- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04521127
Dry Needling and Kinesio Taping in the Treatment of Myofascial Pain Syndrome
Comparison of Dry Needling and Kinesio Taping Methods in the Treatment of Myofascial Pain Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Myofascial pain syndrome (MPS) is a common problem with manifesting itself such as trigger points, taut bands, range of motion limitations and pain. One of the most common place for MPS is neck region and trapezius muscle is the common cause of these symptoms and 9 different trigger point location has been identified on trapezius muscle. Myofascial trigger points, characterized by hypersensitive nodules, can be palpated in stretched bands in the affected muscles. In order to eliminate trigger points fascial releasing, dry needling, kinesio taping and other physical therapy applications can be used.
Although there are several studies investigating the effectiveness of Kinesio taping (KT) and Dry needling(DN) methods in MPS, it is controversial which one is superior to others.
The aim of this study is to compare the effects of exercise, KT, and DN methods on pain and disability in the treatment of upper trapezoidal muscle MPS.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Merkez
-
Bolu, Merkez, Turkey, 14100
- Abant Izzet Baysal University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being diagnosis with MPS and having active myofascial trigger points on trapezius muscle
Exclusion Criteria:
- Fibromyalgia
- a history of myofascial trigger point injection
- acute trauma
- inflammatory joint or muscle disease
- infection or malignancy on cervical region
- neurological disorders
- cervical radiculopathy or myelopathy
- inadequate cooperation for the treatment
- a history of neck surgery or spinal degeneration
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Kinesio Taping Group
Kinesio taping will be applied to trapezius muscle
|
Taping will be performed on sitting position with contralateral lateral flexion and flexion of the neck, using muscle technique with I strip and stretching the head at the maximum level in order to benefit from the muscle release effect.
Kinesio tape was applied directly on muscle with 0% stretching.
|
Active Comparator: Dry needling Group
Dry needling will be applied to trigger point on trapezius muscle
|
The trigger point on the taut band will be held with the thumb and forefinger from below and above.
In the needling technique, a 0.25 * 25-mm with nickel handle, disposable sterile steel acupuncture needle will be used.
The needle tip will be inserted perpendicularly into the subcutaneous tissue and inserted into the muscle until the trigger point in the taut band was found.
The same point will be pinned 8-10 times with fast needle movements inside and out.
Then the needle tip will pulled back so that it did not come out of the skin, and the bottom, top and sides of the first entered point were also pinned.
This procedure was applied to all trigger points in the trapeze muscle.
|
No Intervention: Control Group
Control group will not receive any additional intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pressure Pain Threshold (PPT) Measurement
Time Frame: two weeks
|
Pain pressure threshold (PPT).
was assessed with an analogue algometry (Baseline, FEl Inc. White Plains, NY,USA) with 1 cm2 rubber tip was used to measure the pain pressure threshold.
Algometer perpendicularly placed over spinous process of T1 on prone position and pressure progressively increased 1 kg/s until patients verbally reported pain under the tip of algometer or referring pain.
Measurement repeated three times and average score recorded.
|
two weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Visual analog scale
Time Frame: two weeks
|
The patient was asked to mark the severity of his or her pain with active motion on a horizontal line 100 millimeters in length.
The intensity of the pain was calculated by measuring the area in which the individual marked between 0 (no pain) and 10 (the most severe pain I felt in my life).
|
two weeks
|
Neck Disability Index
Time Frame: two weeks
|
Perceived disability of patients was assessed with 10-item item Neck Disability Index (NDI),which a modified from Oswestry Low Back Pain Disability Index to assess with a score range of 0 to 50.
|
two weeks
|
Global Perceived Effect Scale
Time Frame: two weeks
|
Change in the perception of the symptoms after the treatment was measured by a Global Perceived Effect Scale.
Patients were asked to rate change between 1 completely recovered, 4 unchanged, 7 vastly worse on a horizontal likert scale.
|
two weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Mustafa Fatih Yaşar, MD, Bolu Abant Izzet Baylsa University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Physical Med-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Myofascial Pain Syndrome of Neck
-
Universidad Complutense de MadridRecruitingTrigger Point Pain, Myofascial | Myofascial Pain Syndrome of Neck | Myofacial PainSpain
-
Riphah International UniversityCompletedMyofascial Pain Syndrome of NeckPakistan
-
Medical University of SilesiaCompletedMyofascial Trigger Point Pain | Myofascial Pain Syndrome of Neck | Myofascial Trigger Point SyndromePoland
-
Cairo UniversityCompletedMyofascial Pain Syndrome of NeckEgypt
-
Istanbul UniversityCompletedMyofascial Pain Syndrome of NeckTurkey
-
Istanbul Physical Medicine Rehabilitation Training...CompletedMyofascial Pain Syndrome of NeckTurkey
-
Taipei Medical University WanFang HospitalRecruitingMyofascial Pain Syndrome of NeckTaiwan
-
King Faisal Specialist Hospital & Research CenterRecruitingMyofascial Pain Syndrome of NeckSaudi Arabia
-
Ahi Evran University Education and Research HospitalCompletedMyofascial Pain Syndrome of NeckTurkey
-
China Medical University HospitalCompletedChronic Neck Myofascial Pain Syndrome
Clinical Trials on Kinesio Taping
-
Istanbul Medipol University HospitalNot yet recruitingScapular DyskinesisTurkey
-
Cardenal Herrera UniversityCompletedMobility Limitation | Myofascial Trigger Point PainSpain
-
Cardenal Herrera UniversityCompletedMobility Limitation | Myofascial Trigger Point Pain
-
Ataturk Training and Research HospitalUnknown
-
Norwegian School of Sport SciencesCompletedMuscle Weakness | Anterior Knee Pain | Knee SymptomsNorway
-
Universidade Federal de PernambucoCompleted
-
University of JazanCompletedMeniscus TearSaudi Arabia
-
University of ValenciaCompletedInjury of Musculoskeletal SystemSpain
-
Paulista UniversityCompleted
-
Universidad de GranadaCompletedChronic Venous InsufficiencySpain