CClinicalTrials.gg
Status unknownNCT04258124Updated Sep 29, 2020

Cervical Motor Control Exercises in Strength and Perception of Effort in Electronic Sports Players

An interventional study of Control motor intervention in Sports Physical Therapy, sponsored by Investigación en Hemofilia y Fisioterapia. Status unknown at 1 site in Spain. Open to male participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-09-29.

Sponsored by Investigación en Hemofilia y Fisioterapia · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2020), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
Male
01

Study summary

Introduction. One of the most common injuries in competitive esports professionals is dorsolumbar and neck pain, due to the effort caused by the maintenance of the site for long periods of time. Cervical motor control exercises recruit the deep musculature by increasing its strength and reducing muscle fatigue.

Aim. Evaluate the effectiveness of motor control exercises in cervical muscle fatigue and strength, in electronic athletes from 18 to 25 years.

Study design. Randomized clinical trial, simple blind. Methods. 30 electronic athletes will be randomly assigned in two groups: experimental (which will perform 3 sessions of 3 motor control exercises) and control (which will not perform any type of intervention). The intervention will last 6 weeks, with 3 weekly sessions of 10 minutes each. The study variables are the muscle strength of the deep cervical muscle (measured by a stabilizer pressure gauge) and the subjective perception of the effort (Borg scale).

Expected results. The aim is an improvement in the muscular strength of deep cervical muscles, together with a decrease in subjective perception of exertion.

02

Conditions studied

  • Sports Physical Therapy

Keywords

  • Physiotherapy
  • Motor Control
  • Cervical
  • Stabilizer
  • Esports
03

In context

Lead sponsor

Investigación en Hemofilia y Fisioterapia is the lead sponsor of 54 studies on the registry; 6 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Electronic sportsmen
  • Male sex
  • From 18 to 25 years
  • That at the time of the study participate in national competitions
  • That they have not suffered a musculoskeletal pathology in the last 4 months.

Exclusion criteria

Exclusion Criteria:

  • Athletes taking anti-inflammatory drugs that may influence the intervention
  • Players who are allergic to nylon (main component of the evaluation device)
  • That they have not signed the informed consent document.
05

Study design

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

Study arms

  • Experimental
    Experimental group

    Each session will last 10 minutes, taking place 3 days a week, over a period of 6 weeks. The intervention will take place at the beginning of the training session. The intervention will be carried out in 3 sessions with 3 exercises of 15 repetitions, and with breaks of 40 seconds between each series and exercise. Exercise 1. In quadruped position, keeping the back flat, making an isometric contraction of the transverse muscle, and raising one arm and one leg contralaterally. Exercise 2. Training of the deep cervical flexor muscles, supine. Players will move their heads slowly towards craniocervical flexion. Exercise 3. In standing position, an ocular-cervical coordination exercise by means of a cranio-cervical flexion, adding a rotation, guided by an eye feedback provided by the physiotherapist by means of a laser projected on a wall.

    Other: Control motor intervention

  • No intervention
    Control group

    Athletes in the control group will be asked to follow their usual warm-up routine.

Interventions

  • OtherControl motor intervention

    The intervention through motor control will consist in the application of the protocol described by Hidalgo-Peréz et al. The objective of the application of the technique is to produce an increase in the strength of the deep cervical musculature. The exercises will be performed with the subject in different positions: supine, quadrupedic and standing position. The physiotherapist will be placed in standing position in front of the subject. The intervention will be carried out in 3 sessions with 3 exercises of 15 repetitions, and with breaks of 40 seconds between each series and exercise.

06

What researchers measure

Primary outcomes

  1. Change from baseline strength of the deep cervical musculature after treatment and at 1 month

    An assessment will be carried out with a pressure gauge (Stabilizer model). It will be used according to the protocol indicated by Hudswell et al. The athlete will be positioned supine. The pressure gauge will be placed on the stretcher in the posterior cervical area, asking the subject for a craniocervical flexion. The unit of measure of this measuring instrument is mmHg. A higher score indicates greater strength.

    Time frame: Screening visit, within the first seven days after treatment and after one month follow-up visit

Secondary outcomes

  1. Change from baseline subjective perception of effort after treatment and at 1 month

    It will be done by administering the Borg scale. With this scale, the perception of effort will be measured. After the intervention, we will ask the athlete to assign a number from 0 to 10 to represent the subjective feeling of the amount of work done. The scoring range is from 0 to 10 points, where a higher score will indicate a greater perception of effort.

    Time frame: Screening visit, within the first seven days after treatment and after one month follow-up visit

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 29, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04258124
Lead sponsor
Investigación en Hemofilia y Fisioterapia
Responsible party
Sponsor
First posted
Feb 6, 2020
Start date
Sep 24, 2020 (estimated)
Primary completion
Nov 20, 2020 (estimated)
Completion
Dec 10, 2020 (estimated)
Last update
Sep 29, 2020

Study contacts

Rubén Cuesta-Barriuso, PhD
Contact
ruben.cuestab@gmail.com
+34 913146508
Rubén Cuesta-Barriuso, PhD
principal investigator · Universidad Europea de Madrid

Oversight

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

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