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Myofascial Trigger PointsEarly Phase 1NCT01275482

Effectiveness of Transverse Friction Massage in Latent Myofascial Trigger Points in Anterior Deltoid Muscle

A Early Phase 1 study testing Transverse friction massage (TFM) in people with Myofascial Trigger Points and Myofascial Pain, run by University of Castilla-La Mancha at 1 site in Spain.

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

The purpose of this study is to determine whether Transverse Friction Massage (TFM) in Latent Myofascial Trigger points (MTrP) is more effective making this technique in two different ways. Read more about this study

Who is it for?
Ages 18 years and older, men onlyHealthy volunteers can take part
Conditions the study is for
Myofascial Trigger Points, Myofascial Pain
What is being tested?
Transverse friction massage (TFM)
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteSpain
Study dates
Jan 2011to Mar 2011
Phase
Early Phase 1
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 18 years and older
  • Men only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Having latent myofascial trigger points in anterior deltoid
  • Visual local twitch response

Who cannot join

  • Having active Myofascial trigger points in anterior deltoid
  • Having suffered injuries or surgery in upper limb.
  • Pain in the first evaluation session.
  • Not obtaining local twitch response

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • UCLM

    Toledo, Toledo, 45071

Other trials in Spain

About this study

Official title: Effectiveness of Transverse Friction Massage Causing or Not Local Twitch Response in Anterior Deltoid Muscle Latent Myofascial Trigger Points

The purpose of this study is to determine whether Transverse Friction Massage (TFM) in Latent Myofascial Trigger points (MTrP) is more effective making this technique in two different ways.

Read the detailed description

The investigators divide in two groups. The investigators apply the TFM in similar way in both, but the investigators cause local twitch response (isolated contraction of muscle fibers containing the latent trigger points)just in one group. So the investigators want to know whether the effectiveness of this technique is due to those local twitch responses, comparing both groups. The investigators asses Strength, range of motion, and overall, pressure pain thresholds to evaluate the pain sensitivity progress.

Being tested
Transverse friction massage (TFM)
Keywords
Latent Myofascial trigger point., Transverse friction massage, Local twitch response, Effectiveness

What participants receive

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

  • Transverse friction massage (TFM)Procedure or surgery

    Also called Cyriax massage

    The TFM was describe of Cyriax as an effective method to treat soft tissues. It is a massage done always in perpendicular direction of damage tissue. During the massage, we can caused isolated contractions from the fiber muscles containing the latent trigger points.

  • Transverse friction massage (TFM)Procedure or surgery

    Also called Cyriax massage

    The TFM was describe of Cyriax as an effective method to treat soft tissues. It is a massage done always in perpendicular direction of damage tissue.

Study groups in NCT01275482
Study groupRoleWhat they receive
isolated contractions causedExperimentalThe investigators do TFM causing isolated contractions in de muscle fibers containing de latent trigger point.
Receives: Procedure: Transverse friction massage (TFM)
No isolated contraction causedActive comparatorThe investigators don´t cause contraction during the TFM
Receives: Procedure: Transverse friction massage (TFM)

What is being measured

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

  1. Change from Baseline in Pressure pain Threshold (PPT)during treatment.

    The PPT is defined as the minimal amount of pressure where a sense of pressure first changes to discomfort or pain in a certain point

    Measured: Pre and post treatment every session and 1 week after last session

Timeline

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

  1. First posted12 Jan 2011 (estimated)
  2. Study startJan 2011
  3. Primary completionMar 2011
  4. Study completionMar 2011

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
Early Phase 1
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01275482
Sponsor's protocol ID
deltoid
Status last verified
Apr 2011
First submitted
10 Jan 2011
Last updated
7 Apr 2011
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study testing Transverse friction massage (TFM) in people with Myofascial Trigger Points and Myofascial Pain, run by University of Castilla-La Mancha at 1 site in Spain.

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 2 inclusion and 4 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 7 Apr 2011. 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 Spain. 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.

What does this phase mean?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

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?

Change from Baseline in Pressure pain Threshold (PPT)during treatment. (time frame: Pre and post treatment every session and 1 week after last session). 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 7 Apr 2011.

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