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Ultrasound Achilles Tendon Assessment

U

University of Granada (UGR)

Status

Not yet enrolling

Conditions

Achilles Tendon
Ultrasonography

Treatments

Device: Monopolar 448 kilohertz radiofrequency stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT05498987
MCuevasCervera

Details and patient eligibility

About

448kilohertz capacitive resistive monopolar radiofrequency is a novel technique in physiotherapy and its usefulness and clinical relevance is still to be investigated at both clinical practice and also in performance. Current studies show promising results in different musculoskeletal disorders, however there no studies in the assessment of quality soft tissue in sporty population after the used of this technique.

Full description

Achilles Tendon pain is is one of the most common musculoskeletal disorders, presenting a high prevalence in primary care centers and sport populations. Many factors have been proposed as the cause of pain, however there are no studies analysing possibilities of preventing Achilles Tendon injuries by using a radiofrequency stimulus.

The use of 448kilohertz capacitive resistive monopolar radiofrequency as the focus of the treatment looking for improve the quality of the tissue is still to be explored.

The hypothesis of the present project is that focus treatments on 448kilohertz capacitive resistive monopolar radiofrequency on the Achilles Tendon will produce better outcomes in terms of ultrasound assessment measured by quantified elastography, and this will decreased the possibilities of get injured.

The stimulus will be carried out on the Achilles Tendon region. All interventions will be developed by the same examiner, who is a physiotherapist with 6 years of clinical experience.

Enrollment

28 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18-50 years
  • Sporty people with at least 3 days of training per week and presenting an upper limb dominance.

Exclusion criteria

  • Suffer from any painful Achilles Tendon condition.
  • History of significant Achilles Tendon trauma, such as fracture or ultrasonography Clinically suspected partial thickness cuff tear, following the classification of Wiener and Seitz.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

28 participants in 1 patient group

448 kilohertz Capacitive Resistive Monopolar Radiofrequency stimulus on the dominant Achilles Tendon
Experimental group
Description:
448 kilohertz Capacitive Resistive Monopolar Radiofrequency stimulus on the dominant Achilles Tendon
Treatment:
Device: Monopolar 448 kilohertz radiofrequency stimulation

Trial contacts and locations

1

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Central trial contact

Maria Cuevas Cervera; Santiago Navarro Ledesma, phd

Data sourced from clinicaltrials.gov

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