NCT07642583
Dry Needling and Exercise for Mid-portion Achilles Tendinopathy
Enrolling by Invitation
NAAges 18–64InterventionalTreatmentBrooke Army Medical CenterGovernment-funded
~74 participants
Updated 2026-06-12 on ClinicalTrials.gov
What's tested:Dry needlingSham dry needling
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Victorian Institute of Sport Assessment - Achilles
Measured over From enrollment to 12 weeks
Conditions
Where it's being run
1 sites across 1 statesTexas1
Study leadership
- Benjamin Hando, DSc, PhD · STUDY_CHAIR · Army-Baylor Doctoral Fellowship in Orthopedic Manual Physical Therapy
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
Symptoms in one or both Achilles tendons
Pain reported in Achilles with running, jumping or walking
Symtom duration ≥ 6 weeks
Age 18-64
English-speaking
Exclusion
Score \> 80 on VISA-A
Prior Achilles rupture or surgery
Pain reported in Achilles insertion to calcaneus only
Needle phobia
Self-reported pregnancy
Trainee status
Corticosteroid injection in the past 3 months into the Achilles tendon
Unable to participate in 12 week program
Taken Quinolone antibiotics past three months (e.g. Cipro, Levaquin, Floxin, Baxdela)
Currently undergoing separation from the military
Diagnosis of rheumatoid arthritis, systemic connective tissue disorder, or neurological disorder affecting the lower leg.
Symptoms in Achilles tendon are from another source (e.g. S1 radicular pain, referred pain, sural nerve entrapment)
Currently undergoing active physical therapy elsewhere for Achilles pain
What this trial measures
- Victorian Institute of Sport Assessment - AchillesFrom enrollment to 12 weeks
The Victorian Institute of Sport Assessment - Achilles (VISA-A) is a questionnaire that is validated to measure pain, function and activity for people affected by Achilles tendon pain. It is rated 0-100, with increasing function at higher scores.