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OpenTrials
Completed

NCT Number: NCT03689283

The Effect of Dry Needling on Muscle Stiffness, Gait, Motion, and Strength in Healthy Individuals With Trigger Points

This study would be the first study to assess the immediate effects of dry needling of latent trigger points of the gastrocnemius muscle on muscle stiffness, gait, range of motion, and strength. The study has the potential to demonstrate that dry needling may have immediate effects on mechanical properties of muscle and may thus guide future treatment for individuals with changes in muscle tissue secondary to pain and/or injury.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Regis University

Denver, Colorado, 80221, United States

About this study

Participants will complete the following tests: muscle stiffness testing in both a relaxed and contracted position, GAITRite for spatial and temporal gait characteristics, the Ankle Lunge Test (ALT) to assess range of motion, and calf strength using a dynamometer. Subjects will then receive treatment according to which group they are randomized. Muscle stiffness, gait, motion and strength will be reassessed immediately following treatment at the first session. Four to10 days later, participants will complete the same tests and measures prior to treatment being administered a second time. Another 4-10 days after the second session, participants will complete the tests and measures one final time.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-50 years
  • Able to read and speak sufficient English to complete consent form
  • Symmetrical gait pattern demonstrated through observation
  • Presence of latent trigger point in gastrocnemius muscle

Exclusion criteria

  • Any prior foot/ankle surgery, deformity, or injury on the which would affect strength of the gastrocnemius
  • Any prior acupuncture or dry needling within the past month
  • History of systemic disorder in which dry needling would be contraindicated (i.e. bleeding disorders or anticoagulant medication use)
  • Have fractures of the spine, hip, or knee that would likely affect their weight bearing or gait
  • Restrictions in plantar flexion range of motion which would inhibit performing a heel raise
  • No specific calf injury in the past 6 months
  • Participants known or thought to be pregnant

Treatment and study plan

dry needling

Other

Individuals randomized to the Dry Needling Group will receive dry needling to latent trigger points of the gastrocnemius muscle

Sham Dry Needlling

Other

Individuals randomized to the Control group will receive sham needling to the gastrocnemius muscle

Primary outcomes

  1. MyotonPRO

    Time frame: 2 years

    Muscle stiffness will be measured in both a resting and contracted state utilizing this non-invasive device

Secondary outcomes

  1. Knee to wall

    Time frame: 2 years

    Group by time differences will be assessed for talocrural motion (knee to wall)

  2. GAITRite

    Time frame: 2 years

    Group by time differences will be assessed for gait variables (utilizing the GAITRite 6-meter mat)

  3. Handheld dynamometer

    Time frame: 2 years

    Group by time differences will be assessed for strength of the gastrosoleus complex (utilizing a handheld dynamometer)

Sponsors and collaborators

Lead sponsor

Regis University

Other

Registry information

Official study title

The Effect of Dry Needling on Muscle Stiffness, Gait, Motion, and Strength in Healthy Individuals With Latent Trigger Points

Important dates

Study start
2018
Primary completion
2019
Study completion
2020
First posted
Sep 28, 2018
Registry last updated
Jan 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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