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Deep Friction MassageDFM_AsympNCT03255525

Deep Friction Massage Effects: Asymptomatic

A study testing Deep friction massage P50, Deep friction massage P25 and Deep friction massage P75 in people with Deep Friction Massage, run by Cooperativa de Ensino Superior, Politécnico e Universitário at 1 site in Portugal.

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

Despite DFM being a widely-used technique and the empirical grounding regarding the importance of the pressure applied, there is no study characterizing the pressure applied during DFM, remaining it a discretion of the physiotherapist. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Deep Friction Massage
What is being tested?
Deep friction massage P50, Deep friction massage P25 and Deep friction massage P75
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 sitePortugal
Study dates
26 Jul 2017to 16 Aug 2017
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 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • the participants should have an asymptomatic patellar tendon

Who cannot join

  • history of previous injury of the lower limbs;
  • intake of medication that could interfere with pain mechanisms;
  • presence of any factors or conditions that could interfere with the tendinous tissue as well as with the awareness and sensibility to pain.

Trial locations and contacts

1 site in 1 country.

Portugal1 site
  • Cooperativa Ensino Superior Politécnico e Universitário

    Gandra, Paredes, 4585-116

Other trials in Portugal

About this study

Official title: Deep Friction Massage Effects on Analgesia of the Asymptomatic Patellar Tendon

Despite DFM being a widely-used technique and the empirical grounding regarding the importance of the pressure applied, there is no study characterizing the pressure applied during DFM, remaining it a discretion of the physiotherapist. Additionally, it is not known how the amount of pressure applied may influence pain mechanisms and, consequently how it affects the time needed promote an analgesic response.

Having this, our general objective is to establish a dose-response relationship between the pressure applied during DFM and time of onset of analgesia, in the asymptomatic patellar tendon.

Being tested
Deep friction massage P50, Deep friction massage P25, Deep friction massage P75

What participants receive

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

  • Deep friction massage P50Other

    Deep friction massage as described by Dr. James Cyriax, applied with the mean pressure (P50)

  • Deep friction massage P25Other

    Deep friction massage as described by Dr. James Cyriax, applied with the percentile 25 of the mean pressure (P25)

  • Deep friction massage P75Other

    Deep friction massage as described by Dr. James Cyriax, applied with the percentile 75 of the mean pressure (P75)

Study groups in NCT03255525
Study groupRoleWhat they receive
Deep friction massage P50Active comparatorIn this group it was applied a pressure previously found to be the mean pressure applied by physiotherapists during deep friction massage.
Receives: Other: Deep friction massage P50
Deep friction massage P25ExperimentalIn this group it was applied the percentile 25, of the pressure previously found to be the mean pressure applied by physiotherapists during deep friction massage.
Receives: Other: Deep friction massage P25
Deep friction massage P75ExperimentalIn this group it was applied the percentile 75, of the pressure previously found to be the mean pressure applied by physiotherapists during deep friction massage.
Receives: Other: Deep friction massage P75

What is being measured

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

  1. Time until analgesia

    Self reported sensation of analgesia, controlled by a chronometer

    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 posted21 Aug 2017
  2. Study start26 Jul 2017
  3. Primary completion16 Aug 2017
  4. Study completion16 Aug 2017

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
Crossover
Masking
Single blind
Who is masked
Participant
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03255525
Sponsor's protocol ID
DFM_1
Acronym
DFM_Asymp
Status last verified
Aug 2017
First submitted
18 Aug 2017
Last updated
21 Aug 2017
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Deep friction massage P50, Deep friction massage P25 and Deep friction massage P75 in people with Deep Friction Massage, run by Cooperativa de Ensino Superior, Politécnico e Universitário at 1 site in Portugal.

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 1 inclusion and 3 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 21 Aug 2017. 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 Portugal. 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?

Time until analgesia (time frame: 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 21 Aug 2017.

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