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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04325750
Other study ID # UCV2017-2018-40
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2018
Est. completion date August 28, 2020

Study information

Verified date September 2020
Source Fundación Universidad Católica de Valencia San Vicente Mártir
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study develops the effects of Capacitive and Resistive Energy Transfer Therapy (TECAR) on medial gastrocnemius using thermographic cameras, algometry and lunge tests, in a pre-post study with basketball players using a control group to which placebo is applied. (simulated technique) and an intervention group to which the technique is performed. The main objective of the study is to establish whether the TECAR produces physiological and mechanical changes in the subjects that improve muscle recovery.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date August 28, 2020
Est. primary completion date August 28, 2020
Accepts healthy volunteers No
Gender Male
Age group 16 Years to 39 Years
Eligibility Inclusion Criteria:

- Male players

- Semi-professional players who are currently active

- Not have suffered a lower limb injury in the last 6 months before the study

- Not having suffered a rupture of the triceps surae

- Contain a latent trigger point in the medial gastrocnemius

Exclusion Criteria:

- Players suffering from any disease that could alter the study or be contradictory

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
TECAR Therapy
The intervention will be performed with the T-Care TECAR® therapy machine at the latent trigger points of both gastrocnemius. The professional will apply the therapy with the generator that emits radio frequency signals of 0.5 MHz at a variable power with a maximum of 300W. The frequency to be used will be 500MHz with an intensity of 40% and with direct current.
Other:
Placebo
simulated TECAR Therapy (machine off)

Locations

Country Name City State
Spain Universidad Católica de Valencia San Vicente Mártir Valencia

Sponsors (1)

Lead Sponsor Collaborator
Fundación Universidad Católica de Valencia San Vicente Mártir

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity Visual analogue scale (VAS) of pain 30 minutes
Secondary Back flexion LUNGE Test 30 minutes
Secondary Thermographic evaluation Ymiko Wifi Digital Weather Station with FLIR E60 camera and interpreted with FLIR tools software. 30 minutes
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