Deep Friction Massage Effects: Asymptomatic (DFM_Asymp)

August 18, 2017 updated by: Maria Paço, Cooperativa de Ensino Superior, Politécnico e Universitário

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.

Study Overview

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Paredes
      • Gandra, Paredes, Portugal, 4585-116
        • Cooperativa Ensino Superior Politécnico e Universitário

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Deep friction massage P50
In this group it was applied a pressure previously found to be the mean pressure applied by physiotherapists during deep friction massage.
Deep friction massage as described by Dr. James Cyriax, applied with the mean pressure (P50)
Experimental: Deep friction massage P25
In 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.
Deep friction massage as described by Dr. James Cyriax, applied with the percentile 25 of the mean pressure (P25)
Experimental: Deep friction massage P75
In 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.
Deep friction massage as described by Dr. James Cyriax, applied with the percentile 75 of the mean pressure (P75)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time until analgesia
Time Frame: 10 minutes
Self reported sensation of analgesia, controlled by a chronometer
10 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 26, 2017

Primary Completion (Actual)

August 16, 2017

Study Completion (Actual)

August 16, 2017

Study Registration Dates

First Submitted

August 18, 2017

First Submitted That Met QC Criteria

August 18, 2017

First Posted (Actual)

August 21, 2017

Study Record Updates

Last Update Posted (Actual)

August 21, 2017

Last Update Submitted That Met QC Criteria

August 18, 2017

Last Verified

August 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • DFM_1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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