Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT06729437

Transcranial Direct Current Stimulation on Functionality and Pain in Individuals with Patellar Tendinopathy

Led by University of Valencia · Updated on 2025-02-28

42

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the present study is to investigate the effectiveness of transcranial direct current stimulation (tDCS) prior to a therapeutic eccentric exercise program on parameters related to pain and functionality in individuals with patellar tendinopathy. For this purpose, participants will be randomly divided into two groups: i) experimental group, receiving tDCS prior to a therapeutic exercise program; and ii) control group, receiving sham tDCS and a therapeutic exercise program. The interventions will last for 8 weeks. Additionally, four assessments will be conducted (baseline, week 4, week 8 and week 12). The variables studied are related to pain, functionality, muscle activity and strength, proprioception, and quality of life.

CONDITIONS

Official Title

Transcranial Direct Current Stimulation on Functionality and Pain in Individuals with Patellar Tendinopathy

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 50 years.
  • Diagnosis of patellar tendinopathy (VISA-P score of 80 or lower).
  • Pain lasting more than 3 months.
Not Eligible

You will not qualify if you...

  • Previous knee surgery.
  • Corticosteroid injection in the previous 6 weeks.
  • Systemic inflammatory, autoimmune, or rheumatic diseases.
  • Cognitive or behavioural issues that hinder comprehension and adherence to the intervention.
  • Any neurological disease.
  • Neoplastic disease.
  • Contraindications for tDCS including personal and family history of epilepsy, metallic implants in the head, implanted medication pump, pacemaker, recurrent headaches, skin conditions (psoriasis, eczema), major head surgeries, pregnancy, heart diseases, and certain medications (psychotropic or antihistamines).
  • Pharmacological treatment or knee physical rehabilitation programs in the past year.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Faculty of Physiotherapy, University of Valencia

Valencia, Valencia, Spain, 46022

Actively Recruiting

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Research Team

M

Marta Inglés, Dr

CONTACT

E

Elena Muñoz-Gómez, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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