Back to resultsEfficacy of Peripheral Magnetic Stimulation Compare to Dry Needling in Myofascial Pain Syndrome
Primary Purpose
Myofascial Pain Syndrome
Status
Completed
Phase
Not Applicable
Locations
Thailand
Study Type
Interventional
Intervention
Repetitive Peripheral Magnetic Stimulation
Dry needling
Sponsored by
About this trial
This is an interventional treatment trial for Myofascial Pain Syndrome
Eligibility Criteria
Inclusion Criteria:
- Patients with myofascial pain syndrome at unilateral upper trapezius muscle and had pain score (Visual analog scale) at least 4
Exclusion Criteria:
- Patients with signs and/or symptoms of neurological deficit
- Patients with history of cervical hernia, cervical radiculopathy, cervical myelopathy, fibromyalgia, whiplash spondylosis and cervical spinal stenosis.
- Patients who received physical therapy/injection/surgery at neck or pain area in last 6 months.
- Patients with abnormal coagulopathy and/or currently use anticoagulant medicine.
- Patients with cardiac device.
- Patients with history of aneurysm clip procedure, stent-coils procedure or cochlear implant surgery.
- Pregnancy
Sites / Locations
- Physical medicine and rehabilitation
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Repetitive Peripheral Magnetic Stimulation
Dry Needling
Arm Description
Repetitive Peripheral Magnetic Stimulation 1 session
Dry Needling 1 session
Outcomes
Primary Outcome Measures
Change of Visual analog scale
Pain measurement Score from 0-10, 0 means no pain and 10 means maximum pain. Higher scores mean worse outcome.
Secondary Outcome Measures
Neck disability index
Disability secondary to neck pain Score from 0-50, 0 means no disability and 50 means complete disability. Higher scores mean worse outcome.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05320601
Brief Title
Efficacy of Peripheral Magnetic Stimulation Compare to Dry Needling in Myofascial Pain Syndrome
Official Title
Efficacy of Peripheral Magnetic Stimulation Compare to Dry Needling in Patient With Upper Trapezius Myofascial Pain Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
April 11, 2022 (Actual)
Primary Completion Date
May 1, 2022 (Actual)
Study Completion Date
July 1, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mahidol University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
Compare efficiency between repetitive peripheral magnetic stimulation and dry needling in patient with upper trapezius myofascial pain syndrome.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myofascial Pain Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Repetitive Peripheral Magnetic Stimulation
Arm Type
Experimental
Arm Description
Repetitive Peripheral Magnetic Stimulation 1 session
Arm Title
Dry Needling
Arm Type
Experimental
Arm Description
Dry Needling 1 session
Intervention Type
Device
Intervention Name(s)
Repetitive Peripheral Magnetic Stimulation
Intervention Description
Repetitive Peripheral Magnetic Stimulation at trigger point of upper trapezius muscle
Intervention Type
Procedure
Intervention Name(s)
Dry needling
Intervention Description
Dry needling at trigger point of upper trapezius muscle
Primary Outcome Measure Information:
Title
Change of Visual analog scale
Description
Pain measurement Score from 0-10, 0 means no pain and 10 means maximum pain. Higher scores mean worse outcome.
Time Frame
Change from baseline Visual analog scale at immediately after intervention, Change from Baseline visual analog scale at 1 week and Change from baseline Visual analog scale at 4 weeks
Secondary Outcome Measure Information:
Title
Neck disability index
Description
Disability secondary to neck pain Score from 0-50, 0 means no disability and 50 means complete disability. Higher scores mean worse outcome.
Time Frame
Change from baseline Neck disability index at immediately after intervention, Change from Baseline Neck disability index at 1 week and Change from baseline Neck disability index at 4 weeks
Other Pre-specified Outcome Measures:
Title
Pain pressure threshold
Description
The minimum pressure that induces pain in trigger point. Higher scores mean better outcome.
Time Frame
Change from baseline Pain pressure threshold at immediately after intervention, Change from Baseline Pain pressure threshold at 1 week and Change from baseline Pain pressure threshold at 4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with myofascial pain syndrome at unilateral upper trapezius muscle and had pain score (Visual analog scale) at least 4
Exclusion Criteria:
Patients with signs and/or symptoms of neurological deficit
Patients with history of cervical hernia, cervical radiculopathy, cervical myelopathy, fibromyalgia, whiplash spondylosis and cervical spinal stenosis.
Patients who received physical therapy/injection/surgery at neck or pain area in last 6 months.
Patients with abnormal coagulopathy and/or currently use anticoagulant medicine.
Patients with cardiac device.
Patients with history of aneurysm clip procedure, stent-coils procedure or cochlear implant surgery.
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Apiphan Iamchaimongkol, M.D.
Organizational Affiliation
Mahidol University, Ramathibodi Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Physical medicine and rehabilitation
City
Bangkok
Country
Thailand
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
https://pubmed.ncbi.nlm.nih.gov/9665594/
Description
The effect of repetitive magnetic stimulation on localized musculoskeletal pain
Learn more about this trial
Efficacy of Peripheral Magnetic Stimulation Compare to Dry Needling in Myofascial Pain Syndrome
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