Skip to content

Deep Friction Massage Effects: Asymptomatic

Deep Friction Massage Effects on Analgesia of the Asymptomatic Patellar Tendon

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03255525
Acronym
DFM_Asymp
Enrollment
30
Registered
2017-08-21
Start date
2017-07-26
Completion date
2017-08-16
Last updated
2017-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Deep Friction Massage

Brief 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. 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.

Interventions

OTHERDeep friction massage P25

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

OTHERDeep friction massage P75

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

OTHERDeep friction massage P50

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

Sponsors

Cooperativa de Ensino Superior, Politécnico e Universitário
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* the participants should have an asymptomatic patellar tendon

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Time until analgesia10 minutesSelf reported sensation of analgesia, controlled by a chronometer

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026