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Dry Needling Versus Conventional Physical Therapy in Patients With Plantar Fasciitis

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02373618
Enrollment
108
Registered
2015-02-27
Start date
2015-12-31
Completion date
2017-05-17
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

Plantar Fasciitis

Brief summary

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.

Detailed description

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)

Interventions

OTHERDN and conventional PT

Dry needling to the foot and lower leg. Up to 8 sessions over 4 weeks. Also conventional PT including: ultrasound, stretching, strengthening, cryotherapy and manual therapy to the foot and lower leg.

Conventional physical therapy includes ultrasound, strengthening, cryotherapy, and manual therapy up to 8 sessions over 4 weeks.

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 at least 3 months of heel pain 2. Patient has not had physical therapy, massage therapy, chiropractic treatment, or injections for plantar heel pain in the least 4 weeks. 3. 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 4. Plantar heel pain greater than or equal to 2/10 (NPRS 0-10 Scale)

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 tibia, fibula, ankle joint, or foot. 3. History of arthrosis or arthritis of the ankle and/or foot. 4. History of significant ankle and/or foot instability. 5. 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 6. Involvement in litigation or worker's compensation regarding their foot pain. 7. Any condition that might contraindicate the use of electro---needling 8. The patient is pregnant

Design outcomes

Primary

MeasureTime frameDescription
Change in Foot Functional Index TotalBaseline, 1 week, 4 weeks, 3 months3 questions each worth 0-10 points with maximum score of 30 points possible
Change in Foot Functional Index Activity LimitationBaseline, 1 week, 4 weeks, 3 months3 questions each worth 0-10 points with maximum score of 30 points possible
Change in Pain Intensity (NPRS)Baseline, 1 week, 4 weeks, 3 months
Change in Lower Extremity Functional ScaleBaseline, 1 week, 4 weeks, 3 months20 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 First Step Pain in the Morning (NPRS)Baseline, 1 week, 4 weeks, 3 months
Change in Activity Pain (NPRS)Baseline, 1 week, 4 weeks, 3 monthsAverage pain level during standing and walking.
Change in Foot Functional Index PainBaseline, 1 week, 4 weeks, 3 months5 questions each worth 0-10 points with maximum score of 50 points possible.
Change in Foot Functional Index DisabilityBaseline, 1 week, 4 weeks, 3 months9 questions each worth 0-10 points with maximum score of 90 points possible

Secondary

MeasureTime frameDescription
Change in Global Rating of Change Score1 week, 4 weeks, 3 months
Change in Medicine Intake (Frequency of pain medication)Baseline, 3 monthsFrequency of pain medication, including over-the-counter or narcotics for plantar fasciitis

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026