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临床试验/NCT03157271
NCT03157271撤回不适用

The Addition of Dry Needling in the Treatment of Patients With Patellofemoral Pain Syndrome

Duke University0 个研究点开始时间: 2017年10月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
主要终点
Change in Lower Extremity Functional Scale

研究概览

简要总结

Subjects between 14 and 40 years of age referred to physical therapy with a diagnosis of PFPS will be randomly assigned to one of two groups. The first group (PFPS) will be treated pragmatically. The second group (PFPS+DN) will receive the same pragmatic approach with the addition of dry needling intervention. The dry needling intervention will be delivered based on the treating physical therapist's examination of the patient's soft tissue mobility deficits, muscle activation deficits, or referred pain patterns.

详细描述

All interventions delivered to both study groups will be provided by licensed physical therapists at Duke Sports Medicine. The frequency of visits and duration of physical therapy care will be determined on an individual basis. Both groups will be expected to perform an individualized home exercise program to supplement formal therapy visits. The PFPS group will receive a pragmatic treatment approach reflective of currently accepted interventions. The clinician will have the ability to select appropriate interventions based on the presentation/need of each patient. These interventions may include: stretching (iliotibial band, hip flexor, lateral retinaculum); patellar taping; kinesiology taping; bracing; joint mobilization (patella, ankle, hip); orthotics/footwear recommendations; pain modalities such as Ice, electric stimulation, laser; soft tissue mobilization (manual or instrument assisted) for restricted tissues such as peri-patellar tissues, iliotibial band, tensor fasciae latae, hamstrings, calf, quadriceps, hip flexors, and gluteals. The PFPS+DN group will be treated in the same manner described above with the addition of the dry needling intervention. The dry needling intervention will be prescriptive in that each provider will assess patient for the presence of a trigger point that may be contributing either directly or indirectly to the patient's symptoms and perform the intervention per the following guidelines. First, the presence of a trigger point must be verified by locating a palpable taught band, a hypersensitive tender area, referred pain of the MTrP in response to compression, a Jump Sign - response from patient who winces, may cry out, or withdraw, or a local twitch response provoked by manually snapping the taut band. Second, a muscle may be selected for dry needling if that muscle is assumed to be contributing to tissue extensibility restriction, motor control dysfunction, or hyperactivity.

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
14 Years 至 40 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Anterior or retro-patellar knee pain from at least two of the following: prolonged sitting, stair climbing, squatting, running, kneeling, and hopping/jumping.
  • Insidious onset of symptoms unrelated to trauma
  • Presence of pain on palpation of the patellar facets
  • Pain on compression of the patella

排除标准

  • Signs or symptoms of meniscal or other intra-articular pathologic condition.
  • Self-reported other knee pathology such as cartilage injury or ligamentous tear.
  • Known articular cartilage damage (from previously obtained imaging).
  • Ligament laxity or tenderness.
  • Patellar tendonitis, ITB syndrome, fracture,
  • Tenderness over the patellar tendon, ITB, tibial tubercle, or pes anserinus tendons "if reproduced the pain"
  • Patellar instability (positive apprehension sign and/or self-reported history of dislocations or subluxations.
  • Concurrent Hip Pain
  • Lumbar referred pain
  • Osgood-Schlatters or Sinding-Larsen-Johanssen Syndromes
  • Knee surgery within the past year
  • Evidence of effusion

研究组 & 干预措施

PFPS Treatment

No Intervention

This arm (group of patients) will receive typical/pragmatically designed treatment for patellofemoral pain syndrome.

PFPS Plus Dry Needling Treatment

Experimental

This group will receive the same typical/pragmatically designed treatment for patellofemoral pain syndrome but with the addition of a dry needling intervention.

干预措施: Intramuscular Dry Needling (Other)

结局指标

主要结局

Change in Lower Extremity Functional Scale

时间窗: Baseline, 2 weeks, 1 month, at completion of treatment (average of 10 weeks), 3 months, 6 months

20 Item Survey - Self report of difficulty with 20 lower extremity common tasks

次要结局

  • Change in Pain(Baseline, Days 1-15, 1 month, at completion of treatment (average of 10 weeks), 3 months, 6 months)
  • Change in Global Function Rating(Baseline, Days 1-15, 1 month, at completion of treatment (average of 10 weeks), 3 months, 6 months)
  • Change in Global Rating of Change(Baseline, Days 1-15, 1 month, at completion of treatment (average of 10 weeks), 3 months, 6 months)

研究者

申办方类型
Other
责任方
Sponsor

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