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Effects of Dry Needling Using Spinal and Peripheral Sites Versus Peripheral Sites Only

Emory University logo

Emory University

Status

Completed

Conditions

Plantar Fasciitis
Achilles Tendinitis
Patellofemoral Pain Syndrome

Treatments

Procedure: Peripheral Dry Needling
Procedure: Spinal and Peripheral Dry Needling

Study type

Interventional

Funder types

Other

Identifiers

NCT02646579
IRB00084277

Details and patient eligibility

About

The purpose of this study is to determine if dry needling both low back and extremity areas is more effective for reducing pain and improving strength, balance and functional performance among patients with chronic musculoskeletal conditions compared to dry needling of extremity areas only.

Full description

This study will determine if spinal and peripheral dry needling sites results in decreased pain, increased muscle strength, increased proprioception and increased functional performance among individuals with chronic musculoskeletal conditions of the lower extremities, such as plantar fasciitis, Achilles tendinopathy, and patellofemoral pain syndrome. Specific aims are to determine if individuals with chronic musculoskeletal conditions of the lower extremities receiving dry needling to both spinal and peripheral sites exhibit differences in pain, muscle strength, proprioception, and unilateral hop test scores compared to individuals with chronic musculoskeletal conditions of the lower extremities receiving dry needling to peripheral sites only.

Enrollment

34 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Unilateral chronic lower extremity musculoskeletal condition
  • Ability to perform a unilateral one-quarter squat on involved side without pain
  • Asymptomatic during walking

Exclusion criteria

  • History of systemic neurological or arthritic condition
  • History of bony or peripheral nerve trauma or surgery lower extremities
  • No contraindications to dry needling
  • Not currently receiving treatment for the chronic lower extremity musculoskeletal condition

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

Spinal and Peripheral Dry Needling
Experimental group
Description:
Participants will receive dry needling to the low back and painful areas in the leg.
Treatment:
Procedure: Spinal and Peripheral Dry Needling
Peripheral Dry Needling
Active Comparator group
Description:
Participants will receive dry needling to painful areas in the leg.
Treatment:
Procedure: Peripheral Dry Needling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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