- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04859140
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
Status
Completed
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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