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Clinical Trials/NCT02373631
NCT02373631
Completed
Not Applicable

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

Alabama Physical Therapy & Acupuncture1 site in 1 country105 target enrollmentFebruary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Alabama Physical Therapy & Acupuncture
Enrollment
105
Locations
1
Primary Endpoint
Change in Knee Pain Intensity (NPRS)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this research is to compare the effectiveness of conventional physical therapy (manual physical therapy, exercise, range of motion, and stretching) versus conventional physical therapy combined with dry needling in patients with knee osteoarthritis (OA). Physical therapists commonly use conventional physical therapy techniques and dry needling to treat knee OA, and this study is attempting to find out if the addition of dry needling to conventional physical therapy has an equal, greater, or lesser effect than conventional physical therapy alone.

Detailed Description

Patients with knee OA will be randomized to receive 1-2 treatments per week for 6 weeks (up to 10 sessions total) of either: (1) Dry Needling and conventional physical therapy or the (2) Conventional physical therapy (manual physical therapy, exercise, range of motion and stretching)

Registry
clinicaltrials.gov
Start Date
February 2015
End Date
May 19, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Alabama Physical Therapy & Acupuncture
Responsible Party
Principal Investigator
Principal Investigator

James Dunning, DPT, MSc, FAAOMPT

DPT MSc FAAOMPT

Alabama Physical Therapy & Acupuncture

Eligibility Criteria

Inclusion Criteria

  • Report of knee pain of at least 2/10 per NPRS (0---10 scale) for \>3 months
  • Report of at least 3 of the following per Altman et al. (1986)
  • Over 50 Years of age
  • Less than 30 minutes of morning stiffness
  • Crepitus on active motion
  • Bony tenderness
  • Bony enlargement
  • No palpable warmth of synovium

Exclusion Criteria

  • 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 knee
  • History of physical therapy, massage therapy, chiropractic treatment, or injections for knee pain in the last 4 weeks
  • History of a surgical procedure on either lower extremity in last 6 months
  • Two or more positive neurologic signs consistent with nerve root compression, including any two of the following:
  • Weakness involving a major muscle group of the lower extremity.
  • Diminished patella or achilles tendon reflex
  • Diminished or absent sensation to pinprick in lower extremity dermatome
  • Involvement in litigation or worker's compensation regarding knee pain.
  • Any condition that might contraindicate the use of electro-needling

Outcomes

Primary Outcomes

Change in Knee Pain Intensity (NPRS)

Time Frame: Baseline, 2 Weeks, 6 Weeks, 3 Months

Change in Knee Osteoarthritis Index (Pain)

Time Frame: Baseline, 2 Weeks, 6 Weeks, 3 Months

5 Questions each worth 0-4 points with a maximum score of 20 points possible

Change in Knee Osteoarthritis Index (Stiffness)

Time Frame: Baseline, 2 Weeks, 6 Weeks, 3 Months

2 Questions each worth 0-4 points with a maximum score of 8 points possible

Change in Knee Osteoarthritis Index (Physical Function)

Time Frame: Baseline, 2 Weeks, 6 Weeks, 3 Months

17 Questions each worth 0-4 points with a maximum score of 68 points possible

Change in Knee Osteoarthritis Index (Total)

Time Frame: Baseline, 2 Weeks, 6 Weeks, 3 Months

24 Questions each worth 0-4 points with a maximum score of 96 points possible

Secondary Outcomes

  • Change in Global Rating of Change Score (GROC)(2 Weeks, 6 Weeks, 3 Months)
  • Change in Medicine Intake (Frequency of medication intake)(Baseline, 3 months)

Study Sites (1)

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