About this trial
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.
Eligibility criteria
Qualifiers
Age between 18 and 50 years.
Diagnosis of patellar tendinopathy (VISA-P score of 80 or lower).
Pain lasting more than 3 months.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- tDCS + Therapeutic eccentric exercise
- Sham tDCS + Therapeutic eccentric exercise