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Fasciae (Anatomy)--InflammationNCT03521544

Self-Myofascial Release in the Posterior Myofascial Chain

A study testing Self-myofascial release in people with Fasciae (Anatomy)--Inflammation, run by Universitat Internacional de Catalunya 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 study investigates the relation between different segments of the posterior myofascial chain of the human body. The intervention consists on apply self-myofascial release with a foam roller in one of the segments of the posterior myofascial chain of the participants, and then see if the treatment has produced any… Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Fasciae (Anatomy)--Inflammation
What is being tested?
Self-myofascial release
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteSpain
Study dates
16 Apr 2018to 18 May 2018
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 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

None listed.

Who cannot join

  • Pregnant women
  • Musculoskeletal problems in the last month
  • Surgical interventions in he knee, hip, ankle, back or neck in tha last 6 months
  • Psychological or nervous alterations
  • Uncomprehension of the study protocol

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Universitat Internacional de Catalunya

    Sant Cugat del Vallès, Barcelona, 08195

Other trials in Spain

About this study

Official title: Self-Myofascial Release in the Posterior Myofascial Chain in Healthy Subjects With a Foam Roller

The study investigates the relation between different segments of the posterior myofascial chain of the human body.

The intervention consists on apply self-myofascial release with a foam roller in one of the segments of the posterior myofascial chain of the participants, and then see if the treatment has produced any changes in the hamstrings, gastrocnemius and soleus flexibility.

Read the detailed description

The study investigates the relation between different segments of the posterior myofascial chain of the human body.

The intervention consists on apply self-myofascial release with a foam roller in one of the segments of the posterior myofascial chain, and then see if the treatment has produced any changes in the hamstrings, gastrocnemius and soleus flexibility.

Being tested
Self-myofascial release

What participants receive

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

  • Self-myofascial releaseOther

    Also called Foam rolling

    The subjects roll a foam roller under a determinated part of the body to self-massage that area.

Study groups in NCT03521544
Study groupRoleWhat they receive
Plantar FasciaExperimentalSelf-myofascial release in the plantar fascia.
Receives: Other: Self-myofascial release
Tricep surae fasciaExperimentalSelf-myofascial release in the triceps surae fascia.
Receives: Other: Self-myofascial release
Hamstrings fasciaExperimentalSelf-myofascial release in the hamstrings fascia.
Receives: Other: Self-myofascial release
Spine erectors and lumbar fasciaExperimentalSelf-myofascial release in the spine erectors and lumbar fascia.
Receives: Other: Self-myofascial release
Occipital and suboccipital fasciaExperimentalSelf-myofascial release in the occipital and suboccipital fascia.
Receives: Other: Self-myofascial release
Control groupNo interventionLay on a stretcher.

What is being measured

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

  1. Hamstrings flexibility change

    Measurement of the hamstrings flexibility change through Sit and Reach Test

    Measured: 0 seconds, 30 seconds, 2 minutes, 5 minutes, 10 minutes

Secondary outcomes (2)
  1. Triceps surae flexibility change

    Measurement of the triceps surae flexibility change using the Lunge Test.

    Measured: 0 seconds, 10 minutes

  2. Fatigue

    Fatigue subjective sensation using the Modified Borg Scale

    Measured: 10 minutes

Timeline

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

  1. First posted11 May 2018
  2. Study start16 Apr 2018
  3. Primary completion18 May 2018
  4. Study completion18 May 2018

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
Single blind
Who is masked
Outcomes assessor
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03521544
Sponsor's protocol ID
P1/01
Status last verified
Jun 2018
First submitted
12 Apr 2018
Last updated
20 Jun 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Self-myofascial release in people with Fasciae (Anatomy)--Inflammation, run by Universitat Internacional de Catalunya 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 0 inclusion and 5 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 20 Jun 2018. 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.

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?

Hamstrings flexibility change (time frame: 0 seconds, 30 seconds, 2 minutes, 5 minutes, 10 minutes). 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 20 Jun 2018.

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