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Dry Needling Versus Conventional Physical Therapy in Patients With Knee Osteoarthritis

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02373631
Enrollment
105
Registered
2015-02-27
Start date
2015-02-28
Completion date
2017-05-19
Last updated
2017-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

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)

Interventions

OTHERDry Needling, Conventional PT

Dry needling to the knee and conventional physical therapy (stretching, ROM, strengthening), 1-2 treatments per week X6 weeks (up to 10 sessions total)

Conventional physical therapy to include knee stretching, range of motion, and strengthening exercises,1-2 treatments per week X6 weeks (up to 10 sessions total)

Sponsors

Universidad Rey Juan Carlos
CollaboratorOTHER
Alabama Physical Therapy & Acupuncture
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Report of knee pain of at least 2/10 per NPRS (0---10 scale) for \>3 months 2. 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

1. 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. 2. History of previous surgery to the knee 3. History of physical therapy, massage therapy, chiropractic treatment, or injections for knee pain in the last 4 weeks 4. History of a surgical procedure on either lower extremity in last 6 months 5. 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 6. Involvement in litigation or worker's compensation regarding knee pain. 7. Any condition that might contraindicate the use of electro-needling 8. The patient is pregnant.

Design outcomes

Primary

MeasureTime frameDescription
Change in Knee Osteoarthritis Index (Pain)Baseline, 2 Weeks, 6 Weeks, 3 Months5 Questions each worth 0-4 points with a maximum score of 20 points possible
Change in Knee Osteoarthritis Index (Physical Function)Baseline, 2 Weeks, 6 Weeks, 3 Months17 Questions each worth 0-4 points with a maximum score of 68 points possible
Change in Knee Osteoarthritis Index (Total)Baseline, 2 Weeks, 6 Weeks, 3 Months24 Questions each worth 0-4 points with a maximum score of 96 points possible
Change in Knee Pain Intensity (NPRS)Baseline, 2 Weeks, 6 Weeks, 3 Months
Change in Knee Osteoarthritis Index (Stiffness)Baseline, 2 Weeks, 6 Weeks, 3 Months2 Questions each worth 0-4 points with a maximum score of 8 points possible

Secondary

MeasureTime frameDescription
Change in Medicine Intake (Frequency of medication intake)Baseline, 3 monthsFrequency of medication intake (narcotics and over-the-counter) for knee pain
Change in Global Rating of Change Score (GROC)2 Weeks, 6 Weeks, 3 Months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026