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Treatment of Chronic Back Pain With Focused Vibroacoustic Stimulation

Primary Purpose

Back Pain

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
KKT
sham KKT
Sponsored by
Wilfrid Laurier University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Back Pain

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of chronic low back pain with a disease duration of more than 3 months (further diagnostic results were not required)
  • Aged 18-75.
  • Scored at least 4/10 in pain scale (VAS or Numerical)
  • Written consent

Exclusion Criteria:

  • Acute back pain (< 4 weeks)
  • History of spinal or vertebral surgery
  • History of any vertebral or spinal infection
  • History of significant trauma related to the spine
  • History of IV drug use
  • History of malignancy
  • Congenital deformation of the spine (except mild scoliosis or kyphosis)
  • Pregnancy
  • Previous KKT Treatment
  • Undergoing concurrent treatment Unable to complete all 12 treatment sessions due to travel, distance or transportation issues, etc.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Placebo Comparator

    No Intervention

    Arm Label

    Treatment

    Placebo

    Waitlist period

    Arm Description

    Intervention is applied to the C1 of the spine.

    Intervention is applied in reduced intensity to the trapezius muscle.

    Participants will have a 1 month waitlist period where no intervention takes place.

    Outcomes

    Primary Outcome Measures

    Change from baseline of Visual Analog Scale for Pain
    A scale which measures the intensity of pain. Scored from 0 to 100. 0 means no pain, 100 means maximum pain.
    Change from baseline of Roland Morris Disability Questionnaire
    Measures back pain disability.
    Change in baseline of EuroQol (EQ5D-5L) Questionnaire
    Quality of Life Questionnaire
    Change in Neck Pain Disability Index
    Measures neck pain disability

    Secondary Outcome Measures

    Change in Medication Dosage
    The assessor will ask what medications the participant is taking. They will record the drug and dosage.
    Change in Shoulder and Pelvis tilt
    Measured via calipers
    Change in Leg length
    Change in Cervical range of motion
    Change in Palpatory tenderness of the spine
    The assessor will count and record the number of tender regions along the spine.

    Full Information

    First Posted
    July 3, 2020
    Last Updated
    June 3, 2022
    Sponsor
    Wilfrid Laurier University
    Collaborators
    KKT International
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04468516
    Brief Title
    Treatment of Chronic Back Pain With Focused Vibroacoustic Stimulation
    Official Title
    Treatment of Chronic Back Pain With Focused Vibroacoustic Stimulation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2022 (Anticipated)
    Primary Completion Date
    January 1, 2023 (Anticipated)
    Study Completion Date
    January 1, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Wilfrid Laurier University
    Collaborators
    KKT International

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Chronic back and neck pain is the most common chronic condition worldwide. Unfortunately, the current available treatment options are limited and largely unsuccessful, which is considered as one of the primary drivers for the high cost of back pain management. Systematic reviews show that the results of common treatments including pain medications, surgery, exercise and psychological therapies for back pain demonstrate inconsistent results and moderate improvement. Therefore, non-invasive adjunct therapies can be a useful addition to traditional back pain management. Focused vibroacoustic treatment for back and neck pain is a non-invasive procedure that applies low frequency sound waves to the spine (50Hz-110Hz), and has shown consistent and positive results in early clinical and animal studies. The goal of this project is to test vibroacoustic sound waves delivered to the spine in a double blind randomized controlled trial to demonstrate the efficacy of focused vibroacoustics in treating chronic back pain. Participants with back pain will be recruited and divided into a treatment and placebo group and will undergo treatment at a clinic over a one month period. Outcome measures will be collected before and after the intervention period. Placebo participants will be offered the full treatment without charge after the experiment is over.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Parallel double blind randomized controlled trial
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Masking Description
    There are two groups (treatment and placebo). Participants will not know which group they are in until the end. Masking will be maintained by the following plan: Researcher assigning participants to treatment and control groups: Dr. Abdullah Mosabbir. Researcher(s)/clinician(s) performing pre-treatment/post-treatment assessments: Dr. Aslam Khan, or a Clinician hired by KKT who is NOT doing #3. Researcher(s)/clinician(s) performing treatments or sham procedure: Dr. Peter Dyback, or a Clinician hired by KKT who is NOT doing #2. Researcher who will assemble these data, code it, and do the data analysis: Dr. Abdullah Mosabbir. Researchers who will supervise the design and ethical conduct of the study as well as data analysis: Dr. Heidi Ahonen and Dr. Quincy Almeida. Researchers whose role is conceptual: Dr.Karim Bayanzay, Dr. Lidan You, and Dr. Lee Bartel.
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Treatment
    Arm Type
    Experimental
    Arm Description
    Intervention is applied to the C1 of the spine.
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Intervention is applied in reduced intensity to the trapezius muscle.
    Arm Title
    Waitlist period
    Arm Type
    No Intervention
    Arm Description
    Participants will have a 1 month waitlist period where no intervention takes place.
    Intervention Type
    Device
    Intervention Name(s)
    KKT
    Intervention Description
    Vibroacoustic sound waves applied focally.
    Intervention Type
    Device
    Intervention Name(s)
    sham KKT
    Intervention Description
    sham KKT
    Primary Outcome Measure Information:
    Title
    Change from baseline of Visual Analog Scale for Pain
    Description
    A scale which measures the intensity of pain. Scored from 0 to 100. 0 means no pain, 100 means maximum pain.
    Time Frame
    1 month
    Title
    Change from baseline of Roland Morris Disability Questionnaire
    Description
    Measures back pain disability.
    Time Frame
    1 month
    Title
    Change in baseline of EuroQol (EQ5D-5L) Questionnaire
    Description
    Quality of Life Questionnaire
    Time Frame
    1 month
    Title
    Change in Neck Pain Disability Index
    Description
    Measures neck pain disability
    Time Frame
    1 month
    Secondary Outcome Measure Information:
    Title
    Change in Medication Dosage
    Description
    The assessor will ask what medications the participant is taking. They will record the drug and dosage.
    Time Frame
    1 month
    Title
    Change in Shoulder and Pelvis tilt
    Description
    Measured via calipers
    Time Frame
    1 month
    Title
    Change in Leg length
    Time Frame
    1 month
    Title
    Change in Cervical range of motion
    Time Frame
    1 month
    Title
    Change in Palpatory tenderness of the spine
    Description
    The assessor will count and record the number of tender regions along the spine.
    Time Frame
    1 month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Clinical diagnosis of chronic low back pain with a disease duration of more than 3 months (further diagnostic results were not required) Aged 18-75. Scored at least 4/10 in pain scale (VAS or Numerical) Written consent Exclusion Criteria: Acute back pain (< 4 weeks) History of spinal or vertebral surgery History of any vertebral or spinal infection History of significant trauma related to the spine History of IV drug use History of malignancy Congenital deformation of the spine (except mild scoliosis or kyphosis) Pregnancy Previous KKT Treatment Undergoing concurrent treatment Unable to complete all 12 treatment sessions due to travel, distance or transportation issues, etc.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Abdullah A Mosabbir, PhD
    Phone
    6477875430
    Email
    Abdullah.Mosabbir@kktspinetreatment.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Heidi J Ahonen, PhD
    Phone
    519.884.0710
    Ext
    x2431
    Email
    hahonen@wlu.ca

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    17710007
    Citation
    Desmoulin GT, Yasin NI, Chen DW. Spinal mechanisms of pain control. Clin J Pain. 2007 Sep;23(7):576-85. doi: 10.1097/AJP.0b013e3180e00eb8.
    Results Reference
    background
    PubMed Identifier
    21289569
    Citation
    Desmoulin GT, Hewitt CR, Hunter CJ. Disc strain and resulting positive mRNA expression from application of a noninvasive treatment. Spine (Phila Pa 1976). 2011 Jun 15;36(14):E921-8. doi: 10.1097/BRS.0b013e3181fd78b3.
    Results Reference
    background
    PubMed Identifier
    20386503
    Citation
    Desmoulin GT, Reno CR, Hunter CJ. Free axial vibrations at 0 to 200 Hz positively affect extracellular matrix messenger ribonucleic acid expression in bovine nucleus pulposi. Spine (Phila Pa 1976). 2010 Jul 1;35(15):1437-44. doi: 10.1097/BRS.0b013e3181c2a8ec.
    Results Reference
    background

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    Treatment of Chronic Back Pain With Focused Vibroacoustic Stimulation

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