- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04089228
Kinesio Taping on Trapezius Trigger Points After Integrated Neuromuscular Inhibition Technique (INIT)
September 11, 2019 updated by: Riphah International University
Effects of Kinesio Taping on Upper Trapezius Trigger Points After Integrated Neuromuscular Inhibition Technique (INIT)
The aim of this research is to see the effects of kinesio taping after integrated neuromuscular inhibition technique on pain, disability, pain-pressure threshold and muscle length in patients with upper trapezius trigger points.
There will be two groups experimental and control.
One study group will receive kinesiotaping after integrated neuromuscular inhibition technique and the other group will only receive integrated neuromuscular inhibition technique.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study is Randomized controlled trail done at physiotherapy department of Railway General Hospital Rawalpindi.
The sample size of 26 individuals calculated using open epi tool.
Sampling technique applied was convenience sampling.
Randomization in groups by sealed envelope method.
The subjects were divided into two groups with 13 patients each.
Both groups were treated with Integrated neuromuscular inhibition technique (Muscle energy Technique, sustain pressure, Strain counter-strain) while Kinesio tape was applied after INIT in only experimental group.
Study duration was of 6 months.
Individuals having age between 20-40 years, upper trapezius active or latent trigger points, limited side bending were included in this study.
Tools used in the study were neck disability index (NDI), algometry, numeric pain rating scale (NPRS) and muscle length (side bending through inclinometer).
Assessments were taken on 1st day pre and post intervention and on 4th day.
Study Type
Interventional
Enrollment (Actual)
26
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Federal, Pakistan
-
Islamabad,, Federal, Pakistan, Pakistan, 44000
- Riphah International University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 50 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Upper Trapezius Active or latent trigger points
- Limited range of motion (cervical Side Bending)
Exclusion Criteria:
- Radiculopathies
- Malignancy
- Infection
- Trauma
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Kinesiotape Group and INIT
Kinesiotaping and Integrated Neuromuscular Inhibition Technique (KT + INIT )
|
Total of 4 sessions on upper trapezius trigger points on alternate days.
Sustain Pressure.
Strain Counter-strain (for 90 sec) Passive Isometric Relaxation (PIR) (6-10 sec hold, 4 reps)
|
ACTIVE_COMPARATOR: INIT Group
Integrated Neuromuscular Inhibition Technique (INIT)
|
Sustain Pressure.
Strain Counter-strain (for 90 sec) Passive Isometric Relaxation (PIR) (6-10 sec hold, 4 reps)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Neck disability index
Time Frame: 4th Day
|
Changes from the baseline, The NDI is a modification of the neck disability index and it was developed by Vernon and Mior.
It was designed to measure the neck pain and disability over time.
It consists of 10 items, five parts sections.
At the end, score is calculated by dividing the obtained score by total 50 multiplied by 100.
|
4th Day
|
Pain-Pressure threshold (PPT)
Time Frame: 4th day
|
Changes from the baseline, Pain-pressure threshold was measured with the help of an algometer.
|
4th day
|
NPRS
Time Frame: 4th Day
|
Changes from the baseline, Numeric Pain rating scale is a scale for pain intensity starting from 0-10.
Where 0 indicates no pain and 10 indicate severe pain.
|
4th Day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle length measure
Time Frame: 4th Day
|
Changes from the baseline, Muscle length of upper trapezius was measured with the help of Inclinometer
|
4th Day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Vazquez-Delgado E, Cascos-Romero J, Gay-Escoda C. Myofascial pain syndrome associated with trigger points: a literature review. (I): Epidemiology, clinical treatment and etiopathogeny. Med Oral Patol Oral Cir Bucal. 2009 Oct 1;14(10):e494-8. doi: 10.4317/medoral.14.e494.
- Lluch E, Nijs J, De Kooning M, Van Dyck D, Vanderstraeten R, Struyf F, Roussel NA. Prevalence, Incidence, Localization, and Pathophysiology of Myofascial Trigger Points in Patients With Spinal Pain: A Systematic Literature Review. J Manipulative Physiol Ther. 2015 Oct;38(8):587-600. doi: 10.1016/j.jmpt.2015.08.004. Epub 2015 Sep 19.
- Lavelle ED, Lavelle W, Smith HS. Myofascial trigger points. Anesthesiol Clin. 2007 Dec;25(4):841-51, vii-iii. doi: 10.1016/j.anclin.2007.07.003.
- Alvarez DJ, Rockwell PG. Trigger points: diagnosis and management. Am Fam Physician. 2002 Feb 15;65(4):653-60.
- Shah JP, Gilliams EA. Uncovering the biochemical milieu of myofascial trigger points using in vivo microdialysis: an application of muscle pain concepts to myofascial pain syndrome. J Bodyw Mov Ther. 2008 Oct;12(4):371-384. doi: 10.1016/j.jbmt.2008.06.006. Epub 2008 Aug 13.
- Cerezo-Tellez E, Torres-Lacomba M, Mayoral-Del Moral O, Sanchez-Sanchez B, Dommerholt J, Gutierrez-Ortega C. Prevalence of Myofascial Pain Syndrome in Chronic Non-Specific Neck Pain: A Population-Based Cross-Sectional Descriptive Study. Pain Med. 2016 Dec;17(12):2369-2377. doi: 10.1093/pm/pnw114. Epub 2016 Jun 20.
- Vernon H, Schneider M. Chiropractic management of myofascial trigger points and myofascial pain syndrome: a systematic review of the literature. J Manipulative Physiol Ther. 2009 Jan;32(1):14-24. doi: 10.1016/j.jmpt.2008.06.012.
- Bubnov RV. Evidence-based pain management: is the concept of integrative medicine applicable? EPMA J. 2012 Oct 22;3(1):13. doi: 10.1186/1878-5085-3-13.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
February 1, 2019
Primary Completion (ACTUAL)
June 20, 2019
Study Completion (ACTUAL)
June 30, 2019
Study Registration Dates
First Submitted
September 4, 2019
First Submitted That Met QC Criteria
September 11, 2019
First Posted (ACTUAL)
September 13, 2019
Study Record Updates
Last Update Posted (ACTUAL)
September 13, 2019
Last Update Submitted That Met QC Criteria
September 11, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- RiphahIU Nowal Kamran
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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