NCT06300385

Brief Summary

Motocross, a popular sport, involves riding motorized vehicles on rugged tracks with obstacles. It's physically demanding, with high speeds and a risk of accidents. Grip strength is crucial, especially in the arms and forearms, which are prone to injury. Physiotherapy often employs strength exercises, including electromyostimulation. However, there's little research on their effectiveness for motocross athletes. This study aims to compare electromyostimulation combined with strength training versus strength training alone in relieving pain, fatigue, and improving strength in motocross athletes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 3, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 8, 2024

Completed
24 days until next milestone

Study Start

First participant enrolled

April 1, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2024

Completed
Last Updated

July 5, 2024

Status Verified

July 1, 2024

Enrollment Period

2 months

First QC Date

March 3, 2024

Last Update Submit

July 3, 2024

Conditions

Keywords

sportselectromyostimulationexercisepainfatiguestrength

Outcome Measures

Primary Outcomes (4)

  • Visual analog scale

    Pain assessment: Pain scores of patients will be recorded using 0-100 mm Visual Analog Scale (VAS) to grade pain. For VAS; A measured horizontal line will be created, and definitions such as 'no symptoms' and 'severe symptoms' will be written at both ends. The participant will be instructed to mark a point on the line appropriate to the severity of the symptom. Wrist pain values in the resting position will be recorded before and after the 6-week program.

    6 week

  • Strength measurement

    Lafayette Dynamometer: Lafayette Manual Muscle Testing device will be used to evaluate muscle strength. While the measurements are being made, the device will be kept stationary and the resistance given by the participant will be measured in Newtons. Measurements will be made in the sitting position for wrist flexion/extension and forearm flexion, and total muscle strength will be recorded.

    6 week

  • Fatigue assessment

    Fatigue Severity Scale: The fatigue level of the participants will be evaluated with the Fatigue Severity Scale. It is a survey with 9 questions and 8-point Likert form.A high score means a high level of fatigue.

    6 week

  • Grip strength assessment

    Jamar Hand Grip Dynamometer will be used to evaluate hand grip and finger flexor muscle strength. The participant will sit upright during the assessment. Elbow and knee angle will be 90 degrees. A full force grip will be required with the wrist in the neural position. The measurement will be performed 3 times with an interval of 10 seconds. Increasing values will indicate higher strength. Measurement results will be recorded in kilograms and pounds.

    6 week

Study Arms (2)

Experimental

EXPERIMENTAL

These participants will receive electromyostimulation simultaneously with strengthening exercise.

Device: ElectromyostimulationOther: Strengthening exercises

Sham control

SHAM COMPARATOR

These participants will receive sham electromyostimulation (current turned off) simultaneously with strengthening exercise.

Other: Strengthening exercises

Interventions

Electromyostimulation (EMS), a low-frequency current, will be used for electrical stimulation of the wrist flexor muscle group. Stimulation frequency will be applied as 25 Hertz. Care will be taken to ensure that the current intensity does not cause pain in the patient. The size of the EMS electrodes is 2 cm2 and they will be placed in the form of 4 electrodes on the wrist flexor muscles (inner wrist area) with a distance of 1 cm between them. Each strengthening session will be 15 minutes for 6 weeks, 3 days a week, for a total of 18 sessions. EMS application will be carried out together with strengthening exercises. Laica MD6078 branded device belonging to the researchers will be used.

Experimental

All participants will do resistance exercises for strengthening, 3 sessions per week for 6 weeks. Each movement will be performed in 3 sets and 12 repetitions according to the planned intensity. Wrist curl, reverse wrist curl movements (with 10kg dumbbells) and power web flex grip movements will be applied simultaneously with EMS application. The program will last 15 minutes in total.

ExperimentalSham control

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Having at least 5 years of professional motocross training experience
  • Being between 18 and 30 years old
  • Volunteering to participate in the study

You may not qualify if:

  • To be absent from the 6-week EMS and strengthening program for more than 2 consecutive sessions
  • Having suffered any injury that prevents you from training in the last 6 months
  • Being receiving a physiotherapy program other than the protocol to be used in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul Bilgi University

Istanbul, 34440, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Athletic InjuriesMotor ActivityPainFatigue

Condition Hierarchy (Ancestors)

Wounds and InjuriesBehaviorNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Hulya Sisli, PhD

    Istanbul Bilgi University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: 2 parallel groups randomized controlled study
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 3, 2024

First Posted

March 8, 2024

Study Start

April 1, 2024

Primary Completion

June 1, 2024

Study Completion

July 1, 2024

Last Updated

July 5, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will not share

Locations