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RecruitingNCT03968614Updated May 18, 2025

Electrical DN as an Adjunct to Eccentric Exercise, Stretching + MT for Achilles Tendinopathy

An interventional study of Electric dry needling and conventional PT and Conventional PT in Achilles Tendinopathy, sponsored by Alabama Physical Therapy & Acupuncture. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-05-18.

Sponsored by Alabama Physical Therapy & Acupuncture · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
110
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this research is to compare two different approaches for treating patients with achilles tendinopathy: eccentric exercise, stretching and manual therapy VS Electric dry needling, eccentric exercise, stretching and manual therapy. Physical therapists commonly use all of these techniques to treat achilles tendinopathy. This study is attempting to find out if one treatment strategy is more effective than the other.

Read the detailed description

Patients with achilles tendinopathy will be randomized to receive 8-10 treatments (1-2 treatments per week) over 6 weeks (10 treatments max) of either: (1)Eccentric exercise, stretching, manual therapy and electrical dry needling or 2. eccentric exercise, stretching and manual therapy

02

Conditions studied

  • Achilles Tendinopathy

Browse trials for

03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Adult >18 years old that is able to speak English.
  2. Report of at least 3 months of Achilles pain clinically diagnosed as Achilles tendonitis or Achilles tendinopathy
  3. Patient has not had physical therapy, massage therapy, chiropractic treatment or injections for Achilles pain in the last 6 months:
  4. Diagnosis of noninsertional tendinopathy, defined as the following

    • Subjective report of pain located 2-6 cm proximal to the insertion of Achilles tendon to the calcaneus, particularly with running or jumping
    • Tenderness to palpation of the Achilles tendon while the clinician gently squeezes the tendon between the thumb and index finger in a proximal to distal direction
    • Positive Arc Sign - Intratendinous swelling moves relative to the malleoli with the tendon during active dorsi/plantar Flexion
    • Royal London Test - Tenderness to palpation decreases significantly or disappears with max dorsiflexion

Exclusion criteria

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 vascular disease, malignancy, etc.
  2. History of previous Achilles tendon surgery, ankle arthrodesis, hind foot fracture, or leg length discrepancy of more than one half inch.
  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:

    1. Muscle weakness involving a major lower extremity muscle group
    2. Diminished lower extremity patella or Achilles tendon reflexes
    3. Diminished / absent sensation in any lower extremity dermatome
  6. Involvement in litigation or worker's compensation regarding foot pain
  7. Any condition that might contraindicate the use of electro-needling
  8. The patient is pregnant.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
110 participants (estimated)

Study arms

  • Experimental
    Electrical Dry Needling and conventional PT

    Electrical Dry Needling, Eccentric Exercise, Stretching and Manual Therapy

    Other: Electric dry needling and conventional PT

  • Active comparator
    Conventional PT

    Eccentric Exercise, Stretching and Manual Therapy

    Other: Conventional PT

Interventions

  • OtherElectric dry needling and conventional PT

    Electrical Dry Needling, Eccentric Exercise, Stretching and Manual Therapy

  • OtherConventional PT

    Eccentric Exercise, Stretching and Manual Therapy

05

What researchers measure

Primary outcomes

  1. Change in VISA-A Questionnaire

    Index of severity of Achilles tendinopathy. Lower score means greater severity of condition.

    Time frame: baseline, 2 weeks, 6 weeks, 3 months

Secondary outcomes

  1. Change in achilles pain (NPRS) (Rating Score)

    Higher scores mean greater pain

    Time frame: baseline, 2 weeks, 6 weeks, 3 months

  2. Change in Foot and Ankle Ability Measure - ADL

    activities of daily living (0-84 points) 21 Item 84-point ADL Subscale

    Time frame: baseline, 2 weeks, 6 weeks, 3 months

  3. Change in Foot and Ankle Ability Measure - Sports

    Sports (0-32 points) 8 Item 32-point sports subscale

    Time frame: baseline, 2 weeks, 6 weeks, 3 months

  4. GROC (ranges from -7 to +7). Global Rating of Change score.

    Time frame: 2 weeks, 6 weeks, 3 months

06

Study locations

1 of 1 sites recruiting
  • Prisma Health - Research PT Specialists
    Columbia, South Carolina 29201, United States
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03968614
Lead sponsor
Alabama Physical Therapy & Acupuncture
Collaborators
Universidad Rey Juan Carlos
Responsible party
James Dunning, DPT, MSc, FAAOMPT (Primary Investigator and President of Spinal Manipulation Institute and Dry Needling Institute of the American Academy of Manipulative Therapy, Alabama Physical Therapy & Acupuncture) — Principal investigator
First posted
May 30, 2019
Start date
Jun 10, 2019
Primary completion
May 1, 2026 (estimated)
Completion
May 1, 2026 (estimated)
Last update
May 18, 2025

Study contacts

James Dunning, DPT
Contact
jamesdunning@hotmail.com
18017079056
Raymond Butts, DPT PhD
Contact
fellowship@spinalmanipulation.org
8034223954
James Dunning, DPT
principal investigator · American Academy of Manipulative Therapy

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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