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Myofascial Pain SyndromeNCT02029391

Kinesio Taping in Subjects With Myofascial Pain Syndrome: a Randomized Controlled Trial

A study testing Manual pressure release and Kinesio tape in people with Myofascial Pain Syndrome, run by National Taiwan University Hospital at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Musculoskeletal dysfunction is considered as a major public health problem affecting about one third of the adult population. Myofascial pain syndrome (MPS) characterized by myofacial trigger points as well as fascia tenderness are thought to be the main cause of musculoskeletal dysfunction. Read more about this study

Who is it for?
Ages 20 to 60 years
Conditions the study is for
Myofascial Pain Syndrome
What is being tested?
Manual pressure release and Kinesio tape
Could I receive a placebo?
No, everyone receives an active treatment
How many people
31 participants
Where
1 siteTaiwan
Study dates
Oct 2013to Dec 2013
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • age between 20 and 60 years
  • shoulder or neck pain corresponding with the area covered by the upper trapezius muscle
  • Trigger point (taut band) in the upper trapezius muscle

Who cannot join

  • diagnosis of fibromyalgia syndrome
  • having undergone myofascial therapy within the past month before the study
  • history of cervical spine or shoulder surgery
  • previous history of a whiplash injury;
  • diagnosis of cervical radiculopathy or myelopathy;
  • taking medicine that might change the pain intensity or pain threshold, such as analgesics, sedatives, substance abuse (including alcohol, narcotics);
  • a cognitive impairment that would prevent them from being able to understand and/or participate fully in the intervention or the measures.

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Institute of Physical Therapy, National Taiwan University

    Taipei, Taiwan, 100

Other trials in Taiwan

About this study

Official title: Kinesio Taping on Short Term Changes in Subjects With Myofascial Pain Syndrome: a Randomized Controlled Trial

Musculoskeletal dysfunction is considered as a major public health problem affecting about one third of the adult population. Myofascial pain syndrome (MPS) characterized by myofacial trigger points as well as fascia tenderness are thought to be the main cause of musculoskeletal dysfunction. The aim of the treatment for musculoskeletal dysfunction is to reduce pain and restore normal function. Clinically, some evidence supports the application of kinesio tape in these patients. The underlying mechanism, however, is not clear. The investigators goal was to validate proposed mechanism of kinesio tape in these patients. The primary outcome are muscle stiffness, pain intensity and sensitivity.

Being tested
Manual pressure release, Kinesio tape
Keywords
Myofascial pain syndrome, taping, manual therapies
Medical subject headings
Myofascial Pain Syndromes

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Manual pressure releaseOther

    Therapist applied non-painful pressure with slowly increase over the myofascial trigger point until he felts a tissue resistance barrier.

  • Kinesio tapeOther

    Kinesio tape was adhered from insertion to origin of the upper trapezius muscle

Study groups in NCT02029391
Study groupRoleWhat they receive
Myofascial pain syndrome patientsActive comparatorManual pressure release only
Receives: Other: Manual pressure release
Myofascial pain syndromeExperimentalOne session of manual pressure release and kinesio tape
Receives: Other: Manual pressure release; Other: Kinesio tape

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Muscle stiffness

    Measured: baseline, immediate after intervention and at week 1

Secondary outcomes (2)
  1. Visual analog scale (VAS)

    Measured: baseline, immediate after intervention and at week 1

  2. Pressure pain threshold

    Measured: baseline, immediate after intervention and at week 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Jan 2014 (estimated)
  2. Study startOct 2013
  3. Primary completionNov 2013
  4. Study completionDec 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
31 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02029391
Sponsor's protocol ID
201304048RINB
Status last verified
Jan 2014
First submitted
6 Jan 2014
Last updated
9 Jan 2014
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Manual pressure release and Kinesio tape in people with Myofascial Pain Syndrome, run by National Taiwan University Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Jan 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Muscle stiffness (time frame: baseline, immediate after intervention and at week 1). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2014.

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