  • Non-mechanical anterior knee pain
  • Fear of needles

研究组 & 干预措施

Dry Needling and Exercise

Experimental

Dry Needling to treat gluteus medius trigger points followed by hip and core exercises.

干预措施: Dry Needling (Other)

Dry Needling and Exercise

Experimental

Dry Needling to treat gluteus medius trigger points followed by hip and core exercises.

干预措施: Hip and core strengthening exercises (Other)

Soft Tissue Mobilization

Active Comparator

Soft tissue mobilization to treat gluteus medius trigger points followed by hip and core exercises.

干预措施: Soft Tissue Mobilization (Other)

Soft Tissue Mobilization

Active Comparator

Soft tissue mobilization to treat gluteus medius trigger points followed by hip and core exercises.

干预措施: Hip and core strengthening exercises (Other)

Placebo Control

Placebo Comparator

Placebo to control for hands on time and attention from therapist followed by hip and core exercises.

干预措施: Placebo Control (Other)

Placebo Control

Placebo Comparator

Placebo to control for hands on time and attention from therapist followed by hip and core exercises.

干预措施: Hip and core strengthening exercises (Other)

结局指标

主要结局

Change in Hip Abduction Dynamometer test

时间窗: Baseline,Immediately Post-Intervention (anticipated at 5 minutes after baseline testing), Immediately Post-Execise (anticipated to be 1 hour after baseline testing)

Isometric maximal voluntary contraction strength of the hip abductor muscles will be measured with a portable dynamometer. The dynamometer is placed so as the testing pad is positioned 5cm proximal to the lateral femoral condyle. Two to three maximal voluntary contraction trials will be permitted. The subjects will be instructed to produce their maximal force without any concern for the rate of force development. The duration of these contractions will be 5 seconds, and thirty seconds of rest will be given between trials. A third trial is completed only if the difference between the first two maximal voluntary contractions is \>10%. • Hip abduction strength will be expressed as a percentage of the patient body weight.

次要结局

  • Change in Numeric Pain Rating Scale (NPRS) during single leg squat(Baseline,Immediately Post-Intervention (anticipated at 5 minutes after baseline testing), Immediately Post-Execise (anticipated to be 1 hour after baseline testing))

研究者

发起方
Mitchell Selhorst
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Mitchell Selhorst

Principal Investigator

Nationwide Children's Hospital

研究点 (2)

Loading locations...

相似试验