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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04427553
Other study ID # URJC-UAX-02-2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 12, 2020
Est. completion date December 4, 2020

Study information

Verified date December 2020
Source Universidad Rey Juan Carlos
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Percutaneous Peripheral Nerve Stimulation is a relative new intervention applied by physical therapists. Although it has been hypothesized that this technique could improve pain and function, no studies have investigated changes in physical performance in soccer players. This study will evaluate changes in physical performance after the application of Percutaneous Peripheral Nerve Stimulation in a sample of healthy soccer players.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 4, 2020
Est. primary completion date November 25, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Semiprofessional soccer player - No symptoms or injury in the lower extremity previous 6 months - Training frequency of at least 3 days a week plus soccer game Exclusion Criteria: - fear to needles - presence of pain or any musculoskeletal disease - previous surgery in the lower extremity - underlying medical conditions, e.g., diabetes, hypertension

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Percutaneous Peripheral Nerve Stimulation
Participants assigned to this group will received two sessions (once per week) of ultrasound guided Percutaneous Peripheral Nerve Stimulation targeting the femoral nerve.
Other:
Control Group
No intervention

Locations

Country Name City State
Spain César Fernández-de-las-Peñas Alcorcon Rest Of The World
Spain César Fernández-de-las-Peñas Alcorcón Madrid

Sponsors (1)

Lead Sponsor Collaborator
Universidad Rey Juan Carlos

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Contra-Movement Jump between baseline and follow-up periods The jump will start in an upright position with participants hands in their waists. They will perform a vertical jump after a fast down countermovement. During the knees and hips flexion, the trunk will remain the most upright as possible. The jump is measured using a Chronopump-Boscosystem DIN-A2 contact platform obtaining a jump reliable and valid height in centimeters Baseline and immediately after each session and 1 month after the last treatment session
Secondary Changes in Squat Performance Speed between baseline and follow-up periods The Speed4Lift device will be used. Squats will be performed using a 20kg olympic bar with two 20kg discs in each side. Participants will place the bar over their shoulders in a 90ยบ triple-flexion position. The measurements will be performed during the concentric contraction phase of the squat Baseline and immediately after each session and 1 month after the last treatment session
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