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Quantitative Ultrasound Biomarkers to Assess Upper Trapezius Muscles in Patients With Chronic Pain

Primary Purpose

Chronic Neck Pain

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Quantitative Ultrasound
Osteopathic TART Assessment
Osteopathic Manipulation Treatment
Sponsored by
Rocky Vista University, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Chronic Neck Pain

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Inclusion criteria for the healthy participants include:

  • Age 18 years and older;
  • Healthy. No history of musculoskeletal conditions, such as severe pain, trauma, joint or spine surgery;
  • Able to sign written informed consent,
  • Tolerant to the osteopathic exam, and ultrasound.

Inclusion criteria for patients with chronic neck pain include:

  • Age 18 years and older
  • Having chronic neck pain persisting longer than 12 weeks, meeting TART criteria, diagnosed by an osteopathic physician;
  • Able to sign written informed consent;
  • Tolerant to the osteopathic exam, ultrasound, and OMT.

Exclusion Criteria:

Exclusion criteria for the healthy participants include:

  • Under 18 years of age;
  • Having a medical history of musculoskeletal conditions, joint and/or spine surgery, trauma;
  • Employee of the study investigators;
  • Being unable to competently consent or assent to participation (e.g., mentally disabled, demented, delusional, or a prisoner);
  • Not tolerant to the osteopathic exam, ultrasound.

Exclusion criteria for patients with chronic neck pain include:

  • Age < 18 years,
  • Unable or unqualified to sign an informed consent,
  • Unstable and/or late stage diseases,
  • Not tolerant to the osteopathic exam, ultrasound, OMT.

There is no specific racial/ethnic background limitation in this study.

Sites / Locations

  • Ultrasound Research Laboratory

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Healthy participants

Patients with chronic neck pain

Arm Description

Non-invasive quantitative ultrasound (B-mode image, ultrasound elastography), EMG, and osteopathic assessment (TART assessments) will be performed on the upper trapezius muscle in healthy participants one time at the time of the enrollment.

Non-invasive quantitative ultrasound (B-mode ultrasound, ultrasound elastography), EMG, osteopathic assessment, and osteopathic manipulative treatment (OMT) of the upper trapezius muscle will be performed on participants with chronic neck pain 3 times. All ultrasound, EMG biomarkers and TART assessments will be collected before and after OMT.

Outcomes

Primary Outcome Measures

Ultrasound diagnostic performance evaluation
Evaluation for healthy participants and for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units), shear wave velocity (m/s), and longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Ultrasound diagnostic performance evaluation
Evaluation for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units), shear wave velocity (m/s), and longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.

Secondary Outcome Measures

Ultrasound echo-intensity
Evaluation for healthy participants and for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units) will be recorded. Measured using ultrasound.
Ultrasound echo-intensity
Evaluation for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units) will be recorded. Measured using ultrasound.
Ultrasound echo-intensity
Evaluation for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units) will be recorded. Measured using ultrasound.
Ultrasound shear wave velocity
Evaluation for healthy participants and for patients with chronic neck pain. Changes in shear wave velocity (m/s), will be recorded. Measured using ultrasound.
Ultrasound shear wave velocity
Evaluation for patients with chronic neck pain. Changes in shear wave velocity (m/s), will be recorded. Measured using ultrasound.
Ultrasound shear wave velocity
Evaluation for patients with chronic neck pain. Changes in shear wave velocity (m/s), will be recorded. Measured using ultrasound.
Ultrasound longitudinal strain ratios
Evaluation for healthy participants and for patients with chronic neck pain. Changes in longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Ultrasound longitudinal strain ratios
Evaluation for patients with chronic neck pain. Changes in longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Ultrasound longitudinal strain ratios
Evaluation for patients with chronic neck pain. Changes in longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.

Full Information

First Posted
August 1, 2022
Last Updated
August 24, 2022
Sponsor
Rocky Vista University, LLC
Collaborators
American Osteopathic Association
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1. Study Identification

Unique Protocol Identification Number
NCT05497622
Brief Title
Quantitative Ultrasound Biomarkers to Assess Upper Trapezius Muscles in Patients With Chronic Pain
Official Title
Quantitative Ultrasound Biomarkers to Assess Upper Trapezius Muscles in Patients With Chronic Neck Pain Before and After Osteopathic Manipulative Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
August 24, 2022 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rocky Vista University, LLC
Collaborators
American Osteopathic Association

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this study is to identify and develop multiparametric quantitative ultrasound imaging (QUI) biomarkers for assessing upper trapezius muscle with and without chronic neck pain and their response to treatment. This goal will be achieved by testing the underlying hypothesis that abnormal muscle tissue can be identified based on its physio-mechanical properties, and that changes in these properties can be used to guide and monitor treatment progress. Preliminary results have shown that biomarkers including muscle B-mode ultrasound echo-intensity, shear wave velocity, and longitudinal strain ratios associated with muscle tissue structure, mechanics, and function significantly differ between muscles in low back pain and neuromuscular disorders and normal muscles. This study will determine which biomarkers are best suited to differentiate abnormal muscle in chronic neck pain from healthy muscles and develop a quantitative objective program for chronic neck pain management.
Detailed Description
The main objective will be achieved through two aims: Aim 1: Identify and develop quantitative biomarkers to distinguish structure, mechanics, function, and blood flow in abnormal muscles associated with chronic neck pain from normal muscles, correlated with clinical osteopathic assessments. To determine the diagnostic performances of echo-intensity as a muscle structural biomarker, shear wave velocity and longitudinal strain ratio as muscle mechanics/function biomarkers, and color Doppler microvascular index as a muscle blood flow biomarker will be evaluated. These assessments will be evaluated in healthy subjects to test these quantitative biomarkers on upper trapezius muscle in the neck region to establish normal control values. To determine the clinical utility of these novel biomarkers, subjects with chronic neck pain will receive clinical osteopathic assessments over the neck region using conventional osteopathic examination with qualitative disease scoring by clinicians and subjective pain scales by subjects. The above quantitative biomarkers and qualitative osteopathic assessments of corresponding tissues with and without chronic neck pain will be analyzed using advanced ultrasound processing methods and statistical analyses. Aim 2: Evaluate the abilities of quantitative biomarkers developed in Aim 1 to assess the responses of muscle tissue structure, mechanics, function, and blood flow to osteopathic manipulative treatment (OMT) for chronic neck pain. To determine the prognostic performance of the QUI biomarkers developed in Aim 1 in predicting clinical response to OMT treatment, it will demonstrate that abnormal muscle tissue physio-mechanical properties to be directly linked to the pain of the patients. This trial will determine if improvement in abnormal biomarker values leads to improvement in subject's pain and osteopathic assessments. Subjects with chronic neck pain will be examined at intervals with biomarker measurements and osteopathic assessments. Image processing and statistical analysis will be used to determine the performance of the biomarkers in predicting response to treatment. the approach used in this study is supported by preliminary studies, which show how ultrasound biomarkers change following OMT, returning toward more normal muscle tissue mechanics. This clinical trial will validate at least one clinically useful prognostic biomarker for chronic neck pain management, lay the foundation for further clinical research and treatment based on quantitative, reproducible, well-established methods, and lead to a large grant application.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Neck Pain

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Two groups will be used in the study to evaluate Quantitative Ultrasound Imaging (QUI) biomarkers and TART assessments. Healthy participants. Non-invasive quantitative ultrasound (B-mode image, ultrasound elastography), EMG, and osteopathic assessment (TART assessments) will be performed on the upper trapezius muscle in healthy controls one time at the time of the enrollment. Patients with chromic neck pain. Non-invasive quantitative ultrasound (B-mode ultrasound, ultrasound elastography), EMG, osteopathic assessment, and osteopathic manipulative treatment (OMT) of the upper trapezius muscle will be performed on participants with chronic neck pain 3 times. All ultrasound, EMG biomarkers and TART assessments will be collected before and after OMT.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
108 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Healthy participants
Arm Type
Experimental
Arm Description
Non-invasive quantitative ultrasound (B-mode image, ultrasound elastography), EMG, and osteopathic assessment (TART assessments) will be performed on the upper trapezius muscle in healthy participants one time at the time of the enrollment.
Arm Title
Patients with chronic neck pain
Arm Type
Experimental
Arm Description
Non-invasive quantitative ultrasound (B-mode ultrasound, ultrasound elastography), EMG, osteopathic assessment, and osteopathic manipulative treatment (OMT) of the upper trapezius muscle will be performed on participants with chronic neck pain 3 times. All ultrasound, EMG biomarkers and TART assessments will be collected before and after OMT.
Intervention Type
Diagnostic Test
Intervention Name(s)
Quantitative Ultrasound
Other Intervention Name(s)
QUI
Intervention Description
Ultrasound assessment of Trapezius muscle
Intervention Type
Diagnostic Test
Intervention Name(s)
Osteopathic TART Assessment
Other Intervention Name(s)
TART
Intervention Description
Evaluation of the 4 diagnostic criteria: Tissue Texture abnormality Asymmetry Restriction of Motion Tenderness
Intervention Type
Procedure
Intervention Name(s)
Osteopathic Manipulation Treatment
Other Intervention Name(s)
OMT
Intervention Description
Use of manual techniques such as soft tissue stretching, resisted isometric stretches, fascial relaxation and counter strain.
Primary Outcome Measure Information:
Title
Ultrasound diagnostic performance evaluation
Description
Evaluation for healthy participants and for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units), shear wave velocity (m/s), and longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Baseline, pre-intervention
Title
Ultrasound diagnostic performance evaluation
Description
Evaluation for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units), shear wave velocity (m/s), and longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Immediately after the intervention
Secondary Outcome Measure Information:
Title
Ultrasound echo-intensity
Description
Evaluation for healthy participants and for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Baseline, pre-intervention
Title
Ultrasound echo-intensity
Description
Evaluation for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Immediately after the intervention
Title
Ultrasound echo-intensity
Description
Evaluation for patients with chronic neck pain. Changes in muscle B-mode ultrasound echo-intensity (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Follow- up. Up to 18 weeks after procedure.
Title
Ultrasound shear wave velocity
Description
Evaluation for healthy participants and for patients with chronic neck pain. Changes in shear wave velocity (m/s), will be recorded. Measured using ultrasound.
Time Frame
Baseline, pre-intervention
Title
Ultrasound shear wave velocity
Description
Evaluation for patients with chronic neck pain. Changes in shear wave velocity (m/s), will be recorded. Measured using ultrasound.
Time Frame
Immediately after the intervention
Title
Ultrasound shear wave velocity
Description
Evaluation for patients with chronic neck pain. Changes in shear wave velocity (m/s), will be recorded. Measured using ultrasound.
Time Frame
Follow- up. Up to 18 weeks after procedure.
Title
Ultrasound longitudinal strain ratios
Description
Evaluation for healthy participants and for patients with chronic neck pain. Changes in longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Baseline, pre-intervention
Title
Ultrasound longitudinal strain ratios
Description
Evaluation for patients with chronic neck pain. Changes in longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Immediately after the intervention
Title
Ultrasound longitudinal strain ratios
Description
Evaluation for patients with chronic neck pain. Changes in longitudinal strain ratios (arbitrary units) will be recorded. Measured using ultrasound.
Time Frame
Follow- up. Up to 18 weeks after procedure.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Inclusion criteria for the healthy participants include: Age 18 years and older; Healthy. No history of musculoskeletal conditions, such as severe pain, trauma, joint or spine surgery; Able to sign written informed consent, Tolerant to the osteopathic exam, and ultrasound. Inclusion criteria for patients with chronic neck pain include: Age 18 years and older Having chronic neck pain persisting longer than 12 weeks, meeting TART criteria, diagnosed by an osteopathic physician; Able to sign written informed consent; Tolerant to the osteopathic exam, ultrasound, and OMT. Exclusion Criteria: Exclusion criteria for the healthy participants include: Under 18 years of age; Having a medical history of musculoskeletal conditions, joint and/or spine surgery, trauma; Employee of the study investigators; Being unable to competently consent or assent to participation (e.g., mentally disabled, demented, delusional, or a prisoner); Not tolerant to the osteopathic exam, ultrasound. Exclusion criteria for patients with chronic neck pain include: Age < 18 years, Unable or unqualified to sign an informed consent, Unstable and/or late stage diseases, Not tolerant to the osteopathic exam, ultrasound, OMT. There is no specific racial/ethnic background limitation in this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jing Gao, MD
Organizational Affiliation
Rocky Vista University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ultrasound Research Laboratory
City
Ivins
State/Province
Utah
ZIP/Postal Code
84738
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
De-identified data will be available with reasonable request to principal investigator.

Learn more about this trial

Quantitative Ultrasound Biomarkers to Assess Upper Trapezius Muscles in Patients With Chronic Pain

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