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
About this trial
This is an interventional treatment trial for Back Pain
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.
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
NCT ID
NCT04468516
First Posted
July 3, 2020
Last Updated
June 3, 2022
Sponsor
Wilfrid Laurier University
Collaborators
KKT International
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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