跳至主要内容
临床试验/NCT02373618
NCT02373618已完成不适用

Dry Needling Versus Conventional Physical Therapy in Patients With Plantar Fasciitis: a Multi-center Randomized Clinical Trial

Alabama Physical Therapy & Acupuncture2 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2015年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
108
试验地点
2
主要终点
Change in Pain Intensity (NPRS)

研究概览

简要总结

The purpose of this research is to compare patient outcomes following treatment of plantar fasciitis with conventional physical therapy (stretching, strengthening, ultrasound, manual therapy, and cryotherapy) and conventional physical therapy plus dry needling. Physical therapists commonly use conventional physical therapy techniques and dry needling to treat plantar fasciitis, and this study is attempting to find out if the addition of dry needling to conventional physical therapy is more effective than conventional physical therapy alone.

详细描述

Patients with plantar fasciitis will be randomly assigned to receive 1-2 treatments per week for 4 weeks of either: (1) Dry Needling and conventional physical therapy, or the (2) Conventional physical therapy (stretching, strengthening, ultrasound, manual therapy, and cryotherapy)

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Report of at least 3 months of heel pain
  • Patient has not had physical therapy, massage therapy, chiropractic treatment, or injections for plantar heel pain in the least 4 weeks.
  • Diagnosis of plantar heel pain with ALL of the following positive clinical signs:
  • "First---step" pain upon weight bearing in the morning OR after sitting for a period of time
  • Pain localized over the medial calcaneal tubercle
  • Increased pain with extended walking OR standing >15 minutes
  • Plantar heel pain greater than or equal to 2/10 (NPRS 0-10 Scale)

排除标准

  • Report of red flags to manual physical therapy to include: hypertension, infection, diabetes, peripheral neuropathy, heart disease, stroke, chronic ischemia, edema, severe varicosities, tumor, metabolic disease, prolonged steroid use, fracture, RA, osteoporosis, severe vascular disease, malignancy, etc.
  • History of previous surgery to the tibia, fibula, ankle joint, or foot.
  • History of arthrosis or arthritis of the ankle and/or foot.
  • History of significant ankle and/or foot instability.
  • Two or more positive neurologic signs consistent with nerve root compression, including any two of the following:
  • Muscle weakness involving a major lower extremity muscle group
  • Diminished lower extremity patella or Achilles tendon reflexes
  • Diminished / absent sensation in any lower extremity dermatome
  • Involvement in litigation or worker's compensation regarding their foot pain.
  • Any condition that might contraindicate the use of electro---needling
  • The patient is pregnant

结局指标

主要结局

Change in Pain Intensity (NPRS)

时间窗: Baseline, 1 week, 4 weeks, 3 months

Change in First Step Pain in the Morning (NPRS)

时间窗: Baseline, 1 week, 4 weeks, 3 months

Change in Activity Pain (NPRS)

时间窗: Baseline, 1 week, 4 weeks, 3 months

Average pain level during standing and walking.

Change in Foot Functional Index Total

时间窗: Baseline, 1 week, 4 weeks, 3 months

3 questions each worth 0-10 points with maximum score of 30 points possible

Change in Foot Functional Index Disability

时间窗: Baseline, 1 week, 4 weeks, 3 months

9 questions each worth 0-10 points with maximum score of 90 points possible

Change in Lower Extremity Functional Scale

时间窗: Baseline, 1 week, 4 weeks, 3 months

20 questions each worth 0-4 points with maximum score of 80 points possible. Do not convert to a 20 questions, each worth 0-4 points with maximum score of 80 points possible

Change in Foot Functional Index Activity Limitation

时间窗: Baseline, 1 week, 4 weeks, 3 months

3 questions each worth 0-10 points with maximum score of 30 points possible

Change in Foot Functional Index Pain

时间窗: Baseline, 1 week, 4 weeks, 3 months

5 questions each worth 0-10 points with maximum score of 50 points possible.

次要结局

  • Change in Medicine Intake (Frequency of pain medication)(Baseline, 3 months)
  • Change in Global Rating of Change Score(1 week, 4 weeks, 3 months)

研究者

发起方
Alabama Physical Therapy & Acupuncture
申办方类型
Other
责任方
Principal Investigator
主要研究者

James Dunning, DPT, MSc, FAAOMPT

DPT FAAOMPT

Alabama Physical Therapy & Acupuncture

研究点 (2)

Loading locations...

相似试验