CClinicalTrials.gg
Status unknownNCT03941067Updated May 7, 2019

Effects of Pre-event Massage Over the Neuromuscular Response

An interventional study of Pre-event massage in Neuromuscular Diseases, sponsored by Universitat Internacional de Catalunya. Status unknown at 1 site in Spain. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-05-07.

Sponsored by Universitat Internacional de Catalunya · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2019), so the status shown — last known as Enrolling by invitation — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

The study observes the effect of a pre-event massage on the gastrocnemius muscles over the neuromuscular response of the gastrocnemious muscles.

02

Conditions studied

  • Neuromuscular Diseases

Keywords

  • Neuromuscular response
  • pre-competition massage
  • pre-event massage
03

In context

Neuromuscular Diseases

300 studies on the registry are indexed under Neuromuscular Diseases; 87 are open to participants now.

This study's planned enrollment of 30 is close to the median of 32 across 168 interventional studies indexed under Neuromuscular Diseases.

Browse Neuromuscular Diseases studies →

Lead sponsor

Universitat Internacional de Catalunya is the lead sponsor of 144 studies on the registry; 43 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Exclusion Criteria:

  • Muscle injury in the last two months
  • To not understand the study orders
  • Suffer a musculoskeletal disorder that doesn't allow the subject to do the study protocol
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Pre-event massage

    Other: Pre-event massage

  • No intervention
    Control

Interventions

  • OtherPre-event massage

    Five minutes massage, combining superficial and high-frequency techniques of massage applied with the therapist hands

06

What researchers measure

Primary outcomes

  1. Delay time change

    Time between an electric impulse and 10% of the contraction of the muscle that is being excited with an electric impulse, using an electromyography test (miliseconds).

    Time frame: 2 minutes before the intervention, and 8 minutes after the intervention

  2. Contraction time change

    Time between 10% and 90% of the contraction of the muscle that is being excited with an electric impulse, using an electromyography test (miliseconds).

    Time frame: 2 minutes before the intervention, and 8 minutes after the intervention

  3. Sustain time change

    time between 50% of the contraction and 50% of the relaxation of the muscle after being impulsed with an electric impulse, using an electromyography test (miliseconds).

    Time frame: 2 minutes before the intervention, and 8 minutes after the intervention

  4. Relaxation time change

    time between 90% and 50% of the relaxation of the muscle after being impulsed with an electric impulse, using an electromyography test (miliseconds).

    Time frame: 2 minutes before the intervention, and 8 minutes after the intervention

  5. Maximal displacement change

    Maximal displacement of the muscle after being excited with an electric impulse, using an electromyography test (miliseconds).

    Time frame: 2 minutes before the intervention, and 8 minutes after the intervention

Secondary outcomes

  1. Gastrocnemious strength change

    Isometric strength of the gastrocnemious muscles using a handheld dynamometer "microFET 2" (newtons).

    Time frame: 8 minutes before the intervention, and 2 minutes after the intervention

  2. Passive ankle dorsiflexion change

    Passive range of motion of the ankle dorsiflexion, using an inclinometer (degrees).

    Time frame: 6 minutes before the intervention, and 4 minutes after the intervention

  3. Jump height change

    Maximum jump height with one leg using the application "My Jump 2" (centimeters).

    Time frame: 10 minutes before the intervention, and 1 minute after the intervention

  4. Stiffness change

    Resistance to an external force that deforms its initial shape, using a "Myoton".

    Time frame: 5 minute before the intervention, and 5 minute after the intervention

  5. Elasticity change

    Capacity to recover its initial shape after the removal of the external force that lead to its deformation, using a "Myoton".

    Time frame: 5 minute before the intervention, and 5 minute after the intervention

  6. Relaxation change

    Time for a muscle to recover its shape from deformation after the removal of an external force, using a "Myoton" (miliseconds).

    Time frame: 5 minute before the intervention, and 5 minute after the intervention

07

Study locations

1 site
  • Universitat Internacional de Catalunya
    Sant Cugat Del Vallès, Barcelona 08195, Spain
08

References and documents

Publications

  • Perez-Bellmunt A, Labata-Lezaun N, Llurda-Almuzara L, Rodriguez-Sanz J, Gonzalez-Rueda V, Bueno-Gracia E, Celik D, Lopez-de-Celis C. Effects of a Massage Protocol in Tensiomyographic and Myotonometric Proprieties. Int J Environ Res Public Health. 2021 Apr 8;18(8):3891. doi: 10.3390/ijerph18083891. PubMed 33917668 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 7, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03941067
Lead sponsor
Universitat Internacional de Catalunya
Responsible party
Albert Pérez Bellmunt (Principal investigator, Universitat Internacional de Catalunya) — Principal investigator
First posted
May 7, 2019
Start date
May 2, 2019
Primary completion
Jun 7, 2019 (estimated)
Completion
Jun 7, 2019 (estimated)
Last update
May 7, 2019

Study contacts

Albert Pérez-Bellmunt
principal investigator · Universitat Internacional de Catalunya

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2019. You cannot join it, but the record below documents what was studied.

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