Selective Effect of Foam Rolling and Manual Massage (AUTOMASSEEG)

April 21, 2021 updated by: Prof. Aymeric Guillot, Laboratoire Interuniversitaire de Biologie de la Motricité

Effects of Self-myofascial Release and Manual Massage on Psychometric, Behavioural and Neurophysiological Indexes of Performance and Well-being: a Randomized Control Trial

The present double-blinded randomized controlled design aims at comparing the effects of a full-body manual massage and foam rolling intervention. Sixty-five healthy individuals were randomly allocated to foam rolling, manual massage or a control intervention consisting in an autogenic relaxation routine.

Study Overview

Detailed Description

Self-report ratings of perceived anxiety, muscle pain and relaxation were the psychometric outcome variables. Sit-and-reach, toes-touch and mental calculation performances were the behavioral variables. Resting-state alpha and beta power recorded using electroencephalography and galvanic skin resistance measures were the neurophysiological outcome variables.

Study Type

Interventional

Enrollment (Actual)

65

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

      • Villeurbanne, France, 69622
        • University Claude Bernard Lyon 1

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 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Regular practice of foam rolling (10 min routines, 2-3 times per week over the past 6 months)

Exclusion Criteria:

  • Chronic medical conditions including functional limitations that might affect proprioception and/or pain perception

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Foam rolling
The foam rolling routine consisted in unilateral exercises alternatively performed on both legs and bilateral exercises on lower and back muscles. All participants started with the feet in a standing up position with a lacrosse ball. Then, participants performed on the ground the foam rolling exercises with the foam roller targeting leg and back muscles.
Self-report of perceived anxiety and physical sensations (muscle pain, relaxation and warmth)
Sit-and-reach and toe touch tests
Iterated substractions (for 2 minutes)
Alpha and beta oscillation power (4 minutes recordings)
Skin conductance during the resting state period
Experimental: Manual massage
Participants in the manual massage group received manual massage by a professional physiotherapist who was blinded to the purpose of the experiment (20 years of registered practice). Participants were lying in the prone position on a massage table. To facilitate the physiotherapist's maneuvers, massage oil was used. The manual massage protocol reproduced several features of the foam rolling intervention, i.e., order of the areas massaged, massage time per muscles and total duration of the session.
Self-report of perceived anxiety and physical sensations (muscle pain, relaxation and warmth)
Sit-and-reach and toe touch tests
Iterated substractions (for 2 minutes)
Alpha and beta oscillation power (4 minutes recordings)
Skin conductance during the resting state period
Active Comparator: Autogenic relaxation
Participants in the relaxation group listened to a 16 min relaxation audio tape, based on the autogenic training method. Participants were lying on the massage table in supine position, wearing headphones. During this desensitization-relaxation technique, they were guided to visualize bodily perceptions of heaviness and warmth in their arms, thorax and legs. To facilitate concentration, participants were left alone in a dark room.
Self-report of perceived anxiety and physical sensations (muscle pain, relaxation and warmth)
Sit-and-reach and toe touch tests
Iterated substractions (for 2 minutes)
Alpha and beta oscillation power (4 minutes recordings)
Skin conductance during the resting state period

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in range of motion measures from standardized flexibility tests
Time Frame: Pretest and an immediate posttest after the intervention
Lower back and hamstring flexibility index from sit-and-reach and toe touch tests
Pretest and an immediate posttest after the intervention
Resting-state electroencephalography
Time Frame: Pretest and an immediate posttest after the intervention
Power of alpha and beta neural oscillations
Pretest and an immediate posttest after the intervention
Changes in subjective scores (self-reports on numeric rating scales)
Time Frame: Pretest and an immediate posttest after the intervention
Perceived anxiety and physical sensations (muscle pain, warmth and relaxation) on a numeric rating scale of 10 cm (0: "Complete absence of anxiety/muscle pain/muscle warmth/muscle relaxation"; 10: "Maximal possible levels of anxiety/muscle pain/muscle warmth/muscle relaxation")
Pretest and an immediate posttest after the intervention
Changes in mental calculation performances
Time Frame: Pretest and an immediate posttest after the intervention
Iterated substractions for 2 minutes
Pretest and an immediate posttest after the intervention
Changes in physiological arousal
Time Frame: Pretest and an immediate posttest after the intervention
Skin conductance during resting state periods
Pretest and an immediate posttest after the intervention

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)

April 1, 2021

Primary Completion (Actual)

April 1, 2021

Study Completion (Actual)

April 1, 2021

Study Registration Dates

First Submitted

April 16, 2021

First Submitted That Met QC Criteria

April 21, 2021

First Posted (Actual)

April 26, 2021

Study Record Updates

Last Update Posted (Actual)

April 26, 2021

Last Update Submitted That Met QC Criteria

April 21, 2021

Last Verified

April 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • LIBMNEURO - AUTOMASSEEG

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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