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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04859140
Other study ID # LIBMNEURO - AUTOMASSEEG
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date April 1, 2021

Study information

Verified date April 2021
Source Laboratoire Interuniversitaire de Biologie de la Motricité
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date April 1, 2021
Est. primary completion date April 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Psychometric ratings (Likert-scale)
Self-report of perceived anxiety and physical sensations (muscle pain, relaxation and warmth)
Behavioral:
Range of motion measures
Sit-and-reach and toe touch tests
Mental calculation task
Iterated substractions (for 2 minutes)
Device:
Resting-state electroencephalography
Alpha and beta oscillation power (4 minutes recordings)
Resting-state galvanic skin resistance measures
Skin conductance during the resting state period

Locations

Country Name City State
France University Claude Bernard Lyon 1 Villeurbanne

Sponsors (1)

Lead Sponsor Collaborator
Laboratoire Interuniversitaire de Biologie de la Motricité

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in range of motion measures from standardized flexibility tests Lower back and hamstring flexibility index from sit-and-reach and toe touch tests Pretest and an immediate posttest after the intervention
Primary Resting-state electroencephalography Power of alpha and beta neural oscillations Pretest and an immediate posttest after the intervention
Primary Changes in subjective scores (self-reports on numeric rating scales) 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
Primary Changes in mental calculation performances Iterated substractions for 2 minutes Pretest and an immediate posttest after the intervention
Primary Changes in physiological arousal Skin conductance during resting state periods Pretest and an immediate posttest after the intervention
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