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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04258124
Other study ID # CMOTOR
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 24, 2020
Est. completion date December 10, 2020

Study information

Verified date September 2020
Source Investigación en Hemofilia y Fisioterapia
Contact Rubén Cuesta-Barriuso, PhD
Phone +34 913146508
Email ruben.cuestab@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date December 10, 2020
Est. primary completion date November 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 25 Years
Eligibility 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:

- 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Control 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.

Locations

Country Name City State
Spain European University of Madrid Madrid

Sponsors (1)

Lead Sponsor Collaborator
Investigación en Hemofilia y Fisioterapia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. Screening visit, within the first seven days after treatment and after one month follow-up visit
Secondary 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. Screening visit, within the first seven days after treatment and after one month follow-up visit
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