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CompletedNCT01734577Updated Jun 19, 2013

Effect of Dry Needling Multifidus on Thickness of Transversus Abdominis in Healthy Individuals

An interventional study of Dry needling and Sham needling in Back Pain, sponsored by University of Nevada, Las Vegas. Completed at 1 site in United States. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-06-19.

Sponsored by University of Nevada, Las Vegas · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
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Study summary

Intramuscular therapy (also known as dry needling) has been shown to give dramatic relief of musculoskeletal pain. The mechanisms of action remain unknown, and this study will examine for a neurophysiological effect.

Read the detailed description

Consenting adults will be taught how to contract their abdominal muscles, and to contract transversus abdominis in particular. They will then have real time ultrasound measurements of the resting and contracted thickness of their left transversus abdominis muscle. After this, they will receive actual or sham needling to their left multifidus muscle by another researchers blinded to the real time ultrasound measurements. After needling or sham intervention is complete, the original researchers will return to re-measure transversus abdominis. They will be blind to intervention allocation.

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Conditions studied

  • Back Pain

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Keywords

  • Back pain
03

In context

Back Pain

2,373 studies on the registry are indexed under Back Pain; 284 are open to participants now.

This study's enrollment of 60 is close to the median of 60 across 1,941 interventional studies indexed under Back Pain.

Browse Back Pain studies →

Lead sponsor

University of Nevada, Las Vegas is the lead sponsor of 75 studies on the registry; 22 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 2 (40%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age, absence of back pain or symptoms for greater than 6 months and ability to perform DCC. Subjects must also report they are comfortable with being 'needled'.

Exclusion criteria

Exclusion Criteria:

  • Presence of back pain or symptoms within the last 6 months, history of: abdominal or spinal surgery, significant scoliosis, rheumatoid arthritis, osteoporosis, osteopenia, active ankylosing spondylitis. If a subject reports a fear of needles.
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Active comparator
    Dry needling

    Monofilament needles will be inserted into each subject's left multifidus muscle and stimulated mechanically for a local twitch response

    Procedure: Dry needling

  • Sham comparator
    Sham needling

    Monofilament tubes will be pressed into the left multifidus muscle and mechanically manipulated to give the sensation that needling is occuring.

    Procedure: Sham needling

Interventions

  • ProcedureDry needling

    Sterile monofilament needles

  • ProcedureSham needling

    Applicator tubes from the sterile monofilament needles

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What researchers measure

Primary outcomes

  1. Thickness of transversus abdominis at rest and during contraction

    Real time ultrasound measurement

    Time frame: 1 day

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Study locations

1 site
  • University of Nevada Las Vegas - Department of Physical Therapy
    Las Vegas, Nevada 89154, United States
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References and documents

Publications

  • Puentedura EJ, Buckingham SJ, Morton D, Montoya C, Fernandez de Las Penas C. Immediate Changes in Resting and Contracted Thickness of Transversus Abdominis After Dry Needling of Lumbar Multifidus in Healthy Participants: A Randomized Controlled Crossover Trial. J Manipulative Physiol Ther. 2017 Oct;40(8):615-623. doi: 10.1016/j.jmpt.2017.06.013. PubMed 29187313 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 19, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01734577
Lead sponsor
University of Nevada, Las Vegas
Responsible party
Emilio (Dr. Emilio J. Puentedura, University of Nevada, Las Vegas) — Principal investigator
First posted
Nov 27, 2012
Start date
Aug 2012
Primary completion
Jun 2013
Completion
Jun 2013
Last update
Jun 19, 2013

Study contacts

Daniella Morton, BSc
study director · University of Nevada Las Vegas Physical Therapy
Sarah Buckingham, BSc
study director · University of Nevada Las Vegas Physical Therapy
Crystal Montoya, BSc
study director · Univesity of Nevada Las Vegas Physical Therapy

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2013. You cannot join it, but the record below documents what was studied.

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