FAT-VIB: Effects of Running Shoe Sole Hardness on Vibration and Neuromuscular Fatigue During a Half-marathon Run on a Treadmill

Sponsor
Centre Hospitalier Universitaire de Saint Etienne (Other)
Overall Status
Completed
CT.gov ID
NCT06110637
Collaborator
(none)
20
1
2
6.7
3

Study Details

Study Description

Brief Summary

During running, each contact between the foot and the ground causes an impact. Ground reaction forces (GRF) are considered as an input into the musculoskeletal system. It involves a sudden deceleration in the lower limb packages (including muscles) which generates Soft-Tissue Vibrations (STV). The body is able to attenuate Soft-Tissue Vibrations (STV) but this capability decreases with fatigue. STV could be minimize by improving shoe midsole hardness.

Condition or Disease Intervention/Treatment Phase
  • Other: "hard shoes" runners evaluation
  • Other: "Soft shoes" runners evaluation
N/A

Detailed Description

Only 4 studies have studied Soft-Tissue Vibrations (STV) with a distance not exceeding 10 km and without evaluating the potential influence of the shoe. Thus, the effects of shoe midsole hardness on Soft-Tissue Vibrations (STV) and neuromuscular fatigue at the end of an intense and/or long run remains unknown.

The purpose is to compare two shoes whose only midsole hardness differs during a half-marathon on Soft-Tissue Vibrations (STV), neuromuscular fatigue and running kinetics.

Maybe the shoe ensuring a better STV damping of the medial gastrocnemius muscle would reduce neuromuscular fatigue and improve comfort.

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Effects of Running Shoe Sole Hardness on Vibration and Neuromuscular Fatigue During a Half-marathon Run on a Treadmill
Actual Study Start Date :
Jun 15, 2022
Actual Primary Completion Date :
Dec 15, 2022
Actual Study Completion Date :
Jan 6, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Hard shoes runners

Half-marathon runners with hard shoes preceded and followed by assessment of neuromuscular fatigue.

Other: "hard shoes" runners evaluation
The "hard shoes" runners get on the treadmill for 21 km at a speed corresponding to 70 percent (%) of their the maximum aerobic speed (MAV) and are evaluated.

Active Comparator: Soft shoes runners

Half-marathon runners with soft shoes preceded and followed by assessment of neuromuscular fatigue.

Other: "Soft shoes" runners evaluation
The "soft shoes" runners get on the treadmill for 21 km at a speed corresponding to 70 percent (%) of their the maximum aerobic speed (MAV) and are evaluated.

Outcome Measures

Primary Outcome Measures

  1. Change of the damping coefficient (in percent %). [From the beginning to the end of the 21 km race.]

    The main evaluation criterion will be the relative variation (in percent %) of the damping coefficient (in /s) of the medial gastrocnemius muscle measured with an accelerometer, at the beginning (the first five minutes) and at the end (the last five minutes) of 21 km at a speed corresponding to 70% of the maximum aerobic speed (MAS) on a treadmill, carried out by experienced amateurs during two shoe conditions: soft and firm sole.

Secondary Outcome Measures

  1. Temporal evolution of vibrations measurements. [Kilometers : 1st, 3rd, 6th, 9th, 12th, 15th, 18th, 21st]

    The relative variation (in percent %) of the damping coefficient (in /s) of the medial gastrocnemius muscle will be measured with an accelerometer every 3 km at a speed corresponding to 70% of the maximum aerobic speed (MAS) on a treadmill, carried out by confirmed amateurs during the two shoe conditions. For this outcome, it is not possible to use an unit of time, because the time of the measurements are define only by the distance covered by the subject.

  2. Evaluation of improved vibration damping on neuromuscular fatigue : isometric force [From the beginning to the end of the 21 km race.]

    The relative change (in percent %) in the maximum isometric force (in Newton) of the ankle plantar flexors before and after the 21 km

  3. Evaluation of improved vibration damping on neuromuscular fatigue : jerk amplitude. [From the beginning to the end of the 21 km race.]

    The relative change (in percent %) in jerk amplitudes measured by electrically evoked force (in Newton) after isometric contraction of the plantar flexors of the ankle, before and after the 21 km.

  4. Evaluation of improved vibration damping on neuromuscular fatigue : level of voluntary activation. [From the beginning to the end of the 21 km race.]

    The relative change (percent %) in the maximum level of voluntary activation (percent %) measured in isometric mode of the plantar flexors of the ankle before and after the 21 km

  5. Evaluation of improved vibration damping on neuromuscular fatigue : plantar flexors. [From the beginning to the end of the 21 km race.]

    The relative change (in percent %) in the maximum isometric force (in Newton) of the plantar flexors of the toes before and after the 21 km.

  6. Biomechanical parameters measurement : Ground reaction forces [Kilometers : 1st, 3rd, 6th, 9th, 12th, 15th, 18th, 21st.]

    Ground reaction forces (in Newton, measured by treadmill force platforms): passive peak (PP), active peak (PA), 20-80 percent (%) loading rate (LR). For this outcome, it is not possible to use an unit of time, because the time of the measurements are define only by the distance covered by the subject.

  7. Biomechanical parameters measurement : Spatio-temporal parameters [Kilometers : 1st, 3rd, 6th, 9th, 12th, 15th, 18th, 21st.]

    Spatio-temporal parameters: contact time (CT), flight time (TV), duty factor (DF) defined as the ratio between contact time and stride time (contact time + flight time). For this outcome, it is not possible to use an unit of time, because the time of the measurements are define only by the distance covered by the subject.

  8. Temporal evolution of the energy cost measurement [From the beginning to the end of the 21 km race.]

    This will be the relative variation (in percent %) of the energy cost (in J/kg/m), measured continuously thanks to a portable gas exchange measurement system (ergo spirometer Metamax 3B®, Cortex Medical, Leipzig, Germany), at a speed corresponding to 70% of the maximum aerobic speed (MAS) on a treadmill, carried out by experienced amateurs during the two shoe conditions.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Endurance runners doing a long run of at least 20 km once a week.

  • Affiliated or beneficiaries of a social security plan.

  • Have freely given their written consent.

  • Not participating in a competition during the study period.

  • Shoe size 37 to 46

Exclusion Criteria:
  • Any subject who has been injured in the 3 months preceding the protocol

  • Any subject with chronic joint pathologies (e.g., repeated sprains, patellar or ligament problems) or cardiac pathologies.

  • Any subject with chronic or central neurological pathologies

  • Any subject participating at the same time in another medical interventional experiment

  • Any subject who has taken corticosteroids within 3 months (inhalation, infiltration or history of prolonged corticosteroid therapy).

  • Any subject deprived of liberty or under legal protection (guardianship, curatorship, safeguard of justice, family habilitation).

  • Any subject declaring to have taken products prohibited by the World Anti-Doping Agency

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier Universitaire de Saint-Etienne Saint-Étienne France 42055

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Saint Etienne

Investigators

  • Principal Investigator: LEONARD FEASSON, MDPHD, CHU de Saint-Etienne

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Saint Etienne
ClinicalTrials.gov Identifier:
NCT06110637
Other Study ID Numbers:
  • 21CH248
  • 2022-A00219-34
First Posted:
Oct 31, 2023
Last Update Posted:
Oct 31, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre Hospitalier Universitaire de Saint Etienne
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 31, 2023