Ultrasonography Detection of Local Twitch Response During Dry Needling (US-DN)

November 30, 2023 updated by: Dr. Antonio I Cuesta-Vargas, University of Malaga

Semi-Automatic Ultrasonography Detection of Local Twitch Response Intensities During Dry Needling: Implications on Joint Range of Motion

Background: One treatment of Muscle trigger points (MTrPs) is deep dry needling (DN) with the purpose of obtaining local twitch responses (LTRs), which are highly effective in releasing MTrPs. In DN procedures the mechanisms associated with LTRs and the LTR intensities required for optimal clinical results are poorly understood, especially in relation to range of motion after intervention. Therefore, evaluating the intensity of LTRs is relevant for implementing DN in different clinical settings, such as in patients with muscular or neurological dysfunctions. One way to assess muscle contractions and LTRs is through ultrasound video analysis.

The aim of this report was to evaluate the reliability of semi-automatic LTR intensities tracking during dry needling by assessing ultrasound signals with an image processing method, in addition to evaluating the relationship between LTR intensities and muscle elasticity.

Method: Young males without signs or symptoms of musculoskeletal pain were included. Primary outcome measure was the LTR intensities determined by percentage change of muscle thickness. The secondary outcome measures were the muscle elasticity of medial gastrocnemius and hamstring, previous and posterior DN in both lower limbs for each subject. Three LTRs, detected by a physical therapist and ultrasound assessment, were induced by inserting a filament needle into muscle latent trigger points in medial gastrocnemius. The intensities of LTRs were measured by assessing ultrasound images using an optical flow method and through comparisons with manual detection.

Study Overview

Detailed Description

The aim of this report was to evaluate the reliability of semi-automatically tracking local twitch responses (LTR) intensities during dry needling by assessing ultrasound signals with an optical flow method designed to estimate movement of ROIs, in addition to evaluating the relationship between LTR intensities and muscle elasticity.

Experimental protocol and measurements For each subject, the ROM of the medial gastrocnemius (MG) and hamstring (HA) was determined in both lower limbs using weight bearing and the active knee extension test, respectively, using a universal goniometer. For the knee extension test, 180° were subtracted from the obtained range, and the values were presented as negative. Both tests present excellent intra- and inter-rater reliability.

All participants were placed in a prone position with the ankle locked at 90º. Latent MTrPs were identified in both MG using according the presence of a palpable taut band and hypersensitive spot in the palpable taut band as diagnostic criteria. The ultrasound transducer was positioned over the MG muscle using a fixing device that was composed of a thermoplastic polymer, with enough space for the dry needling (DN) technique to be performed.

The deep DN was administered by a physical therapist with three years of experience in the technique. The ultrasound video (SonoSite Titan; Sonosite, Bothell, WA, USA) was recorded at 60 frames per second captured through an external capture device from Epiphan Systems Inc. (Ottawa, Ontario, Canada). According to the perception of the physical therapist and the ultrasound assessment, the filament needle was inserted into the MTrP to achieve three LTRs. Posterior to DN application, the ROMs of the MG and HA were measured.

The recorded ultrasound video was examined by the Camtasia software (Tech-Smith Corp, Okemos, MI, USA) to select three LTRs for latter analysis. Each LTR was tracked by the Lucas-Kanade optical flow (LKOF) algorithm with affine optic flow extension [12]. All analyses were performed using the Matlab® 2014 software (Mathworks Inc., Natick, MA, USA). For tracking muscle thickness, two ROIs (size 250 x 70 pixels) positioned on the superficial and deep aponeurosis were manually selected.

Muscle thickness was normalized as a percentage of recruitment using the following equation: (thickness contracted-thickness rest/thickness rest)*100. For manual tracking of LTRs, the recorded ultrasound video was analyzed in the Matlab® 2014 software. Peak muscle thickness was determined by selecting muscle borders using hyperechoic aponeurosis lines.

Study Type

Interventional

Enrollment (Actual)

7

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy volunteer

Exclusion Criteria:

  • Participants were excluded if they presented any history of musculoskeletal pain in the last six months, pathological conditions of the vertebral column, neurological diseases, respiratory diseases, a systemic rheumatic condition, heritable connective tissue disorders, and/or any previous abdominal surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Deep Dry Needling

Deep Dry Needling (DN) with the purpose of obtaining local twitch responses (LTRs). Description: Latent MTrPs were identified in both MG using according the presence of a palpable taut band and hypersensitive spot in the palpable taut band as diagnostic criteria.

The deep DN was administered by a physical therapist with three years of experience in the technique. The ultrasound video (SonoSite Titan; Sonosite, Bothell, WA, USA) was recorded at 60 frames per second captured through an external capture device from Epiphan Systems Inc. (Ottawa, Ontario, Canada). According to the perception of the physical therapist and the ultrasound assessment, the filament needle was inserted into the MTrP to achieve three LTRs. Posterior to DN application, the ROMs of the MG and HA were measured

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Size of local twitch responses to Dry Needling with Ultrasonomiography 30 fps
Time Frame: through study completion, an average of 1 year
acute effect based in Range of Interest (RoI) of deep fascia reference
through study completion, an average of 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinimetric Tool
Time Frame: through study completion, an average of 1 year
stratificaction of size of local responses to dry needling thicknessbased, reliability and construct validity study
through study completion, an average of 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Antonio Cuesta-Vargas, PhD, University of Malaga

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2016

Primary Completion (Actual)

March 1, 2016

Study Completion (Actual)

April 1, 2016

Study Registration Dates

First Submitted

June 24, 2016

First Submitted That Met QC Criteria

July 6, 2016

First Posted (Estimated)

July 7, 2016

Study Record Updates

Last Update Posted (Estimated)

December 1, 2023

Last Update Submitted That Met QC Criteria

November 30, 2023

Last Verified

June 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • CH-Sp-01

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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